Transport of activated fatty acids by the peroxisomal ATP-binding-cassette transporter Pxa2 in a semi-intact yeast cell system

被引:95
作者
Verleur, N
Hettema, EH
VanRoermund, CWT
Tabak, HF
Wanders, RJA
机构
[1] UNIV AMSTERDAM,ACAD MED CTR,DEPT CLIN CHEM F0224,NL-1100 DE AMSTERDAM,NETHERLANDS
[2] UNIV AMSTERDAM,ACAD MED CTR,DEPT BIOCHEM,NL-1100 DE AMSTERDAM,NETHERLANDS
[3] UNIV AMSTERDAM,ACAD MED CTR,DEPT PEDIAT,EMMA CHILDREN HOSP,NL-1105 AZ AMSTERDAM,NETHERLANDS
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 1997年 / 249卷 / 03期
关键词
peroxisome; fatty-acid transporter; ATP-binding cassette transporter; Saccharomyces cerevisiae; adrenoleukodystrophy;
D O I
10.1111/j.1432-1033.1997.00657.x
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
In the yeast Saccharomyces cerevisiae, fatty acid beta-oxidation is restricted to peroxisomes. Previous studies have shown two possible routes by which fatty acids enter the peroxisome. The first route involves transport of medium-chain fatty acids across the peroxisomal membrane as free fatty acids, followed by activation within the peroxisome by Faa2p, an acyl-CoA synthetase. The second route involves transport of long-chain fatty acids. Long-chain fatty acids enter the peroxisome via a route that involves activation in the extraperoxisomal space, followed by transport across the peroxisomal membrane. It has been suggested that this transport is dependent upon the peroxisomal ATP-binding-cassette transporters Pxa1p and Pxa2p. In this paper we investigated whether Pxa2p is directly responsible for the transport of C18:1-CoA, a long-chain acyl-CoA ester. Using protoplasts in which the plasma membrane has been selectively permeabilised by digitonin, we show that C18:1-CoA, but not C8:0-CoA, enters the peroxisome via Pxa2p, in an ATP-dependent fashion. The results obtained may contribute to the elucidation of the primary defect in the human disease X-linked adrenoleukodystrophy.
引用
收藏
页码:657 / 661
页数:5
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