Engineering Unspecific Peroxygenases for Enantioselective α‐Hydroxylation of β‐Ketoesters

Unspecific peroxygenases (UPOs) are promising biocatalysts for selective oxyfunctionalization. Compared to cytochrome P450 enzymes (P450s), the catalytic potential of UPOs has been less investigated, largely due to their limited natural diversity and the challenges associated with their optimization...

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Published inAngewandte Chemie International Edition Vol. 64; no. 34; pp. e202509359 - n/a
Main Authors Wang, Zhen‐Yu, Ma, Xin‐Yuan, Wu, Ying, Liu, Yang, Lin, Guang‐Xin, Liu, Xiao‐Qi, Zhang, Chun, Chen, Peng, Zheng, Yongxiang, Jia, Zhi‐Jun
Format Journal Article
LanguageEnglish
Published Germany Wiley Subscription Services, Inc 18.08.2025
EditionInternational ed. in English
Subjects
Online AccessGet full text
ISSN1433-7851
1521-3773
1521-3773
DOI10.1002/anie.202509359

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Abstract Unspecific peroxygenases (UPOs) are promising biocatalysts for selective oxyfunctionalization. Compared to cytochrome P450 enzymes (P450s), the catalytic potential of UPOs has been less investigated, largely due to their limited natural diversity and the challenges associated with their optimization through enzyme engineering. In this study, we engineered an UPO from Aspergillus niger (AniUPO) to catalyze the enantioselective α‐hydroxylation of β‐ketoesters, a valuable transformation yet to be realized in biocatalysis. Through enzyme engineering, two AniUPO variants, AniUPO‐M3 and AniUPO‐M6, were developed to produce a wide range of enantioenriched α‐hydroxy‐β‐ketoesters, achieving up to 97% yield, 4140 total turnover number (TTN), and >99:1 enantiomeric ratio (er). The biocatalytic process operates under mild conditions and is scalable for preparative applications. This study broadens the catalytic repertoire of UPOs and enhances their potential for industrial applications. An unspecific peroxygenase from Aspergillus niger (AniUPO) has been successfully engineered to catalyze the enantioselective α‐hydroxylation of β‐ketoesters. This biocatalytic process demonstrates high efficiency and selectivity with scalability to preparative levels, expanding the catalytic repertoire and synthetic applicability of UPOs in selective oxyfunctionalization.
AbstractList Unspecific peroxygenases (UPOs) are promising biocatalysts for selective oxyfunctionalization. Compared to cytochrome P450 enzymes (P450s), the catalytic potential of UPOs has been less investigated, largely due to their limited natural diversity and the challenges associated with their optimization through enzyme engineering. In this study, we engineered an UPO from Aspergillus niger ( Ani UPO) to catalyze the enantioselective α‐hydroxylation of β‐ketoesters, a valuable transformation yet to be realized in biocatalysis. Through enzyme engineering, two Ani UPO variants, Ani UPO‐M3 and Ani UPO‐M6, were developed to produce a wide range of enantioenriched α‐hydroxy‐β‐ketoesters, achieving up to 97% yield, 4140 total turnover number (TTN), and >99:1 enantiomeric ratio (er). The biocatalytic process operates under mild conditions and is scalable for preparative applications. This study broadens the catalytic repertoire of UPOs and enhances their potential for industrial applications.
Unspecific peroxygenases (UPOs) are promising biocatalysts for selective oxyfunctionalization. Compared to cytochrome P450 enzymes (P450s), the catalytic potential of UPOs has been less investigated, largely due to their limited natural diversity and the challenges associated with their optimization through enzyme engineering. In this study, we engineered an UPO from Aspergillus niger (AniUPO) to catalyze the enantioselective α‐hydroxylation of β‐ketoesters, a valuable transformation yet to be realized in biocatalysis. Through enzyme engineering, two AniUPO variants, AniUPO‐M3 and AniUPO‐M6, were developed to produce a wide range of enantioenriched α‐hydroxy‐β‐ketoesters, achieving up to 97% yield, 4140 total turnover number (TTN), and >99:1 enantiomeric ratio (er). The biocatalytic process operates under mild conditions and is scalable for preparative applications. This study broadens the catalytic repertoire of UPOs and enhances their potential for industrial applications.
Unspecific peroxygenases (UPOs) are promising biocatalysts for selective oxyfunctionalization. Compared to cytochrome P450 enzymes (P450s), the catalytic potential of UPOs has been less investigated, largely due to their limited natural diversity and the challenges associated with their optimization through enzyme engineering. In this study, we engineered an UPO from Aspergillus niger (AniUPO) to catalyze the enantioselective α‐hydroxylation of β‐ketoesters, a valuable transformation yet to be realized in biocatalysis. Through enzyme engineering, two AniUPO variants, AniUPO‐M3 and AniUPO‐M6, were developed to produce a wide range of enantioenriched α‐hydroxy‐β‐ketoesters, achieving up to 97% yield, 4140 total turnover number (TTN), and >99:1 enantiomeric ratio (er). The biocatalytic process operates under mild conditions and is scalable for preparative applications. This study broadens the catalytic repertoire of UPOs and enhances their potential for industrial applications. An unspecific peroxygenase from Aspergillus niger (AniUPO) has been successfully engineered to catalyze the enantioselective α‐hydroxylation of β‐ketoesters. This biocatalytic process demonstrates high efficiency and selectivity with scalability to preparative levels, expanding the catalytic repertoire and synthetic applicability of UPOs in selective oxyfunctionalization.
Unspecific peroxygenases (UPOs) are promising biocatalysts for selective oxyfunctionalization. Compared to cytochrome P450s, the catalytic potential of UPOs has been less investigated, largely due to their limited natural diversity and the challenges associated with their optimization through enzyme engineering. In this study, we engineered an UPO from Aspergillus niger (AniUPO) to catalyze the enantioselective α-hydroxylation of β‑ketoesters, a valuable transformation yet to be realized in biocatalysis. Through enzyme engineering, two AniUPO variants, AniUPO-M3 and AniUPO-M6, were developed to produce a wide range of enantioenriched α-hydroxy β-ketoesters, achieving up to 97% yield, 4140 total turnover number (TTN), and >99:1 enantiomeric ratio (er). The biocatalytic process operates under mild conditions and is scalable for preparative applications. This study broadens the catalytic repertoire of UPOs and enhances their potential for industrial applications.Unspecific peroxygenases (UPOs) are promising biocatalysts for selective oxyfunctionalization. Compared to cytochrome P450s, the catalytic potential of UPOs has been less investigated, largely due to their limited natural diversity and the challenges associated with their optimization through enzyme engineering. In this study, we engineered an UPO from Aspergillus niger (AniUPO) to catalyze the enantioselective α-hydroxylation of β‑ketoesters, a valuable transformation yet to be realized in biocatalysis. Through enzyme engineering, two AniUPO variants, AniUPO-M3 and AniUPO-M6, were developed to produce a wide range of enantioenriched α-hydroxy β-ketoesters, achieving up to 97% yield, 4140 total turnover number (TTN), and >99:1 enantiomeric ratio (er). The biocatalytic process operates under mild conditions and is scalable for preparative applications. This study broadens the catalytic repertoire of UPOs and enhances their potential for industrial applications.
Author Jia, Zhi‐Jun
Chen, Peng
Zhang, Chun
Lin, Guang‐Xin
Wu, Ying
Liu, Yang
Liu, Xiao‐Qi
Wang, Zhen‐Yu
Ma, Xin‐Yuan
Zheng, Yongxiang
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Keywords Oxyfunctionalization
Biocatalysis
Enantioselectivity
Enzyme engineering
Unspecific peroxygenase
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Snippet Unspecific peroxygenases (UPOs) are promising biocatalysts for selective oxyfunctionalization. Compared to cytochrome P450 enzymes (P450s), the catalytic...
Unspecific peroxygenases (UPOs) are promising biocatalysts for selective oxyfunctionalization. Compared to cytochrome P450s, the catalytic potential of UPOs...
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SubjectTerms Aspergillus niger - enzymology
Biocatalysis
Biocatalysts
Catalysis
Cytochrome P450
Cytochromes P450
Enantiomers
Enantioselectivity
Enzyme engineering
Hydroxylation
Industrial applications
Ketoesters
Ketones - chemistry
Ketones - metabolism
Mixed Function Oxygenases - chemistry
Mixed Function Oxygenases - genetics
Mixed Function Oxygenases - metabolism
Oxyfunctionalization
Protein Engineering
Stereoisomerism
Unspecific peroxygenase
Title Engineering Unspecific Peroxygenases for Enantioselective α‐Hydroxylation of β‐Ketoesters
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fanie.202509359
https://www.ncbi.nlm.nih.gov/pubmed/40474860
https://www.proquest.com/docview/3240794641
https://www.proquest.com/docview/3216364472
Volume 64
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