Liu J, Quinn N, Berchtold G A, Walsh C T
Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts 02115.
Biochemistry. 1990 Feb 13;29(6):1417-25. doi: 10.1021/bi00458a012.
Isochorismate synthase (EC 5.4.99.6), the entC gene product of Escherichia coli, catalyzes the conversion of chorismate to isochorismate, the first step in the biosynthesis of the powerful iron-chelating agent enterobactin. A sequence-specific deletion method has been used to construct an EntC overproducer, which allows for the purification and characterization of the E. coli isochorismate synthase for the first time. The N-terminal sequence and the subunit molecular weight (43,000) of the polypeptide derived from SDS-polyacrylamide gel electrophoresis agree with those deduced from DNA sequence data. The enzyme is an active monomer with a native molecular weight of 42,000. It was shown that EntC alone is fully capable of catalyzing the interconversion of chorismate and isochorismate in both directions and the associated activity is not affected by EntA of the same biosynthetic pathway as has recently been speculated [Elkins, M. F., & Earhart, C. F. (1988) FEMS Microbiol. Lett. 56, 35; Liu, J., Duncan, K., & Walsh, C.T. (1989) J. Bacteriol. 171, 791; Ozenberger, B. A., Brickman, T.J., & McIntosh, M. A. (1989) J. Bacteriol. 171, 775]. The kinetic constants were determined with Km = 14 microM and kcat = 173 min-1 for chorismate in the forward direction and Km = 5 microM and kcat = 108 min-1 for isochorismate in the backward direction. The equilibrium constant for the reaction derived from the kinetic data is 0.56 with the equilibrium lying toward the side of chorismate, corresponding to a free energy difference of 0.36 kcal/mol between chorismate and isochorismate.(ABSTRACT TRUNCATED AT 250 WORDS)
异分支酸合成酶(EC 5.4.99.6)是大肠杆菌entC基因的产物,催化分支酸转化为异分支酸,这是强效铁螯合剂肠杆菌素生物合成的第一步。已使用序列特异性缺失方法构建了EntC过量产生菌,首次实现了大肠杆菌异分支酸合成酶的纯化和特性鉴定。从SDS-聚丙烯酰胺凝胶电泳得到的多肽的N端序列和亚基分子量(43,000)与从DNA序列数据推导的结果一致。该酶是一种活性单体,天然分子量为42,000。结果表明,单独的EntC完全能够双向催化分支酸和异分支酸的相互转化,并且相关活性不受同一生物合成途径中EntA的影响,这与最近的推测一致[埃尔金斯,M.F.,& 厄哈特,C.F.(1988年)《FEMS微生物学快报》56卷,35页;刘,J.,邓肯,K.,& 沃尔什,C.T.(1989年)《细菌学杂志》171卷,791页;奥曾伯格,B.A.,布里克曼,T.J.,& 麦金托什,M.A.(1989年)《细菌学杂志》171卷,775页]。正向反应中分支酸的动力学常数测定为Km = 14微摩尔,kcat = 173分钟-1,反向反应中异分支酸的动力学常数测定为Km = 5微摩尔,kcat = 108分钟-1。从动力学数据得出的反应平衡常数为0.56,平衡偏向分支酸一侧,对应分支酸和异分支酸之间的自由能差为0.36千卡/摩尔。(摘要截短于250字)