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铜绿假单胞菌 GB-1 中的锰(II)氧化受鞭毛合成和表面底物的影响。

Mn(II) oxidation in Pseudomonas putida GB-1 is influenced by flagella synthesis and surface substrate.

机构信息

Division of Environmental and Biomolecular Systems, Oregon Health & Science University, Beaverton, OR, 97006-8921, USA.

出版信息

Arch Microbiol. 2011 Aug;193(8):605-14. doi: 10.1007/s00203-011-0702-0. Epub 2011 Apr 11.

Abstract

Bacterially mediated manganese(II) oxidation greatly affects the biogeochemical cycling of Mn and other elements. One species of bacteria that are capable of Mn(II) oxidation is the gamma-proteobacterium Pseudomonas putida GB-1. In this organism, Mn(II) oxidation begins in stationary phase on the outer surface of the cell, forming a layer of insoluble Mn(III,IV) oxides. A random transposon mutagenesis screen isolated 12 mutant strains of P. putida GB-1 that exhibited increased Mn(II) oxidation on solid media relative to wild type. In 8 out of the 12 strains, the transposon had inserted into a putative flagellar gene. Those 8 strains each had motility defects, thus the disrupted genes are part of the P. putida GB-1 flagellar regulon. The flagellar genes identified include putative structural components (FliC, FliD, FlgE, and FlgL) and regulatory proteins (FlgM and FleN). Deletion of either the FleN gene (fleN) or the overlapping gene fliA resulted in increased Mn(II) oxidation, while in-frame deletion of fliF, which encodes an essential component of the basal body, did not. In liquid media, the flagellar mutants exhibited delayed Mn(II) oxidation relative to wild type. These results suggest that bacterial Mn(II) oxidation is regulated in part by flagellar-mediated responses to the surface substrate.

摘要

细菌介导的锰(II)氧化作用极大地影响了锰和其他元素的生物地球化学循环。能够氧化 Mn(II)的细菌物种之一是γ-变形菌假单胞菌 GB-1。在该生物体内,Mn(II)氧化作用始于细胞外表面的静止期,形成一层不溶性的 Mn(III,IV)氧化物。随机转座子诱变筛选分离出 12 株相对于野生型在固体培养基上具有更高 Mn(II)氧化作用的假单胞菌 GB-1 突变株。在 12 株菌株中的 8 株中,转座子插入了一个假定的鞭毛基因。这 8 株菌均存在运动缺陷,因此,被破坏的基因是假单胞菌 GB-1 鞭毛调控子的一部分。鉴定出的鞭毛基因包括假定的结构成分(FliC、FliD、FlgE 和 FlgL)和调节蛋白(FlgM 和 FleN)。缺失 FleN 基因(fleN)或重叠基因 fliA 都会导致 Mn(II)氧化增加,而编码基体基本成分的 fliF 基因的框内缺失则不会。在液体培养基中,与野生型相比,鞭毛突变体的 Mn(II)氧化作用延迟。这些结果表明,细菌 Mn(II)氧化作用部分受到鞭毛介导的对表面底物的反应的调控。

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