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山梨酸胁迫下枯草芽孢杆菌的转录组分析揭示了营养限制反应并表明了质膜重塑。

Transcriptome analysis of sorbic acid-stressed Bacillus subtilis reveals a nutrient limitation response and indicates plasma membrane remodeling.

作者信息

Ter Beek Alex, Keijser Bart J F, Boorsma Andre, Zakrzewska Anna, Orij Rick, Smits Gertien J, Brul Stanley

机构信息

Laboratory for Molecular Biology and Microbial Food Safety, Swammerdam Institute for Life Sciences, University of Amsterdam, Nieuwe Achtergracht 166, 1018 WV Amsterdam, The Netherlands.

出版信息

J Bacteriol. 2008 Mar;190(5):1751-61. doi: 10.1128/JB.01516-07. Epub 2007 Dec 21.

Abstract

The weak organic acid sorbic acid is a commonly used food preservative, as it inhibits the growth of bacteria, yeasts, and molds. We have used genome-wide transcriptional profiling of Bacillus subtilis cells during mild sorbic acid stress to reveal the growth-inhibitory activity of this preservative and to identify potential resistance mechanisms. Our analysis demonstrated that sorbic acid-stressed cells induce responses normally seen upon nutrient limitation. This is indicated by the strong derepression of the CcpA, CodY, and Fur regulon and the induction of tricarboxylic acid cycle genes, SigL- and SigH-mediated genes, and the stringent response. Intriguingly, these conditions did not lead to the activation of sporulation, competence, or the general stress response. The fatty acid biosynthesis (fab) genes and BkdR-regulated genes are upregulated, which may indicate plasma membrane remodeling. This was further supported by the reduced sensitivity toward the fab inhibitor cerulenin upon sorbic acid stress. We are the first to present a comprehensive analysis of the transcriptional response of B. subtilis to sorbic acid stress.

摘要

弱有机酸山梨酸是一种常用的食品防腐剂,因为它能抑制细菌、酵母和霉菌的生长。我们利用轻度山梨酸胁迫下枯草芽孢杆菌细胞的全基因组转录谱,揭示这种防腐剂的生长抑制活性,并确定潜在的抗性机制。我们的分析表明,受山梨酸胁迫的细胞会诱导出在营养限制时通常会出现的反应。这表现为CcpA、CodY和Fur调控子的强烈去阻遏,以及三羧酸循环基因、SigL和SigH介导的基因的诱导,还有严谨反应。有趣的是,这些条件并未导致芽孢形成、感受态或一般应激反应的激活。脂肪酸生物合成(fab)基因和BkdR调控的基因被上调,这可能表明细胞膜重塑。山梨酸胁迫下对fab抑制剂浅蓝菌素的敏感性降低进一步支持了这一点。我们首次对枯草芽孢杆菌对山梨酸胁迫的转录反应进行了全面分析。

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