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  Screening and Engineering the Synthetic Potential of Carboxylating Reductases from Central Metabolism and Polyketide Biosynthesis

Peter, D., Schada von Borzyskowski, L., Kiefer, P., Christen, P., Vorholt, J. A., & Erb, T. J. (2015). Screening and Engineering the Synthetic Potential of Carboxylating Reductases from Central Metabolism and Polyketide Biosynthesis. Angew Chem Int Ed Engl, 54(45), 13457-61. doi:10.1002/anie.201505282.

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Peter, D.1, 2, Author           
Schada von Borzyskowski, L.1, 2, Author           
Kiefer, P., Author
Christen, P., Author
Vorholt, J. A., Author
Erb, T. J.1, 2, Author           
Affiliations:
1Understanding and Building Metabolism, Department of Biochemistry and Synthetic Metabolism, Max Planck Institute for Terrestrial Microbiology, Max Planck Society, ou_3266303              
2Institute of Microbiology, Eidgenössische Technische Hochschule (ETH) Zurich, Zurich, Switzerland, ou_persistent22              

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Free keywords: Models, Molecular Molecular Structure Oxidoreductases Acting on CH-CH Group Donors/chemistry/*metabolism Polyketides/chemistry/*metabolism *Protein Engineering CO2 fixation biotechnology crotonyl-CoA carboxylase/reductase natural product engineering polyketides
 Abstract: Carboxylating enoyl-thioester reductases (ECRs) are a recently discovered class of enzymes. They catalyze the highly efficient addition of CO2 to the double bond of alpha,beta-unsaturated CoA-thioesters and serve two biological functions. In primary metabolism of many bacteria they produce ethylmalonyl-CoA during assimilation of the central metabolite acetyl-CoA. In secondary metabolism they provide distinct alpha-carboxyl-acyl-thioesters to vary the backbone of numerous polyketide natural products. Different ECRs were systematically assessed with a diverse library of potential substrates. We identified three active site residues that distinguish ECRs restricted to C4 and C5-enoyl-CoAs from highly promiscuous ECRs and successfully engineered a selected ECR as proof-of-principle. This study defines the molecular basis of ECR reactivity, allowing for predicting and manipulating a key reaction in natural product diversification.

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 Dates: 2015-09-19
 Publication Status: Issued
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 Identifiers: Other: 26383129
DOI: 10.1002/anie.201505282
ISSN: 1521-3773 (Electronic)1433-7851 (Linking)
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Title: Angew Chem Int Ed Engl
Source Genre: Journal
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Pages: - Volume / Issue: 54 (45) Sequence Number: - Start / End Page: 13457 - 61 Identifier: -