Directed Evolution of (R)-2-Hydroxyglutarate Dehydrogenase Improves 2-Oxoadipate Reduction by 2 Orders of Magnitude
Journal article, 2022

Pathway engineering is commonly employed to improve the production of various metabolites but may incur in bottlenecks due to the low catalytic activity of a particular reaction step. The reduction of 2-oxoadipate to (R)-2-hydroxyadipate is a key reaction in metabolic pathways that exploit 2-oxoadipate conversion via α-reduction to produce adipic acid, an industrially important platform chemical. Here, we engineered (R)-2-hydroxyglutarate dehydrogenase from Acidaminococcus fermentans (Hgdh) with the aim of improving 2-oxoadipate reduction. Using a combination of computational analysis, saturation mutagenesis, and random mutagenesis, three mutant variants with a 100-fold higher catalytic efficiency were obtained. As revealed by rational analysis of the mutations found in the variants, this improvement could be ascribed to a general synergistic effect where mutation A206V played a key role since it boosted the enzyme's activity by 4.8-fold. The Hgdh variants with increased activity toward 2-oxoadipate generated within this study pave the way for the bio-based production of adipic acid.

protein engineering

(R)-2-hydroxyacid dehydrogenase

(R)-2-hydroxyadipate

adipic acid

random mutagenesis

saturation mutagenesis

Author

Veronica Saez Jimenez

Chalmers, Biology and Biological Engineering, Industrial Biotechnology

Simone Scrima

Technical University of Denmark (DTU)

Danish Cancer Research Society Center

Matteo Lambrughi

Danish Cancer Research Society Center

Elena Papaleo

Danish Cancer Research Society Center

Technical University of Denmark (DTU)

Valeria Mapelli

Chalmers, Biology and Biological Engineering, Industrial Biotechnology

Martin Engqvist

Chalmers, Biology and Biological Engineering, Systems and Synthetic Biology

Lisbeth Olsson

Chalmers, Biology and Biological Engineering, Industrial Biotechnology

ACS Synthetic Biology

2161-5063 (eISSN)

Vol. 11 8 2779-2790

Subject Categories

Biochemistry and Molecular Biology

Biocatalysis and Enzyme Technology

Organic Chemistry

DOI

10.1021/acssynbio.2c00162

PubMed

35939387

More information

Latest update

3/7/2024 9