Enantioselective Artificial Metalloenzymes Based on a Bovine Pancreatic Polypeptide Scaffold

Site creation: Enantioselective artificial metalloenzymes have been created by grafting a new active site onto bovine pancreatic polypeptide through the introduction of an amino acid capable of coordinating a copper(II) ion. This hybrid catalyst gave good enantioselectivities in the Diels-Alder and...

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Vydané v:Angewandte Chemie (International ed.) Ročník 48; číslo 28; s. 5159 - 5162
Hlavní autori: Coquière, David, Bos, Jeffrey, Beld, Joris, Roelfes, Gerard
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: Weinheim Wiley-VCH Verlag 29.06.2009
WILEY‐VCH Verlag
Wiley
Predmet:
Amino Acid Sequence
Animals
artificial metalloenzymes
asymmetric catalysis
Catalysis
Cattle
Chemistry
Chemistry, Multidisciplinary
copper
Copper - chemistry
Diels–Alder reactions
Metalloproteins - chemistry
Michael addition
Molecular Sequence Data
Pancreatic Polypeptide - chemistry
Physical Sciences
Science & Technology
Stereoisomerism
Michael addition
OXALOACETATE DECARBOXYLASE
DESIGN
ALPHA,BETA-UNSATURATED 2-ACYL IMIDAZOLES
PROTEIN
asymmetric catalysis
DIRECTED EVOLUTION
BIOTIN-AVIDIN
PEPTIDE
TRIFLATE COMPLEXES
Diels-Alder reactions
HYBRID CATALYSTS
copper
artificial metalloenzymes
ISSN:1433-7851, 1521-3773, 1521-3773
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Abstract Site creation: Enantioselective artificial metalloenzymes have been created by grafting a new active site onto bovine pancreatic polypeptide through the introduction of an amino acid capable of coordinating a copper(II) ion. This hybrid catalyst gave good enantioselectivities in the Diels-Alder and Michael addition reactions in water (see scheme) and displayed a very high substrate selectivity.
AbstractList Site creation : Enantioselective artificial metalloenzymes have been created by grafting a new active site onto bovine pancreatic polypeptide through the introduction of an amino acid capable of coordinating a copper(II) ion. This hybrid catalyst gave good enantioselectivities in the Diels–Alder and Michael addition reactions in water (see scheme) and displayed a very high substrate selectivity. magnified image
Site creation: Enantioselective artificial metalloenzymes have been created by grafting a new active site onto bovine pancreatic polypeptide through the introduction of an amino acid capable of coordinating a copper(II) ion. This hybrid catalyst gave good enantioselectivities in the Diels–Alder and Michael addition reactions in water (see scheme) and displayed a very high substrate selectivity. Site creation: Enantioselective artificial metalloenzymes have been created by grafting a new active site onto bovine pancreatic polypeptide through the introduction of an amino acid capable of coordinating a copper(II) ion. This hybrid catalyst gave good enantioselectivities in the Diels–Alder and Michael addition reactions in water (see scheme) and displayed a very high substrate selectivity.
Site creation: Enantioselective artificial metalloenzymes have been created by grafting a new active site onto bovine pancreatic polypeptide through the introduction of an amino acid capable of coordinating a copper(II) ion. This hybrid catalyst gave good enantioselectivities in the Diels-Alder and Michael addition reactions in water (see scheme) and displayed a very high substrate selectivity.
Site creation: Enantioselective artificial metalloenzymes have been created by grafting a new active site onto bovine pancreatic polypeptide through the introduction of an amino acid capable of coordinating a copper(II) ion. This hybrid catalyst gave good enantioselectivities in the Diels-Alder and Michael addition reactions in water (see scheme) and displayed a very high substrate selectivity.Site creation: Enantioselective artificial metalloenzymes have been created by grafting a new active site onto bovine pancreatic polypeptide through the introduction of an amino acid capable of coordinating a copper(II) ion. This hybrid catalyst gave good enantioselectivities in the Diels-Alder and Michael addition reactions in water (see scheme) and displayed a very high substrate selectivity.
Author Beld, Joris
Bos, Jeffrey
Coquière, David
Roelfes, Gerard
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Issue 28
Keywords Michael addition
OXALOACETATE DECARBOXYLASE
DESIGN
ALPHA,BETA-UNSATURATED 2-ACYL IMIDAZOLES
PROTEIN
asymmetric catalysis
DIRECTED EVOLUTION
BIOTIN-AVIDIN
PEPTIDE
TRIFLATE COMPLEXES
Diels-Alder reactions
HYBRID CATALYSTS
copper
artificial metalloenzymes
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Notes http://dx.doi.org/10.1002/anie.200901134
We wish to thank Dr. W. R. Browne and A. J. Boersma for useful suggestions. Financial support from the NRSC‐Catalysis is gratefully acknowledged.
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  article-title: THE BOVINE SERUM ALBUMIN-2-PHENYLPROPANE-1,2-DIOLATODIOXO-OSMIUM(VI) COMPLEX AS AN ENANTIOSELECTIVE CATALYST FOR CIS-HYDROXYLATION OF ALKENES
  publication-title: JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS
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Snippet Site creation: Enantioselective artificial metalloenzymes have been created by grafting a new active site onto bovine pancreatic polypeptide through the...
Site creation : Enantioselective artificial metalloenzymes have been created by grafting a new active site onto bovine pancreatic polypeptide through the...
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SubjectTerms Amino Acid Sequence
Animals
artificial metalloenzymes
asymmetric catalysis
Catalysis
Cattle
Chemistry
Chemistry, Multidisciplinary
copper
Copper - chemistry
Diels–Alder reactions
Metalloproteins - chemistry
Michael addition
Molecular Sequence Data
Pancreatic Polypeptide - chemistry
Physical Sciences
Science & Technology
Stereoisomerism
Title Enantioselective Artificial Metalloenzymes Based on a Bovine Pancreatic Polypeptide Scaffold
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fanie.200901134
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https://www.ncbi.nlm.nih.gov/pubmed/19557756
https://www.proquest.com/docview/46330008
https://www.proquest.com/docview/67452225
Volume 48
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