Engineering of P450pyr Hydroxylase for the Highly Regio- and Enantioselective Subterminal Hydroxylation of Alkanes
Published 2014 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Engineering of P450pyr Hydroxylase for the Highly Regio- and Enantioselective Subterminal Hydroxylation of Alkanes
Authors
Keywords
-
Journal
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 53, Issue 12, Pages 3120-3124
Publisher
Wiley
Online
2014-02-20
DOI
10.1002/anie.201311091
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Regioselectiveo-Hydroxylation of Monosubstituted Benzenes by P450 BM3
- (2013) Alexander Dennig et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Regio- and Stereoselective Hydroxylation of Optically Active α-Ionone Enantiomers by Engineered Cytochrome P450 BM3 Mutants
- (2012) Harini Venkataraman et al. ADVANCED SYNTHESIS & CATALYSIS
- Novel chiral tool, (R)-2-octanol dehydrogenase, from Pichia finlandica: purification, gene cloning, and application for optically active α-haloalcohols
- (2012) Hiroaki Yamamoto et al. APPLIED MICROBIOLOGY AND BIOTECHNOLOGY
- Amides of 4-hydroxy-8-methanesulfonylamino-quinoline-2-carboxylic acid as zinc-dependent inhibitors of Lp-PLA2
- (2012) Yi Hu et al. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
- Evolving P450pyr hydroxylase for highly enantioselective hydroxylation at non-activated carbon atom
- (2012) Son Quang Pham et al. CHEMICAL COMMUNICATIONS
- Controlled Oxidation of Remote sp3 C–H Bonds in Artemisinin via P450 Catalysts with Fine-Tuned Regio- and Stereoselectivity
- (2012) Kaidong Zhang et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Engineering the third wave of biocatalysis
- (2012) U. T. Bornscheuer et al. NATURE
- P450BM3(CYP102A1): connecting the dots
- (2011) Christopher J. C. Whitehouse et al. CHEMICAL SOCIETY REVIEWS
- Regio- and stereoselectivity of P450-catalysed hydroxylation of steroids controlled by laboratory evolution
- (2011) Sabrina Kille et al. Nature Chemistry
- Regioselective ω-hydroxylation of medium-chain n-alkanes and primary alcohols by CYP153 enzymes from Mycobacterium marinum and Polaromonas sp. strain JS666
- (2011) Daniel Scheps et al. ORGANIC & BIOMOLECULAR CHEMISTRY
- Regio- and Stereoselective Biohydroxylations with a Recombinant Escherichia coli Expressing P450pyr Monooxygenase of Sphingomonas Sp. HXN-200
- (2010) Wei Zhang et al. ADVANCED SYNTHESIS & CATALYSIS
- High-Throughput Method for Determining the Enantioselectivity of Enzyme-Catalyzed Hydroxylations Based on Mass Spectrometry
- (2010) Yongzheng Chen et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Laboratory Evolution of Stereoselective Enzymes: A Prolific Source of Catalysts for Asymmetric Reactions
- (2010) Manfred T. Reetz ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Inverting the enantioselectivity of P450pyr monooxygenase by directed evolution
- (2010) Weng Lin Tang et al. CHEMICAL COMMUNICATIONS
- Enzymatic functionalization of carbon–hydrogen bonds
- (2010) Jared C. Lewis et al. CHEMICAL SOCIETY REVIEWS
- Protein engineering of microbial enzymes
- (2010) Dominique Böttcher et al. CURRENT OPINION IN MICROBIOLOGY
- Efficient stereo- and regioselective hydroxylation of alkanes catalysed by a bulky polyoxometalate
- (2010) Keigo Kamata et al. Nature Chemistry
- Directed Evolution of Enantioselective Enzymes: An Unconventional Approach to Asymmetric Catalysis in Organic Chemistry
- (2009) Manfred T. Reetz JOURNAL OF ORGANIC CHEMISTRY
- In Vivo Evolution of Butane Oxidation by Terminal Alkane Hydroxylases AlkB and CYP153A6
- (2008) D. J. Koch et al. APPLIED AND ENVIRONMENTAL MICROBIOLOGY
- Evolved CYP102A1 (P450BM3) variants oxidise a range of non-natural substrates and offer new selectivity options
- (2008) Christopher J. C. Whitehouse et al. CHEMICAL COMMUNICATIONS
Add your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload NowAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started