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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].微生物学通报,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
基金项目:国家自然科学基金 , 国家高技术研究发展计划(863计划)
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  假单胞菌  调控基因  克隆  功能研究  Pseudomonas  Mutant  gene  Characterization  差异  培养基  积累量  发酵液  野生型  合成  运动能力  泳动  结果  突变株  技术构建  同源重组
修稿时间:2007年3月14日

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].Microbiology,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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