An involvement of yeast peroxisomal channels in transmembrane transfer of glyoxylate cycle intermediates

被引:20
作者
Antonenkov, Vasily D. [1 ,2 ]
Mindthoff, Sabrina [3 ]
Grunau, Silke [1 ,2 ]
Erdmann, Ralf [3 ]
Hiltunen, J. Kalervo [1 ,2 ]
机构
[1] Univ Oulu, Dept Biochem, FIN-90014 Oulu, Finland
[2] Univ Oulu, Bioctr Oulu, FIN-90014 Oulu, Finland
[3] Ruhr Univ Bochum, Inst Physiol Chem, Abt Syst Biochem, D-44780 Bochum, Germany
基金
芬兰科学院;
关键词
Glyoxylate cycle; Peroxisomes; Membrane channels; SACCHAROMYCES-CEREVISIAE; FORMING ACTIVITIES; MEMBRANE-PROTEINS; LEAF PEROXISOMES; OUTER-MEMBRANE; BETA-OXIDATION; PERMEABILITY; PORIN; TRANSPORT;
D O I
10.1016/j.biocel.2009.08.014
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The separate localization of glyoxylate cycle enzymes in the peroxisomes and the cytosol of the yeast Saccharomyces cerevisiae indicates that the peroxisomal membrane must permit the flow of metabolites between the two compartments. The transfer of these metabolites may require peroxisomal membrane channel(s). We used an electrophysiological approach (reconstitution assay in lipid bilayers) to assess the ability of peroxisomal membrane channels to conduct different solutes including metabolites of the glyoxylate cycle. At least two distinct channel-forming activities were detected in peroxisomal preparations. One of these activities was highly inducible by dithiothreitol and showed large-amplitude current increments when I M KCI was used as a bath solution. Single-channel analysis revealed that the inducible channel is anion-selective (P(Cl-)/P(K+) = 2.6; P(citrate)/P(K+) = 1.6) and displays flickering at holding potentials over +/- 30 mV directed upward or downward relative to the main open state of the channel. The channel inducible by DTT facilitates the transfer of solutes with a molecular mass up to 400 Da, sufficient to allow the transmembrane trafficking of glyoxylate cycle intermediates between the peroxisomal lumen and the cytoplasm. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2546 / 2554
页数:9
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