Open AccessTransposon mutations in the flagella biosynthetic pathway of the solvent‐tolerant Pseudomonas putida S12 result in a decreased expression of solvent efflux genes
Author(s) -
Kieboom Jasper,
Bruinenberg Riekje,
KeizerGunnink Ineke,
Bont Jan A.M.
Publication year - 2001
Publication title -
fems microbiology letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.899
H-Index - 151
eISSN - 1574-6968
pISSN - 0378-1097
DOI - 10.1111/j.1574-6968.2001.tb10628.x
Subject(s) - rpon , transposable element , sigma factor , mutant , biology , transposon mutagenesis , pseudomonas putida , efflux , flagellum , gene , mutagenesis , rna polymerase , genetics , microbiology and biotechnology , biochemistry , gene expression , promoter , rna
Fourteen solvent‐sensitive transposon mutants were generated from the solvent‐tolerant Pseudomonas putida strain S12 by applying the Tn Mod ‐KmO mutagenesis system. These mutants were unable to grow in the presence of octanol and toluene. By cloning the region flanking the transposon insertion point a partial sequence of the interrupted genes was determined. Comparison of the deduced amino acid sequences with a protein database revealed the following interrupted putative gene products: organic solvent efflux proteins SrpA and SrpB, the flagellar structural proteins FlgK, FlaG, FliI, FliC, and FliH, the transcriptional activator FleQ, the alternative RNA polymerase sigma factor RpoN, and the flagellum‐specific RNA polymerase sigma factor FliA (RpoF). The transposon mutants, except for the organic solvent efflux mutants, were nonmotile as determined by a swarm assay and the formation of the flagellum was totally impaired. Expression studies with a srp promoter probe showed a decreased expression of the SrpABC efflux pump in the nonmotile mutants.