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Microbiol Res ; 206: 159-167, 2018 Jan.
Article in English | 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)
Anti-Bacterial Agents/metabolism , Bacterial Proteins/genetics , Gene Expression Regulation, Bacterial/genetics , Membrane Proteins/genetics , Pseudomonas fluorescens/genetics , Pseudomonas fluorescens/metabolism , Sigma Factor/genetics , Acetyl-CoA Carboxylase/metabolism , Bacterial Proteins/metabolism , Base Sequence , Chromosome Mapping , DNA, Bacterial , Escherichia coli/genetics , Gene Expression Profiling , Genes, Bacterial/genetics , Genetic Vectors , Membrane Proteins/metabolism , Mutation , Phenotype , Phloroglucinol/analogs & derivatives , Phloroglucinol/metabolism , Protein Biosynthesis , Pseudomonas fluorescens/growth & development , Rhizoctonia , Sigma Factor/metabolism , Transcription, Genetic , Transcriptional Activation
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