Nutritional Composition, Bioactive Compounds and Functional Evaluation of Various Parts of Cajanus cajan (L.) Millsp

The pigeon pea (Cajanus cajan (L.) Millsp.) is one of the major grain legume crops of the tropical world and recent evidence indicates that it possesses various health benefits. However, to the best of our knowledge, no comparison has been made on the nutritional composition and biological functions of its leaves, seeds, and roots. Therefore, the present study investigates which part of the C. cajan (L.) Millsp plant has the highest potential for development as a health food product. Results show that C. cajan (L.) Millsp roots (CCR) have a higher total polyphenol content (TPC) and total flavonoids flavonoid (TFC) contents than leaves and seeds. The antioxidant, anti-hyperglycemic, and anti-bacterial activities of CCR extracted with hot water (HWCR), 50% ethanol (EECR50), and 95% ethanol (EECR95) were determined. We found that EECR95 had the strongest antioxidant activity, as evaluated by 1,1-Diphenyl-2-picrylhydrazyl radical (DPPH) and 2,2′-azino-bis (3-ethylbenzothiazoline-6-sulfonic acid) (ABTS+) scavenging, and reducing power. EECR95 exhibited higher anti-hyperglycemic ability (inhibition of α-glucosidase and α-amylase activities) and anti-glycation effects (IC50 = 39, 120 and 229 μg/mL, respectively) than HWCR and EECR50. EECR95 also exhibited potent anti-bacterial activities on E. coli, Staphylococcus aureus, Porphyromonas gingivalis, and Streptococcus mutans, with minimum inhibitory concentrations of 113, 180, 16, and 100 μg/mL, respectively. Based on above results, we conclude that CCR has considerable potential for health food development and further studies of CCR in animals to confirm these biological effects and safety issues are warranted.


Introduction
Cajanus cajan (L.) Millsp, known as pigeon pea, is one of the major grain legume crops of the tropical world. Taiwanese aborigines have consumed pigeon pea since ancient times and found that the seeds, leaves, and roots of C. cajan have various functions, such as inhibition of swelling of internal organs, utility in healing wound and cancer therapy [1]. A large number of compounds have been isolated from C. cajan that have excellent biological activities. As a traditional folk medicine, the leaves of C. cajan have been widely used to arrest blood, relieve pain and kill worms [2]. C. cajan leaves are rich in flavonoids, stilbenes, saponin, tannin, reducing sugars, resins and terpenoids which are potentially antioxidant,

Microorganisms and Culture Medium
Staphylococcus aureus (BCRC 10781) and Escherichia coli (BCRC 10316) were purchased from the Food Industry Research & Development Institute (Hsin Chu, Taiwan). They were maintained on an agar slant at 4 • C. Each bacterial strain was subcultured overnight at 35 • C in Mueller-Hilton agar slants. The bacterial growth was harvested using 5 mL of sterile saline water, its absorbance was adjusted at 550 nm and diluted to attain viable cell count of 10 7 CFU/mL using spectrophotometer. Porphyromonas gingivalis (BCRC 14417) and Streptococcus mutans (BCRC 10793), proven cariogenic dental pathogens, were used mainly in this study for minimum inhibitory concentrations (MIC) determination. P. gingivalis were grown in ultrafiltered tryptic soy medium (TSM) (containing 5% defibrinated sheep blood) incubated in the anaerobic jar and the jar was kept in the incubator for 48 h. S. mutans were incubated in brain heart infusion (DIFCO 0418; Becton, Dickinson and Company, Sparks, Maryland, USA) broth at 37 • C with shaking at 200 rpm.

Preparation of Hot Water and Ethanol Extracts of Leaves, Seeds, and Roots from C. cajan
Dried roots, leaf and seeds of C. cajan (Taitung No. 3) were collected from Taitung District  Agricultural Research and Extension Station, Council of Agriculture (Taitung, Taiwan). Leaves, seeds, and roots of C. cajan were rinsed with running water to remove soil. The surface of the leaves, seeds, and roots were sterilized in 75% ethanol for 3 min and then rinsed three times in sterile distilled water; then grind to powder. Dried roots, leaf and seeds of C. cajan (500 g) were extracted with 1:20 ratio (w/v) of 98 ± 2 • C hot water (10 L) for 3 h or extracted with 1:20 ratio 50%, 95% ethanol by soaking in the room temperature for 72 h. After filtering through Whatman No. 2 filter paper, the filtrates were concentrated (10-fold) under reduced pressure and lyophilized to obtain the hot water extracts of leaves, seeds, and roots (HWCL, HWCS, HWCR), 50% ethanol extract of leaves, seeds, and roots (EECL50, EECS50, EECR50).

Determination of Basic Nutritional and Amino Acid Compositions
Nutritional values of leaves, seeds, and roots of C. cajan including moisture, protein, fat, fiber, ash, carbohydrate and mineral (Na, Zn, Mg, Mn, Fe, Cu, Ca) contents were analyzed following the Association of Official Analytical Communities (AOAC; (2000)) guidelines [9]. Amino acid compositions of C. cajan were determined as described in AOAC 994.12 [10].

Determination of Total Phenolic Content (TPC)
TPC was determined by the Folin Ciocalteu method following the literature method of Do et al. [11]. Briefly, 1 mL of extract (100-500 µg/mL) solution was mixed with 2.5 mL of 10% (w/v) Folin-Ciocalteu reagent. After 5 min, 2.0 mL of Na 2 CO 3 (75%) was subsequently added to the mixture and incubated at 50 • C for 10 min with intermittent agitation. Afterwards, the sample was cooled and the absorbance was measured utilizing a UV spectrophotometer (UV-1800, Shimadzu, Kyoto, Japan) at 765 nm against a blank without extract. The TPC value was expressed as micrograms of gallic acid equivalent per gram of extract (mg gallic acid (GAE)/g dry extract).

Determination of Total Flavonoid Content (TFC)
TFC of each extract investigated by using the aluminum chloride colorimetric method described in Do et al. [11] with slight modifications. An aliquot of 1 mL of extract solution (1-500 g/mL) or quercetin (25-200 µg/mL) were mixed with 0.2 mL of 10% (w/v) AlCl 3 solution in methanol, 0.2 mL (1 M) potassium acetate and 5.6 mL distilled water. The mixture was incubated for 30 min at room temperature followed with the measurement of absorbance at 415 nm against the blank. Results were expressed as micrograms of quercetin equivalent per gram of extract (mg Quercetin (QUE)/g dry extract). The radical scavenging activity of the extracts was adopted to measure antioxidant activity using the DPPH method [11]. Briefly, 2 mL of extract solution (1-500 µg/mL) in methanol was added to 2 mL of DPPH (0.1 mM) solution. The mixtures were kept aside in a dark area for 30 min and absorbance was measured at max 517 nm against an equal amount of DPPH and methanol as a blank. The percentage of DPPH scavenging was estimated using the equation (1): where A 0 = absorbance of the control and A 1 = absorbance of the test extracts. The IC 50 value is the half-maximal inhibit concentration as the amount of antioxidant required to decrease the initial DPPH concentration by 50%.

Nitric Oxide (NO) Scavenging Effects Assay
The NO radical scavenging activity was measured applying the method presented in Marcocci et al. [12] with slight modifications. Aliquots of 4 mL of extract solutions (1-500 µg/mL) were added to 1 mL of sodium nitroprusside solution (25 mM) in a test tube and then incubated at 37 • C for 2 h. A 0.5-mL portion of the incubation solution was removed and diluted with 0.3 mL of Griess reagent. The absorbance of the chromophore formed during the diazotization of nitrite with sulfanilamide and subsequent coupling with naphthylethylenediamine dihydrochloride was immediately read at 570 nm and referred to the absorbance of standard solutions of sodium nitrite salt treated in the same way with Griess reagent.

ABTS + Scavenging Effects Assay
The antioxidant capacity was determined by applying a spectrophotometric method described in Jeannine et al. [13]. In this assay, 2,20-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt (ABTS) solution was mixed with potassium persulfate and left in the dark for 12 h before use. Samples (10 µL, concentration of 1-500 µg/mL) were added to the ABTS methanol solution (1 mL) and the absorbance was measured after 6 min. The ABTS radical scavenging ability was calculated with this equation: ((A 0 − A 1 )/A 0 ) × 100, where A 0 is the absorbance of the control and A 1 is the absorbance in the presence of the samples. The IC 50 value was half-maximal inhibit concentration as the amount of antioxidant required to decrease the initial ABTS concentration by 50%.

Ferric Reducing Antioxidant Power (FRAP) Assay
FRAP values of the individual extracts that reflect their antioxidant activity were determined using the modified Fe 3+ to Fe 2+ reduction assay [14]. Briefly, 1 mL of extract solution (1-500 µg/mL) in methanol was added to 2.5 mL of 0.2 M sodium phosphate buffer (pH 6.6) and 2.5 mL of 1% (w/v) potassium ferricyanide (K 3 Fe(CN) 6 ) solution. The mixture was vortexed and incubated at 50 • C for 20 min assisted with a vortex shaker followed by the addition of 2.5 mL 10% (w/v) trichloroacetic acid and centrifugation at 3000 rpm. Finally, 2.5 mL of the supernatant was mixed with 2.5 mL deionized water and 0.5 mL 0.1% (w/v) ferric chloride, and Perl's Prussian blue color was measured at 700 nm against a blank. Increased absorbance of the reaction mixture indicated greater reducing power.

Inhibition of α-Amylase Activity Assay
The assay was done as illustrated by Shu et al. [15] with some modifications. Briefly, 50 µL of sample in 0.02 M phosphate buffer (pH 6.9, containing 0.006 M NaCl) was mixed with 25 µL of α-amylase at a final concentration of 2.5 mU/mL and incubated at 25 • C, 10 min. Then, 50 µL of starch solution (0.5% (w/v), 0.02 M phosphate buffer, pH 6.9, containing 0.006 M NaCl) was added and incubated 10 min, 25 • C. Then, 100 µL 3,5-dinitrosalicylic acid (DNS) color reagent was added to stop the reaction (100 mg DNS dissolved in 3 mL distilled water, to this 3 g KNaC 4 H 4 O 6 ·4H 2 O, and 2 mL of NaOH (2 M) were added; the solution was diluted to 10 mL with distilled water) and immediately kept in water bath 100 • C for 10 min. The absorbance of the resultant solution was taken at 540 nm. The uninhibited enzyme was taken as control. A suitable blank (phosphate buffer and starch solution) was used for all the samples.

Inhibition of α-Glucosidase Activity Assay
The slightly modified method of McCue et al. [16]. In brief, in a 96-well microplate, 50 µL α-glucosidase (1.0 U/mL) in phosphate buffer (0.1 M, pH 6.8) for 10 min at 37 • C was incubated with 50 µL of samples of various concentrations. The reaction was prompted by addition of 50 µL of 5 mM, p-Nitrophenyl-α-D-glucopyranoside in a 0.1 M phosphate buffer at pH 6.8. P-nitrophenol's release kinetics were read with a microplate spectrophotometric reader Multiskan MS™ (Labsystems, Minneapolis, MO, USA) for 5 min at intervals of 30 s and absorbance was measured at 405 nm. The half maximal inhibitory concentration (IC 50 ) of extract was then estimated from the concentration-dependent graph. That is the inhibitor concentration against the percent activity is plotted ((I)-Activity % graph). Using the linear (y = mx + n) equation on this graph for y = 50 value × point becomes the IC 50 value.

Anti-Glycation Assay (Advanced Glycation End Products (AGEs) Formation)
The glycosylation of bovine serum albumin BSA was carried out in accordance with a literature method [17] with some modifications. Extract solution (1-500 µg/mL) was incubated in 10 mg/mL BSA with 1.1 M glucose in 0.1 M phosphate buffer at pH 7.4 containing 0.2% sodium azide at 37 • C for 1, 2, 3, and 4 weeks. The formation of glycated BSA was determined at an excitation wavelength of 355 nm and emission of 460 nm (GENios, TECAN, Neustadt, Germany). Aminoguanidine (AMG) was used as a positive control.

Antimicrobial Activity
The MIC of extracts was determined using a micro dilution method, as described by Song et al. [18]. Inoculum suspensions were prepared from 18 to 24 h broth cultures. Diluted 100 µL suspensions of each bacterial strain were added to 100 µL of various concentrations of extracts diluted with broth to obtain a final bacterial count of approximately 1-1.5 × 10 6 CFU/mL. The final concentrations of extracts ranged from 5 µg/mL to 500 µg/mL in a series of two-fold dilutions. The MIC was defined as the lowest concentration that restricted bacterial growth to an absorbance lower than 0.05 at 550 nm.

Statistical Analysis
All statistical analyses were performed using SPSS for Windows, version 18 (SPSS, Inc., Chicago, IL, USA). Data are expressed as means ± standard deviation (SD) and analyzed using one-way ANOVA followed by Duncan's multiple range test. p < 0.05 is considered statistically significant.

Basic Nutritional Composition of C. cajan
The basic nutritional compositions of leaves, seeds, and roots are presented in Table 1. Moisture, ash, protein, and fat contents of seeds were all higher than those of leaves and roots. Roots have higher carbohydrate content (contained carbohydrate and fiber) (90.3 g/100 g) than leaves and seeds. Sugar was not detected in leaves, seeds, and roots of C. cajan. The seeds and roots contained high amounts of magnesium (138.8, 130.0 mg/100 g) and calcium (581, 597 mg/100 g). Table 1. The basic nutritional composition of leaves, seeds, and roots of C. cajan.

Amino Acid Composition of C. cajan
As the results in Table 2 show, the total amino acid contents of leaves, seeds and roots from C. cajan were 6188.0, 6657.9 and 4452.4 mg/100 g, and their essential amino acid contents were 3467.3, 3696.5 and 2232.8 mg/100g, respectively. It is worth noting that the leaves, seeds and roots of C. cajan contain a high content of branched chain amino acids (BCAA), which are 1334, 1743, and 1146 mg/100 g, respectively.  Table 3 shows that yields of leaves, seeds, and root extracts of C. cajan by hot water were in the range from 8.9-10.2% and by 50% ethanol they were in the range from 4.3-7.2%. The extracts from the roots, seeds and leaves of C. cajan extracted with 50% ethanol contain higher TPC and TFC than its hot water extract. In addition, the contents of hot water and 50% ethanol extracts of roots (HWCR, EECR50) have higher TPC and TFC contents than the other parts of C. cajan. EECR50 had higher TPC and TFC contents than those of HWCR, the TPC and TFC contents of EECR50 were 27.15 mg GAE/g dw and 16.87 mg QUE/g dw, respectively, and the TPC and TFC contents of HWCR were only 16.24 mg GAE/g dw and 7.32 mg QUE/g dw.

Antioxidant Activities of C. cajan Extracts
As the result in Table 4 show, the DPPH scavenging effects of 50% ethanol extracts (EECR, EECS, and EECL) were higher than those of hot water extracts of C. cajan (HWCR, HWCS, and HWCL). EECR had a higher effect in the DPPH assay (IC 50 = 640 µg/mL) than the other extracts. In addition, the inhibitory effect of EECR on NO production in LPS-induced macrophage was also better than that of the EECL and EECS, the IC 50 was 51, 217 and 512 µg/g, respectively (p < 0.05).

The Ccorrelation of Antioxidant Activity and Phenolic Compounds of 50% Ethanol Extracts of Leaves, Seeds, and Roots from C. cajan
The correlations between phenolic compounds and antioxidant activity of EECR are shown in Table 5. The antioxidant activity was high and positive correlation with the content of total phenolic compounds. The correlation coefficients (r values) of TPC and TFC for DPPH free radicals scavenging effects were 0.7411 and 0.6340 r values for NO scavenging effects were 0.6069 and 0.5032, respectively. TPC has higher r values with TPC (0.9345) in 50% ethanol extracts of leaves, seeds, and roots of C. cajan, and DPPH scavenging effects and NO scavenging effects also have a fairly high correlation coefficient (r = 0.9023).

Antioxidant Effects of Hot Water and Ethanol Extracts of C. cajan Roots
In order to further explore the antioxidant effects of hot water and ethanol extract of CCR, DPPH, ABTS + scavenger effects and FRAP were evaluated. Table 6 shows that EECR95 had the best antioxidant activity regardless of the different antioxidant evaluation methods, and the IC 50 of DPPH and ABTS scavenger effects were 460, and 100 µg/mL, which were much better than those of HWCR and EECR50. Besides, EECR95 also had higher reducing power on FRAP assay than that of EECR50 and HWCR, their EC 50 were 929, 1131 and 2159 µg/mL, respectively (p < 0.05).  Table 7 shows the inhibiory effects of hypoglycemic effects of HWCR, EECR50 and EECR95. The results indicated that EECR95 had the best hypoglycemic effects on α-glucosidase and α-amylase activities and anti-glycation effects than EECR50 and EECR95 (IC 50 = 39, 120 and 229 µg/mL, respectively). α-glucosidase and α-amylase activities of EECR95 were even better than acarbose (an inhibitor of α-glucosidase activity in the intestine, which is clinically used for the treatment of diabetes). In addition, the anti-glycation effects of EECR95 also was comparable to the ability of aminoguanidine (AMG, a drug known to inhibit the formation of AGEs) (p < 0.05). 39 ± 2 a 120 ± 12 a 229 ± 12 a 1 Acarbose an inhibitor of α-glucosidase activity in the intestine, which is clinically used for the treatment of diabetes; 2 AMG (Aminoguanidine): A drug known to inhibit the formation of AGEs; 3 HWCR: hot water extracts, EECR50, and EECR95 50% and 95% ethanol extracts of C. cajan roots; 4 Value (means ± SD, n = 3) in each column not sharing the same superscript letter are significant difference (p < 0.05).

Anti-Microbial Effects of Hot Water and Ethanol Extracts of C. cajan Roots
As the results in Table 8 show, HWCR had no antibacterial ability, however, EECR50 and EECR95 have excellent antibacterial effects, among which EECR95 still had the best effect, and it has the best inhibitory effect on P. gingivalis periodonogen (anaerobic culture) (MIC = 16 µg/mL), followed by S. mutans and E. coli (MIC was about 100 and 113 µg/mL, respectively). Even though EECR95 had the lowest anti-microbial effect on S. aureus, its MIC was only about 180 µg/mL (p < 0.05). Table 8. The anti-bacterial growth effects of hot water, 50 and 95% ethanol extracts from C. cajan roots.

Discussion
Cajanus cajan can be planted in arid, poor quality soils, which coupled with its high nutritional value, is of great significance in providing the quality and quantity of human proteins. The literature on the leaves, seeds and roots of C. cajan has demonstrated notable anti-inflammatory, anti-bacterial and abirritative properties [3,19]. Pal et al. [3] have reported the biological activities and medicinal properties of C. cajan. However, there is no nutritional and functional comparison between the leaves, seeds, and roots of C. cajan in the same reaction systems at the same time. Thus, the aim of this study was to understand which part of C. cajan (leaves, seeds, and roots) has more potential for product development. We chose extraction solvents that are usually traditional used and non-toxic-hot water or ethanol-to obtain the C. cajan extracts. Next, we analyzed the basic nutrition, minerals and amino acids composition of the different parts of C. cajan. The anti-oxidant activity of leaves, seeds, and roots of C. cajan was examined. Finally, the best potential extracts were evaluated by antioxidant, hypoglycemic and antibacterial assay methods.
Legumes, a major food of the human diet, may contribute to some of the health benefits associated with this eating pattern. Their health benefits include a low saturated fat content, high content of essential nutrients, richness in important micronutrients (including potassium, magnesium, folate, iron, and zinc) [20] and bioactive compounds [21]. They are responsible for different antioxidant, anticarcinogenic, anti-inflammatory, antidiabetic activities, etc. [21]. Previous studied have reported that sprouts, leaves and seeds of soybean and mung bean contain high amounts of crude proteins, amino acids, lipids and minerals [22][23][24]. They have been shown to possess antioxidant, antimicrobial, anti-inflammatory, antidiabetic and antihypertensive effects [23].
In this study, we found that protein contained in leaves and seeds of C. cajan was about 20%, nearly the same as mung bean (20.97-32.6%) [25], and lower than soybean sprouts (46%) [23]. The nutritional value of C. cajan was assessed base on its amino acid composition. The seeds (beans) contained the highest total amino acid (6657.9 mg/100 g), total essential amino acid (3696.5 mg/100 g) and BCAA contents (3696.5 mg/100g). The human body needs BCAAs to function properly but is unable to make them, so dietary intake is essential (about 35% of the BCAAs in our body are concentrated in muscle tissue). This indicated that seeds of C. cajan are an excellent protein source from legumes.
Dietary fiber (soluble and insoluble) has the ability to lower blood cholesterol, improve glucose tolerance and reduce glycemic response. Mallillin et al. [26] indicated that the dietary fiber content of root crops varied from 4.6 to 13.5 g/100 g and in legumes from 20.9 to 46.9 g/100 g, thus root crops and legumes are good sources of dietary fiber. In particular, the dietary fiber, soluble fiber and insoluble fiber of CCR were 21.8, 2.4 and 19.4 g/100 g, respectively [26]. Brown et al. [27] indicated that soluble fiber can decrease total and LDL cholesterol which is evaluated in 67 controlled trials by meta-analysis. Thus, C. cajan roots may play an important role in cholesterol-lowering effects.
Calcium and magnesium are essential minerals found in the body and play an important physiological role in many of its functions. Magnesium deficiency can cause a variety of pathologies including hypocalcaemia, hypokalemia and cardiac and neurological manifestations. Prolonged magnesium deficiency will cause chronic diseases including diabetes, hypertension, coronary heart disease and osteoporosis [28]. Calcium contributes to bone and teeth health, muscle function, blood clotting, neurotransmission, digestive enzyme; especially it is help bones to develop and grow, keeping the body strong and dense. Legumes contain high levels of calcium and magnesium [19]. Our results also indicated that seeds and roots of C. cajan are rich in calcium (about 600 mg/100g) which is much better than soybean (145 mg/100 g), and the magnesium level (about 140 mg/100 g) is comparable to that of soybean (215 mg/100 g). Thus, C. cajan can contribute to health benefits for hypocalcaemia and magnesium deficiency.
Zhao et al. [29] reported that the phenolic compounds are widely distributed in fruits and vegetables have potential antioxidant activities and free radical-scavenging abilities. In this study we found that CCR contains the most abundant content of TPC and TFC, and TPC and TFC obtained by 50% ethanol extracts is better than that of hot water extracts. Pal et al. [3] reported that the cajaninstilbene acid (3-hydroxy-4-prenylmethoxystilbene-2-carboxylic acid), pinostrobin, vitexin and orientin which were contained in the ethanol extract of C. cajan leaves exhibited the antioxidant activities by scavenging DPPH radicals. Vo et al. [8] also indicated that genistein, genistin and cajanol were the major isoflavonoids responsible for the antioxidant and anti-inflammation activity in CCR. The total polyphenol contents in roots and leaves of Astragalus L. (Fabaceae) (a well-known medicinal legumes) ranged from 4.29-7.89 and 5.01-8.25 mg GAE/g DW [30]. Our results found that the content of polyphenols in roots and leaves of C. cajan are approximately 5-and 2.5-folds that of Astragalus L., respectively.
The correlation between TPC and antioxidant activity is considered the most representative among the bioactive substances with the activity [29]. According to Dancey and Reidy [31], correlation coefficient values of 0.1-0.3 are low, 0.4-0.6 are moderate, and 0.7-1.0 are high. We further analysed the correlation between the hot water and 50% ethanol extracts of roots, seeds, leaves of C. cajan with their corresponding antioxidant effects (DPPH and NO scanvenging effects), and found that their antioxidant activities have a moderate correlation with TPC (r = 0.7411, 0.6069) and TFC (r = 0.6340, 0.5032). Therefore, it is speculated that polyphenols and flavonoids should be the main active compounds of C. cajan.
Plants always have been an exemplary source of drugs because they are rich in bioactive compounds and phytochemicals. Plant polyphenols have gained much attention and popularity because of their multiple functions and minimal side/adverse effects [32]. The antidiabetic effect is one of the most intensely studied biological roles of polyphenols, such as flavonoids, terpenoids, saponins, carotenoids, alkaloids, and glycosides [33,34]. An important strategy to control hyperglycemia is by inhibition of the key carbohydrate-digesting enzymes (α-amylase and α-glucosidase). The inhibitors of these enzymes can delay the digestion of carbohydrates to reduce the rate of glucose absorption from the small intestinal tract, so as to reduce postprandial blood glucose levels. Thus, the inhibition of α-amylase and α-glucosidase activities is a key role to evaluate the anti-diabetic potentials of phytochemicals [35].
AGEs are generated as a result of chronic hyperglycemia. Increasing evidence demonstrates that AGEs play a pivotal role in the development and progression of diabetic vascular damage. An effective approach to prevention and treatment must therefore focus not only on early glycemic control, but also on reducing factors related to oxidative stress, and the dietary intake of exogenous AGEs in particular [36]. Thus, we evaluated the anti-diabetic potential of C. cajan by using the inhibition of the key carbohydrate-digesting enzymes (α-amylase and α-glucosidase) and anti-glycation (AGEs formation) activities. Our results revealed that EECR95 exhibited the strongest hypoglycemic effects by inhibition the carbohydrate-digesting enzymes (α-glucosidase, α-amylase) (IC 50 = 39 and 120 µg/mL) which were much better than that of acarbose (IC 50 = 303 and 970 µg/mL), and anti-glycation effects which were approximately equal to that of aminoguanidine (220 µg/mL). Besides, the other C. cajan extracts (EECR50 and HWCR) also present good hypoglycemic potential. Nahar et al. [37] indicated that methanolic extract of CCR had anti-diabetic potential which decreased the blood glucose level in alloxan-induced diabetic mice. They also indicated that the hypoglycemic and antioxidant activity might be closely related with the polyphenolic compounds in methanolic extract of CCR.
In traditional medicine, phytochemicals found in plant extracts have led to the discovery of novel and effective antimicrobial agents. Many studies have pointed out that flavonoids (quercetin, genistein, cajanol etc.) and gallic acid, caffeic acid, etc. have the ability to inhibit the growth of bacteria (such as E. coli, S. aureus) [38,39]. Adamczak et al. [40] also reported that the amount of antibacterial ability in plant extracts is related to the TFC. The present results indicated that EECR95 not only had the most potent antibacterial potential (against P. gingivalis, S. mutans, E. coli, and S. aureus) but also the highest TPC and TFC than other extracts of CR. Thus, it indicated that TPC and TFC are indeed the main active components in the CR.

Conclusions
In summary, the seeds have the best nutritional properties, such as protein, ash and minerals (calcium, magnesium and iron) than the leaves and roots of C. cajan. In addition, the seeds contain a relatively high level of essential amino acids and BCAAs, both of which are even higher than in soybeans. The antioxidant activity of C. cajan roots is better than that of seeds and leaves. Furthermore, the antioxidant, hypoglycemic and antibacterial effects of EECR95 are superior to those of HWCR andEECR50, and these effects should be related to TPC and TFC in EECR95.

Conflicts of Interest:
The authors declare no conflict of interest.