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Enzymes as modular catalysts for redox half-reactions in H2-powered chemical synthesis: from biology to technology.

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journal contribution
posted on 2019-06-03, 13:44 authored by HA Reeve, PA Ash, H Park, A Huang, M Posidias, C Tomlinson, O Lenz, KA Vincent
The present study considers the ways in which redox enzyme modules are coupled in living cells for linking reductive and oxidative half-reactions, and then reviews examples in which this concept can be exploited technologically in applications of coupled enzyme pairs. We discuss many examples in which enzymes are interfaced with electronically conductive particles to build up heterogeneous catalytic systems in an approach which could be termed synthetic biochemistry We focus on reactions involving the H+/H2 redox couple catalysed by NiFe hydrogenase moieties in conjunction with other biocatalysed reactions to assemble systems directed towards synthesis of specialised chemicals, chemical building blocks or bio-derived fuel molecules. We review our work in which this approach is applied in designing enzyme-modified particles for H2-driven recycling of the nicotinamide cofactor NADH to provide a clean cofactor source for applications of NADH-dependent enzymes in chemical synthesis, presenting a combination of published and new work on these systems. We also consider related photobiocatalytic approaches for light-driven production of chemicals or H2 as a fuel. We emphasise the techniques available for understanding detailed catalytic properties of the enzymes responsible for individual redox half-reactions, and the importance of a fundamental understanding of the enzyme characteristics in enabling effective applications of redox biocatalysis.

Funding

We are grateful for financial support from the Biotechnology and Biological Sciences Research Council [BB/L009722/1] and the Innovate UK/BBSRC/EPSRC Industrial Biotechnology Catalyst [EP/N013514/1]. A.H. and H.A.R. are grateful to the Royal Society of Chemistry for an Undergraduate Research Bursary. M.P. is supported by BBSRC iCASE studentship [BB/M017095/1] and Johnson Matthey Catalysis and Chiral Technologies (JM CCT). We are also grateful to Dr Beatriz Dominguez of JM CCT for providing samples of ADH 105 and ADH 101. Ms Elena Nomerotskaia is acknowledged for preparing samples of E. coli Hyd1 and Hyd2. We thank Janina Preissler and Lars Lauterbach for purifying HoxHYFU derivatives from R. eutropha.

History

Citation

Biochemical Journal, 2017, 474 (2), pp. 215-230

Author affiliation

/Organisation/COLLEGE OF SCIENCE AND ENGINEERING/Department of Chemistry

Version

  • VoR (Version of Record)

Published in

Biochemical Journal

Publisher

Portland Press for Biochemical Society

eissn

1470-8728

Acceptance date

2016-11-15

Copyright date

2017

Available date

2019-06-03

Publisher version

http://www.biochemj.org/content/474/2/215

Language

en