Yang S Y, Elzinga M
Laboratory of Neurobiochemistry, New York State Institute for Basic Research in Developmental Disabilities, Staten Island 10314.
J Biol Chem. 1993 Mar 25;268(9):6588-92.
An Escherichia coli mutant multienzyme complex of fatty acid oxidation, composed of two 41-kDa beta-subunits and two 79-kDa mutant alpha-subunits with the alpha/Gly116-->Phe substitution, has been overproduced and purified. The catalytic properties of 3-ketoacyl-coenzyme A (CoA) thiolase and L-3-hydroxyacyl-CoA dehydrogenase were found to be virtually identical with those of the wild type, whereas both enoyl-CoA hydratase and 3-hydroxyacyl-CoA epimerase activities were eliminated by the alpha/Gly116-->Phe mutation. delta 3-cis-delta 2-trans-Enoyl-CoA isomerase was only slightly affected by the mutation. The results of this study, together with the sequence analysis of the large alpha-subunit of the E. coli complex (Yang, X.-Y. H., Schulz, H., Elzinga, M., and Yang, S.-Y. (1991) Biochemistry 30, 6788-6795) and a demonstration of the epimerization of D-3-hydroxyacyl-CoAs in E. coli via a dehydration/hydration mechanism (Smeland, T. E., Cuebas, D., and Schulz, H. (1991) J. Biol. Chem. 266, 23904-23908), lead to the conclusion that enoyl-CoA hydratase and 3-hydroxyacyl-CoA epimerase are associated with a common active site in the amino-terminal domain of the multifunctional fatty acid oxidation protein. Thus the E. coli hydratase and epimerase activities represent two functions of a unique crotonase that converts both L- and D-3-hydroxyacyl-CoAs to 2-trans-enoyl-CoAs. Moreover, the results suggest that the amino-terminal domain of the large alpha-subunit is also involved in the isomerase activity but the key residue(s) required for catalyzing the isomerization is distinct from the crotonase.
一种由两个41 kDa的β亚基和两个79 kDa的α亚基(α亚基的Gly116被Phe取代)组成的大肠杆菌脂肪酸氧化突变多酶复合物已被大量表达并纯化。发现3-酮酰基辅酶A(CoA)硫解酶和L-3-羟酰基辅酶A脱氢酶的催化特性与野生型几乎相同,而烯酰CoA水合酶和3-羟酰基辅酶A差向异构酶的活性都因α/Gly116→Phe突变而消除。δ3-顺式-δ2-反式-烯酰CoA异构酶仅受到该突变的轻微影响。本研究结果,连同对大肠杆菌复合物大α亚基的序列分析(杨,X.-Y. H.,舒尔茨,H.,埃尔津加,M.,和杨,S.-Y.(1991年)《生物化学》30,6788 - 6795)以及对大肠杆菌中D-3-羟酰基辅酶A通过脱水/水合机制进行差向异构化的证明(斯梅兰,T. E.,奎瓦斯,D.,和舒尔茨,H.(1991年)《生物化学杂志》266,23904 - 23908),得出结论:烯酰CoA水合酶和3-羟酰基辅酶A差向异构酶与多功能脂肪酸氧化蛋白氨基末端结构域中的一个共同活性位点相关联。因此,大肠杆菌水合酶和差向异构酶活性代表了一种独特巴豆酸酶的两种功能,该酶将L-和D-3-羟酰基辅酶A都转化为2-反式-烯酰CoA。此外,结果表明大α亚基的氨基末端结构域也参与异构酶活性,但催化异构化所需的关键残基与巴豆酸酶不同。