Berge R K
Biochim Biophys Acta. 1979 Aug 30;574(2):321-33. doi: 10.1016/0005-2760(79)90013-4.
A long-chain acyl-CoA hydrolase from rat liver microsomes has been purified by solvent extraction and gel chromatography to homogeneity as judged by polyacrylamide gel electrophoresis in the presence and absence of sodium dodecyl sulfate. The enzyme was a monomer of molecular weight 59 000. In a sucrose gradient it sedimented at 4.3 S. The isoelectric point, pI was 6.9, and the Stokes radius was approx. 31 A. The enzyme hydrolyzed long-chain fatty acyl-CoA (C7--C18) with maximum activity for palmitoyl-CoA. Bovine serum albumin activation of the enzyme was related to the ratio acyl-CoA/bovine serum albumin, and at high ratios, acyl-CoA inhibited the enzyme activity. Disregarding the substrate inhibition, an apparent Km of 65 nmol/mg protein or 1-10(-7) M and a V of 750 nmol/mg protein per min were calculated. The enzyme was inhibited by p-hydroxymercuribenzoate and N-ethylmaleimide. Reactivation by means of dithiothreitol was not complete.
通过溶剂萃取和凝胶色谱法,从大鼠肝脏微粒体中纯化出一种长链酰基辅酶A水解酶,在有无十二烷基硫酸钠的情况下,经聚丙烯酰胺凝胶电泳判断,该酶已达到同质。该酶是一种分子量为59000的单体。在蔗糖梯度中,它以4.3 S沉降。等电点pI为6.9,斯托克斯半径约为31 Å。该酶水解长链脂肪酰基辅酶A(C7 - C18),对棕榈酰辅酶A具有最大活性。牛血清白蛋白对该酶的激活与酰基辅酶A/牛血清白蛋白的比例有关,在高比例时,酰基辅酶A会抑制酶活性。不考虑底物抑制作用,计算得出表观Km为65 nmol/mg蛋白质或1×10⁻⁷ M,V为750 nmol/mg蛋白质每分钟。该酶受到对羟基汞苯甲酸酯和N - 乙基马来酰亚胺的抑制。通过二硫苏糖醇进行的再激活并不完全。