Olefin Cyclopropanation and Carbon-hydrogen Amination Via Carbene and Nitrene Transfers Catalyzed by Engineered Cytochrome P450 Enzymes

Olefin Cyclopropanation and Carbon-hydrogen Amination Via Carbene and Nitrene Transfers Catalyzed by Engineered Cytochrome P450 Enzymes
Author: Pedro de Souza Leão Coelho
Publisher:
Total Pages: 500
Release: 2013
Genre: Biocatalysis
ISBN:

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Synthetic biology promises to transform organic synthesis by enabling artificial catalysis in living cells. I start by reviewing the state of the art in this young field and recognizing that new approaches are required for designing enzymes that catalyze nonnatural reactions, in order to expand the scope of biocatalytic transformations. Carbene and nitrene transfers to C=C and C-H bonds are reactions of tremendous synthetic utility that lack biological counterparts. I show that various heme proteins, including cytochrome P450BM3, will catalyze promiscuous levels of olefin cyclopropanation when provided with the appropriate synthetic reagents (e.g., diazoesters and styrene). Only a few amino acid substitutions are required to install synthetically useful levels of stereoselective cyclopropanation activity in P450BM3. Understanding that the ferrous-heme is the active species for catalysis and that the artificial reagents are unable to induce a spin-shift-dependent increase in the redox potential of the ferric P450, I design a high-potential serine-heme ligated P450 (P411) that can efficiently catalyze cyclopropanation using NAD(P)H. Intact E. coli whole-cells expressing P411 are highly efficient asymmetric catalysts for olefin cyclopropanation. I also show that engineered P450s can catalyze intramolecular amination of benzylic C-H bonds from arylsulfonyl azides. Finally, I review other examples of where synthetic reagents have been used to drive the evolution of novel enzymatic activity in the environment and in the laboratory. I invoke preadaptation to explain these observations and propose that other man-invented reactions may also be transferrable to natural enzymes by using a mechanism-based approach for choosing the enzymes and the reagents. Overall, this work shows that existing enzymes can be readily adapted for catalysis of synthetically important reactions not previously observed in nature.


Olefin Cyclopropanation and Carbon-hydrogen Amination Via Carbene and Nitrene Transfers Catalyzed by Engineered Cytochrome P450 Enzymes
Language: en
Pages: 500
Authors: Pedro de Souza Leão Coelho
Categories: Biocatalysis
Type: BOOK - Published: 2013 - Publisher:

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Synthetic biology promises to transform organic synthesis by enabling artificial catalysis in living cells. I start by reviewing the state of the art in this yo
Biocatalytic Methods for Carbon-nitrogen Bond Formation Via Hemoprotein-catalyzed Group Transfer Reactions
Language: en
Pages: 254
Authors: Viktoria Steck
Categories:
Type: BOOK - Published: 2019 - Publisher:

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"Our group has recently established that heme-containing proteins, in particular myoglobin and cytochrome P450s, constitute promising biocatalysts for the forma
Transition Metal-Catalyzed Carbene Transformations
Language: en
Pages: 450
Authors: Jianbo Wang
Categories: Science
Type: BOOK - Published: 2021-12-20 - Publisher: John Wiley & Sons

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Presents an up-to-date overview of the rapidly growing field of carbene transformations Carbene transformations have had an enormous impact on catalysis and org
Cytochrome P450
Language: en
Pages: 702
Authors: Paul R. Ortiz de Montellano
Categories: Medical
Type: BOOK - Published: 2007-02-05 - Publisher: Springer Science & Business Media

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Cytochrome P450: Structure, Mechanism, and Biochemistry, third edition is a revision of a review that summarizes the current state of research in the field of d
Biocatalytic Organofluorine Synthesis Via Hemoprotein-catalyzed Carbene Transfer Reactions
Language: en
Pages: 291
Authors: Antonio Tinoco Valencia
Categories:
Type: BOOK - Published: 2020 - Publisher:

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"Protein engineering efforts in our laboratory led to the development of efficient hemoprotein-based biocatalysts for abiological carbene transfer reactions. Th