Lahesaare Andrio, Moor Hanna, Kivisaar Maia, Teras Riho
Institute of Molecular and Cell Biology, University of Tartu, Tartu, Estonia.
PLoS One. 2014 Dec 29;9(12):e115901. doi: 10.1371/journal.pone.0115901. eCollection 2014.
The biofilm matrix of the rhizospheric bacterium Pseudomonas putida consists mainly of a proteinaceous component. The two largest P. putida proteins, adhesins LapA and LapF, are involved in biofilm development but prevail in different developmental stages of the biofilm matrix. LapA is abundant in the initial stage of biofilm formation whereas LapF is found in the mature biofilm. Although the transcriptional regulation of the adhesins is not exhaustively studied, some factors that can be involved in their regulation have been described. For example, RpoS, the major stress response sigma factor, activates, and Fis represses LapF expression. This study focused on the LapF expression control by Fis. Indeed, using DNase I footprint analysis a Fis binding site Fis-F2 was located 150 bp upstream of the lapF gene coding sequence. The mapped 5' end of the lapF mRNA localized the promoter to the same region, overlapping with the Fis binding site Fis-F2. Monitoring the lapF promoter activity by a β-galactosidase assay revealed that Fis overexpression causes a 4-fold decrease in the transcriptional activity. Furthermore, mutations that diminished Fis binding to the Fis-F2 site abolished the repression of the lapF promoter. Thus, these data suggest that Fis is involved in the biofilm regulation via repression of LapF expression.
根际细菌恶臭假单胞菌的生物膜基质主要由蛋白质成分组成。恶臭假单胞菌的两种最大的蛋白质,黏附素LapA和LapF,参与生物膜的形成,但在生物膜基质的不同发育阶段占主导地位。LapA在生物膜形成的初始阶段含量丰富,而LapF存在于成熟生物膜中。尽管对黏附素的转录调控尚未进行详尽研究,但已描述了一些可能参与其调控的因素。例如,主要应激反应σ因子RpoS激活,而Fis抑制LapF的表达。本研究聚焦于Fis对LapF表达的控制。事实上,通过DNase I足迹分析,在lapF基因编码序列上游150 bp处定位到一个Fis结合位点Fis-F2。lapF mRNA的定位5'端将启动子定位于同一区域,与Fis结合位点Fis-F2重叠。通过β-半乳糖苷酶测定监测lapF启动子活性表明,Fis过表达导致转录活性降低4倍。此外,减少Fis与Fis-F2位点结合的突变消除了对lapF启动子的抑制。因此,这些数据表明Fis通过抑制LapF表达参与生物膜调控。