Cloning of genes involved in myo-inositol transport in a Pseudomonas sp
Author(s) -
D Gauchat-Feiss,
Joachim Frey,
M Belet,
J. Deshusses
Publication year - 1985
Publication title -
journal of bacteriology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.652
H-Index - 246
eISSN - 1067-8832
pISSN - 0021-9193
DOI - 10.1128/jb.162.1.324-327.1985
Subject(s) - biology , periplasmic space , cosmid , mutant , escherichia coli , pseudomonas , cloning (programming) , molecular cloning , microbiology and biotechnology , gene , mutagenesis , biochemistry , genetics , bacteria , gene expression , programming language , computer science
A soil isolate of a Pseudomonas sp. can utilize myo-inositol (MI) as the sole carbon source. In this strain, MI is transported through the membrane by a high-affinity transport system in which a periplasmic binding protein is involved. Mutants impaired in the transport system were obtained by mutagenesis with N-methyl-N'-nitro-N-nitrosoguanidine and subsequently identified by their slow growth rate at low MI concentrations. Strains with a low linear initial rate of MI uptake were analyzed. Using a broad-host-range cosmid cloning system, we have constructed a gene bank of the wild-type Pseudomonas sp. in an Escherichia coli recA-host. A rapid mating technique enabled us to screen the gene library for clones which are able to restore the active transport of MI in the mutant. An 11.5-kilobase segment containing genes involved in the MI transport has been isolated, and its restriction enzyme cleavage map has been determined.
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