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Design of a synthetic enzyme cascade for the in vitro fixation of formaldehyde to acetoin.
Cui, Zhenzhen; Ding, Mengnan; Dai, Wei; Zheng, Meiyu; Wang, Zhiwen; Chen, Tao.
Affiliation
  • Cui Z; Department of Biochemical Engineering, School of Chemical Engineering and Technology, Tianjin University, Tianjin, China; Frontier Science Center for Synthetic Biology and Key Laboratory of Systems Bioengineering (MOE), School of Chemical Engineering and Technology, Tianjin University, Tianjin, Chin
  • Ding M; Department of Biochemical Engineering, School of Chemical Engineering and Technology, Tianjin University, Tianjin, China; Frontier Science Center for Synthetic Biology and Key Laboratory of Systems Bioengineering (MOE), School of Chemical Engineering and Technology, Tianjin University, Tianjin, Chin
  • Dai W; Department of Biochemical Engineering, School of Chemical Engineering and Technology, Tianjin University, Tianjin, China; Frontier Science Center for Synthetic Biology and Key Laboratory of Systems Bioengineering (MOE), School of Chemical Engineering and Technology, Tianjin University, Tianjin, Chin
  • Zheng M; Department of Biochemical Engineering, School of Chemical Engineering and Technology, Tianjin University, Tianjin, China; Frontier Science Center for Synthetic Biology and Key Laboratory of Systems Bioengineering (MOE), School of Chemical Engineering and Technology, Tianjin University, Tianjin, Chin
  • Wang Z; Department of Biochemical Engineering, School of Chemical Engineering and Technology, Tianjin University, Tianjin, China; Frontier Science Center for Synthetic Biology and Key Laboratory of Systems Bioengineering (MOE), School of Chemical Engineering and Technology, Tianjin University, Tianjin, Chin
  • Chen T; Department of Biochemical Engineering, School of Chemical Engineering and Technology, Tianjin University, Tianjin, China; Frontier Science Center for Synthetic Biology and Key Laboratory of Systems Bioengineering (MOE), School of Chemical Engineering and Technology, Tianjin University, Tianjin, Chin
Enzyme Microb Technol ; 178: 110446, 2024 Aug.
Article in En | MEDLINE | ID: mdl-38626535
ABSTRACT
Formaldehyde (FALD) has gained prominence as an essential C1 building block in the synthesis of valuable chemicals. However, there are still challenges in converting FALD into commodities. Recently, cell-free biocatalysis has emerged as a popular approach for producing such commodities. Acetoin, also known as 3-hydroxy-2-butanone, has been widely used in food, cosmetic, agricultural and the chemical industry. It is valuable to develop a process to produce acetoin from FALD. In this study, a cell-free multi-enzyme catalytic system for the production of acetoin using FALD as the substrate was designed and constructed. It included three scales FALD utilization pathway, glycolysis pathway and acetoin synthesis pathway. After the optimization of the reaction system, 20.17 mM acetoin was produced from 122 mM FALD, with a yield of 0.165 mol/mol, reaching 99.0% of the theoretical yield. The pathway provides a new approach for high-yield acetoin production from FALD, which consolidates the foundation for the production of high value-added chemicals using cheap one-carbon compounds.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biocatalysis / Formaldehyde / Acetoin Language: En Journal: Enzyme Microb Technol Year: 2024 Document type: Article Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biocatalysis / Formaldehyde / Acetoin Language: En Journal: Enzyme Microb Technol Year: 2024 Document type: Article Country of publication: United States