Regioselectivity Inversion of an <i>O</i> ‐Methyltransferase via Semi‐rational Mutagenesis Combined with Metal Ion Substitution-Reference-Cited by-同舟云学术

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Regioselectivity Inversion of an O ‐Methyltransferase via Semi‐rational Mutagenesis Combined with Metal Ion Substitution

Published:2022-10-27 Issue:23 Volume:14 Page:
ISSN:1867-3880
Container-title:ChemCatChem
language:en
Short-container-title:ChemCatChem

Author:

Su Ying¹,Li Hai‐Peng¹,Zhang Man¹,Ding Xu‐Wei¹,Xu Jian‐He¹,Chen Qi¹,Zheng Gao‐Wei¹^ORCID

Affiliation:

1. State Key Laboratory of Bioreactor Engineering East China University of Science and Technology 130 Meilong Road Shanghai 200237 P. R. China

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cctc.202200844

Reference34 articles.

1. Exploiting the Regioselectivity of Baeyer-Villiger Monooxygenases for the Formation of β-Amino Acids and β-Amino Alcohols

2. Durch Nutzen der Regioselektivität von Baeyer-Villiger- Monooxygenasen zu β-Aminosäuren und β-Aminoalkoholen

3. Biocatalysis in Organic Chemistry and Biotechnology: Past, Present, and Future

4. Enantioselective biocatalysis optimized by directed evolution

5. Near-perfect control of the regioselective glucosylation enabled by rational design of glycosyltransferases

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5. Engineering an O‐methyltransferase for the Regioselective Biosynthesis of Hesperetin Dihydrochalcone;ChemCatChem;2023-09-07

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