Mitochondrial β-oxidation

被引:315
作者
Bartlett, K
Eaton, S
机构
[1] Univ Newcastle Upon Tyne, Royal Victoria Infirm, Sir James Spence Inst Child Hlth, Dept Child Hlth, Newcastle Upon Tyne NE1 4LP, Tyne & Wear, England
[2] UCL, Inst Child Hlth, Biochem Endocrinol & Metab Unit, London WC1E 6BT, England
[3] UCL, Inst Child Hlth, Surg Unit, London WC1E 6BT, England
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 2004年 / 271卷 / 03期
关键词
D O I
10.1046/j.1432-1033.2003.03947.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
Mitochondrial beta-oxidation is a complex pathway involving, in the case of saturated straight chain fatty acids of even carbon number, at least 16 proteins which are organized into two functional subdomains; one associated with the inner face of the inner mitochondrial membrane and the other in the matrix. Overall, the pathway is subject to intramitochondrial control at multiple sites. However, at least in the liver, carnitine palmitoyl transferase I exerts approximately 80% of control over pathway flux under normal conditions. Clearly, when one or more enzyme activities are attenuated because of a mutation, the major site of flux control will change.
引用
收藏
页码:462 / 469
页数:8
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