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嗜酸乳杆菌中参与耐酸性和蛋白水解活性的双组分调节系统的微阵列分析。

Microarray analysis of a two-component regulatory system involved in acid resistance and proteolytic activity in Lactobacillus acidophilus.

作者信息

Azcarate-Peril M Andrea, McAuliffe Olivia, Altermann Eric, Lick Sonja, Russell W Michael, Klaenhammer Todd R

机构信息

Department of Food Science, North Carolina State University, Box 7624, Raleigh, NC 27695, USA.

出版信息

Appl Environ Microbiol. 2005 Oct;71(10):5794-804. doi: 10.1128/AEM.71.10.5794-5804.2005.

Abstract

Two-component regulatory systems are one primary mechanism for environmental sensing and signal transduction. Annotation of the complete genome sequence of the probiotic bacterium Lactobacillus acidophilus NCFM revealed nine two-component regulatory systems. In this study, the histidine protein kinase of a two-component regulatory system (LBA1524HPK-LBA1525RR), similar to the acid-related system lisRK from Listeria monocytogenes (P. D. Cotter et al., J. Bacteriol. 181:6840-6843, 1999), was insertionally inactivated. A whole-genome microarray containing 97.4% of the annotated genes of L. acidophilus was used to compare genome-wide patterns of transcription at various pHs between the control and the histidine protein kinase mutant. The expression pattern of approximately 80 genes was affected by the LBA1524HPK mutation. Putative LBA1525RR target loci included two oligopeptide-transport systems present in the L. acidophilus genome, other components of the proteolytic system, and a LuxS homolog, suspected of participating in synthesis of the AI-2 signaling compound. The mutant exhibited lower tolerance to acid and ethanol in logarithmic-phase cells and poor acidification rates in milk. Supplementation of milk with Casamino Acids essentially restored the acid-producing ability of the mutant, providing additional evidence for a role of this two component system in regulating proteolytic activity in L. acidophilus.

摘要

双组分调控系统是环境感知和信号转导的一种主要机制。对益生菌嗜酸乳杆菌NCFM完整基因组序列的注释显示有九个双组分调控系统。在本研究中,一个与单核细胞增生李斯特菌的酸相关系统lisRK(P.D.科特等人,《细菌学杂志》181:6840 - 6843,1999年)相似的双组分调控系统(LBA1524HPK - LBA1525RR)的组氨酸蛋白激酶被插入失活。使用一个包含嗜酸乳杆菌97.4%注释基因的全基因组微阵列,来比较对照菌株和组氨酸蛋白激酶突变体在不同pH值下全基因组范围的转录模式。大约80个基因的表达模式受到LBA1524HPK突变的影响。推测的LBA1525RR靶位点包括嗜酸乳杆菌基因组中存在的两个寡肽转运系统、蛋白水解系统的其他组分以及一个LuxS同源物,怀疑其参与AI - 2信号化合物的合成。该突变体对数期细胞对酸和乙醇的耐受性较低,在牛奶中的酸化速率也较差。用酪蛋白氨基酸补充牛奶基本上恢复了突变体的产酸能力,为这个双组分系统在调节嗜酸乳杆菌蛋白水解活性中的作用提供了额外证据。

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