DetoxFungiV1, Main, Exploration, bibRecord, 002214

Regulation of arsenate resistance in Desulfovibrio desulfuricans G20 by an arsRBCC operon and an arsC gene.

Identifieur interne : 002214 ( Main/Exploration ); précédent : 002213; suivant : 002215

Regulation of arsenate resistance in Desulfovibrio desulfuricans G20 by an arsRBCC operon and an arsC gene.

Auteurs : Xiangkai Li [États-Unis] ; Lee R. Krumholz

Source :

Journal of bacteriology [ 0021-9193 ] ; 2007.

RBID : pubmed:17337573

Descripteurs français

KwdFr :
- Arsenate Reductases (génétique), Arsenate Reductases (métabolisme), Arséniates (métabolisme), Arséniates (toxicité), Arsénites (métabolisme), Desulfovibrio desulfuricans (enzymologie), Desulfovibrio desulfuricans (génétique), Escherichia coli (MeSH), Génome bactérien (MeSH), Mutagenèse (MeSH), Opéron (MeSH), Oxydoréduction (MeSH), Phylogenèse (MeSH), Protéines bactériennes (génétique), Protéines bactériennes (métabolisme), Régulation de l'expression des gènes bactériens (MeSH), Régulation de l'expression des gènes codant pour des enzymes (MeSH), Résistance bactérienne aux médicaments (MeSH).
MESH :
- enzymologie : Desulfovibrio desulfuricans.
- génétique : Arsenate Reductases, Desulfovibrio desulfuricans, Protéines bactériennes.
- métabolisme : Arsenate Reductases, Arséniates, Arsénites, Protéines bactériennes.
- toxicité : Arséniates.
- Escherichia coli, Génome bactérien, Mutagenèse, Opéron, Oxydoréduction, Phylogenèse, Régulation de l'expression des gènes bactériens, Régulation de l'expression des gènes codant pour des enzymes, Résistance bactérienne aux médicaments.

English descriptors

KwdEn :
- Arsenate Reductases (genetics), Arsenate Reductases (metabolism), Arsenates (metabolism), Arsenates (toxicity), Arsenites (metabolism), Bacterial Proteins (genetics), Bacterial Proteins (metabolism), Desulfovibrio desulfuricans (enzymology), Desulfovibrio desulfuricans (genetics), Drug Resistance, Bacterial (MeSH), Escherichia coli (MeSH), Gene Expression Regulation, Bacterial (MeSH), Gene Expression Regulation, Enzymologic (MeSH), Genome, Bacterial (MeSH), Mutagenesis (MeSH), Operon (MeSH), Oxidation-Reduction (MeSH), Phylogeny (MeSH).
MESH :
- chemical , genetics : Arsenate Reductases, Bacterial Proteins.
- chemical , metabolism : Arsenate Reductases, Arsenates, Arsenites, Bacterial Proteins.
- chemical , toxicity : Arsenates.
- enzymology : Desulfovibrio desulfuricans.
- genetics : Desulfovibrio desulfuricans.
- Drug Resistance, Bacterial, Escherichia coli, Gene Expression Regulation, Bacterial, Gene Expression Regulation, Enzymologic, Genome, Bacterial, Mutagenesis, Operon, Oxidation-Reduction, Phylogeny.

Abstract

Desulfovibrio desulfuricans G20 grows and reduces 20 mM arsenate to arsenite in lactate-sulfate media. Sequence analysis and experimental data show that D. desulfuricans G20 has one copy of arsC and a complete arsRBCC operon in different locations within the genome. Two mutants of strain G20 with defects in arsenate resistance were generated by nitrosoguanidine mutagenesis. The arsRBCC operons were intact in both mutant strains, but each mutant had one point mutation in the single arsC gene. Mutants transformed with either the arsC1 gene or the arsRBCC operon displayed wild-type arsenate resistance, indicating that the two arsC genes were equivalently functional in the sulfate reducer. The arsC1 gene and arsRBCC operon were also cloned into Escherichia coli DH5alpha independently, with either DNA fragment conferring increased arsenate resistance. The recombinant arsRBCC operon allowed growth at up to 50 mM arsenate in LB broth. Quantitative PCR analysis of mRNA products showed that the single arsC1 was constitutively expressed, whereas the operon was under the control of the arsR repressor protein. We suggest a model for arsenate detoxification in which the product of the single arsC1 is first used to reduce arsenate. The arsenite formed is then available to induce the arsRBCC operon for more rapid arsenate detoxification.

DOI: 10.1128/JB.01913-06
PubMed: 17337573
PubMed Central: PMC1913334

Affiliations:

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Le document en format XML

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<term>Arsenates (toxicity)</term>
<term>Arsenites (metabolism)</term>
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<term>Desulfovibrio desulfuricans (genetics)</term>
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<term>Escherichia coli (MeSH)</term>
<term>Gene Expression Regulation, Bacterial (MeSH)</term>
<term>Gene Expression Regulation, Enzymologic (MeSH)</term>
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<term>Arsenate Reductases (métabolisme)</term>
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<term>Desulfovibrio desulfuricans (génétique)</term>
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<term>Protéines bactériennes (métabolisme)</term>
<term>Régulation de l'expression des gènes bactériens (MeSH)</term>
<term>Régulation de l'expression des gènes codant pour des enzymes (MeSH)</term>
<term>Résistance bactérienne aux médicaments (MeSH)</term>
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<term>Bacterial Proteins</term>
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<term>Gene Expression Regulation, Bacterial</term>
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<front><div type="abstract" xml:lang="en">Desulfovibrio desulfuricans G20 grows and reduces 20 mM arsenate to arsenite in lactate-sulfate media. Sequence analysis and experimental data show that D. desulfuricans G20 has one copy of arsC and a complete arsRBCC operon in different locations within the genome. Two mutants of strain G20 with defects in arsenate resistance were generated by nitrosoguanidine mutagenesis. The arsRBCC operons were intact in both mutant strains, but each mutant had one point mutation in the single arsC gene. Mutants transformed with either the arsC1 gene or the arsRBCC operon displayed wild-type arsenate resistance, indicating that the two arsC genes were equivalently functional in the sulfate reducer. The arsC1 gene and arsRBCC operon were also cloned into Escherichia coli DH5alpha independently, with either DNA fragment conferring increased arsenate resistance. The recombinant arsRBCC operon allowed growth at up to 50 mM arsenate in LB broth. Quantitative PCR analysis of mRNA products showed that the single arsC1 was constitutively expressed, whereas the operon was under the control of the arsR repressor protein. We suggest a model for arsenate detoxification in which the product of the single arsC1 is first used to reduce arsenate. The arsenite formed is then available to induce the arsRBCC operon for more rapid arsenate detoxification.</div>
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<Abstract><AbstractText>Desulfovibrio desulfuricans G20 grows and reduces 20 mM arsenate to arsenite in lactate-sulfate media. Sequence analysis and experimental data show that D. desulfuricans G20 has one copy of arsC and a complete arsRBCC operon in different locations within the genome. Two mutants of strain G20 with defects in arsenate resistance were generated by nitrosoguanidine mutagenesis. The arsRBCC operons were intact in both mutant strains, but each mutant had one point mutation in the single arsC gene. Mutants transformed with either the arsC1 gene or the arsRBCC operon displayed wild-type arsenate resistance, indicating that the two arsC genes were equivalently functional in the sulfate reducer. The arsC1 gene and arsRBCC operon were also cloned into Escherichia coli DH5alpha independently, with either DNA fragment conferring increased arsenate resistance. The recombinant arsRBCC operon allowed growth at up to 50 mM arsenate in LB broth. Quantitative PCR analysis of mRNA products showed that the single arsC1 was constitutively expressed, whereas the operon was under the control of the arsR repressor protein. We suggest a model for arsenate detoxification in which the product of the single arsC1 is first used to reduce arsenate. The arsenite formed is then available to induce the arsRBCC operon for more rapid arsenate detoxification.</AbstractText>
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Regulation of arsenate resistance in Desulfovibrio desulfuricans G20 by an arsRBCC operon and an arsC gene.

Regulation of arsenate resistance in Desulfovibrio desulfuricans G20 by an arsRBCC operon and an arsC gene.

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