Nagegowda Dinesh A, Bach Thomas J, Chye Mee-Len
Department of Botany, The University of Hong Kong, Pokfulam, Hong Kong, China.
Biochem J. 2004 Nov 1;383(Pt. 3):517-27. doi: 10.1042/BJ20040721.
3-hydroxy-3-methylglutaryl (HMG)-CoA synthase (HMGS; EC 2.3.3.10) is the second enzyme in the cytoplasmic mevalonate pathway of isoprenoid biosynthesis, and catalyses the condensation of acetyl-CoA with acetoacetyl-CoA (AcAc-CoA) to yield S-HMG-CoA. In this study, we have first characterized in detail a plant HMGS, Brassica juncea HMGS1 (BjHMGS1), as a His6-tagged protein from Escherichia coli. Native gel electrophoresis analysis showed that the enzyme behaves as a homodimer with a calculated mass of 105.8 kDa. It is activated by 5 mM dithioerythreitol and is inhibited by F-244 which is specific for HMGS enzymes. It has a pH optimum of 8.5 and a temperature optimum of 35 degrees C, with an energy of activation of 62.5 J x mol(-1). Unlike cytosolic HMGS from chicken and cockroach, cations like Mg2+, Mn2+, Zn2+ and Co2+ did not stimulate His6-BjHMGS1 activity in vitro; instead all except Mg2+ were inhibitory. His6-BjHMGS1 has an apparent K(m-acetyl-CoA) of 43 microM and a V(max) of 0.47 micromol x mg(-1) x min(-1), and was inhibited by one of the substrates (AcAc-CoA) and by both products (HMG-CoA and HS-CoA). Site-directed mutagenesis of conserved amino acid residues in BjHMGS1 revealed that substitutions R157A, H188N and C212S resulted in a decreased V(max), indicating some involvement of these residues in catalytic capacity. Unlike His6-BjHMGS1 and its soluble purified mutant derivatives, the H188N mutant did not display substrate inhibition by AcAc-CoA. Substitution S359A resulted in a 10-fold increased specific activity. Based on these kinetic analyses, we generated a novel double mutation H188N/S359A, which resulted in a 10-fold increased specific activity, but still lacking inhibition by AcAc-CoA, strongly suggesting that His-188 is involved in conferring substrate inhibition on His6-BjHMGS1. Substitution of an aminoacyl residue resulting in loss of substrate inhibition has never been previously reported for any HMGS.
3-羟基-3-甲基戊二酰辅酶A(HMG)合酶(HMGS;EC 2.3.3.10)是类异戊二烯生物合成细胞质甲羟戊酸途径中的第二种酶,催化乙酰辅酶A与乙酰乙酰辅酶A(AcAc-CoA)缩合生成S-HMG-CoA。在本研究中,我们首次详细鉴定了一种植物HMGS,即芥菜HMGS1(BjHMGS1),它是一种来自大肠杆菌的带有His6标签的蛋白质。天然凝胶电泳分析表明,该酶表现为同型二聚体,计算分子量为105.8 kDa。它被5 mM二硫苏糖醇激活,并被对HMGS酶具有特异性的F-244抑制。其最适pH为8.5,最适温度为35℃,活化能为62.5 J·mol⁻¹。与鸡和蟑螂的胞质HMGS不同,Mg²⁺、Mn²⁺、Zn²⁺和Co²⁺等阳离子在体外不刺激His6-BjHMGS1的活性;相反,除Mg²⁺外,其他阳离子均有抑制作用。His6-BjHMGS1的表观K(m-乙酰辅酶A)为43 μM,V(max)为0.47 μmol·mg⁻¹·min⁻¹,并被其中一种底物(AcAc-CoA)以及两种产物(HMG-CoA和HS-CoA)抑制。对BjHMGS1中保守氨基酸残基进行定点诱变发现,R157A、H188N和C212S取代导致V(max)降低,表明这些残基在催化能力中有所参与。与His6-BjHMGS1及其可溶性纯化突变衍生物不同,H188N突变体未表现出被AcAc-CoA底物抑制的现象。S359A取代导致比活性增加了10倍。基于这些动力学分析,我们构建了一种新型双突变体H188N/S359A,其比活性增加了10倍,但仍不受AcAc-CoA抑制,这强烈表明His-188参与了His6-BjHMGS1的底物抑制作用。此前从未有过关于任何HMGS因氨基酸残基取代而导致底物抑制丧失的报道。