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益生菌菌株瑞士乳杆菌 M92 的蛋白水解活性。

Proteolytic activity of probiotic strain Lactobacillus helveticus M92.

机构信息

Laboratory for Antibiotic, Enzyme, Probiotic and Starter Cultures Technology, Faculty of Food Technology and Biotechnology, University of Zagreb, Pierottijeva 6/IV, 10000 Zagreb, Croatia.

出版信息

Anaerobe. 2013 Apr;20:58-64. doi: 10.1016/j.anaerobe.2013.02.004. Epub 2013 Feb 27.

Abstract

The aim of this research was to investigate the potential of previously defined probiotic strain Lactobacillus helveticus M92 as functional starter culture for fermented dairy products. Therefore, proteolytic activity of L. helveticus M92 was investigated and compared with those of different representatives of probiotic and starter culture strains. Cluster analysis of AFLP fingerprints showed a difference of L. helveticus M92 compared to five other L. helveticus strains, but the percentage of similarity confirmed the identification on species level. Casein hydrolysis by L. helveticus M92 was monitored by agar-well diffusion test, SDS-PAGE and Anson's method. L. helveticus M92 exhibited the highest proteolytic activity among tested probiotic and starter cultures strains with the fastest acidification rate and the highest pH decrease after overnight incubation in skim milk. The presence of prtH2 gene was confirmed by PCR amplification with specific primers, while PCR product was not obtained after amplification with primers specific to prtH. Furthermore, SDS-PAGE LC-MS/MS analysis of insoluble proteome of L. helveticus M92 enabled identification of several proteins involved in proteolytic system of L. helveticus such as protease PrtM as well as proteins involved in Opp peptide transport system and the intracellular peptidases PepE, PepN, and PepQ.

摘要

本研究旨在探讨先前定义的益生菌菌株瑞士乳杆菌 M92 作为发酵乳制品功能性起始培养物的潜力。因此,研究了 L. helveticus M92 的蛋白水解活性,并将其与不同的益生菌和起始培养物菌株进行了比较。AFLP 指纹图谱的聚类分析显示,L. helveticus M92 与其他 5 株 L. helveticus 菌株存在差异,但相似性百分比证实了在种水平上的鉴定。通过琼脂孔扩散试验、SDS-PAGE 和 Anson 法监测 L. helveticus M92 对酪蛋白的水解作用。L. helveticus M92 在测试的益生菌和起始培养物菌株中表现出最高的蛋白水解活性,其在脱脂乳中过夜孵育后的酸化速度最快,pH 值下降幅度最大。通过使用特异性引物的 PCR 扩增证实了 prtH2 基因的存在,而使用特异性引物对 prtH 进行扩增后未获得 PCR 产物。此外,通过 SDS-PAGE LC-MS/MS 分析 L. helveticus M92 的不可溶性蛋白质组,鉴定出了几种参与 L. helveticus 蛋白水解系统的蛋白质,如蛋白酶 PrtM 以及参与 Opp 肽转运系统和细胞内肽酶 PepE、PepN 和 PepQ 的蛋白质。

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