rdf:type |
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lifeskim:mentions |
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pubmed:issue |
3
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pubmed:dateCreated |
2003-8-13
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pubmed:abstractText |
The number of accessible SH-groups was determined in membrane vesicles prepared from Escherichia coli growing in fermentation conditions at slightly alkaline pH on glucose with or without added formate. Addition of ATP or formate to the vesicles caused a approximately 1.4-fold increase in the number of accessible SH-groups. The increase was inhibited by treatment with N-ethylmaleimide or the presence of the F(0)F(1)-ATPase inhibitors N,N(')-dicyclohexylcarbodiimide or sodium azide. The increase in accessible SH-groups was also absent in strains with the ATP synthase operon deleted or with the single F(0) domain cysteine Cysb21 changed to Ala. Using hyc and hyf mutants, it was shown that the increase was also largely dependent on hydrogenase 4 or hydrogenase 3, main components of formate hydrogen lyase, when bacteria were grown in the absence or presence of added formate. These results suggest a relationship between the F(0)F(1)-ATP synthase and hydrogenase 4 or hydrogenase 3 under fermentation conditions.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Adenosine Triphosphate,
http://linkedlifedata.com/resource/pubmed/chemical/Escherichia coli Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Formate Dehydrogenases,
http://linkedlifedata.com/resource/pubmed/chemical/Formic Acids,
http://linkedlifedata.com/resource/pubmed/chemical/Hydrogenase,
http://linkedlifedata.com/resource/pubmed/chemical/Multienzyme Complexes,
http://linkedlifedata.com/resource/pubmed/chemical/Proton-Translocating ATPases,
http://linkedlifedata.com/resource/pubmed/chemical/Sulfhydryl Compounds,
http://linkedlifedata.com/resource/pubmed/chemical/formate hydrogenlyase,
http://linkedlifedata.com/resource/pubmed/chemical/formic acid,
http://linkedlifedata.com/resource/pubmed/chemical/hydrogenase 4, E coli
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0006-291X
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pubmed:author |
|
pubmed:issnType |
Print
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pubmed:day |
29
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pubmed:volume |
308
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
655-9
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:12914800-Adenosine Triphosphate,
pubmed-meshheading:12914800-Cytoplasmic Vesicles,
pubmed-meshheading:12914800-Escherichia coli,
pubmed-meshheading:12914800-Escherichia coli Proteins,
pubmed-meshheading:12914800-Formate Dehydrogenases,
pubmed-meshheading:12914800-Formic Acids,
pubmed-meshheading:12914800-Hydrogenase,
pubmed-meshheading:12914800-Multienzyme Complexes,
pubmed-meshheading:12914800-Mutation,
pubmed-meshheading:12914800-Proton-Translocating ATPases,
pubmed-meshheading:12914800-Sulfhydryl Compounds
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pubmed:year |
2003
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pubmed:articleTitle |
The number of accessible SH-groups in Escherichia coli membrane vesicles is increased by ATP or by formate.
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pubmed:affiliation |
Department of Biophysics of the Biological Faculty, Yerevan State University, Armenia.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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