Abstract

Genetically engineered host bacteria have an extensive history for the production of specific proteins including the synthesis of single enzymes for the modification of compounds produced for industrial purposes by biological or chemical processes. Such processes have been developed largely through the process of discovery. The ability to assemble multiple enzymes into synthetic pathways is a new development aided by the synthetic biology approach of constructing and assembling suitable enzymes into pathways that may or may not occur in Nature to provide a high-impact platform for bio-manufacturing of chemicals, biofuels and pharmaceuticals. Industry has depended on chemical catalysts because of the known constraints experienced frequently with biological catalysts but when high stereochemistry, mild synthesis conditions and environmentally friendly processes are significant, application of enzymes is preferred, especially in the case of drug synthesis where enantioselectivity is important. However, many whole cell production processes are beset by toxicity problems, metabolite competition, the production of side products, sub-optimal enzyme ratios and varying temperature optima. As a result, a cell-free biocatalysis allows the manipulation of substrate ratios, provision of regenerated cofactors and adjustment of high energy flux ratios that are difficult or impossible to control in whole cell synthesis. We discuss here the construction of cell free biocatalytic pathways as added free enzymes or multi-enzyme modules that may contain heterologous catalysts. We examine the status of applications leading to commercialisation, emphasizing the importance of economical cofactor regeneration. Nevertheless, problems remain, particularly protein post-translational modifications including glycosylation, phosphorylation, ubiquination, acetylation, proteolysis, etc. The National Renewable Energy Laboratory and Pacific North West Laboratory have published lists of top value-added chemicals from biomass that include glucaric acid. There have been few reports on the combination of synthetic biology and cell-free protein synthesis to set up pathways for these valuable intermediate compounds. This observation is despite the existence of at least one large scale but specialised cell-free production of antibody conjugates. This review will provide a description of one successful attempt at the cell-free production of glucaric acid and will evaluate progress for other key intermediate and platform chemicals.

Highlights

  • The presentation of the European Commission’s Circular Economy Strategy and Strategic Plan in 2014 and Action Plan in 2015 have generated considerable discussion of the place, role and relationship of the Circular Bioeconomy as discussed in detail by Carus and Dammer (2018) and for a number of other individual and mainly agricultural industries such as forestry (DeBoer et al, 2020), ethanol production (Erickson, 2018), plastics (Blank et al, 2020); textiles (Aznar, 2019) and animals (Horton, 2019) along with many other examples

  • Developments in a variety of tools have resulted in the classical concept of biocatalysis expanding from single enzyme reactions to the incorporation of multiple enzymes allowing the assembly of synthetic biocatalytic pathways (Bornscheuer, 2018; Poppe and Vértessy, 2018)

  • The current literature is replete with top-down and bottom up suggestions on the way forward for cell-free synthesis (CFS) in the synthesis of biocommodities

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Summary

INTRODUCTION

The presentation of the European Commission’s Circular Economy Strategy and Strategic Plan in 2014 and Action Plan in 2015 have generated considerable discussion of the place, role and relationship of the Circular Bioeconomy as discussed in detail by Carus and Dammer (2018) and for a number of other individual and mainly agricultural industries such as forestry (DeBoer et al, 2020), ethanol production (Erickson, 2018), plastics (Blank et al, 2020); textiles (Aznar, 2019) and animals (Horton, 2019) along with many other examples. Developments in a variety of tools have resulted in the classical concept of biocatalysis expanding from single enzyme reactions to the incorporation of multiple enzymes allowing the assembly of synthetic biocatalytic pathways (Bornscheuer, 2018; Poppe and Vértessy, 2018). Single enzyme reactions have been gradually incorporated into industrial processes to complement chemical catalysis for enantioselective steps in a pathway. Several aspects of this challenging field were reviewed recently (Rudroff et al, 2018) and an expanded account of possibilities in the field is included in the review of Petroll et al (2019). Multi-enzyme pathways are assembled with cell-free systems to allow the testing of an enzymatic pathway without the need for genetic alteration of the host organism and interference from other intracellular processes providing flexibility and control (Cherubini, 2010; Schmidt-Dannert and Lopez-Gallego, 2016; Taniguchi et al, 2017; Zhang et al, 2017; Wilding et al, 2018)

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