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Fis过表达通过调节LapA和LapF的比例增强恶臭假单胞菌生物膜的形成。

Fis overexpression enhances Pseudomonas putida biofilm formation by regulating the ratio of LapA and LapF.

作者信息

Moor Hanna, Teppo Annika, Lahesaare Andrio, Kivisaar Maia, Teras Riho

机构信息

Institute of Molecular and Cell Biology, University of Tartu, Riia 23, 51010 Tartu, Estonia.

出版信息

Microbiology (Reading). 2014 Dec;160(Pt 12):2681-2693. doi: 10.1099/mic.0.082503-0. Epub 2014 Sep 24.

DOI:10.1099/mic.0.082503-0
PMID:25253613
Abstract

Bacteria form biofilm as a response to a number of environmental signals that are mediated by global transcription regulators and alarmones. Here we report the involvement of the global transcription regulator Fis in Pseudomonas putida biofilm formation through regulation of lapA and lapF genes. The major component of P. putida biofilm is proteinaceous and two large adhesive proteins, LapA and LapF, are known to play a key role in its formation. We have previously shown that Fis overexpression enhances P. putida biofilm formation. In this study, we used mini-Tn5 transposon mutagenesis to select potential Fis-regulated genes involved in biofilm formation. A total of 90 % of the studied transposon mutants carried insertions in the lap genes. Since our experiments showed that Fis-enhanced biofilm is mostly proteinaceous, the amounts of LapA and LapF from P. putida cells lysates were quantified using SDS-PAGE. Fis overexpression increases the quantity of LapA 1.6 times and decreases the amount of LapF at least 4 times compared to the wild-type cells. The increased LapA expression caused by Fis overexpression was confirmed by FACS analysis measuring the amount of LapA-GFP fusion protein. Our results suggest that the profusion of LapA in the Fis-overexpressed cells causes enhanced biofilm formation in mature stages of P. putida biofilm and LapF has a minor role in P. putida biofilm formation.

摘要

细菌形成生物膜是对多种由全局转录调节因子和警报素介导的环境信号的一种反应。在此,我们报告全局转录调节因子Fis通过调控lapA和lapF基因参与恶臭假单胞菌生物膜的形成。恶臭假单胞菌生物膜的主要成分是蛋白质,已知两种大型粘附蛋白LapA和LapF在其形成过程中起关键作用。我们之前已表明Fis过表达会增强恶臭假单胞菌生物膜的形成。在本研究中,我们使用mini-Tn5转座子诱变来筛选参与生物膜形成的潜在Fis调控基因。总共90%的研究转座子突变体在lap基因中发生了插入。由于我们的实验表明Fis增强的生物膜主要是蛋白质,因此使用SDS-PAGE对恶臭假单胞菌细胞裂解物中的LapA和LapF含量进行了定量。与野生型细胞相比,Fis过表达使LapA的量增加了1.6倍,使LapF的量至少减少了4倍。通过测量LapA-GFP融合蛋白量的FACS分析证实了Fis过表达导致的LapA表达增加。我们的结果表明,Fis过表达细胞中LapA的大量存在导致恶臭假单胞菌生物膜成熟阶段生物膜形成增强,而LapF在恶臭假单胞菌生物膜形成中起次要作用。

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