Laboratory of Food Technology, School of Chemistry and Food, Federal University of Rio Grande, Av. Italy 8 km, Carreiros, Rio Grande, RS, 96203-900, Brazil.
Faculty of Public Health, University of São Paulo, Av. Dr. Arnaldo, 715, São Paulo, SP, 01246-904, Brazil.
Plant Foods Hum Nutr. 2018 Jun;73(2):101-107. doi: 10.1007/s11130-018-0668-z.
In previous studies, it has not been reported that protein isolated from chia interferes favorably with antibacterial activity, and reduces cholesterol synthesis. The objective of this study was to determine whether commonly used commercial microbial proteases can be utilized to generate chia protein-based antibacterial and hypocholesterolemic hydrolysates/peptides, considering the effects of protein extraction method. Alcalase, Flavourzyme and sequential Alcalase-Flavourzyme were used to produce hydrolysates from chia protein (CF), protein-rich fraction (PRF) and chia protein concentrates (CPC1 and CPC2). These hydrolysates were evaluated for their antimicrobial activity against Gram-positive (G) and Gram-negative (G) microorganisms. The protein hydrolysates were purified by ultrafiltration through a membrane with 3 kDa nominal molecular weight, for evaluation of hypocholesterolemic activity. An inhibition zone was observed when the hydrolysate was tested against S. aureus, and minimal inhibitory concentration (MIC) and minimal bactericidal concentration (MBC) values were obtained. Peptides from chia protein with molecular mass lower than 3 kDa reduced up to 80.7% of 3-hydroxy-3-methylglutaryl coenzyme A reductase (HMG-CoA reductase) enzymatic reaction velocity. It was also observed that, independent of the method used to obtain chia proteins, the fractions showed relevant bioactivity. Moreover, the intensity of the bioactivity varied with the method for obtaining the protein and with the enzyme used in the hydrolysis process. This is the first report to demonstrate that chia peptides are able to inhibit cholesterol homeostasis.
在以前的研究中,尚未有报道称从奇亚中分离出的蛋白质会对抑制抗菌活性和降低胆固醇合成产生有利影响。本研究的目的是确定常用的商业微生物蛋白酶是否可用于生成基于奇亚蛋白的具有抗菌和降胆固醇作用的水解产物/肽,同时考虑蛋白质提取方法的影响。使用碱性蛋白酶、风味蛋白酶和顺序碱性蛋白酶-风味蛋白酶从奇亚蛋白(CF)、富含蛋白质的部分(PRF)和奇亚蛋白浓缩物(CPC1 和 CPC2)中生产水解产物。这些水解产物被评估了其对革兰氏阳性(G)和革兰氏阴性(G)微生物的抗菌活性。通过超滤将蛋白质水解产物通过 3 kDa 名义分子量的膜进行纯化,以评估降胆固醇活性。当水解产物被测试对金黄色葡萄球菌时,观察到抑菌圈,并且获得了最小抑菌浓度(MIC)和最小杀菌浓度(MBC)值。分子量低于 3 kDa 的奇亚蛋白肽可降低高达 3-羟基-3-甲基戊二酰辅酶 A 还原酶(HMG-CoA 还原酶)酶促反应速度的 80.7%。还观察到,无论使用何种方法获得奇亚蛋白,各部分都表现出相关的生物活性。此外,生物活性的强度随获得蛋白质的方法和水解过程中使用的酶而变化。这是首次报道表明奇亚肽能够抑制胆固醇稳态。