Simpson H D, Green J, Dalton H
Department of Biological Sciences, University of Warwick, Coventry, U.K.
Biochem J. 1987 Jun 15;244(3):585-90. doi: 10.1042/bj2440585.
cis-Toluene dihydrodiol dehydrogenase was purified 200-fold from cells of a thermotolerant Bacillus species grown with toluene as the sole source of carbon and energy. The purified enzyme preparation was remarkably heat-stable and exhibited a half-life of 100 min at 80 degrees C, the temperature optimum. The activation energy of the reaction was 36 kJ.mol-1. Isoelectric focusing indicated that the pI of the native enzyme was 6.4 and that of the denatured enzyme 6.5. Although the pH optimum was 9.8, the enzyme was most stable at pH 8. The Mr of the enzyme was approx. 172,000 as determined by gel filtration and 166,000 by polyacrylamide-gel electrophoresis. The enzyme was composed of six apparently identical subunits with Mr values of 29,500. Kinetic analysis revealed that the Km for cis-toluene dihydrodiol was 92 microM and for NAD+ was 80 microM. The apparent Km values for cis-benzene dihydrodiol and cis-naphthalene dihydrodiol were 330 microM and 51 microM respectively. The enzyme was inhibited by mercurials but was unaffected by metal-ion chelators. Steady-state kinetics and product-inhibition patterns suggested that the enzyme mechanism was ordered Bi Bi.
顺式甲苯二氢二醇脱氢酶是从以甲苯作为唯一碳源和能源生长的耐热芽孢杆菌属细胞中纯化得到的,纯化倍数为200倍。纯化后的酶制剂具有显著的热稳定性,在最适温度80℃下的半衰期为100分钟。该反应的活化能为36kJ·mol⁻¹。等电聚焦表明天然酶的pI为6.4,变性酶的pI为6.5。尽管最适pH为9.8,但该酶在pH8时最稳定。通过凝胶过滤测定该酶的Mr约为172,000,通过聚丙烯酰胺凝胶电泳测定为166,000。该酶由六个明显相同的亚基组成,亚基的Mr值为29,500。动力学分析表明,顺式甲苯二氢二醇的Km为92μM,NAD⁺的Km为80μM。顺式苯二氢二醇和顺式萘二氢二醇的表观Km值分别为330μM和51μM。该酶受到汞制剂的抑制,但不受金属离子螯合剂的影响。稳态动力学和产物抑制模式表明该酶的作用机制为有序的双底物双产物机制。