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  Machine learning-supported enzyme engineering toward improved CO2-fixation of Glycolyl-CoA carboxylase

Marchal, D. G., Schulz, L., Schuster, I., Ivanovska, J., Paczia, N., Prinz, S., et al. (2023). Machine learning-supported enzyme engineering toward improved CO2-fixation of Glycolyl-CoA carboxylase. ACS Synthetic Biology, 12(12), 3521-3530. doi:10.1021/acssynbio.3c00403.

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https://doi.org/10.1021/acssynbio.3c00403 (Publisher version)
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Verlagsversion
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 Creators:
Marchal, Daniel G.1, Author           
Schulz, Luca1, Author           
Schuster, Ingmar, Author
Ivanovska, Jelena, Author
Paczia, Nicole2, Author                 
Prinz, Simone, Author                 
Zarzycki, Jan1, Author           
Erb, Tobias J.2, 3, Author                 
Affiliations:
1Understanding and Building Metabolism, Department of Biochemistry and Synthetic Metabolism, Max Planck Institute for Terrestrial Microbiology, Max Planck Society, ou_3266303              
2Core Facility Metabolomics and small Molecules Mass Spectrometry, Max Planck Institute for Terrestrial Microbiology, Max Planck Society, ou_3266267              
3Center for Synthetic Microbiology (SYNMIKRO), Philipps University of Marburg, Marburg, ou_persistent22              

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 Abstract: Glycolyl-CoA carboxylase (GCC) is a new-to-nature enzyme that catalyzes the key reaction in the tartronyl-CoA (TaCo) pathway, a synthetic photorespiration bypass that was recently designed to improve photosynthetic CO2 fixation. GCC was created from propionyl-CoA carboxylase (PCC) through five mutations. However, despite reaching activities of naturally evolved biotin-dependent carboxylases, the quintuple substitution variant GCC M5 still lags behind 4-fold in catalytic efficiency compared to its template PCC and suffers from futile ATP hydrolysis during CO2 fixation. To further improve upon GCC M5, we developed a machine learning-supported workflow that reduces screening efforts for identifying improved enzymes. Using this workflow, we present two novel GCC variants with 2-fold increased carboxylation rate and 60% reduced energy demand, respectively, which are able to address kinetic and thermodynamic limitations of the TaCo pathway. Our work highlights the potential of combining machine learning and directed evolution strategies to reduce screening efforts in enzyme engineering.

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Language(s): eng - English
 Dates: 2023-11-012023-07-032023-11-072023-11-20
 Publication Status: Published online
 Pages: 10
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1021/acssynbio.3c00403
 Degree: -

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Title: ACS Synthetic Biology
  Abbreviation : ACS Synth. Biol.
Source Genre: Journal
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Publ. Info: Washington, D.C. : American Chemical Society
Pages: - Volume / Issue: 12 (12) Sequence Number: - Start / End Page: 3521 - 3530 Identifier: ISSN: 2161-5063
CoNE: https://pure.mpg.de/cone/journals/resource/2161-5063