Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/79375
Title: Insight into enzymatic nitrile reduction : QM/MM study of the catalytic mechanism of QueF nitrile reductase
Authors: Ribeiro, António J. M.
Yang, Lifeng
Ramos, Maria J.
Fernandes, Pedro A.
Liang, Zhao-Xun
Hirao, Hajime
Keywords: DRNTU::Science::Chemistry::Physical chemistry::Catalysis
Issue Date: 2015
Source: Ribeiro, A. J. M., Yang, L., Ramos, M. J., Fernandes, P. A., Liang, Z.-X., & Hirao, H. (2015). Insight into enzymatic nitrile reduction : QM/MM study of the catalytic mechanism of QueF nitrile reductase. ACS catalysis, 5(6), 3740-3751.
Series/Report no.: ACS catalysis
Abstract: The NADPH-dependent QueF nitrile reductases catalyze the unprecedented four-electron reduction of nitrile to amine. QueF nitrile reductases can be found in the tRNA biosynthetic pathway of many bacteria and are potential antimicrobial drug targets. QueF enzymes have also attracted great attention as potential industrial biocatalysts for replacing the nitrile-reducing metal hydride catalysts used commonly in the chemical and pharmaceutical industries. Because of their narrow substrate specificity, engineering of the QueF enzymes to generate variants with altered or broadened substrate specificity is crucial for producing practically useful biocatalysts. A better understanding of the catalytic mechanism of the QueF enzymes would expedite rational inhibitor design and enzyme engineering. In this work, we probed the catalytic mechanism of the Vibrio cholerae QueF nitrile reductase by state of the art QM/MM calculations at the ONIOM(B3LYP/6-311+G(2d,2p):AMBER) level. The QM/MM computational results suggest that the nitrile to amine conversion proceeds through four major stages: (a) formation of a C–S covalent bond between the substrate and the catalytic cysteine residue to form the thioimidate intermediate, (b) hydride transfer from NADPH to the substrate to generate the thiohemiaminal intermediate, (c) cleavage of the C–S covalent bond to generate the imine intermediate, and (d) second hydride transfer from NADPH to the imine intermediate to generate the final amine product. The free energy barrier for the rate-limiting step, i.e. the second hydride transfer, was found to be 20.8 kcal/mol. The calculated barrier height and the catalytic residues identified as essential for nitrile reduction are in accordance with the currently available experimental data. The knowledge about the transition states, intermediates, and protein conformational changes along the reaction path will be valuable for the design of enzyme inhibitors as well as the engineering of QueF nitrile reductases.
URI: https://hdl.handle.net/10356/79375
http://hdl.handle.net/10220/34457
DOI: 10.1021/acscatal.5b00528
Rights: © 2015 American Chemical Society. This is the author created version of a work that has been peer reviewed and accepted for publication by ACS Catalysis, American Chemical Society. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: [http://dx.doi.org/10.1021/acscatal.5b00528].
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:SBS Journal Articles
SPMS Journal Articles

SCOPUSTM   
Citations 10

24
Updated on Sep 1, 2020

PublonsTM
Citations 10

26
Updated on Mar 3, 2021

Page view(s) 50

321
Updated on Apr 11, 2021

Download(s) 20

145
Updated on Apr 11, 2021

Google ScholarTM

Check

Altmetric


Plumx

Items in DR-NTU are protected by copyright, with all rights reserved, unless otherwise indicated.