Crosslinked aggregates of Rhizopus oryzae lipase as industrial biocatalysts: Preparation, optimization, characterization, and application for enantioselective resolution reactions

Biotechnology Progress

Volumn 28, Issue 4, 2012, Pages 937-945

  Kartal, Funda ^a   Kilinc, Ali ^a  

^a EGE UNIVERSITY   (Turkey)

Author keywords

Crosslinked enzyme aggregates; Enantioselectivity; Glutaraldehyde; Lipase; Reusability; Schiff base

Indexed keywords

AMMONIUM SULFATE; AQUEOUS MEDIUM; AQUEOUS REACTIONS; CHEMICALLY MODIFIED; CROSS-LINKED ENZYME AGGREGATES; CROSSLINKED; ENANTIOMERIC RATIO; ENANTIOSELECTIVE; ENHANCING EFFECT; ENZYME LEAKAGE; FREE ENZYME; GLUTARALDEHYDES; HIGH POTENTIAL; IMMOBILIZATION PROCESS; IMMOBILIZED ENZYME; INITIAL ACTIVITY; KINETIC RESOLUTION; LIPASE CLEAS; OPTIMUM CONDITIONS; PHENYLETHANOL; PREPARATION PROCESS; RHIZOPUS ORYZAE; RHIZOPUS ORYZAE LIPASE; SCHIFF BASIS; SCHIFF-BASE;

ALDEHYDES; ENANTIOSELECTIVITY; ENZYME ACTIVITY; ETHANOL; FUNCTIONAL GROUPS; LIPASES; REUSABILITY;

AGGREGATES;

CROSS LINKING REAGENT; FUNGAL PROTEIN; GLUTARALDEHYDE; IMMOBILIZED ENZYME; PHENETHYL ALCOHOL; TRIACYLGLYCEROL LIPASE;

ARTICLE; BIOCATALYSIS; CHEMISTRY; ENZYME STABILITY; ENZYMOLOGY; EVALUATION; HEAT; KINETICS; METABOLISM; METHODOLOGY; MICROBIOLOGY; PH; RHIZOPUS; STEREOISOMERISM;

BIOCATALYSIS; CROSS-LINKING REAGENTS; ENZYME STABILITY; ENZYMES, IMMOBILIZED; FUNGAL PROTEINS; GLUTARAL; HOT TEMPERATURE; HYDROGEN-ION CONCENTRATION; INDUSTRIAL MICROBIOLOGY; KINETICS; LIPASE; PHENYLETHYL ALCOHOL; RHIZOPUS; STEREOISOMERISM;

RHIZOPUS ORYZAE;

EID: 84864847938     PISSN: 87567938     EISSN: 15206033     Source Type: Journal    
DOI: 10.1002/btpr.1571     Document Type: Article

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