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Biofilm formation at the air-liquid interface by the Pseudomonas fluorescens SBW25 wrinkly spreader requires an acetylated form of cellulose

机译:荧光假单胞菌SBW25皱纹撒布机在气液界面上形成生物膜需要纤维素的乙酰化形式

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The wrinkly spreader (WS) genotype of Pseudomonas fluorescens SBW25 colonizes the air - liquid interface of spatially structured microcosms resulting in formation of a thick biofilm. Its ability to colonize this niche is largely due to overproduction of a cellulosic polymer, the product of the wss operon. Chemical analysis of the biofilm matrix shows that the cellulosic polymer is partially acetylated cellulose, which is consistent with predictions of gene function based on in silico analysis of wss. Both polar and non-polar mutations in the sixth gene of the wss operon (wssF) or adjacent downstream genes (wssGHIJ) generated mutants that overproduce non-acetylated cellulose, thus implicating WssFGHIJ in acetylation of cellulose. WssGHI are homologues of AlgFIJ from P. aeruginosa, which together are necessary and sufficient to acetylate alginate polymer. WssF belongs to a newly established Pfam family and is predicted to provide acyl groups to WssGHI. The role of WssJ is unclear, but its similarity to MinD-like proteins suggests a role in polar localization of the acetylation complex. Fluorescent microscopy of Calcofluor-stained biofilms revealed a matrix structure composed of networks of cellulose fibres, sheets and clumped material. Quantitative analyses of biofilm structure showed that acetylation of cellulose is important for effective colonization of the air - liquid interface: mutants identical to WS, but defective in enzymes required for acetylation produced biofilms with altered physical properties. In addition, mutants producing non-acetylated cellulose were unable to spread rapidly across solid surfaces. Inclusion in these assays of a WS mutant with a defect in the GGDEF regulator (WspR) confirmed the requirement for this protein in expression of both acetylated cellulose polymer and bacterial attachment. These results suggest a model in which WspR regulation of cellulose expression and attachment plays a role in the co-ordination of surface colonization. [References: 52]
机译:荧光假单胞菌SBW25的皱纹扩散器(WS)基因型定居在空间结构的微观世界的气液界面上,从而形成了厚厚的生物膜。它在这个小生境中定殖的能力主要是由于纤维素操纵子wss操纵子的产物过量生产。生物膜基质的化学分析表明,纤维素聚合物是部分乙酰化的纤维素,这与基于wss的计算机分析对基因功能的预测一致。 wss操纵子的第六个基因(wssF)或相邻下游基因(wssGHIJ)的极性和非极性突变均产生了过量产生非乙酰化纤维素的突变体,从而使WssFGHIJ参与了纤维素的乙酰化。 WssGHI是来自铜绿假单胞菌的AlgFIJ的同源物,它们一起对于乙酰化藻酸盐聚合物是必需的和充分的。 WssF属于一个新建立的Pfam家族,预计将为WssGHI提供酰基。 WssJ的作用尚不清楚,但其与MinD样蛋白的相似性暗示了乙酰化复合物的极性定位中的作用。用Calcofluor染色的生物膜的荧光显微镜显示基质结构由纤维素纤维,薄片和成团的材料组成。生物膜结构的定量分析表明,纤维素的乙酰化对于有效的气-液界面定殖很重要:与WS相同的突变体,但是乙酰化所需的酶缺陷,产生的生物膜具有改变的物理性质。另外,产生非乙酰化纤维素的突变体不能迅速分布在固体表面上。这些检测中包括在GGDEF调节剂(WspR)中存在缺陷的WS突变体,证实了在乙酰化纤维素聚合物表达和细菌附着中都需要这种蛋白质。这些结果提示了一个模型,其中WspR对纤维素表达和附着的调节在表面定植的协调中起作用。 [参考:52]

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