Journal of Bacteriology, April 1999, p. 2059-2066, Vol. 181, No. 7
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Unité de Biochimie Microbienne, Institut Pasteur, URA 1300 du Centre National de la Recherche Scientifique, 75724 Paris Cedex 15, France
Received 8 December 1998/Accepted 22 January 1999
A new gene, bkdR (formerly called yqiR),
encoding a regulator with a central (catalytic) domain was found in
Bacillus subtilis. This gene controls the utilization of
isoleucine and valine as sole nitrogen sources. Seven genes, previously
called yqiS, yqiT, yqiU,
yqiV, bfmBAA, bfmBAB, and
bfmBB and now referred to as ptb, bcd, buk, lpd, bkdA1,
bkdA2, and bkdB, are located downstream from
the bkdR gene in B. subtilis. The products of
these genes are similar to phosphate butyryl coenzyme A transferase,
leucine dehydrogenase, butyrate kinase, and four components of the
branched-chain keto acid dehydrogenase complex: E3 (dihydrolipoamide
dehydrogenase), E1
(dehydrogenase), E1
(decarboxylase), and E2
(dihydrolipoamide acyltransferase). Isoleucine and valine utilization
was abolished in bcd and bkdR null mutants of
B. subtilis. The seven genes appear to be organized as an
operon, bkd, transcribed from a
12,
24 promoter. The
expression of the bkd operon was induced by the presence of
isoleucine or valine in the growth medium and depended upon the
presence of the sigma factor SigL, a member of the sigma 54 family.
Transcription of this operon was abolished in strains containing a null
mutation in the regulatory gene bkdR. Deletion analysis
showed that upstream activating sequences are involved in the
expression of the bkd operon and are probably the target of
bkdR. Transcription of the bkd operon is also
negatively controlled by CodY, a global regulator of gene expression in
response to nutritional conditions.
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