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景天三七中类黄酮抗腐败希瓦氏菌的抗菌机制的转录组分析。

A transcriptome analysis of the antibacterial mechanism of flavonoids from Sedum aizoon L. against Shewanella putrefaciens.

机构信息

Department of Food Science and Engineering, College of Food and Pharmaceutical Science, Ningbo University, Ningbo, 315211, Zhejiang, People's Republic of China.

出版信息

World J Microbiol Biotechnol. 2020 Jun 20;36(7):94. doi: 10.1007/s11274-020-02871-w.

Abstract

Flavonoids from Sedum aizoon L. (FSAL) possess prominent antibacterial activity against Shewanella putrefaciens isolated from sea food. In the current study, the involved molecular mechanisms were investigated using transcriptome analyses combined with bioinformatics analysis in vitro for the first time. Results showed that treatment of FSAL (1.0 MIC) damaged the permeability and integrity of cell membrane and induced 721 differentially expressed genes (DEGs) in tested bacteria at transcriptional levels, including 107 DEGs were up-regulated and 614 DEGs were down-regulated. In addition, the RNA-Seq analysis revealed that the majority of DEGs mainly involved in pathways of lipopolysaccharide biosynthesis, glycerophospholipid metabolism, biosynthesis of amino acids, purine metabolism, ABC transporters and response to stimulus. In summary, the integrated results indicated that the intervention of FSAL induced destruction of cell wall and membrane, disorder of the metabolic process and redox balance, and damage of nucleic acids in S. putrefaciens, at last resulted in the death of cells. This study provided new insights into the anti- S. putrefaciens molecular mechanism underlying the treatment of FSAL, which may be served as the basis guide for identifying potential antimicrobial targets and application of FSAL in food safety.

摘要

景天三七(FSAL)中的类黄酮对从海鲜中分离出的腐生梭菌具有显著的抗菌活性。本研究首次通过体外转录组分析结合生物信息学分析,研究了相关的分子机制。结果表明,FSAL(1.0 MIC)处理破坏了细胞膜的通透性和完整性,并在转录水平上诱导了测试细菌中的 721 个差异表达基因(DEGs),其中 107 个 DEGs 上调,614 个 DEGs 下调。此外,RNA-Seq 分析显示,大多数 DEGs 主要涉及脂多糖生物合成、甘油磷脂代谢、氨基酸生物合成、嘌呤代谢、ABC 转运蛋白和对刺激的反应途径。综上所述,综合结果表明,FSAL 的干预诱导了细胞壁和细胞膜的破坏、代谢过程和氧化还原平衡的紊乱以及腐生梭菌中核酸的损伤,最终导致细胞死亡。本研究为 FSAL 治疗腐生梭菌的抗腐生梭菌分子机制提供了新的见解,可为鉴定潜在的抗菌靶点和 FSAL 在食品安全中的应用提供依据。

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