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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1992-5-20
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pubmed:abstractText |
Amastigotes of Leishmania donovani develop and multiply within the acidic phagolysosomes of mammalian macrophages. Isolated amastigotes are acidophilic; they catabolize substrates and synthesize macromolecules optimally at pH 5.5. Substrate transport in amastigotes has not been characterized. Here we show that amastigotes exhibit an uphill transport of proline (active transport) with an acid pH optimum (pH 5.5). It is dependent upon metabolic energy and is driven by proton motive force. Agents which selectively disturb the component forces of proton motive force, such as carbonyl cyanide chlorophenylhydrazone, nigericin and valinomycin, inhibit proline transport. Transport is sensitive to dicyclohexylcarbodiimide and insensitive to ouabain, demonstrating the involvement of a proton ATPase in the maintenance of proton motive force. It is suggested that the plasma membrane pH gradient probably makes the greatest contribution to proton motive force that drives substrate transport in the amastigote stage.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0166-6851
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
51
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1-8
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:1533014-Adenosine Triphosphatases,
pubmed-meshheading:1533014-Animals,
pubmed-meshheading:1533014-Biological Transport,
pubmed-meshheading:1533014-Enzyme Inhibitors,
pubmed-meshheading:1533014-Hydrogen-Ion Concentration,
pubmed-meshheading:1533014-Ionophores,
pubmed-meshheading:1533014-Leishmania donovani,
pubmed-meshheading:1533014-Membrane Potentials,
pubmed-meshheading:1533014-Proline
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pubmed:year |
1992
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pubmed:articleTitle |
Proline transport in Leishmania donovani amastigotes: dependence on pH gradients and membrane potential.
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pubmed:affiliation |
Department of Biological Sciences, University of Cincinnati, OH 45221.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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