Schlossman D M, Bell R M
J Biol Chem. 1976 Sep 25;251(18):5738-44.
The acyl-CoA:sn-glycerol-3-phosphate acyltransferase (EC 2.3.1.15) (glycerol-P acyltransferase) and acyl-CoA:dihydroxyacetone phosphate acyltransferase (EC 2.3.1.42) (DHAP acyltransferase) activities were investigated in vitro in order to evaluate the quantitative contribution of the glycerol-P and DHAP pathways for the synthesis of triacylglycerols in isolated fat cells and to test the hypothesis that these two activities may be dual catalytic functions of a single enzyme. More than 85% of both acyltransferase activities was associated with the microsomal subcellular fraction. The microsomal glycerol-P acyltransferase activity showed an apparent Km of 8 muM for glycerol-P with a Vmax of 15.6 nmol/min/mg, while the DHAP acyltransferase activity showed an apparent Km of 40 muM for DHAP with a Vmax of 9.7 nmol/min/mg. Glycerol-P was a competitive inhibitor (Ki = 7.2 muM) of the DHAP acyltransferase, and DHAP was a competitive inhibitor (Ki = 92 muM) of the glycerol-P acyltransferase. The two acyltransferase activities showed virtual identity in their pH dependence, acyl-CoA chain length dependence, thermolability, and inactivation by N-ethylmaleimide. Trypsin, detergents, collagenase, phospholipases, and various salts and organic solvents also had similar effects on both activities. Taken as a whole, the data strongly suggest that the microsomal glycerol-P and DHAP acyltransferase activities actually represent dual functions of a single enzyme. Calculations based on the above kinetic constants and previously reported glycerol-P and DHAP pools in adipocytes suggest that the in vivo ratio of glycerol-P to DHAP acylation should be greater than 24:1.
为了评估甘油 - 3 - 磷酸(glycerol - P)和磷酸二羟丙酮(DHAP)途径在分离的脂肪细胞中对三酰甘油合成的定量贡献,并检验这两种活性可能是单一酶的双重催化功能这一假设,对酰基辅酶A:甘油 - 3 - 磷酸酰基转移酶(EC 2.3.1.15)(甘油 - P酰基转移酶)和酰基辅酶A:磷酸二羟丙酮酰基转移酶(EC 2.3.1.42)(DHAP酰基转移酶)的活性进行了体外研究。两种酰基转移酶活性的85%以上与微粒体亚细胞部分相关。微粒体甘油 - P酰基转移酶对甘油 - P的表观Km为8 μM,Vmax为15.6 nmol/min/mg,而DHAP酰基转移酶对DHAP的表观Km为40 μM,Vmax为9.7 nmol/min/mg。甘油 - P是DHAP酰基转移酶的竞争性抑制剂(Ki = 7.2 μM),DHAP是甘油 - P酰基转移酶的竞争性抑制剂(Ki = 92 μM)。两种酰基转移酶活性在pH依赖性、酰基辅酶A链长依赖性、热稳定性以及被N - 乙基马来酰亚胺灭活方面表现出几乎相同的特性。胰蛋白酶、去污剂、胶原酶、磷脂酶以及各种盐和有机溶剂对这两种活性也有类似的影响。总体而言,数据强烈表明微粒体甘油 - P和DHAP酰基转移酶活性实际上代表了单一酶的双重功能。根据上述动力学常数以及先前报道的脂肪细胞中甘油 - P和DHAP库进行的计算表明,体内甘油 - P与DHAP酰化的比例应大于24:1。