Corbell N, Loper J E
Department of Botany and Plant Pathology, Oregon State University, Corvallis 97331, USA.
J Bacteriol. 1995 Nov;177(21):6230-6. doi: 10.1128/jb.177.21.6230-6236.1995.
Mutations in the apdA (for antibiotic production) gene of the plant root-colonizing bacterium Pseudomonas fluorescens Pf-5 pleiotropically abolish the production of an array of antibiotics, including pyrrolnitrin, pyoluteorin, and 2,4-diacetylphloroglucinol, as well as the production of tryptophan side chain oxidase, hydrogen cyanide, and an extracellular protease. The lack of production of secondary metabolites by ApdA- mutants was correlated with the loss of inhibition of the phytopathogenic fungus Rhizoctonia solani in culture. Sequencing of the apdA region identified an open reading frame of 2,751 bp. The predicted amino acid sequence of the apdA gene contains conserved domains of the histidine kinases that serve as sensor components of prokaryotic two-component regulatory systems. The apdA nucleotide and predicted amino acid sequences are strikingly similar to the sequences of lemA and repA, genes encoding putative sensor kinases that are required for the pathogenicity of Pseudomonas syringae pv. syringae and Pseudomonas viridiflava, respectively. Introduction of the cloned apdA+ gene restored the wild-type phenotype to both LemA- mutants of P. syringae and ApdA- mutants of Pf-5. The 101-kDa ApdA protein reacted with an anti-LemA antiserum, further demonstrating the similarity of ApdA to LemA. These results show that apdA encodes a putative sensor kinase component of a classical two-component regulatory system that is required for secondary-metabolite production by P. fluorescens Pf-5.
植物根际定殖细菌荧光假单胞菌Pf-5的apdA(抗生素产生相关)基因突变会多效性地消除一系列抗生素的产生,包括吡咯菌素、绿脓菌素和2,4-二乙酰基间苯三酚,同时还会消除色氨酸侧链氧化酶、氰化氢和一种细胞外蛋白酶的产生。ApdA突变体无法产生次级代谢产物,这与在培养中对植物致病真菌立枯丝核菌抑制作用的丧失相关。对apdA区域进行测序鉴定出一个2751 bp的开放阅读框。apdA基因预测的氨基酸序列包含组氨酸激酶的保守结构域,这些结构域作为原核双组分调节系统的传感组件。apdA核苷酸序列和预测的氨基酸序列与lemA和repA的序列惊人地相似,lemA和repA分别是丁香假单胞菌丁香致病变种和绿黄假单胞菌致病性所需的假定传感激酶的编码基因。导入克隆的apdA+基因可使丁香假单胞菌的LemA突变体和Pf-5的ApdA突变体都恢复野生型表型。101 kDa的ApdA蛋白与抗LemA抗血清发生反应,进一步证明了ApdA与LemA的相似性。这些结果表明,apdA编码一种经典双组分调节系统的假定传感激酶组件,荧光假单胞菌Pf-5产生次级代谢产物需要该组件。