Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:dateCreated
1999-8-2
pubmed:abstractText
Inorganic pyrophosphate promoted the acidification of an intracellular compartment in permeabilized promastigotes of Leishmania donovani, as measured by Acridine Orange uptake. The proton gradient generated by pyrophosphate was collapsed by addition of nigericin or NH4Cl. Pyrophosphate-driven proton translocation was stimulated by potassium ions, and inhibited by NaF, the pyrophosphate analogues imidodiphosphate and aminomethylenediphosphonate (AMDP), dicyclohexylcarbodiimide, and the thiol reagents p-hydroxymercuribenzoate and N-ethylmaleimide, all at concentrations similar to those that inhibit the plant vacuolar proton-pumping pyrophosphatase (H+-PPase). The proton translocation activity had a pH optimum in the range 7.0-7.5, and was unaffected by bafilomycin A1 (40 nM), concanamycin A (5 nM), sodium o-vanadate (500 microM) and KNO3 (200 mM). AMDP-sensitive pyrophosphate hydrolysis was also detected in promastigotes, and potassium ions also stimulated this activity. Sodium ions disrupted pH gradients established in the presence of ATP but not in the presence of pyrophosphate, and sequential addition of ATP and pyrophosphate resulted in partially additive Acridine Orange accumulation, suggesting that the vacuolar H+-PPase is in a different intracellular compartment from the vacuolar H+-ATPase and Na+/H+ exchanger of L. donovani promastigotes. Separation of promastigote extracts on Percoll gradients yielded a dense fraction that contained H+-PPase activity but lacked ATPase activity and markers for mitochondria, glycosomes and lysosomes. The organelles in this fraction appeared by electron microscopy to consist of electron-dense vacuoles. In summary, these results indicate that, in contrast to plant vacuoles, vacuolar H+-PPase and vacuolar ATPase activities are present in different compartments in L. donovani promastigotes.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/10359662-1309654, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359662-1334545, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359662-1534409, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359662-16653187, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359662-16664026, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359662-16664845, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359662-1848180, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359662-2348832, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359662-2543817, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359662-2555340, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359662-3054539, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359662-43092, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359662-610620, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359662-6459452, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359662-7575396, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359662-7575411, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359662-7610161, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359662-7852329, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359662-7876200, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359662-7998937, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359662-8083239, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359662-8120031, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359662-8573106, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359662-8670117, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359662-9083086, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359662-9210392, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359662-9268385, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359662-9346954, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359662-9371704, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359662-9489011, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359662-9528801, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359662-9531501, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359662-9620872, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359662-9696353, http://linkedlifedata.com/resource/pubmed/commentcorrection/10359662-9705361
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0264-6021
pubmed:author
pubmed:issnType
Print
pubmed:day
15
pubmed:volume
340 ( Pt 3)
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
759-66
pubmed:dateRevised
2010-9-13
pubmed:meshHeading
pubmed-meshheading:10359662-Acridine Orange, pubmed-meshheading:10359662-Adenosine Triphosphate, pubmed-meshheading:10359662-Animals, pubmed-meshheading:10359662-Biological Markers, pubmed-meshheading:10359662-Cell Membrane, pubmed-meshheading:10359662-Cell Membrane Permeability, pubmed-meshheading:10359662-Diphosphates, pubmed-meshheading:10359662-Hydrogen, pubmed-meshheading:10359662-Hydrogen-Ion Concentration, pubmed-meshheading:10359662-Kinetics, pubmed-meshheading:10359662-Leishmania donovani, pubmed-meshheading:10359662-Plants, pubmed-meshheading:10359662-Potassium, pubmed-meshheading:10359662-Proton-Translocating ATPases, pubmed-meshheading:10359662-Pyrophosphatases, pubmed-meshheading:10359662-Sodium, pubmed-meshheading:10359662-Sodium-Hydrogen Antiporter, pubmed-meshheading:10359662-Subcellular Fractions, pubmed-meshheading:10359662-Vacuolar Proton-Translocating ATPases, pubmed-meshheading:10359662-Vacuoles
pubmed:year
1999
pubmed:articleTitle
Presence of a vacuolar H+-pyrophosphatase in promastigotes of Leishmania donovani and its localization to a different compartment from the vacuolar H+-ATPase.
pubmed:affiliation
Laboratory of Molecular Parasitology, Department of Pathobiology, College of Veterinary Medicine, University of Illinois at Urbana-Champaign, 2001 South Lincoln Avenue, Urbana, IL 61802, USA.
pubmed:publicationType
Journal Article, Comparative Study, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't