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J. Bacteriol., 10 1997, 6504-6508, Vol 179, No. 20
BJ Beck, LE Connolly, A De Las Penas and DM Downs
In Salmonella typhimurium, the genetic loci and biochemical reactions
necessary for the conversion of aminoimidazole ribotide (AIR) to the 4-
amino-5-hydroxymethyl-2-methyl pyrimidine (HMP) moiety of thiamine remain
unknown. Preliminary genetic analysis indicates that there may be more than
one pathway responsible for the synthesis of HMP from AIR and that the
function of these pathways depends on the availability of AIR, synthesized
by the purine pathway or by the purF-independent alternative pyrimidine
biosynthetic (APB) pathway (L. Petersen and D. Downs, J. Bacteriol.
178:5676-5682, 1996). An insertion in rseB, the third gene in the rpoE
rseABC gene cluster at 57 min, prevented HMP synthesis in a purF mutant.
Complementation analysis demonstrated that the HMP requirement of the purF
rseB strain was due to polarity of the insertion in rseB on the downstream
rseC gene. The role of RseC in thiamine synthesis was independent of rpoE.
Copyright © 1997, American Society for Microbiology
Evidence that rseC, a gene in the rpoE cluster, has a role in thiamine synthesis in Salmonella typhimurium
Department of Bacteriology, University of Wisconsin-Madison, 53706, USA.
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