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Broadening The Substrate Scope of Aldolases Through Metagenomic Enzyme Discovery.

Authors :
Rizzo A
Aranda C
Galman J
Alcasabas A
Pandya A
Bornadel A
Costa B
Hailes HC
Ward JM
Jeffries JWE
Dominguez B
Source :
Chembiochem : a European journal of chemical biology [Chembiochem] 2024 Oct 16; Vol. 25 (20), pp. e202400278. Date of Electronic Publication: 2024 Aug 22.
Publication Year :
2024

Abstract

Bio-processes based on enzymatic catalysis play a major role in the development of green, sustainable processes, and the discovery of new enzymes is key to this approach. In this work, we analysed ten metagenomes and retrieved 48 genes coding for deoxyribose-5-phosphate aldolases (DERAs, EC 4.1.2.4) using a sequence-based approach. These sequences were recombinantly expressed in Escherichia coli and screened for activity towards a range of aldol additions. Among these, one enzyme, DERA-61, proved to be particularly interesting and catalysed the aldol addition of furfural or benzaldehyde with acetone, butanone and cyclobutanone with unprecedented activity. The product of these reactions, aldols, can find applications as building blocks in the synthesis of biologically active compounds. Screening was carried out to identify optimized reaction conditions targeting temperature, pH, and salt concentrations. Lastly, the kinetics and the stereochemistry of the products were investigated, revealing that DERA-61 and other metagenomic DERAs have superior activity and stereoselectivity when they are provided with non-natural substrates, compared to well-known DERAs.<br /> (© 2024 The Authors. ChemBioChem published by Wiley-VCH GmbH.)

Details

Language :
English
ISSN :
1439-7633
Volume :
25
Issue :
20
Database :
MEDLINE
Journal :
Chembiochem : a European journal of chemical biology
Publication Type :
Academic Journal
Accession number :
38953596
Full Text :
https://doi.org/10.1002/cbic.202400278