Abstract:The Brazilian Cerrado presents a wide variety of natural products, including the Pequi (Caryocar brasiliense). The important factor that determines the dietary and nutritional ideality of protein is degestitibility. This work aims to evaluate the protein digestibility of Pequi seeds and the presence of anti-nutritional factors. The protein Pequi almonds were extracted, toasted and untoasted. Evaluation digestibility was structurally characterized by SDS-PAGE 15%, which can be used to analyze simulated gastric … Show more
“…Therefore, the in vitro digestion simulation experiment of the Zihua snap bean lectin was studied. SDS–PAGE has been widely used in simulated gastric fluid (SGF) analysis and simulated intestinal fluid (SIF) analysis [45]. SDS–PAGE analyses of native lectin from the Zihua snap bean in SGF and SIF are shown in Figure 10.…”
A two-step method based on an aqueous two-phase system and Sephadex G-75 was used to separate and purify lectin from the seeds of the Zihua snap bean. The preliminary properties and bioactivity of the Zihua snap bean lectin were characterized by different instrumental methods, such as sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS–PAGE), liquid chromatography-nano electrospray ionization mass spectrometry (Nano LC-ESI-MS/MS), and Fourier transform infrared spectroscopy (FTIR). The hemagglutinating activity of the Zihua snap bean lectin could not be inhibited by glucose, N-acetyl-d-glucosamine, d-galactose, N-acetyl-d-galactosamine, fructose, sucrose, d-maltose, d-trehalose, and lactose. It was found that the hemagglutinating activity of the lectin showed strong dependence on Mn2+ and Ca2+. The thermal and pH stability of the Zihua snap bean lectin was studied by FTIR and fluorescence spectroscopy. Relatively good stability was observed when the temperature was not higher than 70 °C, as well as in the pH range of 2.0 to 10.0. Digestive stability in vitro was investigated. The untreated lectin was relatively stable to pepsin and trypsin activity, but heat treatment could significantly reduce the digestive stability in vitro. Moreover, the lectin showed an inhibitory effect on the tested bacteria (Staphylococcus aureus (S. aureus), Escherichia coli (E. coli), Bacillus subtilis (B. subtilis)), and it also showed a certain inhibitory effect on the growth of Phytophthora infestans (P. infestans) at higher concentrations.
“…Therefore, the in vitro digestion simulation experiment of the Zihua snap bean lectin was studied. SDS–PAGE has been widely used in simulated gastric fluid (SGF) analysis and simulated intestinal fluid (SIF) analysis [45]. SDS–PAGE analyses of native lectin from the Zihua snap bean in SGF and SIF are shown in Figure 10.…”
A two-step method based on an aqueous two-phase system and Sephadex G-75 was used to separate and purify lectin from the seeds of the Zihua snap bean. The preliminary properties and bioactivity of the Zihua snap bean lectin were characterized by different instrumental methods, such as sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS–PAGE), liquid chromatography-nano electrospray ionization mass spectrometry (Nano LC-ESI-MS/MS), and Fourier transform infrared spectroscopy (FTIR). The hemagglutinating activity of the Zihua snap bean lectin could not be inhibited by glucose, N-acetyl-d-glucosamine, d-galactose, N-acetyl-d-galactosamine, fructose, sucrose, d-maltose, d-trehalose, and lactose. It was found that the hemagglutinating activity of the lectin showed strong dependence on Mn2+ and Ca2+. The thermal and pH stability of the Zihua snap bean lectin was studied by FTIR and fluorescence spectroscopy. Relatively good stability was observed when the temperature was not higher than 70 °C, as well as in the pH range of 2.0 to 10.0. Digestive stability in vitro was investigated. The untreated lectin was relatively stable to pepsin and trypsin activity, but heat treatment could significantly reduce the digestive stability in vitro. Moreover, the lectin showed an inhibitory effect on the tested bacteria (Staphylococcus aureus (S. aureus), Escherichia coli (E. coli), Bacillus subtilis (B. subtilis)), and it also showed a certain inhibitory effect on the growth of Phytophthora infestans (P. infestans) at higher concentrations.
“…Hossain;Becker (2001) report the presence of these antinutritional factors in S. aculeata, S. rostrata and S. sesban seeds, but its contents are very low. Although, when isolated, these antinutritional factors have biological relevance, its absence in S. virgata seed is an interesting finding, because lectins and trypsin inhibitors generally do not degrade easily in the gastrointestinal tract and can be complexed with digestive enzymes, interfering in the nutrient absorption (SILVESTRINI et al, 2017). Additionally, the acceptability and use of legumes seeds have been affected by the presence of these antinutritional factors, which reduce the bioavailability nutrients (SHARAN et al, 2021).…”
Sesbania virgata (Cav.) Pers. is a Pantropical legume (Fabaceae) able to colonize riverbanks in Brazilian semiarid regions, commonly used to recover degraded soils. Although its seeds have high nutritional value, are little explored for biotechnological and biological applications. In order to begin to fill the void existing in this theme, the present research described the nutritional composition of the S. virgata seeds, in addition to its antioxidant and antimicrobial activities. The energy value of S. virgata seeds was 366.6 kcal 100g-1, and among the investigated macronutrients, the protein content stands out (60.8%). However, the carbohydrate and crude fat contents are also promising, highlighting the abundance in polyunsaturated fatty acids, especially linoleic acid and linolenic acid. S. virgata seeds are an excellent source of essential (leucine, lysine and valine) and non-essential amino acids (glutamic acid, aspartic acid and arginine). Under the assay conditions, lectins and trypsin inhibitors were not demarcated. Additionally, S. virgata seeds confer antifungal activity against Candida albicans, Candida tropicalis, Aspergillus flavus and Penicillium citrinum, and antioxidant activity, for ABTS•+ and DPPH• scavenging methods. In view of these findings, the nutritional composition of S. virgata seeds encourages its use as natural source of functional products, and its biological activities stimulate its biotechnological and pharmacological application as exogenous antifungal and antioxidant agent.
“…Previous studies showed that Burkina Faso cowpea cultivars are rich in mineral elements (Fe, Zn, Mg, Ca, Se, K, Na), phenolic compounds and have significant antioxidant and anti-lipid peroxidation activities [5,6]. Legumes also contain antinutritional factors like saponin, heamaglutinin, cyanogenic glycoside, phytic acid, tannin, trypsin and chymotrypsin inhibitors that may reduce the bioavailability of nutrients and also cause harmful effects to human health [7,8]. Storage organs of plant such as seeds, tubers and also leaves, flowers, and fruits contain different types of protease inhibitors (PIs) which is able to inhibit some enzymes like trypsin, pepsin and chymotrypsin [9,10,7,11].…”
Section: Introductionmentioning
confidence: 99%
“…Legumes also contain antinutritional factors like saponin, heamaglutinin, cyanogenic glycoside, phytic acid, tannin, trypsin and chymotrypsin inhibitors that may reduce the bioavailability of nutrients and also cause harmful effects to human health [7,8]. Storage organs of plant such as seeds, tubers and also leaves, flowers, and fruits contain different types of protease inhibitors (PIs) which is able to inhibit some enzymes like trypsin, pepsin and chymotrypsin [9,10,7,11]. PIs are small proteins or peptides that inhibit the catalytic action of proteases by forming stoichiometric and stable complexes with their proteolytic enzymes blocking or altering the active site [11][12][13].…”
Cowpea is an important protein crop widespread in Africa. The purpose of this research was to determine the content of trypsin and chymotrypsin inhibitors in different genotypes of cowpea seeds. Trypsin percentage inhibition showed about 13.5-fold variation (5.12% ± 1.47 to 70.52% ± 6.58) between the cowpea genotypes respectively for KVx 421-2J and Kondèsyoungo local. The chymotrypsin inhibitory activity varies among cowpea genotypes from 21.19 to 76.94%. The highest percent inhibitory activity was exhibited by KVx 396-4-5-2D on chymotrypsin. This study also showed significant correlations between type of cowpea genotype and trypsin inhibition potential and also between colour and chymotrypsin inhibition potential of cowpea seeds. Kondèsyoungo local, a landraceae genotype exhibited the high potential to inhibit the trypsin enzyme. Coloured seeds of cowpea genotypes possess higher percentage inhibition of chymotrypsin than the colourless ones (p < 0.05). The calculated mean of trypsin and chymotrypsin inhibition activities showed that Labagela local genotype possess the highest inhibition activity of both protease enzymes. The PCA components analysis and the dendrogram performed basis on the protease inhibitory activities divided the thirty-one genotypes of cowpea used in this study into three classes. The results presented in this work can contribute greatly to the planning of a cowpea breeding program aimed at reducing the content of proteases inhibitors in order to improve the nutritional value of seeds or to increase PI content for tolerance to stored grain pests.
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