Department of Biochemistry, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, NY 10461, USA.
Biochemistry. 2013 Jun 11;52(23):4097-104. doi: 10.1021/bi400177y. Epub 2013 May 30.
The constitutively expressed, chromosomally encoded β-lactamase (BlaC) is the enzyme responsible for the intrinsic resistance to β-lactam antibiotics in Mycobacterium tuberculosis. Previous studies from this laboratory have shown that the enzyme exhibits an extended-spectrum phenotype, with very high levels of penicillinase and cephalosporinase activity, as well as weak carbapenemase activity [Tremblay, L. W., et al. (2008) Biochemistry 47, 5312-5316]. In this report, we have determined the pH dependence of the kinetic parameters, revealing that the maximal velocity depends on the ionization state of two groups: a general base exhibiting a pK value of 4.5 and a general acid exhibiting a pK value of 7.8. Having defined a region where the kinetic parameters are pH-independent (pH 6.5), we determined solvent kinetic isotope effects (SKIEs) for three substrates whose kcat values differ by 5.5 orders of magnitude. Nitrocefin is a highly activated, chromogenic cephalosporin derivative that exhibits steady-state solvent kinetic isotope effects of 1.4 on both V and V/K. Cefoxitin is a slower cephalosporin derivative that exhibits a large SKIE on V of 3.9 but a small SKIE of 1.8 on V/K in steady-state experiments. Pre-steady-state, stopped-flow experiments with cefoxitin revealed a burst of β-lactam ring opening with associated SKIE values of 1.6 on the acylation step and 3.4 on the deacylation step. Meropenem is an extremely slow substrate for BlaC and exhibits burst kinetics in the steady-state experiments. SKIE determinations with meropenem revealed large SKIEs on both the acylation and deacylation steps of 3.8 and 4.0, respectively. Proton inventories in all cases were linear, indicating the participation of a single solvent-derived proton in the chemical step responsible for the SKIE. The rate-limiting steps for β-lactam hydrolysis of these substrates are analyzed, and the chemical steps responsible for the observed SKIE are discussed.
本构表达的、染色体编码的β-内酰胺酶(BlaC)是导致结核分枝杆菌对β-内酰胺类抗生素固有耐药的酶。本实验室之前的研究表明,该酶表现出广谱表型,具有非常高的青霉素酶和头孢菌素酶活性,以及较弱的碳青霉烯酶活性[ Tremblay,L. W.等。(2008)生物化学47,5312-5316]。在本报告中,我们确定了动力学参数的 pH 依赖性,表明最大速度取决于两个基团的离解状态:具有 pK 值为 4.5 的通用碱和具有 pK 值为 7.8 的通用酸。定义了一个动力学参数与 pH 无关的区域(pH 6.5),我们测定了三个底物的溶剂动力学同位素效应(SKIEs),其 kcat 值相差 5.5 个数量级。硝基头孢菌素是一种高度激活的显色头孢菌素衍生物,在 V 和 V/K 上均表现出 1.4 的稳态溶剂动力学同位素效应。头孢西丁是一种较慢的头孢菌素衍生物,在稳态实验中 V 上表现出 3.9 的大 SKIE,但 V/K 上的 SKIE 较小,为 1.8。头孢西丁的预稳态、停流实验显示出β-内酰胺环打开的爆发,酰化步骤的 SKIE 值为 1.6,去酰化步骤的 SKIE 值为 3.4。美罗培南是 BlaC 的极慢底物,在稳态实验中表现出爆发动力学。美罗培南的 SKIE 测定显示,酰化和去酰化步骤的 SKIE 分别为 3.8 和 4.0。在所有情况下,质子库存都是线性的,表明在负责 SKIE 的化学步骤中,只有一个溶剂衍生的质子参与。分析了这些底物的β-内酰胺水解的限速步骤,并讨论了负责观察到的 SKIE 的化学步骤。