Abstract

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.

Highlights

  • Metalloenzyme moieties are combined, adapted and reused in Nature to build up the modular redox circuits that provide metabolic flexibility in microorganisms

  • We have demonstrated a related approach for coupling H2 oxidation to NADH generation on carbon particles, shown schematically in Figure 7A [44,45]

  • The present paper has reviewed the biological and technological applications of redox enzymes as modular catalysts for linking selective redox half-reactions, with a focus on connecting the H+/H2 couple to other redox couples

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Summary

Introduction

Metalloenzyme moieties are combined, adapted and reused in Nature to build up the modular redox circuits that provide metabolic flexibility in microorganisms. We have demonstrated a related approach for coupling H2 oxidation to NADH generation on carbon particles, shown schematically in Figure 7A [44,45].

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