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肠炎沙门氏菌的SdiA是一种检测混合微生物群落的LuxR同源物。

SdiA of Salmonella enterica is a LuxR homolog that detects mixed microbial communities.

作者信息

Michael B, Smith J N, Swift S, Heffron F, Ahmer B M

机构信息

Department of Microbiology, The Ohio State University, Columbus, Ohio 43210-1292, USA.

出版信息

J Bacteriol. 2001 Oct;183(19):5733-42. doi: 10.1128/JB.183.19.5733-5742.2001.

DOI:10.1128/JB.183.19.5733-5742.2001
PMID:11544237
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC95466/
Abstract

Proteins of the LuxR family detect the presence of N-acylhomoserine lactones (AHLs) and regulate transcription accordingly. When AHLs are synthesized by the same species that detects them, the system allows a bacterium to measure the population density of its own species, a phenomenon known as quorum sensing. The sdiA genes of Escherichia coli and Salmonella enterica serovar Typhimurium are predicted to encode LuxR homologs. However, these species do not appear to synthesize AHLs or any other molecule detected by SdiA. It has previously been demonstrated that overexpression of sdiA results in the activation of the ftsQAZ locus in E. coli and four other loci in Salmonella serovar Typhimurium. Here we report that transcriptional fusions to these five loci fall into two classes. The first class requires overexpression of sdiA for activation. The second class responds to sdiA expressed from its natural position in the chromosome if the appropriate AHLs are added to the culture. The only member of the second class is a series of Prck-luxCDABE fusions in Salmonella serovar Typhimurium. SdiA responds with highest sensitivity to AHLs that have a keto modification at the third carbon and an acyl chain length of 6 or 8 (half-maximal response between 1 and 5 nM). Growth of Salmonella in proximity to species known to synthesize these AHLs results in sdiA-dependent activation of the Prck-luxCDABE fusions. SdiA appears to be the first AHL receptor discovered that detects signals emanating exclusively from other species.

摘要

LuxR家族蛋白可检测N-酰基高丝氨酸内酯(AHLs)的存在,并据此调节转录。当AHLs由能够检测到它们的同一物种合成时,该系统使细菌能够测量自身物种的群体密度,这一现象称为群体感应。预计大肠杆菌和鼠伤寒沙门氏菌的sdiA基因编码LuxR同源物。然而,这些物种似乎不合成AHLs或任何其他可被SdiA检测到的分子。此前已证明,sdiA的过表达会导致大肠杆菌中ftsQAZ位点以及鼠伤寒沙门氏菌中其他四个位点的激活。在此我们报告,与这五个位点的转录融合可分为两类。第一类需要sdiA过表达才能激活。如果向培养物中添加适当的AHLs,第二类则对从其在染色体上的天然位置表达的sdiA作出反应。第二类的唯一成员是鼠伤寒沙门氏菌中的一系列Prck-luxCDABE融合。SdiA对在第三个碳上具有酮修饰且酰基链长度为6或8的AHLs反应最为敏感(半数最大反应在1至5 nM之间)。在已知合成这些AHLs的物种附近生长的沙门氏菌会导致Prck-luxCDABE融合的sdiA依赖性激活。SdiA似乎是发现的第一个专门检测来自其他物种发出信号的AHL受体。

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本文引用的文献

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