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J. Biol. Chem., Vol. 276, Issue 44, 40502-40509, November 2, 2001
From the Department of Molecular and Cellular Biochemistry,
Ohio State University Medical Center, Columbus, Ohio 43210
The accumulation and retention of
Ca2+ by yeast mitochondria (Saccharomyces
cerevisiae) mediated by ionophore ETH 129 occurs with a
variable efficiency in different preparations. Ineffective Ca2+ transport and a depressed membrane potential occur in
parallel, are exacerbated in parallel by exogenous free fatty acids,
and are corrected in parallel by the addition of bovine serum
albumin. Bovine serum albumin is not required to develop a high
membrane potential when either Ca2+ or ETH 129 are absent,
and when both are present membrane potential is restored by the
addition of EGTA in a concentration-dependant manner. Respiration and
swelling data indicate that the permeability transition pore does not
open in yeast mitochondria that are treated with Ca2+ and
ETH 129, whereas fatty acid concentration studies and the inaction of
carboxyatractyloside indicate that fatty acid-derived uncoupling does
not underlie the other observations. It is concluded that yeast
mitochondria contain a previously unrecognized
Ca2+:2H+ antiporter that is highly active in
the presence of free fatty acids and leads to a futile cycle of
Ca2+ accumulation and release when exogenous
Ca2+ and ETH 129 are available. It is also shown that
isolated yeast mitochondria degrade their phospholipids at a relatively
rapid rate. The activity responsible is also previously unrecognized. It is Ca2+-independent, little affected by the presence or
absence of a respiratory substrate, and leads to the hydrolysis of
ester linkages at both the sn-1 and sn-2
positions of the glycerophospholipids. The products of this activity,
through their actions on the antiporter, explain the variable behavior
of yeast mitochondria treated with Ca2+ plus ETH 129.
To whom correspondence should be addressed: Dept. of Molecular and
Cellular Biochemistry, Ohio State University, 1645 Neil Ave., Hamilton
Hall 310A, Columbus, Ohio 43210-1218. Tel.: 614-292-8774; Fax:
614-292-4118; E-mail: pfeiffer.17@osu.edu.
Copyright © 2001 by The American Society for Biochemistry and Molecular Biology, Inc. This article has been cited by other articles:
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