Antioxidant indices and amino acid composition of phenolic containing Lima beans (Phaseolus lunatus) after simulated human gastrointestinal digestion

Sule O. Salawu ,
Sule O. Salawu
Contact Sule O. Salawu

Department of Biochemistry, Federal University of Technology, Akure, Nigeria

Department of Biochemistry, Osun State University, Osogbo, Nigeria

Oluwaseun M. Folorunso ,
Oluwaseun M. Folorunso

Department of Biochemistry, Federal University of Technology, Akure, Nigeria

Akintunde A. Akindahunsi ,
Akintunde A. Akindahunsi

Department of Biochemistry, Federal University of Technology, Akure, Nigeria

Aline A. Boligon
Aline A. Boligon

Departamento de Farm´acia Industrial, Centro de Ciˆencias da Sa´ude, Universidade Federal de Santa Maria, Santa Maria, Brazil

Published: 18.04.2019.

Volume 8, Issue 1 (2019)

pp. 97-110;

https://doi.org/10.7455/ijfs/8.1.2019.a9

Abstract

The present investigation was designed to characterize the phenolic profile of Lima beans (Phaseolus Lunatus) and also to evaluate the antioxidant indices: total phenolic content (TPC), total flavonoid content (TFC), ferric reducing antioxidant power (FRAP), 2,2-Diphenyl-1-picrylhydrazyl (DPPH) radical scavenging activity and amino acid composition at different stages of simulated gastrointestinal digestion (oral, gastric, intestinal). High Performance Liquid Chromatography (HPLC-DAD) analysis revealed the presence of some phenolic compounds (gallic acid, catechin, caffeic acid, rutin, quercitrin, quercetin, kaempferol and apigenin), with a reduced amount (mg/g) after cooking: gallic acid (raw: 1.96 ± 0.02; cooked: 1.82 ± 0.01); catechin (raw: 0.83 ± 0.01; cooked: 0.73 ± 0.01); rutin (raw: 2.61 ± 0.03; cooked:1.74 ± 0.03); quercitrin (raw: 5.73 ± 0.01; cooked: 5.68 ± 0.01); apigenin (raw: 2.09 ± 0.01; cooked: 1.79 ± 0.02), with exception of quercetin (raw: 2.11 ± 0.02; cooked: 5.73 ± 0.02) and caffeic acid (raw: 2.08±0.04; cooked 2.95 ± 0.04). The results of the antioxidant indices of in vitro enzyme digested lima beans revealed higher values for cooked Lima beans compared to the raw counterpart, with a stepwise increase at the different stages of in vitro digestion, with the exception of ferric reducing antioxidant power; TPC (oral digestion: 65.44 ± 0.96; gastric digestion:134.87 ± 0.46; intestinal digestion: 517.72 ± 4.70; mg/g tannic acid equivalent), TFC (oral digestion: 199.30 ± 6.43; gastric digestion: 1065.97± 1.22; intestinal digestion: 3691.87 ± 4.2; mg/g quercetin equivalent), DPPH (oral digestion: 85800.00 ± 305.50; gastric digestion: 99066.66 ± 115.47; intestinal digestion: 211354.20 ± 360.84; µmol TE/g sample). The results also revealed a progressive increase in the antioxidant indices and amino acid composition (mg/kg) for both raw and processed lima beans at various stages of the in vitro digestion, with the intestinal phase of simulated digestion ranking higher. This implied that the Lima beans contained some essential amino acids and antioxidant molecules that would be readily available after passing through the gastrointestinal tract and could therefore be explored as functional food in the management of free radical mediated diseases.

Keywords

References

1.
Akond A, Khandaker L, Berthold J, Gates L, Peters K, Delong H, et al. Anthocyanin, total polyphenols and antioxidant activity of common bean. American Journal of Food Technology. 2011. p. 385–94.
2.
Attree R, Du B, Xu B. Distribution of phenolic compounds in seed coat and cotyledon, and their contribution to antioxidant capacities of red and black seed coat peanuts (arachis hypogaea l.) Industrial Crops and Products. 2015. p. 448–56.
3.
Babatunde R, Adejobi A, Fakayode S. Income and calorie intake among farming households in rural Nigeria: results of parametric and nonparametric analysis. Journal of Agricultural Science. 2010. p. 135.
4.
Bain L, Awah P, Geraldine N, Kindong N, Siga Y, Bernard N, et al. Malnutrition in Sub-Saharan Africa: burden, causes and prospects. Pan African Medical Journal. 2013.
5.
Baldermann S, Blagojevic L, Frede K, Klopsch R, Neugart S, Neumann A.
6.
Schreiner M. Are neglected plants the food for the future? Critical Reviews in Plant Sciences. 2016. p. 106–19.
7.
Boligon A, Piana M, Kubica T, Mario D, Dalmolin T, Bonez P, et al. HPLC analysis and antimicrobial, antimycobacterial and antiviral activities of Tabernaemontana catharinensis A. DC. Journal of Applied Biomedicine. 2015. p. 7–18.
8.
Bouayed J, Hoffmann L, Bohn T. Total phenolics, flavonoids, anthocyanins and antioxidant activity following simulated gastro-intestinal digestion and dialysis of apple varieties: Bioaccessibility and potential uptake. Food Chemistry. 2011. p. 14–21.
9.
Brand-Williams W, Cuvelier M, Berset C. Food Science and Technology-lebensmittelwissenschaft & Technologie. 1995. p. 25–30.
10.
Brand T, Brandt D, Cruywagen C. Chemical composition, true metabolisable energy content and amino acid availability of grain legumes for poultry. South African Journal of Animal Science. 2004. p. 116–22.
11.
Delgado-Andrade C, Conde-Aguilera A, Haro J, Pastoriza De La Cueva A, Angel Rufian-Henares S, J. A combined procedure to evaluate the global antioxidant response of bread. Journal of Cereal Science. 2010. p. 239–46.
12.
Escarpa A, Gonzalez M. Identification and quantitation of phenolics from green beans by high-performance liquid chromatography. Chromatographia. 2000. p. 33–8.
13.
Faller A, Fialho E, Liu R. Cellular antioxidant activity of feijoada whole meal coupled with an in vitro diges-tion. Journal of agricultural and food chemistry. 2012. p. 4826–32.
14.
Fanzo J. Global Food Security-agriculture Policy Economics and Environment. 2015. p. 15–23.
15.
Fao. Women, men and nutrition. 2011.
16.
Gimenez B, Moreno S, Lopez-Caballero M, Montero P, Gomez-Guillen M. Antioxidant properties of green tea extract incorporated to fish gelatin films after simulated gastrointestinal enzymatic digestion. LWT -Food Science and Technology. 2013. p. 445–51.
17.
Gujral H, Angurala M, Sharma P, Singh J. Phenolic content and antioxidant activity of germinated and cooked pulses. International Journal of Food Properties. 2011. p. 1366–74.
18.
Han S, Xu B. Bioactive components of leafy vegetable edible amaranth (Amaranthus mangostanus l.) as affected by home cooking manners. American Journal of Food Science and Technology. 2014. p. 122–7.
19.
Huang WY, Cai YZ, Zhang Y. Natural phenolic compounds from medicinal herbs and dietary plants: Potential use for cancer prevention. Nutrition and Cancer-an International Journal. 2010. p. 1–20.
20.
Iriti M, Varoni E. Pulses, healthy, and sustainable food sources for feeding the planet. International Journal of Molecular Sciences. 2017.
21.
Jeong S, Kim S, Kim D, Jo S, Nam K, Ahn D, et al. Effect of heat treatment on the antioxidant activity of extracts from citrus peels. Journal of Agricultural and Food Chemistry. 2004. p. 3389–93.
22.
Jin B, Zhou X, Li B, Lai W, Li X. Influence of in vitro digestion on antioxidative activity of coconut meat protein hydrolysates. Tropical Journal of Pharmaceutical Research. 2015. p. 441–7.
23.
Joseph O, Phelomene M, Helene N, Valens H, Patrick O, Thavarajah D, et al. Phenolic compound profiles of two common beans consumed by rwandans. American Journal of Plant Sciences. 2014. p. 2943–7.
24.
Karamac M, Amarowicz R. Antioxidant activity of phenolic fractions of white bean (phaseolus vulgaris). Journal of Food Lipids. 2004. p. 165–77.
25.
Khang D, Dung T, Elzaawely A, Xuan T. Phenolic profiles and antioxidant activity of germinated legumes. Foods. 2016.
26.
Lisanti A, Formica V, Ianni F, Albertini B, Marinozzi M, Sardella R, et al. Antioxidant activity of phenolic extracts from different cultivars of italian onion (Allium cepa) and relative human immune cell proliferative induction. Pharmaceutical Biology. 2016. p. 799–806.
27.
Lombardi-Boccia G, Schlemmer U, Cappelloni M, Di Lullo G. The inhibitory effect of albumin extracts from white beans (phaseolus vulgaris l.) on in vitro iron and zinc dialysability: Role of phytic acid. Food Chemistry. 1998. p. 1–7.
28.
Luthria D, Pastor-Corrales M. Phenolic acids content of fifteen dry edible bean (phaseolus vulgaris l.) varieties. Journal of Food Composition and Analysis. 2006. p. 205–11.
29.
Meda A, Lamien C, Romito M, Millogo J, Nacoulma O. Determination of the total phenolic, flavonoid and proline contents in burkina fasan honey, as well as their radical scavenging activity. IJFS April. 2005. p. 97–110.
30.
Food Chemistry. p. 571–7.
31.
Miguel M. Antioxidant activity of medicinal and aromatic plants. a review. Flavour and Fragrance Journal. 2010. p. 291–312.
32.
Mole S, Waterman S. Analysis of phenolic plant metabolites. Blackwell Scientific Publications; 1994.
33.
Nyau V, Prakash S, Rodrigues J, Farrant J. Antioxidant activities of bambara groundnuts as assessed by frap and dpph assays. American Journal of Food and Nutrition. 2015. p. 7–11.
34.
Oboh G, Ademiluyi A, Akindahunsi A. Changes in polyphenols distribution and antioxidant activity during fermentation of some underutilized legumes. Food Science and Technology International. 2009. p. 41–6.
35.
Obreshkova D, Tsvetkova D, Ivanov K. Simultaneous identification and determination of total content of aminoacids in food supplements-tablets by gas chromatography. 2012. p. 57–68.
36.
Oluwaniyi O, Dosumu O, Awolola G. Effect of local processing methods (boiling, frying and roasting) on the amino acid composition of four marine fishes commonly consumed in nigeria. Food Chemistry. 2010. p. 1000–6.
37.
Omoba O, Obafaye R, Salawu S, Boligon A, Athayde M. Hplc-dad phenolic characterization and antioxidant activities of ripe and unripe sweet orange peels. Antioxidants. 2015. p. 498–512.
38.
Oomah B, Tiger N, Olson M, Balasubramanian P. Phenolics and antioxidative activities in narrow-leafed lupins (lupinus angustifolius l.) Plant Foods for Human Nutrition. 2006. p. 91–7.
39.
Oyaizu M. Studies on products of browning reaction: Antioxidative activity of products of browning reaction prepared from glucosamine. Japanese Journal of Nutrition. 1986. p. 307–16.
40.
Ozcan T, Yilmaz-Ersan A, Delikanli L, B. Phenolics in human health. 2014. p. 393–6.
41.
Pastor-Cavada E, Juan R, Pastor J, Alaiz M, Vioque J. = true & AuthType = ip. Journal of Botany. 2016. p. 1–6.
42.
Rahman M, Khan F, Das R, Hossain M. Antioxidant activity and total phenolic content of some indigenous fruits of bangladesh. International Food Research Journal. 2016. p. 2399–404.
43.
Reyes-Martinez A, Almaraz-Abarca N, Gallardo-Velazquez T, Del S, Gonzalez-Elizondo M, Herrera-Arrieta Y, et al. Evaluation of foliar phenols of 25 mexican varieties of common bean (phaseolus vulgaris l.) as antioxidants and varietal markers. Natural Product Research. 2014. p. 2158–62.
44.
Ryan L, Prescott S. Stability of the antioxidant activity of twenty-five commercially available fruit juices subjected to an in vitro digestion. International Journal of Food Science & Technology. 2010. p. 1191–7.
45.
Sadeghi Z, Valizadeh J, Shermeh O, Akaberi M. Antioxidant activity and total phenolic content of boerhavia elegans (choisy) grown in baluchestan, iran. Avicenna Journal of Phytomedicine. 2015. p. 1–9.
46.
Salawu S, Bester M, Duodu K. Phenolic composition and bioactive properties of cell wall preparations and whole grains of selected cereals and legumes. Journal of Food Biochemistry. 2014. p. 62–72.
47.
Salawu S, Innocenti M, Giaccherini C, Akindahunsi A, Mulinacci N. Phenolic profiles of four processed tropical green leafy vegetables commonly used as food. Natural Product Communications. 2008. p. 2043–8.
48.
Saleem Z, Ahmed S, Hasan M. Phaseolus lunatus linn: Botany, medicinal uses, phytochemistry and pharmacology. World Journal of Pharmacy and Pharmaceutical Sciences. 2016. p. 87–93.
49.
Scalbert A, Manach C, Morand C, Remesy C, Jimenez L. Dietary polyphenols and the prevention of diseases. Critical Reviews in Food Science and Nutrition. 2005. p. 287–306.
50.
Tagliazucchi D, Verzelloni E, Bertolini D, Conte A. In vitro bio-accessibility and antioxidant activity of grape polyphenols. Food Chemistry. 2010. p. 599–606.
51.
Tavares L, Figueira I, Macedo D, Mcdougall G, Leirao M, Vieira H, et al. Neuroprotective effect of blackberry (rubus sp.) polyphenols is potentiated after simulated gastrointestinal digestion. Food Chemistry. 2012. p. 1443–52.
52.
Trehan I, Manary M. Management of severe acute malnutrition in low-income and middle-income countries. Archives of Disease in Childhood. 2015. p. 283–7.
53.
Wootton-Beard P, Moran A, Ryan L. Stability of the total antioxidant capacity and total polyphenol content of 23 commercially available vegetable juices before and after in vitro digestion measured by frap, dpph, abts and folin-ciocalteu methods. Food Research International. 2011. p. 217–24.
54.
Yellavila S, Agbenorhevi J, Asibuo J, Sampson G. Proximate composition, minerals content and functional properties of five lima bean accessions. Journal of Food Security. 2015.
55.
Zou Y, Chang S, Gu Y, Qian S. Antioxidant activity and phenolic compositions of lentil (lens culinaris var. morton) extract and its fractions. Journal of Agricultural and Food Chemistry. 2011. p. 2268–76.

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