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NarK1和NarK2蛋白在反硝化细菌铜绿假单胞菌PAO1中对硝酸盐和亚硝酸盐的转运作用。

Involvement of NarK1 and NarK2 proteins in transport of nitrate and nitrite in the denitrifying bacterium Pseudomonas aeruginosa PAO1.

作者信息

Sharma Vandana, Noriega Chris E, Rowe John J

机构信息

Department of Biology, University of Dayton, 300 College Park, Dayton, OH 45469-2320, USA.

出版信息

Appl Environ Microbiol. 2006 Jan;72(1):695-701. doi: 10.1128/AEM.72.1.695-701.2006.

Abstract

Two transmembrane proteins were tentatively classified as NarK1 and NarK2 in the Pseudomonas genome project and hypothesized to play an important physiological role in nitrate/nitrite transport in Pseudomonas aeruginosa. The narK1 and narK2 genes are located in a cluster along with the structural genes for the nitrate reductase complex. Our studies indicate that the transcription of all these genes is initiated from a single promoter and that the gene complex narK1K2GHJI constitutes an operon. Utilizing an isogenic narK1 mutant, a narK2 mutant, and a narK1K2 double mutant, we explored their effect on growth under denitrifying conditions. While the DeltanarK1::Gm mutant was only slightly affected in its ability to grow under denitrification conditions, both the DeltanarK2::Gm and DeltanarK1K2::Gm mutants were found to be severely restricted in nitrate-dependent, anaerobic growth. All three strains demonstrated wild-type levels of nitrate reductase activity. Nitrate uptake by whole-cell suspensions demonstrated both the DeltanarK2::Gm and DeltanarK1K2::Gm mutants to have very low yet different nitrate uptake rates, while the DeltanarK1::Gm mutant exhibited wild-type levels of nitrate uptake. Finally, Escherichia coli narK rescued both the DeltanarK2::Gm and DeltanarK1K2::Gm mutants with respect to anaerobic respiratory growth. Our results indicate that only the NarK2 protein is required as a nitrate/nitrite transporter by Pseudomonas aeruginosa under denitrifying conditions.

摘要

在假单胞菌基因组计划中,两种跨膜蛋白被初步归类为NarK1和NarK2,并推测它们在铜绿假单胞菌的硝酸盐/亚硝酸盐转运中发挥重要的生理作用。narK1和narK2基因与硝酸盐还原酶复合体的结构基因位于一个基因簇中。我们的研究表明,所有这些基因的转录均从单个启动子起始,并且基因复合体narK1K2GHJI构成一个操纵子。利用同基因的narK1突变体、narK2突变体和narK1K2双突变体,我们探究了它们在反硝化条件下对生长的影响。虽然ΔnarK1::Gm突变体在反硝化条件下的生长能力仅受到轻微影响,但ΔnarK2::Gm和ΔnarK1K2::Gm突变体在依赖硝酸盐的厌氧生长中均受到严重限制。所有三个菌株均表现出野生型水平的硝酸盐还原酶活性。全细胞悬浮液对硝酸盐的摄取表明,ΔnarK2::Gm和ΔnarK1K2::Gm突变体的硝酸盐摄取率非常低但有所不同,而ΔnarK1::Gm突变体表现出野生型水平的硝酸盐摄取。最后,大肠杆菌narK在厌氧呼吸生长方面挽救了ΔnarK2::Gm和ΔnarK1K2::Gm突变体。我们的结果表明,在反硝化条件下,铜绿假单胞菌仅需要NarK2蛋白作为硝酸盐/亚硝酸盐转运体。

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