Modulation of the properties of immobilized CALB by chemical modification with 2,3,4-trinitrobenzenesulfonate or ethylendiamine. Advantages of using adsorbed lipases on hydrophobic supports

Process Biochemistry

Volumn 47, Issue 5, 2012, Pages 867-876

  Barbosa, Oveimar ^a,b   Ruiz, Monica ^a   Ortiz, Claudia ^a   Fernández, Marisol ^c   Torres, Rodrigo ^a   Fernandez Lafuente, Roberto ^b  

^a UNIVERSIDAD INDUSTRIAL DE SANTANDER   (Colombia)

^b CSIC   (Spain)

^c CENTRO NACIONAL DE BIOTECNOLOGÍA   (Spain)

Author keywords

2,4,6 Trinitrobenzensulfonic acid; Lipase amination; Modulation of lipases properties; Muli step chemical modification of proteins; Octyl agarose; Solid phase chemical modification of lipases

Indexed keywords

ADSORBED ENZYME; AGAROSE; CYANOGEN BROMIDE; ENZYME SPECIFICITY; ETHYLENE DIAMINE; EXPERIMENTAL CONDITIONS; HYDROPHOBIC SUPPORTS; IMMOBILIZED ENZYME; IMMOBILIZED LIPASE; LIPASE B FROM CANDIDA ANTARCTICA; MODIFIED ENZYMES; MULI-STEP CHEMICAL MODIFICATION OF PROTEINS; OCTYL-AGAROSE; REACTION CONDITIONS; SOLID-PHASE;

BROMINE COMPOUNDS; ENZYME ACTIVITY; ENZYME IMMOBILIZATION; ISOMERS; LIPASES; ORGANIC SOLVENTS; PH;

CHEMICAL MODIFICATION;

CANDIDA ANTARCTICA;

EID: 84859424745     PISSN: 13595113     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.procbio.2012.02.026     Document Type: Article

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