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A new concept of biocatalytic synthesis of acrylic monomers for obtaining water-soluble acrylic heteropolymers.
- Source :
-
Metabolic engineering communications [Metab Eng Commun] 2023 Dec 19; Vol. 18, pp. e00231. Date of Electronic Publication: 2023 Dec 19 (Print Publication: 2024). - Publication Year :
- 2023
-
Abstract
- Rhodococcus strains were designed as model biocatalysts (BCs) for the production of acrylic acid and mixtures of acrylic monomers consisting of acrylamide, acrylic acid, and N-alkylacrylamide (N-isopropylacrylamide). To obtain BC strains, we used, among other approaches, adaptive laboratory evolution (ALE), based on the use of the metabolic pathway of amide utilization. Whole genome sequencing of the strains obtained after ALE, as well as subsequent targeted gene disruption, identified candidate genes for three new amidases that are promising for the development of BCs for the production of acrylic acid from acrylamide. New BCs had two types of amidase activities, acrylamide-hydrolyzing and acrylamide-transferring, and by varying the ratio of these activities in BCs, it is possible to influence the ratio of monomers in the resulting mixtures. Based on these strains, a prototype of a new technological concept for the biocatalytic synthesis of acrylic monomers was developed for the production of water-soluble acrylic heteropolymers containing valuable N-alkylacrylamide units. In addition to the possibility of obtaining mixtures of different compositions, the advantages of the concept are a single starting reagent (acrylamide), more unification of processes (all processes are based on the same type of biocatalyst), and potentially greater safety for personnel and the environment compared to existing chemical technologies.<br />Competing Interests: The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (© 2023 The Authors.)
Details
- Language :
- English
- ISSN :
- 2214-0301
- Volume :
- 18
- Database :
- MEDLINE
- Journal :
- Metabolic engineering communications
- Publication Type :
- Academic Journal
- Accession number :
- 38222043
- Full Text :
- https://doi.org/10.1016/j.mec.2023.e00231