Design of a synthetic enzyme cascade for the in vitro fixation of a C1 carbon source to a functional C4 sugar

Realizing a sustainable future requires intensifying the waste stream conversion, such as converting the greenhouse gas carbon dioxide into value-added products. In this paper, we focus on utilizing formaldehyde as a C-1 carbon source for enzymatic C-C bond formation. Formaldehyde can be sustainably derived from other C-1 feedstocks, and in this work, we designed a synthetic enzyme cascade for producing the functional C-4 sugar erythrulose. This involved tailoring the enzyme formolase, which was optimized for fusing formaldehyde, from a three-carbon producer (dihydroxyacetone) to sets of variants with enhanced two-carbon (glycolaldehyde) or four-carbon (erythrulose) activity. To achieve this, a high-throughput combinatorial screening was developed, and every single variant was evaluated in terms of glycolaldehyde, dihydroxyacetone and erythrulose activity. By applying the two most promising variants in an enzyme cascade, we were able to show for the first time production of ERY starting from a C-1 carbon source. In addition, we demonstrated that one of our tailored formolase variants was able to convert 25.0 g L-1 glycolaldehyde to 24.6 g L-1 erythrulose (98% theoretical yield) in a fully atom-economic biocatalytic process. This represents the highest achieved in vitro concentration of erythrulose to date.

Automated summary

This paper focuses on utilizing formaldehyde as a C-1 carbon source for enzymatic C-C bond formation, successfully designing a synthetic enzyme cascade for producing the functional C-4 sugar erythrulose. Through high-throughput combinatorial screening, optimized enzyme variants were developed, and it was shown for the first time that erythrulose can be produced from a C-1 carbon source. Tailored formolase variants were able to convert glycolaldehyde to erythrulose with a 98% theoretical yield, representing the highest achieved in vitro concentration of erythrulose to date.