DuPont Nutrition & Biosciences, Brabrand, Aarhus, Denmark.
PLoS One. 2020 Sep 21;15(9):e0239080. doi: 10.1371/journal.pone.0239080. eCollection 2020.
Two commercial proteases (subtilisin-typed FNA from Bacillus amyloliquefaciens, and chymotrypsin-like NPP from Nocardiopsis prasina), porcine pepsin, porcine pancreatin having protease activity and their combinations were studied in vitro by LC-MS for their ability to digest soy protein isolate (SPI) under conditions close to those found in the stomach (pH 3.7) and small intestine (pH 6.5). The total number of peptides generated, and their size distribution were obtained under each set of the digestion conditions. These peptides were grouped according to their C-terminal amino acid (AA) residue (P1) and mass, based on which two concepts were proposed, i.e., Normalized Peptide Bond Cleavage Frequency (NPBCF) and Protease Substrate Broadness Index (PSBI). At pH 3.7, FNA+pepsin increased PSBI vs. pepsin alone by 2.7 and 4.9 percentage points (p.p.) at a SPI:protease ratio of 20:1 and 100:1, respectively. At pH 6.5, FNA+pancreatin improved PSBI by 9.1 and 10.2 p.p. at SPI:protease 20:1 and 100:1, respectively, vs. pancreatin alone. NPP generated 38% more peptides than FNA when administered with pancreatin at SPI:protease 200:1:1 and pH 6.5, but FNA alone (28.9) or FNA+pancreatin (29.1) gave a higher PSBI than pancreatin (22.2), NPP (20.3) and NPP+pancreatin (22.0). At pH 3.7 FNA generated 59% and 39% of peptides of pepsin at SPI:protease of 20:1 and 100:1, respectively, and both groups of peptides had similar size distribution. At pH 6.5 more small sized peptides were generated by FNA or FNA+pancreatin than pancreatin and NPP alone or pancreatin+NPP. In conclusion, FNA showed complementary effects with pepsin and pancreatin in terms of PSBI and generated more small sized peptides compared to NPP.
两种商业蛋白酶(来自解淀粉芽孢杆菌的枯草菌素型 FNA 和来自类诺卡氏菌的糜蛋白酶样 NPP)、猪胃蛋白酶、猪胰蛋白酶具有蛋白酶活性,它们在 LC-MS 下进行了研究,以研究它们在接近胃(pH3.7)和小肠(pH6.5)条件下消化大豆分离蛋白(SPI)的能力。在每组消化条件下,获得了生成的肽的总数及其大小分布。这些肽根据其 C 末端氨基酸(AA)残基(P1)和质量进行分组,基于此提出了两个概念,即归一化肽键切割频率(NPBCF)和蛋白酶底物广谱指数(PSBI)。在 pH3.7 下,与单独使用胃蛋白酶相比,FNA+胃蛋白酶在 SPI:蛋白酶比为 20:1 和 100:1 时分别增加了 2.7 和 4.9 个百分点(p.p.)的 PSBI。在 pH6.5 下,与单独使用胰酶相比,FNA+胰酶在 SPI:蛋白酶比为 20:1 和 100:1 时分别提高了 9.1 和 10.2 个百分点(p.p.)的 PSBI。在 SPI:蛋白酶比为 200:1:1 和 pH6.5 下,当与胰酶一起使用时,NPP 生成的肽比 FNA 多 38%,但 FNA 单独(28.9)或 FNA+胰酶(29.1)的 PSBI 高于胰酶(22.2)、NPP(20.3)和 NPP+胰酶(22.0)。在 pH3.7 下,与 SPI:蛋白酶比为 20:1 和 100:1 相比,FNA 分别生成了胃蛋白酶的 59%和 39%的肽,并且这两组肽具有相似的大小分布。在 pH6.5 下,与单独使用胰酶和 NPP 相比,FNA 或 FNA+胰酶产生了更多的小肽。总之,FNA 在 PSBI 方面与胃蛋白酶和胰酶表现出互补作用,并与 NPP 相比生成了更多的小肽。