Future Directions in Biocatalysis
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portes grátis
Future Directions in Biocatalysis
Matsuda, Tomoko
Elsevier Science & Technology
08/2017
460
Dura
Inglês
9780444637437
15 a 20 dias
1110
Descrição não disponível.
1. X-ray crystal structure determination 2. Simulation for prediction of enzyme functions 3. Biotransformation in ionic liquid 4. Utilization of light energy for reactions using biocatalysis 5. Utilization of liquid and supercritical CO2 as solvents for biocatalysis
Este título pertence ao(s) assunto(s) indicados(s). Para ver outros títulos clique no assunto desejado.
(de)carboxylases; 2-arylpropanoic acid; Activation; Acyl-CoA synthetase; Alcohol; Alcohol dehydrogenase; Amidation; Asymmetric reaction; Asymmetric reduction; Biocatalysis; Biocatalytic promiscuity; Bioluminescence; Bioprospecting; Boron-cluster carborane; C-chiral phosphorus compounds; C-chiral sulfur compounds; CO2; Carboxylase; Catalytic reaction; Chiral alcohols; Chiral cyclic amine; Cofactor; Cofactor recycling; Covalent flavinylation; Deazaflavin; Desymmetrization; Domain decomposition; Domino reaction; Dynamic kinetic resolution; Electronegativity; Enantiomer; Enantioselective; Enantioselectivity; Enzyme; Enzymology; Extradiol ring-cleavage dioxygenase; Firefly luciferase; Flavin; Fluorinated compounds; Ge-chiral germanium compounds; Homology modeling; Hydrolase; Hydrolytic enzymes; Imine reductase; Ionic liquids; Ketoreductase; Kinetic resolution; Light emission; Lipase; Lipase-catalyzed reaction; Medicinal chemistry; Metagenomics; Molecular dynamics; Monooxygenases; Nicotinamide; Nonaqueous solvent; Odorous compound; Optically active compound; Oxidases; P-chiral phosphorus compounds; Peptide bond formation; Photobiocatalysis; Prenylated flavin; Racemization; Reaction intermediate; Reactivity; Redox enzymes; Reduction; Ruthenium; S-GAM; S-chiral sulfur compounds; Sequence alignment; Si-chiral silicon compounds; Substrate specificity; Subtilisin; Synchrotron radiation; Thioester formation; Thioesterification; Vanadium; Various biotransformation; X-ray crystallography; X-ray free electron laser (XFEL)
1. X-ray crystal structure determination 2. Simulation for prediction of enzyme functions 3. Biotransformation in ionic liquid 4. Utilization of light energy for reactions using biocatalysis 5. Utilization of liquid and supercritical CO2 as solvents for biocatalysis
Este título pertence ao(s) assunto(s) indicados(s). Para ver outros títulos clique no assunto desejado.
(de)carboxylases; 2-arylpropanoic acid; Activation; Acyl-CoA synthetase; Alcohol; Alcohol dehydrogenase; Amidation; Asymmetric reaction; Asymmetric reduction; Biocatalysis; Biocatalytic promiscuity; Bioluminescence; Bioprospecting; Boron-cluster carborane; C-chiral phosphorus compounds; C-chiral sulfur compounds; CO2; Carboxylase; Catalytic reaction; Chiral alcohols; Chiral cyclic amine; Cofactor; Cofactor recycling; Covalent flavinylation; Deazaflavin; Desymmetrization; Domain decomposition; Domino reaction; Dynamic kinetic resolution; Electronegativity; Enantiomer; Enantioselective; Enantioselectivity; Enzyme; Enzymology; Extradiol ring-cleavage dioxygenase; Firefly luciferase; Flavin; Fluorinated compounds; Ge-chiral germanium compounds; Homology modeling; Hydrolase; Hydrolytic enzymes; Imine reductase; Ionic liquids; Ketoreductase; Kinetic resolution; Light emission; Lipase; Lipase-catalyzed reaction; Medicinal chemistry; Metagenomics; Molecular dynamics; Monooxygenases; Nicotinamide; Nonaqueous solvent; Odorous compound; Optically active compound; Oxidases; P-chiral phosphorus compounds; Peptide bond formation; Photobiocatalysis; Prenylated flavin; Racemization; Reaction intermediate; Reactivity; Redox enzymes; Reduction; Ruthenium; S-GAM; S-chiral sulfur compounds; Sequence alignment; Si-chiral silicon compounds; Substrate specificity; Subtilisin; Synchrotron radiation; Thioester formation; Thioesterification; Vanadium; Various biotransformation; X-ray crystallography; X-ray free electron laser (XFEL)
