Directed Evolution of (R)-2-Hydroxyglutarate Dehydrogenase Improves 2-Oxoadipate Reduction by 2 Orders of Magnitude
Artikel i vetenskaplig tidskrift, 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

Författare

Veronica Saez Jimenez

Chalmers, Biologi och bioteknik, Industriell bioteknik

Simone Scrima

Danmarks Tekniske Universitet (DTU)

Danish Cancer Research Society Center

Matteo Lambrughi

Danish Cancer Research Society Center

Elena Papaleo

Danish Cancer Research Society Center

Danmarks Tekniske Universitet (DTU)

Valeria Mapelli

Chalmers, Biologi och bioteknik, Industriell bioteknik

Martin Engqvist

Chalmers, Biologi och bioteknik, Systembiologi

Lisbeth Olsson

Chalmers, Biologi och bioteknik, Industriell bioteknik

ACS Synthetic Biology

2161-5063 (eISSN)

Vol. 11 8 2779-2790

Ämneskategorier

Biokemi och molekylärbiologi

Biokatalys och enzymteknik

Organisk kemi

DOI

10.1021/acssynbio.2c00162

PubMed

35939387

Mer information

Senast uppdaterat

2024-03-07