Escalate protein plates from legumes for sustainable human nutrition (2024)

As a library, NLM provides access to scientific literature. Inclusion in an NLM database does not imply endorsem*nt of, or agreement with, the contents by NLM or the National Institutes of Health.
Learn more: PMC Disclaimer | PMC Copyright Notice

Escalate protein plates from legumes for sustainable human nutrition (1)

Link to Publisher's site

Front Nutr. 2022; 9: 977986.

Published online 2022 Nov 4. doi:10.3389/fnut.2022.977986

PMCID: PMC9672682

PMID: 36407518

Author information Article notes Copyright and License information PMC Disclaimer

Abstract

Protein is one of the most important, foremost, and versatile nutrients in food. The quantity and quality of protein are determinants of its nutritional values. Therefore, adequate consumption of high-quality protein is essential for optimal growth, development, and health of humans. Based on short-term nitrogen balance studies, the Recommended Dietary Allowance of protein for the healthy adult with minimal physical activity is 0.8 g protein/kg body weight (BW) per day. Proteins are present in good quantities in not only animals but also in plants, especially in legumes. With the growing demand for protein, interest in plant proteins is also rising due to their comparative low cost as well as the increase in consumers’ demand originating from health and environmental concerns. Legumes are nutrient-dense foods, comprising components identified as “antinutritional factors” that can reduce the bioavailability of macro and micronutrients. Other than nutritive value, the physiochemical and behavioral properties of proteins during processing plays a significant role in determining the end quality of food. The term “complete protein” refers to when all nine essential amino acids are present in the correct proportion in our bodies. To have a balanced diet, the right percentage of protein is required for our body. The consumption of these high protein-containing foods will lead to protein sustainability and eradicate malnutrition. Here, we shed light on major opportunities to strengthen the contribution of diversity in legume crops products to sustainable diets. This review will boost awareness and knowledge on underutilized proteinous foods into national nutritional security programs.

Keywords: amino acid, balanced diet, legumes, nutrition security, physico chemical properties, plant protein

Introduction

The world’s population is expected to reach 10 billion people by 2050. Already, one-third of the current population is affected by malnutrition and undernutrition, which are mostly caused by a lack of healthy foods and a shift in lifestyle (1). There is a need for research into healthy and diversified crops that can grow in harsh or substandard conditions (2, 3). Only three crops provide half of the world’s calories (wheat, rice, and corn), however these grains are low in protein and several minerals (4). Legumes supplement cereals in the diet; they provide significant protein, necessary amino acids and minerals, and can be used in place of meat when it is unavailable or pricey. The Leguminosae belongs to the Fabaceae family (beans or legumes) and is the third biggest and most economically important flowering plant family, with 650 genera and almost 20,000 species of herbs, shrubs, trees, and climbers (5). The legume subfamily includes the Papilionoideae, Caesalpinoideae, Mimosoideae, and Swartzioideae. As an essential component of the human diet, people have been growing legumes as crops for millennia. Alfalfa, clover, lupines, green beans and peas, peanuts, soybeans, dry beans, broad beans, dry peas, chickpeas, mung beans, lentils, and moth beans are all important parts of the human diet, especially in underdeveloped nations (6). Therefore, it is important to add these nutritional diets to people’s daily routine.

Legumes are pod/fruit containing dry grains and have the tendency of nitrogen fixation because the roots of leguminous plants contain rhizobium bacteria which take the nitrates and convert them into nitrogen. This helps to make protein-rich food and, therefore, leguminous plants are considered as a source of protein (7). Since human civilization developed, pulses and cereals were linked, and proteins in both pulses and cereals were able to meet the essential amino-acid requirements of humans and animals (8). Legumes provide approximately one-third dietary protein nitrogen for (9) and average legume consumption is 21 g/person/day, worldwide (10). Pulses belong to the Legume family and, hence, every pulse is a legume, but this is not true vice versa; for example, dry beans, dry peas, chickpeas, lentils, etc. are pulses while legumes are peanuts, soybeans, fresh peas, etc. (11). Pulses have been consumed for many years as part of traditional diets around the world. Approximately 1,000 legumes have been identified but only 20 of them are widely cultivated. These legumes are all grown extensively across Asia and the Pacific. Protein-rich legumes are also cholesterol-free, high in dietary fiber, and low in saturated fat. Legume seeds crude protein ranges from 15.5 to 42% (Table 1). India accounts for 26% of global yield and is the largest producer as well as consumer of pulses (12, 13). The degree of inclusion vs. avoidance of animal-based foods varies widely among human dietary habits around the world (14, 15). The argument that specific amino acids are “missing” from certain plant meals are patently untrue. All 20 amino acids, including the nine essential amino acids, are found in plant diets (16).

TABLE 1

Protein content, PD, PER, CS, BV, NPU, micronutrients and amino acids information of cultivated legumes.

Sr. No.NameScientific nameProtein content (g/100 g)PD (%)PERCSBV (%)NPU (%)Micronutrients valueAmino acidsReferences
1.Field peaPisum sativum L.26802.4NA7560Zinc-34 mg, Copper-6.3 mg, Manganese-15.6 mg, Iron-58.1 mg, Nickel-3.4mgRich in all essential amino acids except methionine, lysine, and threonine(24, 158, 159)
2.SoybeansGlycine max13801.7NA7461.5Iron-3.21 mg, Molybdenum-0.11 mg, Copper-0.23 mg, Phosphorous-19 mg, Sodium-2.35 mgRich in all essential amino acids(31, 32, 85, 160)
3.Mung beanVigna radiata L.2370.24.2976.26456.3Iron-4.4 mg, Magnesium-166 mg, Sodium-13.2 mg, Calcium-114 mg Zinc-2.1 mg, Potassium-414 mgRich in leucine, phenylalanine, valine, lysine, and histidine(37, 40, 95, 161)
4.CowpeaVigna unguiculata2455.492.6550.88NANAZinc-1.29 mg, Iron-2.51 mg, Potassium-278 mg, Calcium-24 mg, Magnesium-53 mg, Sodium-4 mg, Phosphorous-156 mgRich in leucine, lysine and phenylalanine; limited in methionine and cysteine(50, 53, 162, 163)
5.Common beanPhaseolus vulgaris2467⋅472.9539.07NANAPotassium-355 mg, Phosphorous-40 mg, Zinc-1.12 mg, Iron-2.1 mg, Magnesium-70 mg, Copper-0.209 mgHigher in methionine compared to most legumes except soybean(58, 164)
6.Pigeon peaCajanus cajan L.2259.21.876568.540.6Sodium–32.5 mg, Magnesium–138.8 mg, Iron—51.5 mg, Calcium–581 mgLimited in isoleucine, lysine, methionine, and tryptophan(67, 68, 165, 166)
7.ChickpeaCicer arietinum L.2183.82.32NA67.5158.63Calcium- 49 mg, Magnesium-48 mg, Potassium-291 mg, Phosphorus-168 mg, Iron-2.89 mg, Zinc-1.53 mg, manganese-1.03 mgLimited in tryptophan, methionine, and cysteine(75, 167)

*PD, Protein Digestibility; PER, Protein efficiency ratio; CS, Protein chemical score; BV, Biological value; NPU, net protein utilization; NA, Not available.

Legumes contribute to agriculture and the environment in addition to being a key source of food and nourishment for the population. Their nitrogen-fixing ability, for example, can improve soil fertility and assist in avoiding soil erosion as a crop cover. Some legumes are supposed to prevent or treat hypertension, diabetes, and cancer; therefore, they have medical benefits as well (17). As a result, their effects on essential dietary components such as amino acids, lipids, carbs, vitamins, and minerals are given specific attention. Furthermore, in recent years, more individuals have substituted vegetable protein for animal protein, increasing demand for legumes, which are the primary source of plant proteins. To meet this demand, researchers must focus on nutritional profiling of various legumes, increase the use of underutilized legumes, develop low-cost, innovative value-added legume products, educate consumers about the nutritional value of legumes, and find new ways to encourage the use of existing legumes (10). The current review paper also focuses on the proven and potential health advantages connected with legume consumption.

Important legume food crops with nutritional composition and their applications

Legumes have been grown in both the “Old and New Worlds” for thousands of years. It’s probable that their long history as food crops is due to their easy-to-harvest seeds, which have a low water content and can be stored for long periods of time when dry. These characteristics, together with their high protein content and simplicity of cultivation, make legumes attractive crops (Figure 1) (6). Legumes have a range of bioactivities, ultimately leading to various health-promoting benefits (Figure 2).

Escalate protein plates from legumes for sustainable human nutrition (5)

Depicting multi-uses of legume crops.

Escalate protein plates from legumes for sustainable human nutrition (6)

Different bioactivities of the legumes. A summary of the legume plant (pigeonpea): A multifunctional crop containing roots, seeds, and leaves that can be used in a variety of ways.

Pea (Pisum sativum)

The pea is the only species in the Leguminosae family, under the genus Pisum. Pea is one of the world’s most important legumes, with global annual production estimated at roughly 13.5 million metric tons and a producer price of over 200 USD/ton, and at present it is grown in over 90 countries (18). In peas, protein content largely varies based on genetic and environmental factors (Table 1). Peas also contain high quantities of lysine, which might help to compensate for lysine shortage in cereal-based diets (19). The nutritional values are defined by amino acid content. Peas have a good content of valine, arginine, and methionine, although a poor content of cysteine and glutamic acid. In raw pea, the protease inhibitors present are responsible for decreasing in vitro digestion (20). Because of their high carbohydrate, protein, and other nutrient content, peas have long been an important part of the human diet. The content and characteristics of starch, protein, fiber, vitamins, minerals, and phytochemicals in peas are primarily responsible for their health advantages (21). Fiber from the seed coat and cotyledon cell walls improves gastrointestinal function. Pea starch decreases the glycemic index and lowers starch digestibility due to its intermediate amylose level (22). Peas include several phytochemicals that were previously thought to be antinutritive. Polyphenolics, found in colored seed coat types, have antioxidant and anticarcinogenic properties, as well as saponins, which have hypocholesterolemia and anticarcinogenic properties, and galactose oligosaccharides, which have beneficial prebiotic effects in the large intestine (23, 24). Other than protein, peas also contain minerals like zinc (27.4–34 mg kg–1), copper (5.2–6.3 mg kg–1), manganese (9.0–15.6 mg kg–1), nickel (2.3–3.4 mg kg–1), and iron (47.7–58.1 mg kg–1), while potassium and magnesium are somewhat lower (25). Peas are a good source of vitamin C, E, and other antioxidants; these help to improve the immune system, reduce inflammation, and lower the risk of chronic condition like diabetes, heart disease, and arthritis (26).

Soyabean (Glycine max)

The soybean (Glycine max) is one of the world’s most important crops. It is known as the “world’s miracle crop” because of its nutrient-dense content, which makes it ideal for animal feed and human diets. In addition to serving as an oil seed crop and cattle feed, the crop is a good source of protein for human diets and as a biofuel feedstock (27). Soybean is a type of oil seed that contains a variety of nutrients such as protein, carbohydrates, vitamins, and minerals. Soybeans are composed of 36% protein, 19% oil, 35% carbohydrate (17% dietary fiber), 5% minerals, and a variety of other nutrients, including vitamins (28). Mineral content in soybean is in the higher range (0.2–2.1%) for chloride, sodium, potassium, calcium, and phosphorus, while in the lower range (0.01–140 ppm) for chromium, magnesium, copper, iron, arsenic, silicon, cobalt, lead, sulfur, and zinc (29). Soybean contains all essential amino acids required for the balanced functioning of the human body like lysine, isoleucine, leucine, phenylalanine, tyrosine, threonine, methionine, cysteine, tryptophan, histidine, and valine (Table 1). It is a good crop for preventing protein deficiency and serving as a bridge for vitamin “A” absorption (30). Soybeans have many health benefits: it keeps you full for a long time, lowers cholesterol level, boosts digestive health, effects on insulin secretion and energy metabolism, reduces the risk of breast cancer, and is compatible with many specialized diets (3133).

Mung bean (Vigna radiata)

Mung bean (Vigna radiata L.) is a popular pulse eaten around the world, particularly in Asian countries, and has a long history of use in traditional medicine. It has long been recognized as a high-quality source of protein, dietary fiber, minerals, vitamins, and considerable levels of bioactive substances such as polyphenols, polysaccharides, and peptides, making it a preferred functional food for maintaining good health (34). The essential amino acids like leucine (1.847%), phenylalanine (1.443%), valine (1.237%), tryptophan (0.26%), isoleucine (1.008%), arginine (1.672%), lysine (1.664%), methionine (0.286%), threonine (0.782%), and histidine (0.695%) are highly present in mung bean (35, 36). The proteins present in mung bean (60%) have higher in vitro digestibility compared to soybean protein (65%) (37). Apart from protein content, mung bean also serves as a good source of minerals that are found in different ranges like magnesium (129–166 mg/100 g), sodium (8.7–13.2 mg/100 g), iron (3.4–4.4 mg/100 g), calcium (81–114 mg/100 g), zinc (1.2–2.1 mg/100 g), and potassium (363–414 mg/100 g) (29). Our body requires mineral for various crucial functions, including enzyme reactions, protein synthesis, glucose control, and muscle and nerve function (15, 38). The polyphenols, polysaccharides, and polypeptides found in mung beans all have antioxidant properties, which can help to prevent various diseases (39) by lowering bad LDL cholesterol levels and reducing chronic disease risk (37, 40). The mung bean and its extracts have demonstrated excellent health benefits, including hypoglycemic and hypolipidemic effects, as well as having antihypertensive, anticancer, anti-melanogenesis, and immunomodulatory properties (41).

Cowpea (Vigna unguculata L.)

Cowpeas (Vigna unguculata L.) are a member of the Fabaceae family. Cowpeas are grown for both grains and veggies. It is one of the most nutrient-dense African indigenous vegetables with the potential to improve food and nutrition security. The crop originated in West and Central Africa, from where it expanded to Latin America and Southeast Asia through cultivation and production (42). Cowpea has high protein content, and it differs with variety (43). The protein profile of cowpea is complex and unique. Cowpea leaves are high in protein, vitamins like provitamin A, folate, thiamine, riboflavin, and vitamin C, as well as minerals like calcium, phosphorus, and iron (44). The essential amino acids present in cowpea are cysteine, histidine, methionine, leucine, isoleucine, lysine, threonine, and tryptophan. Cowpea proteins are composed of amino acids like phenylalanine, valine, leucine, and lysine, which are found in higher levels than sulfur-containing amino acids. The amino acids are utilized during seed development; because of this, the free amino acid content is higher in immature seeds compared to mature seeds (45, 46). Cowpea leaves have long been used to produce food and feeds, nutraceuticals, micronutrients, and natural antioxidants. (47). Alpha-tocopherols, flavonoids, lycopene, and anticancer agents are among the antioxidants found in the leaves (48). In cowpea (AccessionOAA96/30), the mean value of the mineral elements calcium, chloride, sodium, magnesium, and potassium is 892.1, 177.7, 106.4, 2477.0, and 14710.0 μg/g, respectively (49). Cowpea seeds have different ranges of micronutrients in different genotypes. The range for Zn is 33.9–69.2 μg.g–1, for Fe is 45.1–67.0 μg.g–1, 5.2–8.1 μg.g–1 for Cu, and 10.1–17.4 μg.g–1 for Mn (50). Cowpea possesses iron in high quantities, which eliminates anemia and assists in protein metabolism, which is essential for RBCs and hemoglobin production. Manganese also maintains the structure and strengthening of bones (51). It assists in the formation of bone by regulating the enzymes and hormones which are involved in the process of bone metabolism (50).

Proteins, peptides, and protease inhibitors in cowpea have been shown to improve lipid profile, blood glucose levels, and blood pressure, as well as help to prevent cancer by reducing the growth of various cancer cell lines (50, 52, 53). Cowpea protein isolate can be used in food items as an alternative. Protein isolation is a viable option for reducing antinutritive effects and increasing digestibility and bioavailability of leguminous amino acids. In impoverished nations, a mixed meal of legumes and grains can compensate for inadequacies or low levels of lysine and sulfur amino acids in cereals and grain legumes, respectively (46, 54).

Common bean (Phaseolus vulgaris)

Domestication of the common bean began around 8,000 years ago in central Mexico and South America. These were isolated events that led to the formation of two large genetic pools: Mesoamerican, which stretches from northern Mexico to Colombia, and Andean, which stretches from Peru to Argentina (55). Common beans are an important dietary proteinaceous source to large populations of these semi-dry global regions, contributing to about 15% of calorie intake and up to 36% of total daily protein in parts of Africa and the Americas (56). Seeds of common bean have ∼25% protein along with minerals like Mg, Cu, Ca, Fe, Zn, and vitamins such as folate (“FoodData Cent.,” n.d.). Beans have useful levels of mineral micronutrients like copper (9.1–11.6 mg kg–1), selenium (381–500 μg kg–1), potassium (18,854–23,175 mg kg–1), magnesium (1,845–2,383 mg kg–1), and zinc (24.8–33.3 mg kg–1) (26). Common beans have 25–30% of the recommended content levels of iron in food and are known as rich sources of several other minerals (57). Common bean has a lesser genetic complexity than soybean, and the new genetic information available for the Andean and Mesoamerican pools makes it an appealing model for studying molecular mechanisms like symbiosis and nutritional deficiency adaptation (56). Common beans, without a doubt, have a lot of potential as a nutraceutical food. Encouragement of its consumption could aid in the prevention of chronic diseases, diabetes, and high cholesterol, which are on the rise around the world (58). The processing of ordinary beans into a range of goods may expand the number of products available for consumption (59).

Pigeon pea (Cajanus cajan)

Pigeon pea is a perennial plant in the Fabaceae family. Pigeon pea is a popular legume crop in South Asia, providing high protein content and nutritional benefits for over a billion people (60). Red gram, congo pea, gungo pea, and no-eye pea are some of the other frequent names for this tropical legume. Due to its higher yield under extreme environmental circ*mstances, such as heat, drought, and low soil fertility, this hardy legume has a significant potential positive influence on the lives of impoverished farmers when compared to other legumes (61). Pigeon pea contains higher amounts of amino acid like aspartic acid, lysine, leucine, arginine, and glutamic acid (Table 1) (62). The sulfur-containing amino acids (methionine and cystine) are limited in major legumes but are found in pigeon pea (63). It has a good number of health-promoting phytochemicals in addition to protein and fiber. Phenolic acids, flavonoids, tannins, saponins, and phytic acid are the most common phytochemicals identified in pigeon pea seeds. Antioxidant, antidiabetic, and anti-inflammatory properties are the most common bioactivity of these components (64, 65). The functional characteristics of pigeon pea flour make it a good ingredient for culinary products such as bread, pasta, and nutritional bars, and it can be used as a gluten-free cereal substitute (66). Recent data suggests that bioactive compounds found in pigeon peas play an important role in modifying the gut microbiota and, as a result, can lower inflammation. Animal models have also been used to examine the prebiotic potential of non-digestible raffinose family oligosaccharides (67). Pigeon pea helps in maintaining blood pressure, preventing anemia, aiding weight loss, and boosting energy (67, 68).

Pigeon pea can also be used as a substitute for artificial nutrition formulae that cause low-level inflammation. Now it is used as a unique nutritional ingredient in foods such as biscuits, noodles, pasta, and sausages because of its high fiber and protein content, gluten-free status, low glycemic index, antioxidant levels, and functional features such as fat absorption and water-binding capability (69).

Chickpeas (Cicer arietinum L.)

Chickpeas (Cicer arietinum L), often known as garbanzo beans or Bengal gram, are the third most significant variety of legume. The chickpea is divided into two types: Kabuli and Desi. Desi grain has 327 kcal/100 g of energy, while Kabuli grain has 365 kcal/100 g (70). Chickpea grains have a greater protein content than any other pulse crop, with 60–65% carbohydrate, 6% fat, and between 12 and 31% protein. Chickpeas are high in protein, carbohydrates, and all the essential amino acids. Chickpea seed has the highest digestibility as compared to other dry edible legume, with 23% protein, 64% total carbohydrates, 47% starch, 5% fat, 6% crude fiber, 6% soluble sugar, and 3% ash. Calcium, magnesium, potassium, phosphorus, iron, zinc, and manganese are all abundant in chickpeas (71). When compared to legumes like the common bean and soybean, chickpea seeds have a similar protein content. Chickpea protein has a high bioavailability and digestibility (48–89.01%) (72). Chickpea is a rich source of several minerals like manganese (21.9–25.4 mg kg–1), copper (6.6–8.7 mg kg–1), iron (48.6–55.6 mg kg–1), (73) zinc (21.1–28.3 mg kg–1), selenium (629–864 μg kg–1), and magnesium (1,525–1,902 mg kg–1) (26). These micronutrients are responsible for a variety of health benefits like improving digestion, aiding weight management, and reducing the risk of heart disease. Chickpeas have higher levels of selenium (731 μg kg–1) but lower levels of calcium compared to other legumes (26). Chickpeas can boost a food’s nutritional value while also lowering its acrylamide concentration. Acrylamide is a toxic chemical that can be found in meals including bread, crackers, and chips. The application of chickpea flour and protein could be a novel technique to lower the amount of acrylamide in these goods. The sensory and textural qualities are affected by the inclusion of chickpea flour (74). The protein quality of legumes is improved by heat treatment because heat inactivates several heat liable anti-nutritional factors Chickpeas have several possible health benefits, and when combined with other pulses and grains, they may be able to reduce the risk of cardiovascular disease, type 2 diabetes, digestive illnesses, and several other malignancies. It regulates blood pressure, improves digestion, and boosts immune health and hemoglobin level (75). Overall, chickpeas are a valuable pulse crop with a wide range of nutritional and health benefits (Table 1 and Figure 2) (76).

Functional properties of legume proteins

Legumes are a low-cost protein source, which makes them valuable and healthy components whether utilized as flours, concentrates, or protein isolates (PIs) (77). The protein content of legumes differs based on the legume species. Seed proteins are divided into three categories: structural, storage, and physiologically active. Enzymes, lectins, and enzyme inhibitors are the most physiologically active proteins (78).

Legume protein type

The predominant protein components in legume seeds are globulins (35–80%) and albumins (2–37%). The primary globulins include legumin (11S) and vicilin (7S), while albumins include enzymes, enzyme inhibitors, and lectins (79, 80). Albumins are water-soluble proteins that contain enzymes, protease inhibitors, amylase inhibitors, and lectins. Globulins account for nearly 70% of legume seed proteins, are predominantly composed of the 7S, 11S, and 15S proteins, and are defined as protein extractable in dilute salt solutions. Pea protein is mostly made up of the 7S/11S globulin (salt-soluble, 65–80% of total) and albumin 2S (water-soluble, 10–20%) protein classes, whereas soybean has large number of storage proteins like globulin and prolamin. Mung bean is enriched with storage proteins like albumin (25%) and globulin (60%) (81). Cowpea includes albumins, globulins, prolamin, and glutelin as major protein types while common bean is mainly composed of albumin and globulin (47.56 and 44.64%, respectively). Pigeon pea storage protein found within pulses are globulins, albumins, and glutelin. Albumins and globulins are the primary proteins present in chickpeas, with tiny amounts of glutelins and prolamines present. Legumin and vicilin belong to globulins. The primary storage protein, legumin (360 kDa), accounts for 97% of all globulins. A detailed description of all the legume “protein type” and their comparison with the lentil and peanut is presented in Table 2.

TABLE 2

Protein composition of different legumes and their comparison with lentil and peanut.

LegumesProtein content (%)Albumin (%)Globulin (%)Prolamin (%)Glutelin (%)References
Pisum sativum26185543(168, 169)
Glycine max13835215(72, 170)
Vigna radiata2325401010(95)
Vigna unguiculata2410.2510.259.276.92(171)
Phaseolus vulgaris2447.5644.640.980.74(172, 173)
Cajanus cajan L.221029.2163(174176)
Cicer arietinum L.2112562.818.1(86, 175)
Lens culinaris10.5–27.12644220(177)
Arachis hypogaea47–556–912–169.32.5(178)

Physico-chemical and functional properties of the legume proteins

Proteins function as both nutritional and structural building blocks (82). Physical and chemical features of legume proteins, including molecular weight (MW), amino acid content and sequence, structure, surface electrostatic charge, and effective hydrophobicity, are all linked to their functioning. Protein functioning can be altered by physical, chemical, enzymatic, or genetic alterations. The isoelectric points (PIs) are increasingly being used in food products due to their functional characteristics (83, 84). Amino acid profile information on all the legumes under study is provided in the Table 1. Essential amino acids are present in many legumes, while non-essential amino acids, like glutamic acid and aspartic acid, are also present, except in chickpeas (24, 53, 85). MW- Leguminous seeds’ primary storage protein is legumin. Legumin has a MW between 300 and 400 kDa and is a hexamer. Peas are the source of lectin or agglutinin known as Pisum sativum (PSA). PSA is a heterodimer made up of four subunits and has a MW of about 53 kDa. Chickpea legumin has a molecular weight (MW) of between 320 and 400 kDa (86). The amino acid sequence yielded a MW of 20.1 kDa in Glycine max. Cajanus cajan has a MW of 14 KDa (87). The molecular mass of Phaseolus vulgaris is 126 kDa. MBL I and MBL II, two significant lectins, make up the VRA (Vigna radiata agglutinin) protein. 132 kDa is the MW of the tetramer MBL I. In Vigna unguiculata, three globulin subunits with MWs of 110, 76, and 41 kD were discovered to be made up of disulfide-linked polypeptides (88).

Isoelectric point- The pH level at which a specific molecule has no net electrical charge is known as the isoelectric point (89). The protein isoelectric point of legume globulins is thought to be about pH 4.5 (90). Major pea proteins are globulins, which are most soluble above and least soluble below the isoelectric point (4.5), respectively (77). The majority of chickpea proteins have an isoelectric point of 4.5, which is the point at which there is no net charge and no repelling interactions between protein molecules (91). Glycine’s isoelectric point is at pH 6.082, and its isoelectric zone ranges from around pH 4.5 to pH 7.5 (92). Cajanus cajan proteins have an isoelectric point of pH 4.5 where there is no net electrical charge on them (93). Cowpea (Vigna unguiculata) has a conventional solubility pattern with an isoelectric point at pH 6 (94) while Phaseolus vulgaris has an isoelectric point between pH 5.2 and pH 6.2 and the isoelectric point of Vigna radiata is at pH 4.5 (95).

Hydrophobicity-Food proteins’ structural and functional characteristics, such as hydration, gelation, emulsification, foaming, and adhesion, are known to be significantly influenced by hydrophobicity. Hydrophobicity is anticipated to have a significant impact on the physicochemical characteristics, bioavailability, and overall nutritional quality of proteins found in legumes. Comparing the surface characteristics of myoglobin, bovine serum albumin, and lactoglobulin with those of soybean trypsin inhibitor, concanavalin A, and 7S globulin, legume proteins have a higher hydrophobic surface area than myoglobin and serum albumin, according to molecular surface coloring by amino acid hydrophobicity. Numerous hydrophobic regions on the protein surface of lactoglobulin have been linked to the binding of tiny ligands, particularly phenolics (96). Studies on the specific legumes are scarce.

Solubility-In Legume, globulins protein has reduced solubility at pHs close to the protein isoelectric point and have a hydrophobic nature. The solubility of pulse protein is very low (pH 4 and 6) and the solubility is influenced by ionic strength, pH, freezing, temperature, and heating (97). In Soybean, globular protein forms gel (83) when heated and due to this functional group of globular protein get exposed (79). Gelification is affected by the amount of water, concentration of protein, temperature, and pH. The soy PIs change with the alteration of pH and by proteolytic enzymes. Acylation of legume proteins increases the foaming and emulsifying capacity of protein.

Thermal stability- Thermal behavior and thermal stability are the two major properties of the legume’s PIs. Thermal behavior of protein denaturation (Td) in chickpeas with 70% purity and faba beans with 88% purity was recorded as 205 and 183°C, respectively (98). Td values for bean isolates at 55 and 75% purity were 211.5 and 193.8°C and lentil isolates at 45 and 75% purity were 199.5 and 183.4°C, respectively. The thermal stability of legumes rises with purity (99).

Oil Holding Capacity (OHC) and Water Holding Capacity (WHC)- The OHC and WHC of the legumes ranges from 3.5 to 6.8 gm/gm and 1.8 to 6.8 gm/gm, respectively. Legume PIs have good foaming, emulsion, solubility, and emulsifying activity indexes, and these qualities are maintained even at a high pH (2.0 and 10.0) (100).

Encapsulation has made considerable use of legume proteins. Vitamin B9 (folate), tocopherol, ascorbic acid, and phytase are encapsulated independently using legume PIs (e.g., from pea and chickpea), with encapsulation efficiencies ranging from 62 to 100% (101, 102). In simulated gastric and intestinal fluids, phytase encapsulation with pea protein isolate resulted in a low release rate and high bioaccessibility (103). To encapsulate the vegetable oils and flaxseed and soybean oils, respectively, lentil and red kidney bean protein isolate are utilized (104). Apart from these, melting temperatures can vary greatly depending on the particular main amino acid sequence linked to the particular protein type. The pH and salt concentration of the solution, as well as post-translational changes, such as glycosylation, can significantly affect the stability of the protein structure and, consequently, the melting point. Protein shape, charge, and hydrophobicity, as well as the neutrality of dipoles and the hydration of polar groups, all affect their ability to emulsify. The strength of these interactions influences the stability of emulsions (105).

Du et al. (106) studied the bulk densities, water absorption indices, water solubility indices, oil absorption capacities, emulsion activities, and emulsion stabilities in the whole legume floor and found that these properties ranged from 0.543 to 0.816 g/mL, 4.09 to 6.13 g/g, 19.44 g/100 g to 29.14 g/100 g, 0.93 g/g to 1.38 g/g, 61.14 to 92.20%, and 84.15 to 96.90%, respectively. Further, high hydrostatic pressure (HHP), ultrasound, enzymatic hydrolysis, and a combination of these technologies can be used to increase the functioning of legume proteins (107109). Another way to change the characteristics of legume proteins is to use enzyme hydrolysis. The antioxidant and anti-inflammatory activities of PIs from pigeon pea, lentil, and chickpea were improved by alcalase and bromelain hydrolysis (109). The above functional modifications change the structural, chemical, and physicochemical properties of proteins (84).

Impacts of processing techniques on physicochemical properties of legume proteins

Raw bean consumption can be time-consuming, difficult, and, in the worst-case scenario, unsuccessful in terms of the gut’s ability to absorb amino acids. Lupin PIs and defatted wheat meet the required amino acid requirements. Pigeon pea and PIs derived from it are also potential sources of sulfur-containing amino acids that are suitable for human consumption. A range of domestic processing procedures are used empirically to facilitate the absorption of legumes in general, but without understanding the impact on protein digestibility per se. Many bean cultivars and processing methods have been examined to assess the potential for enhancing nutritional value and protein utilization (110). The recent plant protein revolution has pushed legumes to the center of consumer and food industry attention (111). These goods can also be used to fortify foods, boost their content, and produce healthy products that are reduced in calories, cholesterol, and fat. Food protein content is also increased by various food processing procedures that may alter its chemical and physical qualities (112). Some of these may potentially boost protein functioning. As a result, they can also be used as functional additives to improve physical qualities such as hydration, oil-holding capacity, and viscosity (113). Soaking, thermal processing, and microwave radiation enhances the bioavailability of the legume proteins (114116). Other high-intensity thermal procedures include pressure cooking and autoclaving. Both rely on exceeding the typical, ambient boiling point of water in a sealed vessel (pressure cooker) or pressure chamber (autoclave) (117). These rely on milling the legumes into flour before treating them. Baking is an old, conventional thermal process that applies heat using dry air at atmospheric pressure. In general, a dough based on bean flour is produced, rested for some time (leavening), and then baked for more than 30 min at temperatures ranging from 180 to 220°C. Extrusion is likewise based on the transformation of bean flour into a food product (118). Impact of different processing techniques on legume proteins is enumerated in the Table 3. These different processing methods that could affect the legume protein different ways are presented as:

TABLE 3

Effect of processing techniques on protein in different legumes.

LegumesDehullingSoakingCookingHHPFermentationReferences
Pisum sativumTotal protein content increased by 2.2% after germination via de-huskerNAIVPD increased by cooking in water bath.Protein digestibility, oligosaccharides, phytic acid and trypsin inhibitor activity reducedIVPD increased by 2–3%.(179)
Glycine maxincreased the oil holding, foaming and functional propertiesRaffinose content reduced to 22% after soaking seed in water for 16 hCooking of seeds reduced the tannin content and improved its IVPDNAFermentation with Lactobacillus bulgaricus, the IP6 contents in the seed decreased(180)
Vigna radiataNo change in protein content After manually removing post-soakingProtein content decreased by 0.2% after soaking in distilled water for 12 h at room temperatureNADecreased isoleucine, tryptophan, total sulfur amino acid, and lysineIncreases the protein digestibility(79)
Vigna unguculataIncreased the oil holding, foaming and functional properties.Soaking seeds in alkaline water for 16 h eliminated raffinose and reduced stachyose by more than 80%Cooking reduces anti-nutritional content and increase IVPDNAFermentation with Lactobacillus bulgaricus, the IP6 contents in the seeds decreased(180, 181)
Phaseolus VulgarisNADecrease in the protein content 0.2% after soaking in distilled water for 16 h at 30°CNASoaked see drained, mix with oil and salt, boil for 3 h would increase protein digestibilityIncreased the potential of flours as functional ingredients by increasing polyphenol and their anti-oxidant activity(182)
Cajanus cajanNASoaking for 6 h helped in detoxification of trypsin inhibitor and tannins and protein content increased by 6.34%Cooking was more efficient in reducing the levels of lectins, oxalates, saponins and tanninsNAFermentation improved the protein solubility(183)
Cicer arietinumTotal protein content increased by 5% after germination via de-huskerSoaked seed and mixed with oil and salt, boil for 3 h. increase the protein content up to 4.51%Cooking reduced the RFO contents, with the elimination of verbascoseNAGround mix with inoculum and fermented for 24 h, increased the protein digestibility by 13.4%(184)

*HHP, high hydrostatic pressure; IVPD, in vitro protein digestibility; NA, Not available.

Cooking- Unprocessed bean, pea, and lentil flour have similar amounts of protein in them, ranging from 24.8 to 28.7%. However, when contrasting different subtypes of cooked legumes, the impact on the protein content varied greatly. Phaseolus vulgaris beans that had protein levels of 24.8 and 26.2% before processing were dramatically reduced to 23.0 and 21.3% (117). All cooked legumes showed a considerable rise in In vitro Protein Digestibility (IVPD). The IVPD of the raw samples of peas (Pisum sativum L.) varied between 79.9 and 83.5%, while that of the processed samples ranged between 85.9 and 86.8%. After 90 min of heating, the unprocessed chickpea’s IVPD—which was 83.61%—rose to 88.52%. The IVPD was shown to depend on the cooking time (118).

Autoclaving- When compared to the raw form, the crude protein content of beans, peas, and lentils was significantly reduced after autoclaving. Comparatively to cooking, autoclaving raw beans has a different impact on their protein content (119). Like this, autoclaving dramatically raised the IVPD for all species of legumes studied, with the exception of faba bean and lentil. When compared to cooking, autoclaving did not clearly improve protein digestibility. The more severe and intense heat treatment provided by autoclaving did not always appear to be beneficial. Additionally, the IVPD of four distinct legumes was considerably decreased when the autoclaving time was increased from 10 to 90 min (117).

Fermentation- Black beans fermented with the fungus showed a protein digestibility of 48.13%, which is comparable to figures for black beans fermented with Bacillus. The fungus’ capacity to lessen tannins contributed to the improvement in protein digestibility (120, 121).

Baking- The steps involved in making dough, including mixing, rising, and baking, compared to cooking, meant the IVPD was decreased in all but the red lentil. The protein content of green split peas was decreased by this processing procedure while the protein content of yellow split peas increased. Protein content of untreated yellow split peas was 179.23.78%, and after extrusion and baking, it increased to 24.56% (115, 116).

High hydrostatic pressure- HHP treatment enhanced the kidney bean, lentil, and protein hydrolysates’ solubility and emulsifying activity index (107). Following HHP treatment, there were noticeable changes in the secondary structure, including a shift of the amide I and amide II, which demonstrated a decrease in the emulsion stability of lentil PI and kidney bean protein hydrolysate. Chickpea PIs were treated with high-intensity ultrasound, which greatly enhanced their solubility, emulsifying, foaming, and heat-induced gel characteristics (107, 108).

Extrusion- Due to the strong shear and compression, extrusion is a thermal process with a high energy efficiency and is likely the most severe thermal treatment technique. However, the method of extrusion enhanced the nutritious value of legumes (122). The IVPD was markedly enhanced by extruding kidney bean, pea seed, common bean, and faba flour. Extruded kidney beans (100–300 g/kg) were added to broiler diets, and this increased apparent ileal digestibility (AID), which was 77.23–79.03% with feed based on raw kidney beans (117).

There are numerous processing processes available to lower the amount of antinutritional components contained in legumes, boost the bioavailability of macro- and micronutrients, and expand the range of pulse-based products available to consumers (123). To achieve the required outcomes, the processing procedures can be adjusted to the purpose and kind of legumes (124).

Extraction methods used for legume protein type

Proteomics is a cutting-edge approach for analyzing the protein profiling of a tissue in order to interpret the molecular entities that could be changed in order to generate crops that are resistant to stresses. Because of its high protein content (18–30%) in legumes and ease of digestion (68%), it is a key source of protein, especially for a substantial portion of the Indian population who closely follow vegetarian diets (125). Protein extraction technologies can aid in increasing the yield of extracted protein as well as its nutritional and functional qualities. As a result, a suitable protein extraction method should be used (15). Globulins and albumins are the two main proteins found in legumes. These proteins have a minimal solubility at pH values ranging from four to five (isoelectric point). Protein concentrates and isolates with varied purity and functionality can be generated by modifying protein solubility and utilizing filtration procedures that take advantage of their hydrodynamic properties (84).

Various extraction techniques are used for the extraction of different protein types in the legumes. Air classification and pin milling fractionation of legumes into a light or fine fraction (protein concentrate, defined as having protein contents of 60–75%) and a heavy or coarse fraction (starch concentrate, defined as having protein contents of 90–95%) is done. Using this procedure, whole or dehulled legume seeds are pin milled and then fractionated into “protein” and “starch” concentrations using an air classifier (126). However, the quality of the protein fraction obtained through this procedure is low (38–65%), and additional processing is frequently necessary (127). Alkaline extraction and acidic (isoelectric) precipitation method involves the use of distinct protein solubility and precipitation characteristics. The alkaline and acid pH ranges have higher solubility, but the isoelectric point (about pH 4–5) has the lowest solubility (127). The salt extraction process, also known as micellization, is based on the salting-in and salting-out of dietary proteins. After extracting the protein using a suitable salt solution of the necessary ionic strength, the solution is diluted, producing protein precipitation that can then be recovered by centrifugation or filtration, followed by drying (128).

Legume protein in human nutrition

Legumes have been a staple of many traditional cuisines around the world for thousands of years. Some of the food uses of the different legumes have been presented in Table 4. Per capita legume consumption has been stable over the last three decades, whereas meat consumption has increased, particularly in several LMIC (low- and middle-income countries). Plant-forward diets, which involve a move away from meat and toward alternate protein sources such as legumes, are seen as a way to reduce greenhouse gas emissions, water usage, and deforestation (129, 130). These legumes have a high vitamin and mineral content, particularly potassium and calcium (in the case of lupines and soybeans), magnesium, iron, and zinc, as well as vitamin B1 (thiamine) and folates. Soybean is a good source of both linoleic acid and α-linolenic acid (15). Due to their low-fat content, the remaining legumes do not play a significant role as providers of fatty acids. Legumes have a high fiber content. Disaccharide and oligosaccharide levels are very high. Sulfur-containing amino acids (methionine and cystine) limit amino acids in faba beans and lupines (131133). Protein digestibility in all legumes is relatively high, ranging from 89 to 96%. As a result, the Protein Digestibility Corrected Amino Acid Score (PDCAAS) values vary from 81 (lupines) to 96 (peas). These high PDCAAS levels are comparable to animal proteins. Peas and beans, and to a lesser extent lupines, are high in lysine, making them an excellent supplement to cereal proteins, which are poor in lysine. Arginine is also abundant in lupine protein (134). In the future, legumes may provide a sustainable solution to the challenge of providing high-quality dietary protein to the world’s growing population, but this may necessitate significant increases in global legume yields and directing the majority of legume production toward human consumption rather than livestock feed (10).

TABLE 4

Food uses of different legumes across the world.

Common nameFood uses
Adzuki beans (Vigna angularis)Japanese desserts and confections, soup ingredients for therapeutic purposes
Anasazi beans (Phaseolus vulgaris)Boiled meal, snack, soup
Black gram (Vigna mungo)Dhal, fermented products (idli, dosa, papad)
Black turtle beans (Phaseolus vulgaris)Bean soup popular in latin American cuisine
Black-eyed peas (Vigna unguiculata)Boiled snack/part of meal, fried cake akara, steamed pudding moi moi in West Africa
Chickpea (Cicer arietinum)Middle Eastern and Mediterranean foods such as falafel and hummus, Boiled/fried/cooked/crushed snacks, dhal, curry, flour used in bread making, fermented food (dhokla)
Faba bean (Vicia faba)Whole food
Kidney beans (Phaseolus vulgaris)Ingredient in Mexican chili; most-consumed legume in America
Lentils (Lens culinaris)Soups and stews; most important legume in India
Mung beans/Green gram (Vigna radiata)Bean sprouts, cooked whole or with sugar into a dessert, soup, flour used for baking, transparent noodles, patties, sweets
Peanut/Groundnut (Arachis hypogaea)Peanut butter, peanut bar, flour, roasted/boiled snacks
Peas (Pisum sativum)Soup, dhal
Soybean (Glycine max)Asian dishes (tofu, natto miso), roasted snacks, milk, yoghurt, sprouted beans, curd, yuba, soy sauce, soy paste, TVP
Tamarind (Tamarindus indica)Pulp used for food and beverage preparation, flour used as soup thickener, remedy in diarrhea and dysentery

Compiled from Semba et al. (10) and Kouris-Blazos and Belski (185).

In recent years, there has been increased interest in the bioactive characteristics of legume-derived proteins and peptides. Furthermore, because legume starch has a low glycemic index, it contributes to a gradual release of glucose. Dietary fibers from legumes help to normalize bowel function and gastrointestinal health Given the present demand, it is likely demand for diverse legume ingredients will increase in the future. The better functionality of legume-based products will contribute to these developments since legume ingredients can produce specialty food products in addition to meeting daily nutritional requirements (111). Legumes will continue to play an important part in human nutrition and health as the recognition of their potential for improved crop environmental sustainability grows.

Therapeutic use and mechanism of the legume proteins

Due to improved nutritional and functional characteristics of legumes, they can be used in food and nutraceutical applications (135) as well as for various health benefits (108). Products generated from the production or processing of plant-based foods are rich in nutrients. Nutrient-rich diets have been linked to a lower risk of cardiovascular disease, diabetes, hypertension, obesity, and gastrointestinal diseases (136). In addition to the nutritional superiority, legumes are high in bioactive phytochemicals, such as phenolic compounds, and have various bioactivities like antiviral, anticarcinogenic, anti-inflammatory, and antimutagenic, as well as lowering blood cholesterol, blood glucose, blood pressure, and body weight (BW), which is beneficial in coronary heart disease (CHD), osteoporosis, and other degenerative diseases (Figure 2). The therapeutic uses/health benefits of different legume proteins have been explored in Table 5.

TABLE 5

Health benefits of various legume proteins.

Legume sourceInvolved metabolismType of studyBeneficial effectReferences
Dry beans, peas and peanutsCardiovascular and colorectal cancerEpidemiologic Follow-up study22% reduction in coronary heart disease (CHD) and 11% reduction in cardiovascular disease (CVD)(185)
LegumesCardiovascularMeta-analysis10% decreased risk of CVD and CHD(186)
CowpeaHypocholesterolemicEndogenous biosynthesis of cholesterolLowers blood cholesterol, blood glucose, blood pressure, and body weight(52)
Cooked beans, chickpeas or lentilsCardiovascular and diabetesrandomized controlled trialReduced hemoglobinA1c (HbA1c) level and reduction in coronary heart disease (CHD) risk(187)
Five cups/week yellow peas, chickpeas, navy beans, and lentils)Metabolic syndromeRandomized controlled trialReduced risk factors of the metabolic syndrome(188)
Beans with low-GI dietGlycaemia and obesityrandomized, crossover studyImprovement in metabolic control in type-2 obese diabetic patients in weight loss(188)
Legumecoronary diseaseNutritional intervention and/or dietary manipulationPrevent the generation of superoxide radical and boost the immune system(189)
Legume seed extractsColon cancerTest-tube lab researchInhibition of MMP-9 activity and cell migration in colon carcinoma cells(190)
Protein isolates of germinated soybeanCervical cancerAnimal research studiesDecreased in the expression of PTTG1 and TOP2A (therapeutic targets) causing apoptosis of cancer cells(191)
Common beanHypolipidemic propertiesBio-active constituents’ studyPhytosterols, dietary fibers, and resistant starch.(192)

The quantitative and qualitative protein composition is one of the fundamental aspects in selecting plants for nutritional value, and because globulins are the predominant proteins in legumes, there have been an abundance of studies on their characterization in various species (137). In chickpea, during the germination stage, the increase in proteolytic activity was followed by a modest decrease in trypsin inhibitor activity, which is connected to albumin fraction. Protein properties and mobilization during seed germination have been widely examined, revealing gradual hydrolysis with an unknown mechanism of degradation regulation (138). Many plant species contain basic 7S globulin (Bg7S)-like proteins from soybean seeds. Bg7S was previously assumed to be one of the key seed storage proteins, but later investigations revealed that it was not a storage protein, but rather a protein with multiple activities such as stress response, antimicrobial activity, hormone receptor-like activity, and so on. Bg7S and leginsulin, on the other hand, were discovered to have functional effects on humans, rats, and mice, such as blood glucose management, blood pressure control, and plasma cholesterol control, as well as cancer cell antiproliferative properties (139). It also suggested that seed storage protein consumption may affect adipocyte differentiation in vivo, although this mechanism’s effect adipocyte differentiation is not fully understood (72). Peas and lentils include a variety of potentially bioactive components, including protease inhibitors and lectins, which can affect human metabolism in either a favorable or negative way. Some bioactive substances, on the other hand, may be helpful to health. The nutritious quality of the seeds is considerably improved by thermal treatment. Raw and treated seeds are both hypo-cholesterolemic (140). Peas are hypo-cholesterolemic in rats, pigs, and humans. The processes are unknown, but they may be related to fiber and saponins in the seeds (141). On the other hand, Lectins can activate multiple pathways that restrict cancer cell development, with the apoptosis pathway being more effective in specific cell lines by increasing the synthesis of caspases or other proteins involved in the mechanism. Specific genes in this pathway can be down-regulated or up-regulated, resulting in apoptotic suppression or activation, respectively (142). Chickpea lectin inhibited cell growth in human oral cancer cells (KB cells) at a concentration of 37.5 g/mL (IC50) but had no harmful effect on normal human peripheral blood mononuclear cells at a concentration of 600 g/mL (143). Based on the findings and information available, it is possible to conclude that legume protein type (globulins, albumin, prolamin, and glutelin) are effective antibacterial and bioactive agents that can be successfully and efficiently used to understand the therapeutic effects and nutritional benefits of plant legumes, particularly because they are safe natural products that can be prepared at a low-cost, in addition to their well-known rich nutritional value as legume proteins.

Underutilized and neglected legumes

Obtaining food resources for the world’s growing population is getting increasingly difficult. In this situation, each country must make the most of its existing food supplies (144). However, in most African and Asian nations, where underutilized crops could have addressed malnutrition, hunger, and rural poverty, several legume crops that were formerly essential sources of proteins, edible lipids, fiber, minerals, and other nutritional components are on the verge of extinction (29). In reality, some of these crops—namely marama bean, bambara groundnut, yambean, and lablab—offer enormous promise in terms of climate adaptation and nutritional content. Because of their nutritional makeup, these crops have a lot of potential as future food or feed sources (145). However, these potentially essential crops are in danger of becoming uncommon due to a lack of agronomic, genetic, and food research (146).

The African yam bean (Sphenostylis stenocarpa) (AYB) is a popular tropical African food crop with medicinal and pesticidal properties. Although lower than soybean (38%), AYB has around 29 and 19% crude protein in its grain and tuber, respectively (147). Bambara groundnut (Vigna subterranea) is not widely consumed in many parts of Africa, although its nutritional and health benefits are well known. In recent years, there has been increasing interest in cultivating V. subterranea in arid savannah zones to reduce stress and boost protein availability to the local population (148). The winged bean (Psophocarpus tetragonolobus) is a multipurpose legume plant with edible and medicinal portions (149). Vitamins, minerals, protein, and secondary metabolites including phenolic, and flavonoids are abundant in all parts of the plant. Furthermore, winged bean is very resistant to biotic and abiotic stressors, allowing it to thrive in a variety of environments (150).

With help in breeding, transgenic techniques, and agronomic practices, nutritional value of the crops can be enhanced by using biofortification methods (3, 151). In comparison to rice, wheat, and maize, limited analysis has been conducted on biofortification of pulses and legumes in the last decade (29). Biofortification, on the other hand, is one of the more cost-effective ways to address the malnutrition problem among underprivileged and impoverished rural populations (152154).

These neglected crops are becoming increasingly scarce around the world, and their genetic resources are fast disappearing in all of their natural habitats. As a result, a paradigm shift from the current state of neglect to sustainable cultivation, exploitation, and consumption of the species is required (155). The genetic resources accessible among and within neglected crops have not been fully explored to enhance sustainable use for future food and nutritional security, as well as biodiversity preservation to mitigate the detrimental effects of climate change and abiotic stress. Similarly, a species’ ability to tolerate abiotic stress in the face of biological limiting conditions is critical to its continuing use and survival (156, 157).

Conclusion

For a healthier lifestyle, legumes are an inexpensive and long-term source of protein, micronutrients, complex carbohydrates, and essential phytochemicals. Their composition is suitable for celiac and diabetes patients as well as consumers concerned with satiety. The variety and versatility of legumes means that they can be added to a wide range of dishes, including soups, stews, curries, and salads (70). Legumes are great crops for reaching the Sustainable Development Goals due to their nutritional, health, and environmental benefits. Therefore, the genetic resources of legumes should be explored using characterization, evaluation, and documentation. This will provide the identification of trait-specific germplasm for further utilization of the same in the national food basket. Legumes impart various health-promoting bioactivities like reduced risk of CHD, lowered cholesterol, and maintained blood sugar level, blood pressure, and metabolic syndrome. There are only a few reports on the mechanism of action, so it would be important to conduct more studies to verify biological activities, not only in vivo models but also in situ or ex vivo, performed not only in the whole seed but with each of its bioactive compounds, to reveal the benefits of its consumption and importance as a functional food. Various plant components, such as carotenoids and flavonoids, have been shown to have beneficial health advantages. Furthermore, research on plant proteins and bioactive compounds is needed for sustainable human nutrition. More research is needed to determine the best ways to introduce plant proteins safely and effectively into the diet because the incorporation of legumes in the diets of school-going children could play a vital role in eradicating protein-energy malnutrition (PEM), especially in developing countries and in developing Afro-Asian countries.

Author contributions

NS conceived and edited the final manuscript. PJ contributed to initial draft writing and editing. MU contributed to initial draft, tables, and figures. SL contributed to initial draft writing and editing. All authors contributed to the writing and editing, and approved the manuscript.

Funding

NS acknowledged the funding from Department of Science and Technology, Government of India through DST INSPIRE Faculty Award (Grant DST/INSPIRE/04/2018/003674).

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

1. UNDP.TOWARDS 2021/2022 HDR. (2022). Available online at: https://hdr.undp.org/towards-hdr-2022. (accessed February 15, 2022). [Google Scholar]

2. Chaudhary DP, Sapna MS, Kumar R. Interrelationship among nutritional quality parameters of maize (Zea mays) genotypes.Indian J Agric Sci. (2012) 82:681–6. [Google Scholar]

3. Langyan S, Bhardwaj R, Kumari J, Jacob SR, Bisht IS, Singh A, et al.Nutritional diversity in native germplasm of maize collected from three different fragile ecosystems of India.Front Nutr. (2021) 9:812599. 10.3389/fnut.2022.812599 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

4. Campbell BM, Vermeulen SJ, Aggarwal PK, Corner-Dolloff C, Girvetz E, Loboguerrero AM, et al.Reducing risks to food security from climate change.Glob Food Security. (2016) 11:34–43. 10.1016/j.gfs.2016.06.002 [CrossRef] [Google Scholar]

5. Saxena KB, Choudhary AK, Saxena RK, Varshney RK. Breeding pigeonpea cultivars for intercropping: Synthesis and strategies.Breed Sci. (2018) 68:159–67. 10.1270/jsbbs.17105 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

6. Verma N, Sehrawat KD, Ahlawat A, Sehrawat AR. Legumes: The natural products for industrial and medicinal importance-A review.Int J Cell Sci Biotechnol. (2017) 6:6–13. [Google Scholar]

7. Gilbert JA, Bendsen NT, Tremblay A, Astrup A. Effect of proteins from different sources on body composition.Nutr Metab Cardiovasc Dis. (2011) 21:B16–31. 10.1016/j.numecd.2010.12.008 [PubMed] [CrossRef] [Google Scholar]

8. Bennetau-Pelissero C. Plant proteins from Legumes. In: Mérillon JM, Ramawat K.editors. Bioactive Molecules in Food. Reference Series in Phytochemistry. (Cham: Springer; ) (2019). p. 223–65. 10.1007/978-3-319-54528-8_3-1 [CrossRef] [Google Scholar]

9. Pirman T, Stibilj V, Stekar JM, Combe E. Amino acid composition of beans and lentil.Zb Bioteh Fak Univ Ljubl, Kmet Zooteh. (2001) 78:57–68. [Google Scholar]

10. Semba RD, Ramsing R, Rahman N, Kraemer K, Bloem MW. Legumes as a sustainable source of protein in human diets.Glob Food Security. (2021) 28:100520. 10.1016/j.gfs.2021.100520 [CrossRef] [Google Scholar]

11. Asif M, Rooney LW, Ali R, Riaz MN. Application and opportunities of pulses in food system: A review.Crit Rev Food Sci Nutr. (2013) 53:1168–79. 10.1080/10408398.2011.574804 [PubMed] [CrossRef] [Google Scholar]

12. Langyan S, Bhardwaj R, Radhamani J, Yadav R, Gautam RK, Kumar A. A quick analysis method for protein quantification in oilseed crops: A comparison with standard protocol.Front Nutr. (2022) 9:892695. 10.3389/fnut.2022.892695 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

13. Langyan S, Yadava P, Khan FN, Bhardwaj R, Tripathi K, Bhardwaj V, et al.Nutritional and food composition survey of major pulses toward healthy, sustainable, and biofortified diets.Front Sustain Food Syst. (2022) 6:878269. 10.3389/fsufs.2022.878269 [CrossRef] [Google Scholar]

14. Mariotti F, Gardner CD. Dietary protein and amino acids in vegetarian diets—A review.Nutrients. (2019) 11:2661. 10.3390/nu11112661 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

15. Langyan S, Yadava P, Khan FN, Dar ZA, Singh R, Kumar A. Sustaining protein nutrition through plant-based foods.Front Nutr. (2022) 8:1237. 10.3389/fnut.2021.772573 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

16. Gardner CD, Hartle JC, Garrett RD, Offringa LC, Wasserman AS. Maximizing the intersection of human health and the health of the environment with regard to the amount and type of protein produced and consumed in the United States.Nutr Rev. (2019) 77:197–215. 10.1093/nutrit/nuy073 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

17. Bukya MA.A Hand Book on Legumes in Indian Agriculture and Health Benefits.Indore: International E - Publication; (2014). [Google Scholar]

18. Food and Agriculture Organization of the United Nations.FAOSTAT Statistical Database. The State of Food Security and Nutrition in the World 2018. Building Climate Resilience for Food Security and Nutrition.Rome: FAO; (2018). [Google Scholar]

19. Burger TG, Zhang Y. Recent progress in the utilization of pea protein as an emulsifier for food applications.Trends Food Sci Technol. (2019) 86:25–33. 10.1016/j.tifs.2019.02.007 [CrossRef] [Google Scholar]

20. Rungruangmaitree R, Jiraungkoorskul W. Pea, Pisum sativum, and its anticancer activity.Pharm Rev. (2017) 11:39. [PMC free article] [PubMed] [Google Scholar]

21. Krefting J. The appeal of pea protein.J Renal Nutr. (2017) 27:e31–3. 10.1053/j.jrn.2017.06.009 [CrossRef] [Google Scholar]

22. Dahl WJ, Foster LM, Tyler RT. Review of the health benefits of peas (Pisum sativum L.).Br J Nutr. (2012) 108:S3–10. 10.1017/S0007114512000852 [PubMed] [CrossRef] [Google Scholar]

23. Liao W, Fan H, Liu P, Wu J. Identification of angiotensin converting enzyme 2 (ACE2) up-regulating peptides from pea protein hydrolysate.J Funct Foods. (2019) 60:103395. 10.1016/j.jff.2019.05.051 [CrossRef] [Google Scholar]

24. Beitane I, Krumina-Zemture G. Dietary micronutrient content in pea (Pisum sativum L.) and buckwheat (fa*gopyrum esculentum M.) flour.Proceedings of the 11th Baltic Conference on Food Science and Technology “Food science and technology in a changing world” FOODBALT.Jelgava: (2017). p. 56–60. [Google Scholar]

25. Diapari M, Sindhu A, Warkentin TD, Bett K, Tar’an B. Population structure and marker-trait association studies of iron, zinc, and selenium concentrations in seed of field pea (Pisum sativum L.).Mol Breed. (2015) 35:30. 10.1007/s11032-015-0252-2 [CrossRef] [Google Scholar]

26. Ray H, Bett K, Tar’an B, Vandenberg A, Thavarajah D, Warkentin T. Mineral micronutrient content of cultivars of field pea, chickpea, common bean, and lentil grown in Saskatchewan, Canada.Crop Sci. (2014) 54:1698–708. 10.2135/cropsci2013.08.0568 [CrossRef] [Google Scholar]

27. Delele TA. Review on the role soybean on animal feed and human nutrition in ethiopia.Am J Zool. (2021) 4:25–31. 10.11648/j.ajz.20210403.11 [CrossRef] [Google Scholar]

28. Hassan SM.Soybean, nutrition, and health. Soybean–bio-active compounds.London: InTech; (2013). p. 453–73. [Google Scholar]

29. Kumar S, Pandey G. Biofortification of pulses and legumes to enhance nutrition.Heliyon. (2020) 6:e03682. [PMC free article] [PubMed] [Google Scholar]

30. Mengistu A, Kebede G, Feyissa F, Assefa G. Review on major feed resources in Ethiopia: Conditions, challenges, and opportunities.Acad Res J Agric Sci Res. (2017) 5:176–85. 10.14662/ARJASR2017.013 [CrossRef] [Google Scholar]

31. Zahoor F, Ahmed M, Malik MA, Mubeen K, Siddiqui MH, Rasheed M, et al.Soybean (Glycine maxL.) Response to micro-nutrients.Turkish J Field Crops. (2013) 18:134–8. [Google Scholar]

32. Peiretti PG, Meineri G, Longato E, Tassone S. Nutritive value and fatty acid content of soybean plant [Glycine max (L.) Merr.] during its growth cycle.Ital J Anim Sci. (2018) 17:347–52. [Google Scholar]

33. Noreen A, Tabasum S, Ghaffar S, Somi T, Sultan N, Aslam N, et al.Protein- based bionanocomposites.Bionanocomposites.Amsterdam: Elsevier; (2020). p. 267–320. 10.1016/B978-0-12-816751-9.00012-X [CrossRef] [Google Scholar]

34. Hou D, Yousaf L, Xue Y, Hu J, Wu J, Hu X, et al.Mung bean (Vigna radiata L.): Bioactive polyphenols, polysaccharides, peptides, and health benefits.Nutrients. (2019) 11:1238. 10.3390/nu11061238 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

35. Mubarak AE. Nutritional composition and antinutritional factors of mung bean seeds (Phaseolus aureus) as affected by some home traditional processes.Food chem. (2005) 89:489–95. 10.1016/j.foodchem.2004.01.007 [CrossRef] [Google Scholar]

36. United States Department of Agriculture [USDA].Agriculturalresearch service, national nutrient database for standard reference release. (2016). Available online at: https://data.nal.usda.gov/dataset/usda-nationalnutrient-database-standard-reference-legacy-release(accessed February 9, 2020). [Google Scholar]

37. Nair RM, Yang RY, Easdown WJ, Thavarajah D, Thavarajah P, Hughes JDA, et al.Biofortification of mungbean (Vigna radiata) as a whole food to enhance human health.J Sci Food Agric. (2013) 93:1805–13. 10.1002/jsfa.6110 [PubMed] [CrossRef] [Google Scholar]

38. De Jager I, Borgonjen-Van Den Berg KJ, Giller KE, Brouwer ID. Current and potential role of grain legumes on protein and micronutrient adequacy of the diet of rural Ghanaian infants and young children: Using linear programmin.Nutr J. (2019) 18:1–16. 10.1186/s12937-019-0435-5 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

39. Chai WM, Wei QM, Deng WL, Zheng YL, Chen XY, Huang Q, et al.Anti-melanogenesis properties of condensed tannins from Vigna angularis seeds with potent antioxidant and DNA damage protection activities.Food Funct. (2019) 10:99–111. 10.1039/C8FO01979G [PubMed] [CrossRef] [Google Scholar]

40. Dhakal Y, Meena RS, De N, Verma SK, Singh A. Growth, yield and nutrient content of mungbean (Vigna radiata L.) in response to INM in eastern Uttar Pradesh, India.Bangladesh J Bot. (2015) 44:479–82. [Google Scholar]

41. Gupta N, Srivastava N, Bhagyawant SS. Vicilin—A major storage protein of mungbean exhibits antioxidative potential, antiproliferative effects and ACE inhibitory activity.PLoS One. (2018) 13:e0191265. 10.1371/journal.pone.0191265 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

42. Sayeed VKI, Satish S, Kumar A, Hegde K. Pharmacological activities of Vigna unguiculata (L) Walp: A review.Int J Pharma Chem Res. (2017) 3:44–9. [Google Scholar]

43. Vasconcelos IM, Maia FMM, Farias DF, Campello CC, Carvalho AFU, de Azevedo Moreira R, et al.Protein fractions, amino acid composition and antinutritional constituents of high-yielding cowpea cultivars.J Food Compos Anal. (2010) 23:54–60. 10.1016/j.jfca.2009.05.008 [CrossRef] [Google Scholar]

44. Xiong H, Shi A, Mou B, Qin J, Motes D, Lu W, et al.Genetic diversity and population structure of cowpea (Vigna unguiculata L. Walp).PLoS One. (2016) 11:e0160941. 10.1371/journal.pone.0160941 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

45. Rangel A, Saraiva K, Schwengber P, Narciso MS, Domont GB, Ferreira ST, et al.Biological evaluation of a protein isolates from cowpea (Vigna unguiculata) seeds.Food Chem. (2004) 87:491–9. 10.1016/j.foodchem.2003.12.023 [CrossRef] [Google Scholar]

46. Elharadallou SB, Khalid II, Gobouri AA, Abdel-Hafez SH. Amino acid composition of cowpea (Vigna ungiculata L. Walp) flour and its protein isolates.Food Nutr Sci. (2015) 6:790. 10.4236/fns.2015.69082 [CrossRef] [Google Scholar]

47. Baptista A, Pinho O, Pinto E, Casal S, Mota C, Ferreira IM. Characterization of protein and fat composition of seeds from common beans (Phaseolus vulgaris L.), cowpea (Vigna unguiculata L. Walp) and bambara groundnuts (Vigna subterranea L. Verdc) from Mozambique.J Food Meas Charact. (2017) 11:442–50. 10.1007/s11694-016-9412-2 [CrossRef] [Google Scholar]

48. Shetty AA, Magadum S, Managanvi K. Vegetables as sources of antioxidants.J Food Nutr Disord. (2013) 2:2. 10.4172/2324-9323.1000104 [CrossRef] [Google Scholar]

49. Asante IK, Acheampong AO, Adu-Dapaah H. Determination of some mineral components of cowpea (Vigna unguiculata (L.) Walp) using instrumental neutron activation analysis.West Afr J Appl Ecol. (2007) 11:119–23. [Google Scholar]

50. Dakora FD, Belane AK. Evaluation of protein and micronutrient levels in edible cowpea (Vigna Unguiculata L. Walp.) leaves and seeds.Front Sustain Food Syst. (2019) 3:70. 10.3389/fsufs.2019.00070 [CrossRef] [Google Scholar]

51. Sapna C, Chaudhary DP, Dar ZA, Sayyed RZ, El Enshasy HA. Correlation studies among nutritional quality parameters of baby corn.J Sci Ind Res. (2020) 79:804–9. [Google Scholar]

52. Jayathilake C, Visvanathan R, Deen A, Bangamuwage R, Jayawardana BC, Nammi S, et al.Cowpea: An overview on its nutritional facts and health benefits.J Sci Food Agric. (2018) 98:4793–806. 10.1002/jsfa.9074 [PubMed] [CrossRef] [Google Scholar]

53. Enyiukwu DN, Chukwu LA, Bassey IN. Nutrient and anti-nutrient compositions of cowpea (Vigna unguiculata) and mung bean (Vigna radiata) seeds grown in humid Southeast Nigeria: A comparison.Int J Trop Drylands. (2020) 4:41–5. [Google Scholar]

54. Frota KDMG, Lopes LAR, Silva ICV, Arêas JAG. Nutritional quality of the protein of Vigna unguiculata L. Walp and its protein isolate1.Rev Ciência Agronômica. (2017) 48:792–8. 10.5935/1806-6690.20170092 [CrossRef] [Google Scholar]

55. Rodriguez M, Rau D, Bitocchi E, Bellucci E, Biagetti E, Carboni A, et al.Landscape genetics, adaptive diversity, and population structure in Phaseolus vulgaris.New Phytol. (2016) 209:1781–94. 10.1111/nph.13713 [PubMed] [CrossRef] [Google Scholar]

56. Vlasova A, Capella-Gutiérrez S, Rendón-Anaya M, Hernández-Oñate M, Minoche AE, Erb I, et al.Genome and transcriptome analysis of the Mesoamerican common bean and the role of gene duplications in establishing tissue and temporal specialization of genes.Genome Biol. (2016) 17:1–18. 10.1186/s13059-016-0883-6 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

57. Pirman T, Stibilj V, Stekar JM, Combe E. Amino acid composition of beans and lentil.Zb Bioteh Fak Univ Ljubl Kmet Zooteh. (2001) 78:57–68. [Google Scholar]

58. Celmeli T, Sari H, Canci H, Sari D, Adak A, Eker T, et al.The nutritional content of common bean (Phaseolus vulgaris L.) landraces in comparison to modern varieties.Agronomy. (2018) 8:166. [Google Scholar]

59. Nyau V. Nutraceutical perspectives and utilization of common beans (Phaseolus vulgaris L.): A review.Afr J Food Agric Nutr Dev. (2014) 14:9483–96. 10.18697/ajfand.66.12990 [CrossRef] [Google Scholar]

60. Singh N, Narula B, Ujinwal M, Langyan S. Pigeonpea sterility mosaic virus a green plague-Current status of available drug and new potential targets.Ann Proteomics Bioinformatics. (2021) 5:008–026. 10.29328/journal.apb.1001013 [CrossRef] [Google Scholar]

61. Singh N, Rai V, Singh NK. Multi-omics strategies and prospects to enhance seed quality and nutritional traits in pigeonpea.Nucleus. (2020) 63:249–56. 10.1007/s13237-020-00341-0 [CrossRef] [Google Scholar]

62. Ade-Omowaye BIO, Tucker GA, Smetanska I. Nutritional potential of nine underexploited legumes in South west Nigeria.Int Food Res J. (2015) 22:798–806. 10.1080/10408398.2020.1871319 [PubMed] [CrossRef] [Google Scholar]

63. Longvah T, Ananthan R, Bhaskara Chary K, Venkaiah K.Indian food composition tables.New Delhi: ICMR; (2017). [Google Scholar]

64. Devi RR, Premalatha R, Saranya A. Comparative analysis of phytochemical constituents and antibacterial activity of leaf, seed and root extract of Cajanus cajan (L.) Mill sp.Int J Curr Microbiol Appl Sci. (2016) 5:485–94. [Google Scholar]

65. Rani S, Poswal G, Yadav R, Deen MK. Screening of pigeon pea (Cajanus cajan L.) seeds for study of their flavonoids, total phenolic content and antioxidant properties.Int J Pharm Sci Rev Res. (2014) 28:90–4. [Google Scholar]

66. Syed R, Wu Y. A review article on health benefits of Pigeon pea (Cajanus cajan (L.) Millsp).Nutr Res. (2018) 2:15. [Google Scholar]

67. Talari A, Shakappa D. Role of pigeon pea (Cajanus cajan L.) in human nutrition and health: A review.Asian J Dairy Food Res. (2018) 37:212–20. 10.18805/ajdfr.DR-1379 [CrossRef] [Google Scholar]

68. Solomon SG, Okomoda VT, Oda SO. Nutritional value of toasted pigeon pea, Cajanus cajan seed and its utilization in the diet of Clarias gariepinus (Burchell, 1822) fingerlings.Aquac Rep. (2017) 7:34–9. [Google Scholar]

69. Keshav KB. Optimization of high fiber bun formula and its nutritional evaluation.Int J Food Nutr Diet. (2015) 3:89. [Google Scholar]

70. Faridy JCM, Stephanie CGM, Gabriela MMO, Cristian JM. Biological activities of chickpea in human health (Cicer arietinum L.). A review.Plant Foods Hum Nutr. (2020) 75:142–53. 10.1007/s11130-020-00814-2 [PubMed] [CrossRef] [Google Scholar]

71. Ujinwal M, Sahani PA, Singh N. Comparative sequence and structural analysis of lectin protein in chickpea (Cicer arietinum L.) and their relationship with fabaceae family.J Biomed Res Environ Sci. (2019) 5:001–006. [Google Scholar]

72. James AT, Yang A. Interactions of protein content and globulin subunit composition of soybean proteins in relation to tofu gel properties.Food Chem. (2016) 194:284–9. 10.1016/j.foodchem.2015.08.021 [PubMed] [CrossRef] [Google Scholar]

73. Diapari M, Sindhu A, Bett K, Deokar A, Warkentin TD, Tar’an B. Genetic diversity and association mapping of iron and zinc concentrations in chickpea (Cicer arietinum L.).Genome. (2014) 57:459–68. 10.1139/gen-2014-0108 [PubMed] [CrossRef] [Google Scholar]

74. Madurapperumage A, Tang L, Thavarajah P, Bridges W, Shipe E, Vandemark G, et al.Chickpea (Cicer arietinum L.) as a source of essential fatty acids–a biofortification approach.Front Plant Sci. (2021) 12:734980. 10.3389/fpls.2021.734980 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

75. Jukanti AK, Gaur PM, Gowda CLL, Chibbar RN. Nutritional quality and health benefits of chickpea (Cicer arietinum L.): A review.Br J Nutr. (2012) 108:S11–26. [PubMed] [Google Scholar]

76. Yegrem L. Nutritional Composition, Antinutritional Factors, and Utilization Trends of Ethiopian Chickpea (Cicer arietinum L.).Int J Food Sci. (2021) 2021:5570753. 10.1155/2021/5570753 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

77. Barać MB, Pešić MB, Stanojević SP, Kostić AŽ, Èabrilo SB. Techno-functional properties of pea (Pisum sativum) protein isolates: A review.Acta Period Technol. (2015) 46:1–18. 10.2298/APT1546001B [CrossRef] [Google Scholar]

78. Gorissen SH, Crombag JJ, Senden JM, Waterval WH, Bierau J, Verdijk LB, et al.Protein content and amino acid composition of commercially available plant-based protein isolates.Amino Acids. (2018) 50:1685–95. 10.1007/s00726-018-2640-5 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

79. Hall C, Hillen C, Garden Robinson J. Composition, nutritional value, and health benefits of pulses.Cereal Chem. (2017) 94:11–31. 10.1094/CCHEM-03-16-0069-FI [CrossRef] [Google Scholar]

80. Venkidasamy B, Selvaraj D, Nile AS, Ramalingam S, Kai G, Nile SH. Indian pulses: A review on nutritional, functional and biochemical properties with future perspectives.Trends Food Sci Technol. (2019) 88:228–42. 10.1016/j.tifs.2019.03.012 [CrossRef] [Google Scholar]

81. Ganesan K, Xu B. A critical review on phytochemical profile and health promoting effects of mung bean (Vigna radiata).Food Sci Hum Wellness. (2018) 7:11–33. 10.1016/j.fshw.2017.11.002 [CrossRef] [Google Scholar]

82. Kaur C, Singh A, Sethi M, Devi V, Chaudhary DP, Phagna RK, et al.Optimization of protein quality assay in normal, opaque-2, and quality protein maize.Front Sustain Food Syst. (2022) 6:743019. 10.3389/fsufs.2022.743019 [CrossRef] [Google Scholar]

83. Shevkani K, Singh N, Kaur A, Rana JC. Structural and functional characterization of kidney bean and field pea protein isolates: A comparative study.Food Hydrocoll. (2015) 43:679–89. 10.1016/j.foodhyd.2014.07.024 [CrossRef] [Google Scholar]

84. Klupšaitė D, Juodeikienė G. Legume: Composition, protein extraction and functional properties. A review.Chem Technol. (2015) 66:5–12. 10.5755/j01.ct.66.1.12355 [CrossRef] [Google Scholar]

85. Assefa Y, Bajjalieh N, Archontoulis S, Casteel S, Davidson D, Kovács P, et al.Spatial characterization of soybean yield and quality (amino acids, oil, and protein) for United States.Sci Rep. (2018) 8:1–11. 10.1038/s41598-018-32895-0 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

86. Chang YW, Alli I, Konishi Y, Ziomek E. Characterization of protein fractions from chickpea (Cicer arietinum L.) and oat (Avena sativa L.) seeds using proteomic techniques.Food Res Int. (2011) 44:3094–104. [Google Scholar]

87. Shamsi TN, Parveen R, Ahamad S, Fatima S. Structural and biophysical characterization of Cajanus cajan protease inhibitor.J Nat Sci Biol Med. (2017) 8:186. 10.4103/0976-9668.210018 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

88. Fotso M, Azanza JL, Pasquet R, Raymond J. Molecular heterogeneity of cowpea (Vigna unguiculata Fabaceae) seed storage proteins.Plant Syst Evol. (1994) 191:39–56. [Google Scholar]

89. Mohanta TK, Khan A, Hashem A, Abd_Allah EF, Al-Harrasi A. The molecular mass and isoelectric point of plant proteomes.BMC Genomics. (2019) 20:631. 10.1186/s12864-019-5983-8 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

90. Johnston SP, Nickerson MT, Low NH. The physicochemical properties of legume protein isolates and their ability to stabilize oil-in-water emulsions with and without genipin.J Food Sci Technol. (2015) 52:4135–45. 10.1007/s13197-014-1523-3 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

91. Díaz O, Ferreiro T, Rodríguez-Otero JL, Cobos Á. Characterization of chickpea (Cicer arietinum L.) flour films: Effects of pH and plasticizer concentration.Int J Mol Sci. (2019) 20:1246. 10.3390/ijms20051246 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

92. Borsook H, Mac Fadyen DA. The effect of isoelectric amino acids on the ph+ of a phosphate buffer solution: A contribittion in support of the “zwitter ion” hypothesis.J Gen Physiol. (1930) 13:509. 10.1085/jgp.13.5.509 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

93. Olagunju AI, Omoba OS. Pigeon peas possess significant protein and starch fractions with potential as a functional ingredient in food applications. In: Bangar SP, Siroha AK, Kumar M.editors. Handbook of cereals, pulses, roots, and tubers. (Boca Raton, FL: CRC Press; ) (2021). p. 343–56. [Google Scholar]

94. Chel-Guerrero L, Maldonado-Hoil M, Burgos-Pérez A, Castellanos-Ruelas A, Betancur-Ancona D. Functional and some nutritional properties of an isoelectric protein isolate from Mexican cowpea (Vigna unguiculata) seeds.J Food Nutr Res. (2011) 50:210–20. [Google Scholar]

95. Yi-Shen Z, Shuai S, FitzGerald R. Mung bean proteins and peptides: nutritional, functional and bioactive properties.Food Nutr Res. (2018) 15:62. 10.29219/fnr.v62.1290 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

96. Carbonaro M, Maselli P, Nucara A. Structural aspects of legume proteins and nutraceutical properties.Food Res Int. (2015) 76:19–30. [Google Scholar]

97. Raikos V, Campbell L, Euston SR. Rheology and texture of hen’s egg protein heat-set gels as affected by pH and the addition of sugar and/or salt.Food Hydrocoll. (2007) 21:237–44. 10.1016/j.foodhyd.2006.03.015 [CrossRef] [Google Scholar]

98. Ahmed J, Mulla MZ, Siddiq M, Dolan KD. Micromeritic, thermal, dielectric, and microstructural properties of legume ingredients: A review.Legume Sci. (2022) 4:e123. [Google Scholar]

99. Ricci L, Umiltà E, Righetti MC, Messina T, Zurlini C, Montanari A, et al.On the thermal behavior of protein isolated from different legumes investigated by DSC and TGA.J Sci Food Agric. (2018) 98:5368–77. 10.1002/jsfa.9078 [PubMed] [CrossRef] [Google Scholar]

100. Lafarga T, Álvarez C, Villaró S, Bobo G, Aguiló-Aguayo I. Potential of pulse-derived proteins for developing novel vegan edible foams and emulsions.Int J Food Sci Ttechnol. (2020) 55:475–81. 10.1111/ijfs.14286 [CrossRef] [Google Scholar]

101. Ariyarathna IR, Karunaratne DN. Use of chickpea protein for encapsulation of folate to enhance nutritional potency and stability.Food Bioprod Process. (2015) 95:76–82. 10.1016/j.fbp.2015.04.004 [CrossRef] [Google Scholar]

102. Gharibzahedi SMT, Smith B. Legume proteins are smart carriers to encapsulate hydrophilic and hydrophobic bioactive compounds and probiotic bacteria: a review.Compr Rev Food Sci Food Saf. (2021) 20:1250–79. [PubMed] [Google Scholar]

103. Gharibzahedi SMT, Smith B. Legume proteins are smart carriers to encapsulate hydrophilic and hydrophobic bioactive compounds and probiotic bacteria: A review.Compr Rev Food Sci Food Saf. (2021) 20:1250–79. 10.1111/1541-4337.12699 [PubMed] [CrossRef] [Google Scholar]

104. Liu F, Chen Z, Tang C-H. Microencapsulation properties of protein isolates from three selected Phaseolus legumes in comparison with soy protein isolate.Lwt. (2014) 55:74–82. 10.1016/j.lwt.2013.09.008 [CrossRef] [Google Scholar]

105. Zayas JF. Emulsifying properties of proteins.Functionality of Proteins in Food.Berlin: Springer; (1997). p. 134–227. [Google Scholar]

106. Du Sk, Jiang H, Yu X, Jay-lin J. Physicochemical and functional properties of whole legume flour.LWT Food Sci Technol. (2014) 55:308–13. 10.1016/j.lwt.2013.06.001 [CrossRef] [Google Scholar]

107. Al-Ruwaih N, Ahmed J, Mulla MF, Arfat YA. High-pressure assisted enzymatic proteolysis of kidney beans protein isolates and characterization of hydrolysates by functional, structural, rheological and antioxidant properties.Lwt. (2019) 100:231–6. 10.1016/j.lwt.2018.10.074 [CrossRef] [Google Scholar]

108. Wang Y, Wang Y, Li K, Bai Y, Li B, Xu W. Effect of high intensity ultrasound on physicochemical, interfacial and gel properties of chickpea protein isolate.Lwt. (2020) 129:109563. 10.1016/j.lwt.2020.109563 [CrossRef] [Google Scholar]

109. Xu X, Qiao Y, Shi B, Dia VP. Alcalase and bromelain hydrolysis affected physicochemical and functional properties and biological activities of legume proteins.Food Struct. (2021) 27:100178. 10.1016/j.foostr.2021.100178 [CrossRef] [Google Scholar]

110. Langyan S, Yadava P, Sharma S, Gupta NC, Bansal R, Yadav R, et al.Food and nutraceutical functions of Sesame: An underutilized crop for nutritional and health benefits.Food Chem. (2022) 389:132990. 10.1016/j.foodchem.2022.132990 [PubMed] [CrossRef] [Google Scholar]

111. Keskin SO, Ali TM, Ahmed J, Shaikh M, Siddiq M, Uebersax MA. Physico-chemical and functional properties of legume protein, starch, and dietary fiber—A review.Legume Sci. (2022) 4:e117. [Google Scholar]

112. Cargo-Froom C, Shoveller AK, Marinangeli CP, Columbus DA. Methods for processing pulses to optimize nutritional functionality and maximize amino acid availability in foods and feeds.Cereal Foods World. (2020):65. [Google Scholar]

113. Ozyurt VH, Ötles S. Effect of food processing on the physicochemical properties of dietary fibre.Acta Sci Pol Technol Aliment. (2016) 15:233–45. [PubMed] [Google Scholar]

114. Rosenfeld DL, Burrow AL. Vegetarian on purpose: Understanding the motivations of plant-based dieters.Appetite. (2017) 116:456–63. 10.1016/j.appet.2017.05.039 [PubMed] [CrossRef] [Google Scholar]

115. Nosworthy MG, Franczyk AJ, Medina G, Neufeld J, Appah P, Utioh A, et al.Effect of processing on the in Vitro and in Vivo protein quality of yellow and green split peas (Pisum sativum).J Agric Food Chem. (2017) 65:7790–6. [PubMed] [Google Scholar]

116. Nosworthy MG, Medina G, Franczyk AJ, Neufeld J, Appah P, Utioh A, et al.Effect of processing on the in vitro and in vivo protein quality of red and green lentils (Lens culinaris).Food Chem. (2018) 240:588–93. [PubMed] [Google Scholar]

117. Drulyte D, Orlien V. The effect of processing on digestion of legume proteins.Foods. (2019) 8:224. [PMC free article] [PubMed] [Google Scholar]

118. Kaewtapee C, Eklund M, Wiltafsky M, Piepho HP, Mosenthin R, Rosenfelder P. Influence of wet heating and autoclaving on chemical composition and standardized ileal crude protein and amino acid digestibility in full-fat soybeans for pigs.J Anim Sci. (2017) 95:779–88. 10.2527/jas.2016.0932 [PubMed] [CrossRef] [Google Scholar]

119. Frikha M, Valencia DG, de Coca-Sinova A, Lázaro R, Mateos GG. Ileal digestibility of amino acids of unheated and autoclaved pea protein concentrates in broilers.Poult Sci. (2013) 92:1848–57. 10.3382/ps.2013-03007 [PubMed] [CrossRef] [Google Scholar]

120. Mojica L, Chen K, de Mejía EG. Impact of commercial precooking of common bean (Phaseolus vulgaris) on the generation of peptides, after pepsin–pancreatin hydrolysis, capable to inhibit dipeptidyl peptidase-IV.J Food Sci. (2015) 80:H188–98. 10.1111/1750-3841.12726 [PubMed] [CrossRef] [Google Scholar]

121. Da Luz JMR, Paes SA, Torres DP, Nunes MD, da Silva JS, Mantovani HC, et al.Production of edible mushroom and degradation of antinutritional factors in jatropha biodiesel residues.LWT Food Sci Technol. (2013) 50:575–80. [Google Scholar]

122. Hejdysz M, Kaczmarek SA, Rutkowski A. Effect of extrusion on the nutritional value of peas for broiler chickens.Arch Anim Nutr. (2016) 70:364–77. 10.1080/1745039X.2016.1206736 [PubMed] [CrossRef] [Google Scholar]

123. Gilani GS, co*ckell KA, Sepehr E. Effects of antinutritional factors on protein digestibility and amino acid availability in foods.J AOAC Int. (2005) 88:967–87. 10.1093/jaoac/88.3.967 [PubMed] [CrossRef] [Google Scholar]

124. Acquah C, Ohemeng-Boahen G, Power KA, Tosh SM. The effect of processing on bioactive compounds and nutritional qualities of pulses in meeting the sustainable development goal 2.Front Sustain Food Syst. (2021) 5:681662. 10.3389/fsufs.2021.68166 [CrossRef] [Google Scholar]

125. Singh N, Jain N, Kumar R, Jain A, Singh NK, Rai V. A comparative method for protein extraction and 2-D gel electrophoresis from different tissues of Cajanus cajan.Front Plant Sci. (2015) 6:606. 10.3389/fpls.2015.00606 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

126. Moses O, Olawuni I, Iwouno JO. The proximate composition and functional properties of full-fat flour, and protein isolate of lima bean (Phaseolus lunatus).Open Access Sci Rep. (2012) 1:1–5. [Google Scholar]

127. Bayram M, Alameen A. Protein extraction techniques from cereals and legumes.Int Gap Agric Livest Congr. (2018). [Google Scholar]

128. Kenmoe LR, Kotue TC, Chandra K, Djouhou FM, Pieme AC, Kansci G, et al.Albumin and globulin fractions from black bean seeds (Phaseolus vulgaris L.) used in the management of sickle cell disease (SCD) in the west region of Cameroon have antisickling and antioxidant properties.J Biotechnol Biomed. (2020) 3:78–92. [Google Scholar]

129. Willett W, Rockström J, Loken B, Springmann M, Lang T, Vermeulen S, et al.Food in the Anthropocene: The EAT–Lancet Commission on healthy diets from sustainable food systems.Lancet. (2019) 393:447–92. 10.1016/S0140-6736(18)31788-4 [PubMed] [CrossRef] [Google Scholar]

130. Kim BF, Santo RE, Scatterday AP, Fry JP, Synk CM, Cebron SR, et al.Country-specific dietary shifts to mitigate climate and water crises.Glob Environ Change. (2020) 62:101926. 10.1016/j.gloenvcha.2019.05.010 [CrossRef] [Google Scholar]

131. Price RK, Welch RW.Cereal grains. In encyclopedia of human nutrition.3rd ed. Cambridge, MA: Academic Press; (2013). p. 307–16. [Google Scholar]

132. Schlegel K, Sontheimer K, Hickisch A, Wani AA, Eisner P, Schweiggert-Weisz U. Enzymatic hydrolysis of lupin protein isolates—Changes in the molecular weight distribution, techno-functional characteristics, and sensory attributes.Food Sci Nutr. (2019) 7:2747–59. 10.1002/fsn3.1139 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

133. Söderberg J.Functional properties of legume proteins compared to egg proteins and their potential as egg replacers in vegan food.Uppsala: Swedish University of Agricultural Sciences; (2013). [Google Scholar]

134. Erbersdobler HF, Barth CA, Jahreis G. Legumes in human nutrition. Nutrient content and protein quality of pulses.Ernahrungs Umschau. (2017) 64:134–9. [Google Scholar]

135. Carbonaro M, Nucara A. Legume proteins and peptides as compounds in nutraceuticals: A structural basis for dietary health effects.Nutrients. (2022) 14:1188. 10.3390/nu14061188 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

136. Kumar M, Tomar M, Punia S, Dhakane-Lad J, Dhumal S, Changan S, et al.Plant-based proteins and their multifaceted industrial applications.LWT. (2022) 154:112620. 10.1016/j.lwt.2021.112620 [CrossRef] [Google Scholar]

137. Kapoor S. Bioactives and therapeutic potential of legumes: A review.Int J Pharm Biol Sci. (2015) 5:65–74. [Google Scholar]

138. Portari GV, Tavano OL, Silva MAD, Neves VA. Effect of chickpea (Cicer arietinum L.) germination on the major globulin content and in vitro digestibility.Food Sci Technol. (2005) 25:807–12. [Google Scholar]

139. Hirano H. Basic 7S globulin in plants.J Proteomics. (2021) 240:104209. [PubMed] [Google Scholar]

140. Messina MJ. Potential public health implications of the hypocholesterolemic effects of soy protein.Nutrition. (2003) 19:280. 10.1016/S0899-9007(02)00995-4 [PubMed] [CrossRef] [Google Scholar]

141. Wang N, Warkentin TD, Vandenberg B, Bing DJ. Physicochemical properties of starches from various pea and lentil varieties, and characteristics of their noodles prepared by high temperature extrusion.Food Res Int. (2014) 55:119–27. [Google Scholar]

142. Gautam AK, Sharma D, Sharma J, Saini KC. Legume lectins: Potential use as diagnostics and therapeutics against the cancer.Int J Biol Macromol. (2020) 142:474–83. 10.1016/j.ijbiomac.2019.09.119 [PubMed] [CrossRef] [Google Scholar]

143. Kumar S, Kapoor V, Gill K, Singh K, Xess I, Das SN, et al.Antifungal and antiproliferative protein from Cicer arietinum: A bioactive compound against emerging pathogens.BioMed Res Int. (2014) 2014:387203. 10.1155/2014/387203 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

144. Gulzar M, Minnaar A. Underutilized protein resources from African legumes. In: Nadathur SR, Wanasundara JPD, Scanlin L.editors. Sustainable protein sources. (London: Academic Press; ) (2017). p. 197–208. 10.1016/B978-0-12-802778-3.00012-3 [CrossRef] [Google Scholar]

145. Cheng A, Raai MN, Zain NAM, Massawe F, Singh A, Wan WAAQI. In search of alternative proteins: Unlocking the potential of underutilized tropical legumes.Food Security. (2019) 11:1205–15. 10.1007/s12571-019-00977-0 [CrossRef] [Google Scholar]

146. Cullis C, Kunert KJ. Unlocking the potential of orphan legumes.J Exp Bot. (2017) 68:1895–903. 10.12691/jfs-5-5-3 [PubMed] [CrossRef] [Google Scholar]

147. Popoola JO, Obembe OO, Adegbite AE. Cytological studies on some accessions of African yam bean (AYB) (Sphenostylis stenocarpa Hochst. Ex. A. Rich. Harms).Int Res J Plant Sci. (2011) 2:249–53. [Google Scholar]

148. Aliyu S, Massawe F, Mayes S. Beyond landraces: Developing improved germplasm resources for underutilized species–a case for Bambara groundnut.Biotechnol Genet Eng Rev. (2014) 30:127–41. 10.1080/02648725.2014.992625 [PubMed] [CrossRef] [Google Scholar]

149. Yang S, Grall A, Chapman MA. Origin and diversification of winged bean (Psophocarpus tetragonolobus (L.) DC.), a multipurpose underutilized legume.Am J Bot. (2018) 105:888–97. 10.1002/ajb2.1093 [PubMed] [CrossRef] [Google Scholar]

150. Singh V, Goel R, Pande V, Asif MH, Mohanty CS. De novo sequencing and comparative analysis of leaf transcriptomes of diverse condensed tannin-containing lines of underutilized Psophocarpus tetragonolobus (L.) DC.Sci Rep. (2017) 7:1–13. 10.1038/srep44733 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

151. Langyan S, Dar ZA, Chaudhary DP, Shekhar JC, Herlambang S, El-Enshasy H, et al.Analysis of nutritional quality attributes and their inter-relationship in maize inbred lines for sustainable livelihood.Sustainability. (2021) 13:1–12. 10.3390/su131161370 [CrossRef] [Google Scholar]

152. Changan S, Chaudhary DP, Kumar S, Kumar B, Kaul J, Guleria S, et al.Biochemical characterization of elite maize (Zea mays) germplasm for carotenoids composition.Indian J Agric Sci. (2017) 87:46–50. [Google Scholar]

153. Kumar S, Sangwan S, Yadav R, Langyan S, Singh M. Maize carotenoid composition and biofortification for provitamin A activity. In: Chaudhary D, Kumar S, Langyan S.editors. Maize: Nutrition dynamics and novel uses. (New Delhi: Springer; ) (2014). p. 83–91. [Google Scholar]

154. Tan GZ, Das Bhowmik SS, Hoang TM, Karbaschi MR, Johnson AA, Williams B, et al.Finger on the pulse: Pumping iron into chickpea.Front Plant Sci. (2017) 8:1755. 10.3389/fpls.2017.01755 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

155. Foyer CH, Siddique KH, Tai AP, Anders S, Fodor N, Wong FL, et al.Modelling predicts that soybean is poised to dominate crop production across Africa.Plant Cell Environ. (2019) 42:373–85. 10.1111/pce.13466 [PubMed] [CrossRef] [Google Scholar]

156. Ogunsola KE, Ojuederie OB, Emmanuel B. In vitro morphogenic responses of African yam bean (Sphenostylis stenocarpa (Hochst ex. A. Rich.) Harms) accessions to plant growth regulators.Plant Cell Tissue Organ Cult. (2016) 127:613–22. 10.1007/s11240-016-1036-z [CrossRef] [Google Scholar]

157. Popoola J, Ojuederie O, Omonhinmin C, Adegbite A. Neglected and underutilized legume crops: Improvement and future prospects. In: Shah F, Khan Z, Iqbal A, Turan M, Olgun M.editors. Recent advances in grain crops research. (London: Intech Open; ) (2019). 10.1093/aob/mcu024 [CrossRef] [Google Scholar]

158. Grant G, Duncan M, Alonso R, Marzo F.Peas and Lentils. (2003). 10.1016/B0-12-227055-X/00899-3 [CrossRef] [Google Scholar]

159. Brunsgaard G, Kidmose U, Kaack K, Eggum BO. Protein quality and energy density of green peas as influenced by seed size and time of harvest.J Sci Food Agric. (1994) 65:363–70. [Google Scholar]

160. Astawan M, Muchtadi D.Nutritional Contents and Protein Nutritional Value of Local and Imported Soybean Tempe Flours and Their Antioxidant Activities. Scientific Repository. (2014). Available online at: http://repository.ipb.ac.id/handle/123456789/68369 [Google Scholar]

161. Dahiya PK, Linnemann AR, Van Boekel MAJS, Khetarpaul N, Grewal RB, Nout MJR. Mung bean: Technological and nutritional potential.Crit Rev Food Sci Nutr. (2015) 55:670–88. [PubMed] [Google Scholar]

162. Jackson JC. Protein nutritional quality of cowpea and navy bean residue fractions.Afr J Food, Agric Nutr Dev. (2009) 9:764–78. [Google Scholar]

163. Mensa-Wilmot Y, Phillips RD, Hargrove JL. Protein quality evaluation of cowpea-based extrusion cooked cereal/legume weaning mixtures.Nutr Res. (2001) 21:849–57. [Google Scholar]

164. Barampama Z, Simard RE. Nutrient composition, protein quality and antinutritional factors of some varieties of dry beans (Phaseolus vulgaris) grown in Burundi.Food Chem. (1993) 47:159–67. [Google Scholar]

165. Singh U. Protein quality of pigeonpea (Cajanus cajan (L.) Millsp.) as influenced by seed polyphenols and cooking process.Plant Foods Hum Nutr. (1993) 43:171–9. 10.1007/BF01087921 [PubMed] [CrossRef] [Google Scholar]

166. Saxena KB, Vijaya Kumar R, Sultana R. Quality nutrition through pigeonpea—a review.Health. (2010) 2:1335–44. [Google Scholar]

167. Clemente A, Vioque J, Sánchez-Vioque R, Pedroche J, Bautista J, Millán F. Protein quality of chickpea (Cicer arietinum L.) protein hydrolysates.Food Chem. (1999) 67:269–74. [Google Scholar]

168. Reinkensmeier A, Bußler S, Schlüter O, Rohn S, Rawel HM. Characterization of individual proteins in pea protein isolates and air classified samples.Food Res Int. (2015) 76:160–7. [Google Scholar]

169. Lu ZX, He JF, Zhang YC, Bing DJ. Composition, physicochemical properties of pea protein and its application in functional foods.Crit Rev Food Sci Nutr. (2020) 60:2593–605. [PubMed] [Google Scholar]

170. Zhao Y, Tian R, Xu Z, Jiang L, Sui X. Recent advances in soy protein extraction technology.Authorea. (2022). [Google Scholar]

171. Gonçalves FV, Medici LO, Fonseca MPSD, Gaziola SA, Lima GR, Macedo DC, et al.Characterization of the development of cowpea cultivars and of the quantity and quality of proteins in their grains.Pesqui Agropecu Bras. (2020):55–66. [Google Scholar]

172. Yang Y, He S, Zhang Y, Li X, Liu H, Li Q, et al.Comparison of crude prolamins from seven kidney beans (Phaseolus vulgaris L.) based on composition, structure and functionality.Food Chem. (2021) 357:129748. 10.1016/j.foodchem.2021.129748 [PubMed] [CrossRef] [Google Scholar]

173. Oliveira AP, Andrade GF, Mateó BS, Naozuka J. Protein and metalloprotein distribution in different varieties of beans (Phaseolus vulgaris L.): effects of cooking.Int J Food Sci. (2017) 2017:5957178. 10.1155/2017/5957178 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

174. Cheboi JJ, Kinyua MG, Kimurto PK, Kiplagat OK, Ng’an’ga F, Ghimire SR. Biochemical composition of pigeonpea genotypes in Kenya.Aust J Crop Sci. (2019) 13:1848–55. [Google Scholar]

175. Tripathi A, Iswarya V, Rawson A, Singh N, Oomah BD, Patras A. Chemistry of pulses—macronutrients.Pulse Foods.Cambridge, MA: Academic Press; (2021). p. 31–59. [Google Scholar]

176. Saxena KB, Sawargaonkar SL. Genetic enhancement of seed proteins in pigeonpea–methodologies, accomplishments, and opportunities.Int J Sci Res. (2015) 4:03–07. [Google Scholar]

177. Khazaei H, Subedi M, Nickerson M, Martínez-Villaluenga C, Frias J, Vandenberg A. Seed protein of lentils: Current status, progress, and food applications.Foods. (2019) 8:391. 10.3390/foods8090391 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

178. Singh A, Raina SN, Sharma M, Chaudhary M, Sharma S, Rajpal VR. Functional uses of peanut (Arachis hypogaea L.) seed storage proteins.Grain Seed Proteins Funct. (2021). [Google Scholar]

179. Linsberger-Martin G, Weiglhofer K, Phuong TPT, Berghofer E. High hydrostatic pressure influences antinutritional factors and in vitro protein digestibility of split peas and whole white beans.LWT Food Sci Technol. (2017) 51:331–6. [Google Scholar]

180. Rasha Mohamed K, Abou-Arab EA, Gibriel AY, Rasmy NM, Abu-Salem FM. Effect of legume processing treatments individually or in combination on their phytic acid content.Afr J Food Sci Technol. (2011) 2:36–46. [Google Scholar]

181. Pedrosa MM, Guillamón E, Arribas C. Autoclaved and extruded legumes as a source of bioactive phytochemicals: A review.Foods. (2021) 10:379. 10.3390/foods10020379 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

182. Espinosa-Páez E, Alanis-Guzmán MG, Hernández-Luna CE, Báez-González JG, Amaya-Guerra CA, Andrés-Grau AM. Increasing antioxidant activity and protein digestibility in Phaseolus vulgaris and Avena sativa by fermentation with the Pleurotus ostreatus Fungus.Molecules. (2017) 22:2275. 10.3390/molecules22122275 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

183. Rizvi QUEH, Kumar K, Ahmed N, Yadav AN, Chauhan D, Thakur P, et al.Influence of soaking and germination treatments on the nutritional, anti-nutritional, and bioactive composition of pigeon pea (Cajanus cajan L.).J Appl Biol Biotechnol. (2022) 10:1–3. [Google Scholar]

184. Çabuk B, Nosworthy MG, Stone AK, Korber DR, Tanaka T, House JD, et al.Effect of fermentation on the protein digestibility and levels of non-nutritive compounds of pea protein concentrate.Food Technol Biotechnol. (2018) 56:257. 10.17113/ftb.56.02.18.5450 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

185. Kouris-Blazos A, Belski R. Health benefits of legumes and pulses with a focus on Australian sweet lupins.Asia Pacific J Clin Nutr. (2016) 25:1–17. 10.6133/apjcn.2016.25.1.23 [PubMed] [CrossRef] [Google Scholar]

186. Marventano S, Pulido MI, Sanchez-Gonzalez C, Godos J, Speciani A, Galvano F, et al.Legume consumption and CVD risk: A systematic review and meta-analysis.Public Health Nutr. (2017) 20:245–54. 10.1017/S1368980016002299 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

187. Matemu A, Nakamura S, Katayama S. Health benefits of antioxidative peptides derived from legume proteins with a high amino acid score.Antioxidants. (2021) 10:316. 10.3390/antiox10020316 [PMC free article] [PubMed] [CrossRef] [Google Scholar]

188. Rebello CJ, Greenway FL, Finley JW. A review of the nutritional value of legumes and their effects on obesity and its related co-morbidities.Obes Rev. (2014) 15:392–407. 10.1111/obr.12144 [PubMed] [CrossRef] [Google Scholar]

189. Oghbaei M, Prakash J. Effect of primary processing of cereals and legumes on its nutritional quality: A comprehensive review.Cogent Food Agric. (2016) 2:1136015. 10.1111/j.1740-8709.2007.00124.x [PMC free article] [PubMed] [CrossRef] [Google Scholar]

190. Lima AIG, Mota J, Monteiro SAVS, Ferreira RMSB. Legume seeds and colorectal cancer revisited: Protease inhibitors reduce MMP-9 activity and colon cancer cell migration.Food Chemistry (2016) 197(Pt A):30–8. 10.1016/j.foodchem.2015.10.063 [PubMed] [CrossRef] [Google Scholar]

191. Martini D, Godos J, Marventano S, Tieri M, Ghelfi F, Titta L, et al.Nut and legume consumption and human health: An umbrella review of observational studies.Int J Food Sci Nutr. (2021) 72:871–8. 10.1080/09637486.2021.1880554 [PubMed] [CrossRef] [Google Scholar]

192. Ramírez-Jiménez AK, Reynoso-Camacho R, Tejero ME, León-Galván F, Loarca-Piña G. Potential role of bioactive compounds of Phaseolus vulgaris L. on lipid-lowering mechanisms.Food Res Int. (2015) 76:92–104. [Google Scholar]

Articles from Frontiers in Nutrition are provided here courtesy of Frontiers Media SA

Escalate protein plates from legumes for sustainable human nutrition (2024)

FAQs

How do you obtain complete protein when eating legumes? ›

Combining incomplete proteins to form a complete protein

Whole grains with beans (beans and rice; hummus and pita bread; bean-based chili and crackers; refried beans and tortillas) Beans with nuts or seeds (salad with chickpeas and sunflower seeds)

Which legume is the highest in protein? ›

Some legumes with the highest protein content per 100 g serving include :
  • field peas (26 g)
  • cowpeas (24 g)
  • common beans (24 g)
  • mung beans (23 g)
  • pigeon peas (22 g)
  • chickpeas (21 g)
  • soybeans (13 g)

What is the sustainability of legumes? ›

They can be grown in a variety of climates and soil types, and they require less water and fertilizer than other crops, making them a sustainable option for farmers.

What is the role of legumes in human nutrition in functional food improve health through adequate food? ›

The consumption of legumes, as a part of a balanced diet, can bring human health benefits, including a reduced risk of cardiovascular disease (CVD; Marventano et al., 2017) and related CVD issues, like obesity, high blood pressure, type-2 diabetes, dyslipidemia, and stroke (Polak et al., 2015; Becerra-Tomás et al., ...

What to eat with lentils to make a complete protein? ›

Alternatively, a full complement of amino acids can be achieved by pairing lentils with whole grains such as rice or wheat. Lentils are also a great source of fiber, vitamin B1 and folic acid, and are naturally gluten-free.

Can you get enough protein from legumes? ›

Beans and legumes

“Beans and legumes are fiber-rich nutrient powerhouses and an excellent source of protein,” says Hopsecger. “One serving (1/2 cup cooked) of beans provides about 7 grams of protein, the same as 1 ounce of meat.”

What is the most critical plant nutrient in legumes? ›

5.3 Legumes for crop and soil improvement

For most effective yield, plants require a furnish of mineral nutrients, the most essential of which is nitrogen.

What are the best legumes for anti inflammatory? ›

Beans such as chickpeas, black beans, red kidney beans, and lentils are high in fiber and phytonutrients, which reduce inflammation. They are an inexpensive and excellent source of protein, especially for vegetarians or vegans, and they're a low-glycemic carbohydrate. Aim to eat at least one cup of beans twice a week.

Why eliminate legumes? ›

Grains, pseudograins, and legumes are not nutrient-dense foods. They can actually prevent you from absorbing the amino acids you need for a healthy immune system. Even varieties promoted as wheat-free alternatives are just as devoid of nutrients.

Why don't people eat legumes? ›

Antinutrients. Legumes contain compounds that some people refer to as antinutrients. These compounds protect the plant from being eaten by animals or insects and from infections. However, when humans eat foods containing these compounds, they can bind to essential minerals and prevent the body from absorbing them.

What are 3 very important reasons to keep legumes in your diet? ›

They provide fiber, protein, carbohydrate, B vitamins, iron, copper, magnesium, manganese, zinc, and phosphorous. Legumes are naturally low in fat, are practically free of saturated fat, and because they are plant foods, they are cholesterol free as well.

Should you eat legumes every day? ›

Scientific studies have definitively linked a diet high in legumes with a lower risk of developing obesity, diabetes, high blood pressure, high cholesterol, heart disease, or strokes. As a matter of fact, eating legumes every day can effectively treat these diseases in people who already have them.

What nutrients do legumes lack? ›

Legumes contain relatively low quantities of the essential amino acid methionine (which is found in higher amounts in grains).

Are legumes good or bad for you? ›

Legumes are linked to various health benefits. They have an impressive nutritional profile and are one of the best plant-based sources of protein. While they harbor antinutrients, you can use methods like soaking, sprouting, and boiling to reduce their levels of these compounds.

How do you extract protein from legumes? ›

Several methods comprising wet and dry processes are used to extract protein from legumes. Choice of extraction method mainly depends on legume type and desired purity and functionality of extracted protein. Dry processing is suitable for starch-rich legumes, and involves fine milling and air classification.

What to eat with chickpeas for complete protein? ›

You can toss chickpeas with whole grains like farro or barley, or add chickpeas to salads for a plant-based protein boost. Chickpeas also work well in soups, like in the Daily Harvest Tomato + Zucchini Minestrone Soup.

What is the ratio of rice to lentils for complete protein? ›

The content and MA of methionine are low in lentils. However, combination of lentils with rice in a 1:1 ratio can improve the protein quality of lentil-based diets, resulting in increased protein synthesis in young healthy adults.

Top Articles
Latest Posts
Article information

Author: Dean Jakubowski Ret

Last Updated:

Views: 5947

Rating: 5 / 5 (50 voted)

Reviews: 89% of readers found this page helpful

Author information

Name: Dean Jakubowski Ret

Birthday: 1996-05-10

Address: Apt. 425 4346 Santiago Islands, Shariside, AK 38830-1874

Phone: +96313309894162

Job: Legacy Sales Designer

Hobby: Baseball, Wood carving, Candle making, Jigsaw puzzles, Lacemaking, Parkour, Drawing

Introduction: My name is Dean Jakubowski Ret, I am a enthusiastic, friendly, homely, handsome, zealous, brainy, elegant person who loves writing and wants to share my knowledge and understanding with you.