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蛋白质组学研究强调了与海洋细菌假交替单胞菌 D41 生物膜发育相关的外膜蛋白。

Proteomic studies highlight outer-membrane proteins related to biofilm development in the marine bacterium Pseudoalteromonas sp. D41.

机构信息

Laboratoire de Biotechnologie et Chimie Marines, Université de Bretagne-Sud (UEB), IUEM, Lorient, France.

出版信息

Proteomics. 2012 Nov;12(21):3180-92. doi: 10.1002/pmic.201100644. Epub 2012 Oct 12.

DOI:10.1002/pmic.201100644
PMID:22965736
Abstract

Bacterial biofilm development is conditioned by complex processes involving bacterial attachment to surfaces, growth, mobility, and exoproduct production. The marine bacterium Pseudoalteromonas sp. strain D41 is able to attach strongly onto a wide variety of substrates, which promotes subsequent biofilm development. Study of the outer-membrane and total soluble proteomes showed ten spots with significant intensity variations when this bacterium was grown in biofilm compared to planktonic cultures. MS/MS de novo sequencing analysis allowed the identification of four outer-membrane proteins of particular interest since they were strongly induced in biofilms. These proteins are homologous to a TonB-dependent receptor (TBDR), to the OmpW and OmpA porins, and to a type IV pilus biogenesis protein (PilF). Gene expression assays by quantitative RT-PCR showed that the four corresponding genes were upregulated during biofilm development on hydrophobic and hydrophilic surfaces. The Pseudomonas aeruginosa mutants unable to produce any of the OmpW, OmpA, and PilF homologues yielded biofilms with lower biovolumes and altered architectures, confirming the involvement of these proteins in the biofilm formation process. Our results indicate that Pseudoalteromonas sp. D41 shares biofilm formation mechanisms with human pathogenic bacteria, but also relies on TBDR, which might be more specific to the marine environment.

摘要

细菌生物膜的形成受到复杂过程的影响,包括细菌附着在表面、生长、移动和外产物的产生。海洋细菌假交替单胞菌 D41 能够强烈附着在各种基质上,这促进了随后的生物膜的形成。对其外膜和总可溶性蛋白质组的研究表明,与浮游培养相比,当这种细菌在生物膜中生长时,有 10 个斑点的强度变化显著。MS/MS 从头测序分析允许鉴定出 4 种外膜蛋白,因为它们在生物膜中强烈诱导。这些蛋白与一个 TonB 依赖性受体(TBDR)、OmpW 和 OmpA 孔蛋白以及一种 IV 型菌毛生物发生蛋白(PilF)同源。通过定量 RT-PCR 的基因表达分析表明,在疏水性和亲水性表面上形成生物膜的过程中,这四个相应基因的表达上调。不能产生任何 OmpW、OmpA 和 PilF 同源物的铜绿假单胞菌突变体产生的生物膜的生物量较低且结构发生改变,这证实了这些蛋白参与了生物膜的形成过程。我们的结果表明,假交替单胞菌 D41 与人类病原菌共享生物膜形成机制,但也依赖于 TBDR,这可能更特定于海洋环境。

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