Abstract
In Salmonella typhimurium, thiamine is a required nutrient that is synthesized de novo. Labeling studies have demonstrated probable precursors for both the 4-amino-5-hydroxymethyl-2-methylpyrimidine pyrophosphate moiety and the 4-methyl-5-(beta-hydroxyethyl) thiazole monophosphate moiety. The isolation of thiamine auxotrophs with mutations in at least five different genetic loci is reported. The majority (22 of 25) of the mutants required only the thiazole moiety of thiamine to satisfy their growth requirement. Most (14 of 25) of the mutants were affected in the thi cluster at min 90 on the S. typhimurium genetic map. Data provided herein indicate that this cluster encodes an operon whose transcription is regulated by thiamine and suggest that thiamine pyrophosphate, or a molecule derived form it, is the effector molecule. Mutants with altered regulation of this operon were isolated, and we propose that they are defective in thiamine phosphate kinase, the product of the thiL gene.
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- Abstracts of papers presented at the 1980 meetings of the Genetic Society of America. Boulder, Colorado August 18-20, 1980. Genetics. 1980;94(4 Pt 2 Suppl):1–16. [PMC free article] [PubMed] [Google Scholar]
- Archer C. D., Elliott T. Transcriptional control of the nuo operon which encodes the energy-conserving NADH dehydrogenase of Salmonella typhimurium. J Bacteriol. 1995 May;177(9):2335–2342. doi: 10.1128/jb.177.9.2335-2342.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Benson N. R., Goldman B. S. Rapid mapping in Salmonella typhimurium with Mud-P22 prophages. J Bacteriol. 1992 Mar;174(5):1673–1681. doi: 10.1128/jb.174.5.1673-1681.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Castilho B. A., Olfson P., Casadaban M. J. Plasmid insertion mutagenesis and lac gene fusion with mini-mu bacteriophage transposons. J Bacteriol. 1984 May;158(2):488–495. doi: 10.1128/jb.158.2.488-495.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chen P., Ailion M., Weyand N., Roth J. The end of the cob operon: evidence that the last gene (cobT) catalyzes synthesis of the lower ligand of vitamin B12, dimethylbenzimidazole. J Bacteriol. 1995 Mar;177(6):1461–1469. doi: 10.1128/jb.177.6.1461-1469.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ciampi M. S., Roth J. R. Polarity effects in the hisG gene of salmonella require a site within the coding sequence. Genetics. 1988 Feb;118(2):193–202. doi: 10.1093/genetics/118.2.193. [DOI] [PMC free article] [PubMed] [Google Scholar]
- DeMoll E., Shive W. Determination of the metabolic origin of the sulfur atom in thiamin of Escherichia coli by mass spectrometry. Biochem Biophys Res Commun. 1985 Oct 15;132(1):217–222. doi: 10.1016/0006-291x(85)91010-1. [DOI] [PubMed] [Google Scholar]
- Downs D. M. Evidence for a new, oxygen-regulated biosynthetic pathway for the pyrimidine moiety of thiamine in Salmonella typhimurium. J Bacteriol. 1992 Mar;174(5):1515–1521. doi: 10.1128/jb.174.5.1515-1521.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Downs D. M., Petersen L. apbA, a new genetic locus involved in thiamine biosynthesis in Salmonella typhimurium. J Bacteriol. 1994 Aug;176(16):4858–4864. doi: 10.1128/jb.176.16.4858-4864.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Escalante-Semerena J. C., Roth J. R. Regulation of cobalamin biosynthetic operons in Salmonella typhimurium. J Bacteriol. 1987 May;169(5):2251–2258. doi: 10.1128/jb.169.5.2251-2258.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Estramareix B., David S. Conversion of 5-aminoimidazole ribotide to the pyrimidine of thiamin in enterobacteria: study of the pathway with specifically labeled samples of riboside. Biochim Biophys Acta. 1990 Aug 17;1035(2):154–160. doi: 10.1016/0304-4165(90)90110-i. [DOI] [PubMed] [Google Scholar]
- Estramareix B., Therisod M. La tyrosine, facteur de la biosynthèse du thiazole de la thiamine chez Escherichia coli. Biochim Biophys Acta. 1972 Jul 19;273(2):275–282. [PubMed] [Google Scholar]
- Groenen M. A., Timmers E., van de Putte P. DNA sequences at the ends of the genome of bacteriophage Mu essential for transposition. Proc Natl Acad Sci U S A. 1985 Apr;82(7):2087–2091. doi: 10.1073/pnas.82.7.2087. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hong J. S., Ames B. N. Localized mutagenesis of any specific small region of the bacterial chromosome. Proc Natl Acad Sci U S A. 1971 Dec;68(12):3158–3162. doi: 10.1073/pnas.68.12.3158. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hughes K. T., Roth J. R. Directed formation of deletions and duplications using Mud(Ap, lac). Genetics. 1985 Feb;109(2):263–282. doi: 10.1093/genetics/109.2.263. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Imamura N., Nakayama H. thiK and thiL loci of Escherichia coli. J Bacteriol. 1982 Aug;151(2):708–717. doi: 10.1128/jb.151.2.708-717.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kawasaki T., Nose Y. Thiamine regulatory mutants in Escherichia coli. J Biochem. 1969 Mar;65(3):417–425. doi: 10.1093/oxfordjournals.jbchem.a129029. [DOI] [PubMed] [Google Scholar]
- Kawasi T., Iwashima A., Nose Y. Regulation of thiamine biosynthesis in Escherichia coli. J Biochem. 1969 Mar;65(3):407–416. doi: 10.1093/oxfordjournals.jbchem.a129028. [DOI] [PubMed] [Google Scholar]
- Kleckner N., Roth J., Botstein D. Genetic engineering in vivo using translocatable drug-resistance elements. New methods in bacterial genetics. J Mol Biol. 1977 Oct 15;116(1):125–159. doi: 10.1016/0022-2836(77)90123-1. [DOI] [PubMed] [Google Scholar]
- Mizote T., Nakayama H. The thiM locus and its relation to phosphorylation of hydroxyethylthiazole in Escherichia coli. J Bacteriol. 1989 Jun;171(6):3228–3232. doi: 10.1128/jb.171.6.3228-3232.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nakayama H., Hayashi R. Biosynthetic pathway of thiamine pyrophosphate: a special reference to the thiamine monophosphate-requiring mutant and the thiamine pyrophosphate-requiring mutant of Escherichia coli. J Bacteriol. 1972 Dec;112(3):1118–1126. doi: 10.1128/jb.112.3.1118-1126.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Newell P. C., Tucker R. G. Precursors of the pyrimidine moiety of thiamine. Biochem J. 1968 Jan;106(1):271–277. doi: 10.1042/bj1060271. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sanderson K. E., Hessel A., Rudd K. E. Genetic map of Salmonella typhimurium, edition VIII. Microbiol Rev. 1995 Jun;59(2):241–303. doi: 10.1128/mr.59.2.241-303.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sanger F., Nicklen S., Coulson A. R. DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci U S A. 1977 Dec;74(12):5463–5467. doi: 10.1073/pnas.74.12.5463. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schmieger H. Phage P22-mutants with increased or decreased transduction abilities. Mol Gen Genet. 1972;119(1):75–88. doi: 10.1007/BF00270447. [DOI] [PubMed] [Google Scholar]
- VOGEL H. J., BONNER D. M. Acetylornithinase of Escherichia coli: partial purification and some properties. J Biol Chem. 1956 Jan;218(1):97–106. [PubMed] [Google Scholar]
- Vander Horn P. B., Backstrom A. D., Stewart V., Begley T. P. Structural genes for thiamine biosynthetic enzymes (thiCEFGH) in Escherichia coli K-12. J Bacteriol. 1993 Feb;175(4):982–992. doi: 10.1128/jb.175.4.982-992.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Way J. C., Davis M. A., Morisato D., Roberts D. E., Kleckner N. New Tn10 derivatives for transposon mutagenesis and for construction of lacZ operon fusions by transposition. Gene. 1984 Dec;32(3):369–379. doi: 10.1016/0378-1119(84)90012-x. [DOI] [PubMed] [Google Scholar]
- Youderian P., Sugiono P., Brewer K. L., Higgins N. P., Elliott T. Packaging specific segments of the Salmonella chromosome with locked-in Mud-P22 prophages. Genetics. 1988 Apr;118(4):581–592. doi: 10.1093/genetics/118.4.581. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zurlinden A., Schweingruber M. E. Cloning, nucleotide sequence, and regulation of Schizosaccharomyces pombe thi4, a thiamine biosynthetic gene. J Bacteriol. 1994 Nov;176(21):6631–6635. doi: 10.1128/jb.176.21.6631-6635.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]