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J. Biol. Chem., Vol. 265, Issue 14, 7721-7724, 05, 1990
P Dimroth and A Thomer
The citrate carrier of Klebsiella pneumoniae fermenting this substrate has
been solubilized from the bacterial membranes with Triton X-100. The
transport function was reconstituted by incorporation of the carrier into
proteoliposomes using a freeze-thaw sonication procedure. Citrate uptake
into these proteoliposomes required the presence of Na+ ions on the
outside; the amount of citrate accumulated increased as the external Na+
concentration increased from 0 to 100 mM. Proteoliposomes preloaded with
citrate catalyzed citrate counterflow when added to external [14C] citrate.
Sodium ions were required for counterflow activity. The kinetics of citrate
uptake, counterflow, or efflux were not influenced by an inside negative
membrane potential, and the presence of the uncoupler carbonyl cyanide p-
trifluoromethoxyphenylhydrazone was without effect on citrate uptake. The
data therefore suggest an electroneutral Na(+)-citrate symport mechanism
for the transport of this tricarboxylic acid into K. pneumoniae.
Solubilization and reconstitution of the Na(+)-dependent citrate carrier of Klebsiella pneumoniae
Institut fur Physiologische Chemie, Technischen Universitat Munchen, Federal Republic of Germany.
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