The metabolic strategies used by bacteria to cope with life in the absence of oxygen have been primarily studied in strict anaerobes. Little effort has been made to approach this problem in facultative anaerobes like enterobacteria (e.g., E. coli and Salmonella) for which genetic methods have been developed. Most work on the biochemistry and genetics of enterobacteria has been done using cells growing under aerobic conditions. We propose to investigate the anaerobic metabolism of the facultative anaerobe Salmonella typhimurium. Vitamin B12 (cobalamin) is a essential nutrient for many forms of life (excluding plants) including man. The biosynthesis of this important macromolecule is not well understood, and practically nothing is known about the environmental factors, and the mechanisms that regulate the synthesis of B12 at the molecular level. Salmonella makes B12 de novo but only during anaerobic growth conditions. The use of sophisticated genetics in this bacterium has yielded important information about the genomic organization and transcriptional regulation of the cobalamin biosynthetic (cob) genes. We will initiate a comprehensive approach to the characterization of the B12 biosynthetic enzymes. For this purpose, we will use modern chemical, biochemical, molecular biological, and genetic techniques. Genetic and molecular biological experiments will be performed to determine the number of gene products involved in the biosynthesis of the lower ligand of B12 (i.e., dimethylbenzimidazole, DMB), and in the synthesis of the nucleotide loop, which links DMB to the rest of the molecule. We will use biochemical and genetic techniques to establish the metabolic precursors of DMB, and its biosynthetic route(s). We have isolated a large number of mutants that will help us identify enzymic as well as regulatory functions of this pathway. Assays for a number of proposed enzymes will be set up, and used in their purification in order to understand the underlying chemical events leading to the synthesis of this macromolecule. We plan to study the role of newly discovered cob genes that map outside the reported cob operons, and which have different phenotypes in response to oxygen. These genes may be involved in interactions between the biosynthetic pathway and the sophisticated transport systems for this vitamin. We propose to continue investigating B12 biosynthesis in hopes of increasing our understanding of this vitamin and the anaerobic lifestyle of Salmonella.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM040313-02
Application #
3297733
Study Section
Microbial Physiology and Genetics Subcommittee 2 (MBC)
Project Start
1988-09-01
Project End
1992-08-31
Budget Start
1989-09-01
Budget End
1990-08-31
Support Year
2
Fiscal Year
1989
Total Cost
Indirect Cost
Name
University of Wisconsin Madison
Department
Type
Earth Sciences/Resources
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
Mattes, Theodoric A; Escalante-Semerena, Jorge C (2018) Facile isolation of ?-ribazole from vitamin B12 hydrolysates using boronate affinity chromatography. J Chromatogr B Analyt Technol Biomed Life Sci 1090:52-55
Park, Kiyoung; Mera, Paola E; Moore, Theodore C et al. (2015) Unprecedented Mechanism Employed by the Salmonella enterica EutT ATP:Co(I)rrinoid Adenosyltransferase Precludes Adenosylation of Incomplete Co(II)rrinoids. Angew Chem Int Ed Engl 54:7158-61
Newmister, Sean A; Otte, Michele M; Escalante-Semerena, Jorge C et al. (2011) Structure and mutational analysis of the archaeal GTP:AdoCbi-P guanylyltransferase (CobY) from Methanocaldococcus jannaschii: insights into GTP binding and dimerization. Biochemistry 50:5301-13
Mera, Paola E; Escalante-Semerena, Jorge C (2010) Dihydroflavin-driven adenosylation of 4-coordinate Co(II) corrinoids: are cobalamin reductases enzymes or electron transfer proteins? J Biol Chem 285:2911-7
Gray, Michael J; Escalante-Semerena, Jorge C (2010) A new pathway for the synthesis of ?-ribazole-phosphate in Listeria innocua. Mol Microbiol 77:1429-38
Claas, Kathy R; Parrish, J R; Maggio-Hall, L A et al. (2010) Functional analysis of the nicotinate mononucleotide:5,6-dimethylbenzimidazole phosphoribosyltransferase (CobT) enzyme, involved in the late steps of coenzyme B12 biosynthesis in Salmonella enterica. J Bacteriol 192:145-54
Otte, Michele M; Escalante-Semerena, Jorge C (2009) Biochemical characterization of the GTP:adenosylcobinamide-phosphate guanylyltransferase (CobY) enzyme of the hyperthermophilic archaeon Methanocaldococcus jannaschii. Biochemistry 48:5882-9
Gray, Michael J; Escalante-Semerena, Jorge C (2009) The cobinamide amidohydrolase (cobyric acid-forming) CbiZ enzyme: a critical activity of the cobamide remodelling system of Rhodobacter sphaeroides. Mol Microbiol 74:1198-210
Gray, Michael J; Escalante-Semerena, Jorge C (2009) In vivo analysis of cobinamide salvaging in Rhodobacter sphaeroides strain 2.4.1. J Bacteriol 191:3842-51
Mera, Paola E; St Maurice, Martin; Rayment, Ivan et al. (2009) Residue Phe112 of the human-type corrinoid adenosyltransferase (PduO) enzyme of Lactobacillus reuteri is critical to the formation of the four-coordinate Co(II) corrinoid substrate and to the activity of the enzyme. Biochemistry 48:3138-45

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