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一个参与荧光假单胞菌ATCC 17400中绿脓菌素产生的细胞色素c生物合成基因。

A cytochrome c biogenesis gene involved in pyoverdine production in Pseudomonas fluorescens ATCC 17400.

作者信息

Gaballa A, Koedam N, Cornelis P

机构信息

Laboratorium Plantenfysiologie, Vrije Universiteit Brussel, Sint Genesius Rode, Belgium.

出版信息

Mol Microbiol. 1996 Aug;21(4):777-85. doi: 10.1046/j.1365-2958.1996.391399.x.

Abstract

Pseudomonas fluorescens ATCC 17400 produces pyoverdine under iron-limiting conditions. A Tn5 mutant, 2G11, produced lower amounts of different pyoverdine forms and was unable to grow under iron limitation caused by ethylenediamine-di(o-hydroxy-phenylacetic acid) (EDDHA) or zinc. This mutant was complemented by a 9.6 kb HindIII-BamHI DNA fragment that contained eight contiguous open reading frames (ORFs cytA to cytH). The proteins possibly encoded by this polycistronic gene cluster were all similar to the products of cytochrome c biogenesis genes from, amongst others, Rhodobacter capsulatus and Bradyrhizobium japonicum, not only in terms of amino acid sequence, but also in the overall hydropathy index of these proteins. By TnphoA mutagenesis and site-specific gene replacement it was found that the first three ORFs (cytA to cytC) were essential for cytochrome c production while only the product of cytA was needed for normal pyoverdine production. The presence of a putative haem-binding site in the CytA protein (WGSWWVWD) was confirmed. From analysis of a constructed phoA fusion, a periplasmic location was found for this motif. The ability of the cytA gene to restore both cytochrome c and pyoverdine production suggests the involvement of this particular gene both in haem and in pyoverdine transport in P. fluorescens.

摘要

荧光假单胞菌ATCC 17400在铁限制条件下产生吡咯菌素。一个Tn5突变体2G11产生的不同形式的吡咯菌素量较低,并且在由乙二胺 - 二(邻羟基苯乙酸)(EDDHA)或锌引起的铁限制下无法生长。该突变体由一个9.6 kb的HindIII - BamHI DNA片段互补,该片段包含八个连续的开放阅读框(ORF cytA至cytH)。这个多顺反子基因簇可能编码的蛋白质不仅在氨基酸序列方面,而且在这些蛋白质的整体亲水性指数方面,都与来自红假单胞菌和日本慢生根瘤菌等的细胞色素c生物合成基因的产物相似。通过TnphoA诱变和位点特异性基因置换发现,前三个ORF(cytA至cytC)对于细胞色素c的产生是必需的,而正常吡咯菌素的产生仅需要cytA的产物。在CytA蛋白(WGSWWVWD)中确认了一个假定的血红素结合位点。通过对构建的phoA融合体的分析,发现该基序位于周质中。cytA基因恢复细胞色素c和吡咯菌素产生的能力表明该特定基因参与了荧光假单胞菌中血红素和吡咯菌素的转运。

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