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Journal of Bacteriology, September 1998, p. 4757-4759, Vol. 180, No. 17
Department of Bacteriology, University of
Wisconsin-Madison, Madison, Wisconsin 53706
Received 13 April 1998/Accepted 21 June 1998
In Salmonella typhimurium, precursors to the pyrimidine
moiety of thiamine are synthesized de novo by the purine biosynthetic pathway or the alternative pyrimidine biosynthetic (APB) pathway. The
apbA gene was the first locus defined as required for
function of the APB pathway (D. M. Downs and L. Petersen, J. Bacteriol. 176:4858-4864, 1994). Recent work showed the ApbA protein
catalyzes the NADPH-specific reduction of ketopantoic acid to pantoic
acid. This activity had previously been associated with the
pantothenate biosynthetic gene panE. Although previous
reports placed panE at 87 min on the Escherichia
coli chromosome, we show herein that apbA and
panE are allelic and map to 10 min on both the S. typhimurium and E. coli chromosomes. Results
presented here suggest that the role of ApbA in thiamine synthesis is
indirect since in vivo labeling studies showed that pantoic acid, the
product of the ApbA-catalyzed reaction, is not a direct precursor to
thiamine via the APB pathway.
0021-9193/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
The panE Gene, Encoding Ketopantoate
Reductase, Maps at 10 Minutes and Is Allelic to apbA in
Salmonella typhimurium
*
Corresponding author. Mailing address: University of
Wisconsin-Madison, 1550 Linden Dr., Madison, WI 53706. Phone: (608)
265-4630. Fax: (608) 262-9865. E-mail:
Downs{at}macc.wisc.edu.
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