Bartlett Kim, Eaton Simon
Department of Child Health, Sir James Spence Institute of Child Health, University of Newcastle upon Tyne, Royal Victoria Infirmary, Newcastle upon Tyne, UK.
Eur J Biochem. 2004 Feb;271(3):462-9. doi: 10.1046/j.1432-1033.2003.03947.x.
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.
线粒体β-氧化是一条复杂的途径,对于偶数碳原子的饱和直链脂肪酸而言,该途径至少涉及16种蛋白质,这些蛋白质被组织成两个功能亚结构域;一个与线粒体内膜的内表面相关,另一个位于线粒体基质中。总体而言,该途径在多个位点受到线粒体内的调控。然而,至少在肝脏中,在正常条件下,肉碱棕榈酰转移酶I对途径通量的控制作用约占80%。显然,当由于突变导致一种或多种酶活性减弱时,通量控制的主要位点将会改变。