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细胞壁中 O-乙酰化和 N-脱乙酰化的增加通过提高乳球菌细胞壁的完整性来促进其耐酸性和乳链菌肽的产生。

The increase of O-acetylation and N-deacetylation in cell wall promotes acid resistance and nisin production through improving cell wall integrity in Lactococcus lactis.

机构信息

Key Laboratory of Systems Bioengineering (Ministry of Education), Tianjin University, Tianjin, 300072, People's Republic of China.

Department of Pharmaceutical Engineering, School of Chemical Engineering and Technology, Tianjin University, Tianjin, 300072, People's Republic of China.

出版信息

J Ind Microbiol Biotechnol. 2018 Sep;45(9):813-825. doi: 10.1007/s10295-018-2052-2. Epub 2018 Jun 6.

DOI:10.1007/s10295-018-2052-2
PMID:29876686
Abstract

Cell wall is closely related to bacterial robustness and adsorption capacity, playing crucial roles in nisin production in Lactococcus lactis. Peptidoglycan (PG), the essential component of cell wall, is usually modified with MurNAc O-acetylation and GlcNAc N-deacetylation, catalyzed by YvhB and XynD, respectively. In this study, increasing the two modifications in L. lactis F44 improved autolysis resistance by decreasing the susceptibility to PG hydrolases. Furthermore, both modifications were positively associated with overall cross-linkage, contributing to cell wall integrity. The robust cell wall rendered the yvhB/xynD-overexpression strains more acid resistant, leading to the increase of nisin production in fed-batch fermentations by 63.7 and 62.9%, respectively. Importantly, the structural alterations also reduced nisin adsorption capacity, resulting in reduction of nisin loss. More strikingly, the co-overexpression strain displayed the highest nisin production (76.3% higher than F44). Our work provides a novel approach for achieving nisin overproduction via extensive cell wall remodeling.

摘要

细胞壁与细菌的坚固性和吸附能力密切相关,在乳球菌产乳酸链球菌素中起着至关重要的作用。肽聚糖(PG)是细胞壁的主要成分,通常通过 YvhB 和 XynD 分别催化 MurNAc O-乙酰化和 GlcNAc N-脱乙酰化进行修饰。在本研究中,通过降低 PG 水解酶的敏感性,增加 L. lactis F44 中的这两种修饰可提高自溶抗性。此外,两种修饰均与总交联呈正相关,有助于维持细胞壁的完整性。坚固的细胞壁使 yvhB/xynD 过表达菌株更耐酸,导致补料分批发酵中产乳酸链球菌素的产量分别增加了 63.7%和 62.9%。重要的是,结构改变还降低了乳酸链球菌素的吸附能力,从而减少了乳酸链球菌素的损失。更引人注目的是,共过表达菌株表现出最高的乳酸链球菌素产量(比 F44 高 76.3%)。我们的工作为通过广泛的细胞壁重塑实现乳酸链球菌素的过量生产提供了一种新方法。

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