Chemistry Department, Khalifa University, PO Box 127788, Abu Dhabi, United Arab Emirates.
CIVE Department, Khalifa University, PO Box 127788, Abu Dhabi, United Arab Emirates.
J Mol Model. 2021 Jan 28;27(2):53. doi: 10.1007/s00894-020-04646-4.
L-6-Hydroxynicotine oxidase (LHNO) is a member of monoamine oxidase (MAO) family and catalyzes conversion of (S)-6-hydroxynicotine to 6-hydroxypseudooxynicotine during bacterial degradation of nicotine. Recent studies indicated that the enzyme catalyzes oxidation of carbon-nitrogen bond instead of previously proposed carbon-carbon bond. Based on kinetics and mutagenesis studies, Asn166, Tyr311, and Lys287 as well as an active site water molecule have roles in the catalysis of the enzyme. A number of studies including experimental and computational methods support hydride transfer mechanism in MAO family as a common mechanism in which a hydride ion transfer from amine substrate to flavin cofactor is the rate-limiting step. In this study, we formulated computational models to study the hydride transfer mechanism using crystal structure of enzyme-substrate complex. The calculations involved ONIOM and DFT methods, and we evaluated the geometry and energetics of the hydride transfer process while probing the roles of active site residues. Based on the calculations involving hydride, radical, and polar mechanisms, it was concluded that hydride transfer mechanism is the only viable mechanism for LHNO.
L-6-羟基烟碱氧化酶(LHNO)是单胺氧化酶(MAO)家族的一员,在尼古丁的细菌降解过程中催化(S)-6-羟基烟碱转化为 6-羟基假氧烟碱。最近的研究表明,该酶催化碳-氮键的氧化,而不是以前提出的碳-碳键。基于动力学和诱变研究,Asn166、Tyr311、Lys287 以及一个活性位点水分子在酶的催化中起作用。许多研究包括实验和计算方法支持 MAO 家族中的氢化物转移机制作为一种共同机制,其中氢化物离子从胺底物转移到黄素辅因子是限速步骤。在这项研究中,我们使用酶-底物复合物的晶体结构来制定计算模型以研究氢化物转移机制。计算涉及 ONIOM 和 DFT 方法,我们评估了氢化物转移过程的几何形状和能量学,同时探测活性位点残基的作用。基于涉及氢化物、自由基和极性机制的计算,得出结论认为氢化物转移机制是 LHNO 的唯一可行机制。