Molecular cloning, DNA sequence analysis, and characterization of the Corynebacterium diphtheriae dtxR homolog from Brevibacterium lactofermentum

Author:

Oguiza J A1,Tao X1,Marcos A T1,Martín J F1,Murphy J R1

Affiliation:

1. Area of Microbiology, Faculty of Biology, University of León, Spain.

Abstract

A homolog of the Corynebacterium diphtheriae dtxR gene was isolated from Brevibacterium lactofermentum. The product of the B. lactofermentum dtxR gene was immunoreactive with polyclonal anti-DtxR antibodies and functioned as an iron-activated repressor capable of regulating the expression of beta-galactosidase from a diphtheria tox promoter/operator transcriptional fusion in recombinant Escherichia coli. The extents of induction by increasing concentrations of the chelator 2,2'-dipyridyl were identical in cells expressing DtxR from either C. diphtheriae or B. lactofermentum.

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

Reference15 articles.

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4. Martín J. F. R. F. Cadenas M. Malumbres L. M. Mateos C. Guerrero and J. A. Gil. 1990. Construction and utilization of promoter-probe and expression vectors in corynebacteria. Characterization of corynebacterial promoters p. 283-292. In H. Heslot J. Davies J. Florent L. Bobichon G. Durant and L. Penasse (ed.) Genetics of industrial microorganisms '90. Société Française de Microbiologie Strasbourg France.

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