PMID:7665460

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Citation

Maupin-Furlow, JA, Rosentel, JK, Lee, JH, Deppenmeier, U, Gunsalus, RP and Shanmugam, KT (1995) Genetic analysis of the modABCD (molybdate transport) operon of Escherichia coli. J. Bacteriol. 177:4851-6

Abstract

DNA sequence analysis of the modABCD operon of Escherichia coli revealed the presence of four open reading frames. The first gene, modA, codes for a 257-amino-acid periplasmic binding protein enunciated by the presence of a signal peptide-like sequence. The second gene (modB) encodes a 229-amino-acid protein with a potential membrane location, while the 352-amino-acid ModC protein (modC product) contains a nucleotide-binding motif. On the basis of sequence similarities with proteins from other transport systems and molybdate transport proteins from other organisms, these three proteins are proposed to constitute the molybdate transport system. The fourth open reading frame (modD) encodes a 231-amino-acid protein of unknown function. Plasmids containing different mod genes were used to map several molybdate-suppressible chlorate-resistant mutants; interestingly, none of the 40 mutants tested had a mutation in the modD gene. About 35% of these chlorate-resistant mutants were not complemented by mod operon DNA. These mutants, designated mol, contained mutations at unknown chromosomal location(s) and produced formate hydrogenlyase activity only when cultured in molybdate-supplemented glucose-minimal medium, not in L broth. This group of mol mutants constitutes a new class of molybdate utilization mutants distinct from other known mutants in molybdate metabolism. These results show that molybdate, after transport into cells by the ModABC proteins, is metabolized (activated?) by the products of the mol gene(s).

Links

PubMed PMC177257

Keywords

Amino Acid Sequence; Base Sequence; Biological Transport/genetics; Chlorates/pharmacology; Drug Resistance, Microbial/genetics; Escherichia coli/genetics; Formate Dehydrogenases/biosynthesis; Genes, Bacterial/genetics; Hydrogenase/biosynthesis; Molecular Sequence Data; Molybdenum/metabolism; Multienzyme Complexes/biosynthesis; Mutation; Open Reading Frames/genetics; Operon/genetics; Sequence Analysis, DNA

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