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假单胞菌M18调控基因ppbR的克隆及功能研究
引用本文:郑 斐,黄显清,许煜泉,张雪洪.假单胞菌M18调控基因ppbR的克隆及功能研究[J].微生物学报,2008,35(2):0235-0240.
作者姓名:郑 斐  黄显清  许煜泉  张雪洪
作者单位:上海交通大学生命科学技术学院 微生物代谢教育部重点实验室 上海 200240;上海交通大学生命科学技术学院 微生物代谢教育部重点实验室 上海 200240;上海交通大学生命科学技术学院 微生物代谢教育部重点实验室 上海 200240;上海交通大学生命科学技术学院 微生物代谢教育部重点实验室 上海 200240
基金项目:国家自然科学基金项目(No.30370041和No.20676081); 863计划项目(No. 2006AA10A209)
摘    要:假单胞菌 (Pseudomonas sp.) M18 是促进植物生长的根际细菌, 能产生吩嗪-1-羧酸 (PCA) 和藤黄绿菌素 (Plt) 两种不同的抗生素。根据生物信息学分析, 铜绿假单胞菌PA2572基因编码蛋白可能是一个双元调控系统的应答调节子。本研究从假单胞菌M18基因组中扩增出PA2572同源基因片段ppbR, 利用体外定点插入突变和同源重组技术构建了M18 的ppbR突变株M18P。研究结果表明, 突变株M18P在泳动能力和群集运动能力上有显著的下降。突变株合成PCA 的能力比野生型有显著的下降, 在发酵液中PCA积累量仅为野生型的50%。在KMB培养基中, 突变株Plt的积累量和野生型没有显著的差异。

关 键 词:假单胞菌M18    ppbR    双元调控系统    泳动能力    群集运动能力    吩嗪-1-羧酸

Construction and Characterization of a ppbR gene Mutant of Pseudomonas sp. M18
ZHENG Fei,HUANG Xian-Qing,XU Yu-Quan and ZHANG Xue-Hong.Construction and Characterization of a ppbR gene Mutant of Pseudomonas sp. M18[J].Acta Microbiologica Sinica,2008,35(2):0235-0240.
Authors:ZHENG Fei  HUANG Xian-Qing  XU Yu-Quan and ZHANG Xue-Hong
Institution:Key Laboratory of Microbial Metabolism, Ministry of Education, College of Life Science and Biotechnology, Shanghai Jiaotong University, Shanghai 200240;Key Laboratory of Microbial Metabolism, Ministry of Education, College of Life Science and Biotechnology, Shanghai Jiaotong University, Shanghai 200240;Key Laboratory of Microbial Metabolism, Ministry of Education, College of Life Science and Biotechnology, Shanghai Jiaotong University, Shanghai 200240;Key Laboratory of Microbial Metabolism, Ministry of Education, College of Life Science and Biotechnology, Shanghai Jiaotong University, Shanghai 200240
Abstract:Pseudomonas sp. M18, one of plant-growth-promoting rhizobacteria, can produce secondary metabolites including phenazine-1-carboxylic acid (PCA) and pyoluteorin (Plt). PA2572 gene coding protein is a probable two-component response regulator in Pseudomonas according to homologous speculations. In order to investigate its genetic function, PA2572 homologous gene, ppbR, was amplified from M18 genome, inactivated by inserting a Gm cassette. The resulting reconstruct was introduced into the M18 genome using homologous recombination technique, so as to obtain the null mutant M18P. The results showed that the M18P has less flagellar swimming and swarming motility, and yielded fewer PCA. The production of PCA was only 50% of the wild type. However, there was no remarkable difference between mutant and wild type in producing pyoluteorin in KMB medium.
Keywords:Pseudomonas sp  M18  ppbR  Two-component regulatory system  Swimming mobility  Swarming mobility  Phenazine-1-carboxic acid
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