Engineering of fructose-6-phosphate aldolase for one-carbon conversion to mannitol in a designed biotransformation system.

The engineered FSA variants showed a 34-fold increase in efficiency and achieved an 88% yield in converting methanol to mannitol, but these findings are limited to in vitro conditions.

Summary and findings

This study investigates the engineering of fructose-6-phosphate aldolase (FSA) to enhance its catalytic efficiency for converting methanol to mannitol. The engineered variants exhibited a 34-fold increase in catalytic efficiency compared to the wildtype, achieving a yield of 88% in an in vitro cascade. No therapeutic claims are made.

Abstract

Developing artificial synthetic pathways for converting one-carbon compounds into value-added chemicals represents a promising strategy for carbon-neutral manufacturing. Enzymatic C-C bond formation plays a central role in carbon-chain extension and structural diversification. Fructose-6-phosphate aldolase (FSA) has been employed in <i>in vitro</i> multienzyme systems for producing starch and sugars from methanol. However, its atomistic catalytic mechanism has remained unclear, limiting rational enzyme engineering. Here, we elucidate the aldol reaction mechanism between dihydroxyacetone (DHA) and glyceraldehyde-3-phosphate (GALP) catalyzed by FSA using QM/MM calculations, identifying the Schiff-base/iminium formation step as the rate-limiting step in the aldol condensation. Guided by this mechanism, we engineered FSA variants with a 34-fold increase in catalytic efficiency compared with the wildtype. We further integrated the engineered FSA into a designed <i>in vitro</i> cascade converting methanol to mannitol, achieving a high yield of 88%. Collectively, these mechanistic insights and improved biocatalysts expand the toolkit for green enzymatic C-C bond formation and one-carbon utilization.

Key findings

• Not reported in abstract.
• Not reported in abstract.
• Not reported in abstract.

Limitations

• Not reported in abstract.
• Not reported in abstract.
• Not reported in abstract.

Elsewhere in the NAD+ (Nicotinamide Adenine Dinucleotide) corpus