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Journal of Bacteriology, June 1999, p. 3810-3815, Vol. 181, No. 12
Department of Biochemistry and Food
Chemistry, University of Turku, FIN-20014 Turku,
Finland,1 and Department of
Biochemistry, Purdue University, West Lafayette, Indiana
479072
Received 25 March 1998/Accepted 14 April 1999
Regulation of the purine biosynthetic gene purA was
examined by using a transcriptional fusion to a luciferase reporter
gene. Transcription was repressed about 10-fold by the addition of
adenine and increased approximately 4.5-fold by the addition of
guanosine. This regulation is mediated by a purine repressor (PurR). In
a purR mutant, basal expression was increased 10-fold, and
there was no further stimulation by guanosine or repression by adenine. An open reading frame, yabJ, immediately downstream from
purR was found to have a role in the repression of
purA by adenine. Repression by adenine was perturbed in a
purR+ yabJ mutant, although guanosine
regulation was retained. Mutations in the PurR PRPP binding motif
abolished guanosine regulation in the yabJ mutant. Thus,
PRPP appears to be required for upregulation by guanosine. The amino
acid sequence of YabJ is homologous to the YER057c/YjgF protein family
of unknown function.
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
A Role for a Highly Conserved Protein of Unknown
Function in Regulation of Bacillus subtilis purA by the
Purine Repressor

*
Corresponding author. Mailing address: Department of
Biochemistry and Food Chemistry, University of Turku, Vatselankatu 2, FIN-20014 Turku, Finland. Phone: 358-2 333 6856. Fax: 358-2 333 6860. E-mail: pekrappu{at}utu.fi.
Present address: Bacterial Molecular Genetics Research
Unit, Korea Research Institute of Bioscience and Biotechnology, P.O. Box 115, Yusong, Taejon 305-600, Korea.
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