Directed evolution of phosphite dehydrogenase to cycle noncanonical redox cofactors via universal growth selection platform

Engineering enzymes to utilize the noncanonical redox cofactors such as nicotinamide mononucleotide (NMN + ) is challenging. Here, the authors report a growth-based selection platform for NMN + -reducing enzyme engineering and show its application in developing a phosphite dehydrogenase with improve...

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Main Authors: Linyue Zhang, Edward King, William B. Black, Christian M. Heckmann, Allison Wolder, Youtian Cui, Francis Nicklen, Justin B. Siegel, Ray Luo, Caroline E. Paul, Han Li
Format: Article
Language:English
Published: Nature Portfolio 2022-08-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-022-32727-w
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author Linyue Zhang
Edward King
William B. Black
Christian M. Heckmann
Allison Wolder
Youtian Cui
Francis Nicklen
Justin B. Siegel
Ray Luo
Caroline E. Paul
Han Li
author_facet Linyue Zhang
Edward King
William B. Black
Christian M. Heckmann
Allison Wolder
Youtian Cui
Francis Nicklen
Justin B. Siegel
Ray Luo
Caroline E. Paul
Han Li
author_sort Linyue Zhang
collection DOAJ
description Engineering enzymes to utilize the noncanonical redox cofactors such as nicotinamide mononucleotide (NMN + ) is challenging. Here, the authors report a growth-based selection platform for NMN + -reducing enzyme engineering and show its application in developing a phosphite dehydrogenase with improved catalytic efficiency.
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spelling doaj.art-75d6e8408c81418bb081b0cb20fbd5ad2022-12-22T03:08:35ZengNature PortfolioNature Communications2041-17232022-08-0113111210.1038/s41467-022-32727-wDirected evolution of phosphite dehydrogenase to cycle noncanonical redox cofactors via universal growth selection platformLinyue Zhang0Edward King1William B. Black2Christian M. Heckmann3Allison Wolder4Youtian Cui5Francis Nicklen6Justin B. Siegel7Ray Luo8Caroline E. Paul9Han Li10Department of Chemical and Biomolecular Engineering, University of California IrvineDepartment of Molecular Biology and Biochemistry, University of California IrvineDepartment of Chemical and Biomolecular Engineering, University of California IrvineBiocatalysis, Department of Biotechnology, Delft University of TechnologyBiocatalysis, Department of Biotechnology, Delft University of TechnologyDepartment of Chemistry, University of California, Davis, One Shields AvenueDepartment of Chemical and Biomolecular Engineering, University of California IrvineDepartment of Chemistry, University of California, Davis, One Shields AvenueDepartment of Chemical and Biomolecular Engineering, University of California IrvineBiocatalysis, Department of Biotechnology, Delft University of TechnologyDepartment of Chemical and Biomolecular Engineering, University of California IrvineEngineering enzymes to utilize the noncanonical redox cofactors such as nicotinamide mononucleotide (NMN + ) is challenging. Here, the authors report a growth-based selection platform for NMN + -reducing enzyme engineering and show its application in developing a phosphite dehydrogenase with improved catalytic efficiency.https://doi.org/10.1038/s41467-022-32727-w
spellingShingle Linyue Zhang
Edward King
William B. Black
Christian M. Heckmann
Allison Wolder
Youtian Cui
Francis Nicklen
Justin B. Siegel
Ray Luo
Caroline E. Paul
Han Li
Directed evolution of phosphite dehydrogenase to cycle noncanonical redox cofactors via universal growth selection platform
Nature Communications
title Directed evolution of phosphite dehydrogenase to cycle noncanonical redox cofactors via universal growth selection platform
title_full Directed evolution of phosphite dehydrogenase to cycle noncanonical redox cofactors via universal growth selection platform
title_fullStr Directed evolution of phosphite dehydrogenase to cycle noncanonical redox cofactors via universal growth selection platform
title_full_unstemmed Directed evolution of phosphite dehydrogenase to cycle noncanonical redox cofactors via universal growth selection platform
title_short Directed evolution of phosphite dehydrogenase to cycle noncanonical redox cofactors via universal growth selection platform
title_sort directed evolution of phosphite dehydrogenase to cycle noncanonical redox cofactors via universal growth selection platform
url https://doi.org/10.1038/s41467-022-32727-w
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