J. Bacteriol., 09 1996, 5540-5542, Vol 178, No. 18
Copyright © 1996, American Society for Microbiology
M Kataoka, T Tatsuta, I Suzuki, S Kosono, T Seki and T Yoshida
International Center for Biotechnology, Osaka University, Japan. mkataoka@nch.go.jp
PCR mutagenesis of a 0.9-kbp fragment, containing a repressor gene, traR, and its target promoter, Ptra, from Streptomyces nigrifaciens plasmid pSN22, produced Streptomyces lividans clones with temperature- inducible Ptra expression. Using the promoterless gene for the thermostable Thermus flavus malate dehydrogenase as an indicator, an induction of enzyme activity of as much as was observed in a temperature shift from 28 to 37 degrees C. Temperature downshift reestablished repression of Ptra, making these promoter cassettes very attractive for the temporally regulated expression of cloned genes in Streptomyces spp.
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