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microbiology, Vol 145, 67-73, Copyright © 1999 by Society for General Microbiology
ARTICLES |
IM Solovieva, RA Kreneva, DJ Leak and DA Perumov
Department of Molecular and Radiation Biophysics, Petersburg Nuclear Physics Institute of the Russian Academy of Sciences, Gatchina, Leningrad District. solovyov@math-atom.pti.spb.su
A 3.5 kb EcoRI-BamHI fragment of Bacillus subtilis chromosomal DNA carrying the ribR gene, involved in regulation of the B. subtilis riboflavin operon, was cloned in the B. subtilis-Escherichia coli shuttle vector pCB20. DNA sequence analysis of this fragment revealed several ORFs, one of which encodes a polypeptide of 230 amino acids with up to 45% sequence identity with FAD synthetases from a number of micro-organisms, such as Corynebacterium ammoniagenes, E. coli and Pseudomonas fluorescens, and also to the ribC gene product of B. subtilis. The ribR gene was amplified by PCR, cloned and expressed in E. coli. Measurement of flavokinase activity in cell extracts demonstrated that ribR encodes a monofunctional flavokinase which converts riboflavin into FMN but not to FAD, and is specific for the reduced form of riboflavin.
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