4.6 Article

A new heterofunctional amino-vinyl sulfone support to immobilize enzymes: Application to the stabilization of beta-galactosidase from Aspergillus oryzae

期刊

PROCESS BIOCHEMISTRY
卷 64, 期 -, 页码 200-205

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.procbio.2017.09.020

关键词

Divinylsulfone; Heterofunctional supports; Enzyme immobilization; Enzyme stabilization; Ion exchange; Enzyme orientation

资金

  1. MINECO from Spanish Government [CTQ2013-41507-R, CTQ2017-86170-R]
  2. Algerian Ministry of higher education and scientific research

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The paper shows the preparation of a new heterofunctional agarose support: amino-vinylsulfone. This has been employed to immobilize the interesting enzyme beta-galactosidase from Aspergillus oryzae. The enzyme cannot be immobilized on just vinylsulfone activated support a pH values ranging from 5.0 to 9.0. Neither the enzyme was immobilized using 200 mM of NaCl on amino-vinylsulfone support. However, the enzyme was readily immobilized at moderate ion strength at pH values from 5.0 to 9.0 via ion exchange on amino-vinylsulfone support, and later some covalent enzyme-support bonds could be formed, more rapidly at alkaline pH value. After optimization of immobilization pH, incubation pH and time, and blocking reagent, several immobilized biocatalysts on amino-vinylsulfone support having 50-80% of the initial activity and a stabilization factor of around 8-15 were prepared, depending on the exact immobilization conditions.

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