Your browser doesn't support javascript.
loading
The outer membrane protein OprF and the sigma factor SigX regulate antibiotic production in Pseudomonas fluorescens 2P24.
Li, Xu; Gu, Gao-Qi; Chen, Wei; Gao, Li-Juan; Wu, Xue-Hong; Zhang, Li-Qun.
Affiliation
  • Li X; Department of Plant Pathology, China Agricultural University, Beijing, China.
  • Gu GQ; Department of Plant Pathology, China Agricultural University, Beijing, China.
  • Chen W; Department of Plant Pathology, China Agricultural University, Beijing, China.
  • Gao LJ; Beijing Centre for Physical and Chemical Analysis, Beijing, 100089, China.
  • Wu XH; Department of Plant Pathology, China Agricultural University, Beijing, China; Key Laboratory of Pest Monitoring and Green Management, Ministry of Agriculture, Beijing, China.
  • Zhang LQ; Department of Plant Pathology, China Agricultural University, Beijing, China; Key Laboratory of Pest Monitoring and Green Management, Ministry of Agriculture, Beijing, China. Electronic address: zhanglq@cau.edu.cn.
Microbiol Res ; 206: 159-167, 2018 Jan.
Article in En | MEDLINE | ID: mdl-29146252
ABSTRACT
Pseudomonas fluorescens 2P24 produces 2,4-diacetylphloroglucinol (2,4-DAPG) as the major antibiotic compound that protects plants from soil-borne diseases. Expression of the 2,4-DAPG biosynthesis enzymes, which are encoded by the phlACBD locus, is under the control of a delicate regulatory network. In this study, we identified a novel role for the outer membrane protein gene oprF, in negatively regulating the 2,4-DAPG production by using random mini-Tn5 mutagentsis. A sigma factor gene sigX was located immediately upstream of the oprF gene and shown to be a positive regulator for oprF transcription and 2,4-DAPG production. Genetic analysis of an oprF and sigX double-mutant indicated that the 2,4-DAPG regulation by oprF was dependent on SigX. The sigX gene did not affect PhlA and PhlD expression, but positively regulated the level of malonyl-CoA, the substrate of 2,4-DAPG synthesis, by influencing the expression of acetyl-CoA carboxylases. Further investigations revealed that sigX transcription was induced under conditions of salt starvation or glycine addition. All these findings indicate that SigX is a novel regulator of substrate supplements for 2,4-DAPG production.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sigma Factor / Bacterial Proteins / Pseudomonas fluorescens / Gene Expression Regulation, Bacterial / Membrane Proteins / Anti-Bacterial Agents Type of study: Prognostic_studies Language: En Journal: Microbiol Res Journal subject: MICROBIOLOGIA / SAUDE AMBIENTAL Year: 2018 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sigma Factor / Bacterial Proteins / Pseudomonas fluorescens / Gene Expression Regulation, Bacterial / Membrane Proteins / Anti-Bacterial Agents Type of study: Prognostic_studies Language: En Journal: Microbiol Res Journal subject: MICROBIOLOGIA / SAUDE AMBIENTAL Year: 2018 Document type: Article Affiliation country: China