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首页> 外文期刊>International Dairy Journal >Degradation of alpha s1-CN f1-23 by aminopeptidase N and endopeptidases E, O, O2, and O3 of Lactobacillus helveticus WSU19 under cheese ripening conditions.
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Degradation of alpha s1-CN f1-23 by aminopeptidase N and endopeptidases E, O, O2, and O3 of Lactobacillus helveticus WSU19 under cheese ripening conditions.

机译:干酪成熟条件下瑞士乳杆菌WSU19的氨基肽酶N和内肽酶E,O,O2和O3降解α s1 -CN f1-23。

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摘要

This study determined specificities of aminopeptidase N (PepN), endopeptidase E (PepE), endopeptidase O (PepO), endopeptidase O2 (PepO2), and endopeptidase O3 (PepO3), from Lactobacillus helveticus WSU19 on the alpha < sub>s1-CN f1-23 peptide, formed by residual chymosin during cheese ripening. Cell-free extracts (CFEs) were prepared from Escherichia coli DH5 alpha derivatives expressing peptidase genes of Lb. helveticus WSU19. The alpha < sub>s1-CN f1-23 peptide was digested by CFEs under cheese ripening conditions. Degradation pattern was analyzed qualitatively using MALDI-TOF mass spectrometry. PepN exhibited activity on alpha < sub>s1-CN f1-23 only in the presence of an endopeptidase, particularly PepO-like endopeptidases. PepO, PepO2, and PepO3 cleaved alpha < sub>s1-CN f1-23 predominantly at Glu< sub>14-Val< sub>15, forming the bitter peptide alpha < sub>s1-CN f1-14. PepE cleaved alpha < sub>s1-CN f1-23 primarily at Lys< sub>3-His< sub>4, suggesting a role for PepE in degrading bitter peptides from the N-terminus of alpha < sub>s1-CN f1-23. Combinations of PepE/PepO and PepE/PepO2 were determined to have the potential to decrease the accumulation of alpha < sub>s1-CN f1-14.
机译:这项研究确定了α s1 上来自瑞士乳杆菌WSU19的氨肽酶N(PepN),内肽酶E(PepE),内肽酶O(PepO),内肽酶O2(PepO2)和内肽酶O3(PepO3)的特异性。 > -CN f1-23肽,由干酪成熟过​​程中残留的凝乳酶形成。从表达Lb肽酶基因的大肠杆菌DH5α衍生物制备无细胞提取物(CFE)。 helveticus WSU19。 α s1 -CN f1-23肽在干酪成熟条件下被CFE消化。使用MALDI-TOF质谱定性分析了降解模式。 PepN仅在存在内肽酶特别是PepO样内肽酶的情况下才对α s1 -CN f1-23表现出活性。 PepO,PepO2和PepO3主要在Glu 14 -Val 15 处切割alpha s1 -CN f1-23,形成苦味肽alpha s1 -CN f1-14。 PepE主要在Lys 3 -His 4 处切割alpha s1 -CN f1-23,表明PepE在降解N中的苦肽中的作用- s1 -CN f1-23的末端。确定PepE / PepO和PepE / PepO2的组合具有降低α s1 -CN f1-14积累的潜力。

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