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Volumn 342, Issue 1, 2007, Pages 55-64
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Formation of covalent β-linked carbohydrate-enzyme intermediates during the reactions catalyzed by α-amylases
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Author keywords
Alpha amylases; Covalent intermediates; Mechanism; Methyl 6 3H maltooligosaccharide glycosides; Proton NMR; SN2 double displacement reaction
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Indexed keywords
ACETONE;
CARBOHYDRATES;
CATALYSIS;
NUCLEAR MAGNETIC RESONANCE;
PROTEINS;
REACTION KINETICS;
COVALENT INTERMEDIATES;
DENATURED ENZYME;
GLYCOSIDES;
PROTON NUCLEAR MAGNETIC RESONANCE;
SATURATION TRANSFER ANALYSIS;
ENZYME KINETICS;
ACETONE;
ALPHA 6 MALTOOLIGOSACCHARIDE GLYCOSIDE DERIVATIVE;
AMYLASE;
CARBOHYDRATE;
ARTICLE;
BACILLUS AMYLOLIQUEFACIENS;
CATALYSIS;
COVALENT BOND;
ENZYME DENATURATION;
ENZYME MECHANISM;
HYDROLYSIS;
PRECIPITATION;
PRIORITY JOURNAL;
PROTON NUCLEAR MAGNETIC RESONANCE;
ALPHA-AMYLASE;
ANIMALS;
BACILLUS;
CARBOHYDRATE CONFORMATION;
CATALYSIS;
GLYCOSIDES;
HYDROLYSIS;
MAGNETIC RESONANCE SPECTROSCOPY;
OLIGOSACCHARIDES;
PANCREAS;
SWINE;
BACILLUS AMYLOLIQUEFACIENS;
SUIDAE;
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EID: 33845520086
PISSN: 00086215
EISSN: None
Source Type: Journal
DOI: 10.1016/j.carres.2006.10.028 Document Type: Article |
Times cited : (9)
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References (51)
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