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线性渗透调节周质葡聚糖由铜绿假单胞菌的opgGH基因座编码。

Linear osmoregulated periplasmic glucans are encoded by the opgGH locus of Pseudomonas aeruginosa.

作者信息

Lequette Yannick, Rollet Eglantine, Delangle Aurélie, Greenberg E Peter, Bohin Jean-Pierre

机构信息

Department of Microbiology, University of Washington, Seattle, WA 98195, USA.

Unité de Glycobiologie Structurale et Fonctionnelle CNRS UMR 8576, Université des Sciences et Technologies de Lille, 59655 Villeneuve d'Ascq Cedex, France.

出版信息

Microbiology (Reading). 2007 Oct;153(Pt 10):3255-3263. doi: 10.1099/mic.0.2007/008953-0.

Abstract

Osmoregulated periplasmic glucans (OPGs) are produced by many proteobacteria and are important for bacterial-host interactions. The opgG and opgH genes involved in the synthesis of OPGs are the most widely distributed genes in proteobacterial genomes. Two other non-homologous genes, both named ndvB, are also involved in OPG biosynthesis in several species. The Pseudomonas aeruginosa genome possesses two ORFs, PA5077 and PA5078, that show similarity to opgH and opgG of Pseudomonas syringae, respectively, and one ORF, PA1163, similar to ndvB of Sinorhizobium meliloti. Here, we report that the opgGH locus of P. aeruginosa PA14 is involved in the synthesis of linear polymers with beta-1,2-linked glucosyl residues branched with a few beta-1,6 glucosyl residues. Succinyl residues also substitute this glucose backbone. Transcription of opgGH is repressed by high osmolarity. Low osmolarity promotes the formation of highly structured biofilms, but biofilm development is slower and the area of biomass is reduced under high osmolarity. Biofilm development of an opgGH mutant grown under low osmolarity presents a similar phenotype to the wild-type biofilm grown under high osmolarity. These results suggest that OPGs are important for biofilm formation under conditions of low osmolarity. A previous study suggested that the P. aeruginosa ndvB gene is involved in the resistance of biofilms to antibiotics. We have shown that ndvB is not involved in the biosynthesis of the OPG described here, and opgGH do not appear to be involved in the resistance of P. aeruginosa PA14 biofilms to antibiotics.

摘要

渗透调节周质葡聚糖(OPG)由许多变形菌产生,对细菌与宿主的相互作用很重要。参与OPG合成的opgG和opgH基因是变形菌基因组中分布最广泛的基因。另外两个非同源基因,都命名为ndvB,也参与了几种细菌的OPG生物合成。铜绿假单胞菌基因组有两个开放阅读框,PA5077和PA5078,分别与丁香假单胞菌的opgH和opgG相似,还有一个开放阅读框PA1163,与苜蓿中华根瘤菌的ndvB相似。在此,我们报道铜绿假单胞菌PA14的opgGH基因座参与了线性聚合物的合成,该聚合物具有以β-1,2-连接的葡萄糖残基为主链,并带有一些β-1,6葡萄糖残基作为分支。琥珀酰残基也取代了这个葡萄糖主链。opgGH的转录受到高渗透压抑制。低渗透压促进高度结构化生物膜的形成,但在高渗透压下生物膜形成较慢且生物量面积减小。在低渗透压下生长的opgGH突变体的生物膜形成呈现出与在高渗透压下生长的野生型生物膜相似的表型。这些结果表明,OPG在低渗透压条件下对生物膜形成很重要。先前的一项研究表明,铜绿假单胞菌的ndvB基因参与生物膜对抗生素的抗性。我们已经表明,ndvB不参与此处描述的OPG的生物合成,并且opgGH似乎也不参与铜绿假单胞菌PA14生物膜对抗生素的抗性。

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