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  4. Cell-Free Reaction System for ATP Regeneration from d-Fructose
 
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Cell-Free Reaction System for ATP Regeneration from d-Fructose

Citation Link: https://doi.org/10.15480/882.15055
Publikationstyp
Journal Article
Date Issued
2025
Sprache
English
Author(s)
Kraußer, Franziska  
Rabe, Kenny  
Topham, Christopher  
Voland, Julian
Lilienthal, Laura
Kundoch, Jan-Ole 
Technische Biokatalyse V-6  
Ohde, Daniel  orcid-logo
Technische Biokatalyse V-6  
Liese, Andreas  orcid-logo
Technische Biokatalyse V-6  
Walther, Thomas  
TORE-DOI
10.15480/882.15055
TORE-URI
https://hdl.handle.net/11420/55291
Journal
ACS synthetic biology  
Volume
14
Issue
4
Start Page
1250
End Page
1263
Citation
ACS Synthetic Biology 14 (4): 1250-1263 (2025)
Publisher DOI
10.1021/acssynbio.4c00877
Scopus ID
2-s2.0-105001135528
Publisher
American Chemical Society
Adenosine triphosphate (ATP)-dependent in vitro bioprocesses, such as cell-free protein synthesis and the production of phosphorylated fine chemicals, are of considerable industrial significance. However, their implementation is mainly hindered by the high cost of ATP. We propose and demonstrate the feasibility of a cell-free ATP regeneration system based on the in situ generation of the high-energy compound acetyl phosphate from low-cost d-fructose and inorganic phosphate substrates. The enzyme cascade chains d-fructose phosphoketolase, d-erythrose isomerase, d-erythrulose phosphoketolase, and glycolaldehyde phosphoketolase activities theoretically enabling production of 3 mol ATP per mol of d-fructose. Through a semirational engineering approach and the screening of nine single-mutation libraries, we optimized the phosphoketolase (PKT) from Bifidobacterium adolescentis, identifying the improved variant Bad.F6Pkt H548N. This mutant exhibited a 5.6-fold increase in d-fructose activity, a 2.2-fold increase in d-erythrulose activity, and a 1.3-fold increase in glycolaldehyde activity compared to the wild-type enzyme. The Bad.F6Pkt H548N mutant was initially implemented in a cell-free reaction system together with an acetate kinase from Geobacillus stearothermophilus and a glycerol kinase from Cellulomonas sp. for the production of glycerol-3 phosphate from ADP and glycerol. We demonstrated the feasibility of ATP regeneration from 25 mM d-fructose with a stoichiometry of 1 mol of ATP per mol of C6 ketose. Subsequently, the reaction system was enhanced by incorporating d-erythrose isomerase activity provided by a l-rhamnose isomerase from Pseudomonas stutzeri. In the complete system, the ATP yield increased to 2.53 mol molfructose-1 with a maximum productivity of 7.2 mM h-1
Subjects
acetyl phosphate synthesis | ATP cofactor regeneration | in vitro biocatalysis | molecular modeling | phosphoketolase | semirational enzyme engineering
DDC Class
660: Chemistry; Chemical Engineering
572: Biochemistry
Publication version
publishedVersion
Lizenz
https://creativecommons.org/licenses/by/4.0/
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