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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
4837
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pubmed:dateCreated |
1988-2-17
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pubmed:abstractText |
The MotB protein of Escherichia coli is an essential component of the force generators that couple proton movement across the cytoplasmic membrane to rotation of the flagellar motors. The membrane topology of MotB was examined to explore the possibility that it might form a proton channel. MotB--alkaline phosphatase fusion proteins were constructed to identify likely periplasmic domains of the MotB molecule. Fusions distal to a putative membrane-spanning segment near the amino terminus of MotB exhibited alkaline phosphatase activity, indicating that an extensive carboxyl-terminal portion of MotB may be located on the periplasmic side of the membrane. Protease treatment of MotB in spheroplasts confirmed this view. The simple transmembrane organization of MotB is difficult to reconcile with a role as a proton conductor.
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pubmed:grant |
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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 |
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pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
0036-8075
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
239
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
276-8
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:2447650-Alkaline Phosphatase,
pubmed-meshheading:2447650-Bacterial Proteins,
pubmed-meshheading:2447650-Cell Membrane,
pubmed-meshheading:2447650-Cell Movement,
pubmed-meshheading:2447650-Escherichia coli,
pubmed-meshheading:2447650-Flagella,
pubmed-meshheading:2447650-Ion Channels,
pubmed-meshheading:2447650-Membrane Proteins,
pubmed-meshheading:2447650-Peptide Fragments,
pubmed-meshheading:2447650-Recombinant Fusion Proteins,
pubmed-meshheading:2447650-Serine Endopeptidases,
pubmed-meshheading:2447650-Structure-Activity Relationship,
pubmed-meshheading:2447650-Trypsin
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pubmed:year |
1988
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pubmed:articleTitle |
Bacterial motility: membrane topology of the Escherichia coli MotB protein.
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pubmed:affiliation |
Biology Department, University of Utah, Salt Lake City 84112.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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