Quantitative Comparison of Chiral Catalysts Selectivity and Performance: A Generic Concept Illustrated with Cyclododecanone Monooxygenase as Baeyer–Villiger Biocatalyst
- 21 November 2012
- journal article
- research article
- Published by Wiley in Advanced Synthesis & Catalysis
- Vol. 354 (18) , 3491-3500
Abstract
Within this work a generic tool for chiral catalyst evaluation is established based on the application‐oriented properties activity and selectivity; the concept aims at quantitatively comparing catalyst performance in general on a multitude of substrates. It is designed and intended to serve as decision guidance for challenges in catalysis and comprehensible information extraction from already recorded but unrefined data sets. The underlying algorithm assigns function points to catalytic entities via a statistically solid model possessing high flexibility and generates a relative ranking. This is coupled to an automated iterative refinement process towards maximum information content of results employing Shannon entropy optimization. Consequently, the developed work‐flow facilitates high distinguishability between catalysts even in low‐scattering data sets. The numerical ranking is complemented by a clearly arranged graphic representation permitting facile and reliable visual interpretation of generality or niche capabilities of catalysts. Usefulness of the title concept is demonstrated by the performance evaluation of cyclododecanone monooxygenase, a highly versatile Baeyer–Villiger enzyme. To retain broad applicability, an open‐source MATLAB® script is provided in electronic form.Keywords
This publication has 53 references indexed in Scilit:
- Quantum Mechanical/Molecular Mechanical Study on the Mechanism of the Enzymatic Baeyer–Villiger ReactionJournal of the American Chemical Society, 2012
- Blending Baeyer–Villiger monooxygenases: using a robust BVMO as a scaffold for creating chimeric enzymes with novel catalytic propertiesChemical Communications, 2012
- Extensive substrate profiling of cyclopentadecanone monooxygenase as Baeyer–Villiger biocatalyst reveals novel regiodivergent oxidationsJournal of Molecular Catalysis B: Enzymatic, 2011
- Snapshots of Enzymatic Baeyer-Villiger CatalysisJournal of Biological Chemistry, 2011
- Introduction to Enzymes in SynthesisChemical Reviews, 2011
- Baeyer−Villiger Monooxygenases: More Than Just Green ChemistryChemical Reviews, 2011
- Introduction to Frontiers in Transition Metal Catalyzed Reactions (and a Brief Adieu)Chemical Reviews, 2011
- Cloning, Expression, Characterization, and Biocatalytic Investigation of the 4-Hydroxyacetophenone Monooxygenase from Pseudomonas putida JD1Applied and Environmental Microbiology, 2009
- Stereoselective Desymmetrizations by Recombinant Whole Cells Expressing the Baeyer–Villiger Monooxygenase from Xanthobacter sp. ZL5: A New Biocatalyst Accepting Structurally Demanding SubstratesEuropean Journal of Organic Chemistry, 2008
- A “Designer Yeast” That Catalyzes the Kinetic Resolutions of 2-Alkyl-Substituted Cyclohexanones by Enantioselective Baeyer−Villiger OxidationsThe Journal of Organic Chemistry, 1996