Laccase mediator system for activation of agarose gel: Application for immobilization of proteins
(2011) In Journal of Molecular Catalysis B: Enzymatic 68(3-4). p.270-274- Abstract
- Cross-linked Sepharose beads were treated with laccase-TEMPO system for oxidation of the primary alcohol groups on the sugar moieties. Optimal activation conditions using Trametes versicolor laccase were at pH 5 and 22 degrees C, giving an aldehyde content of 55 mu mol g(-1) Sepharose with 28 units g(-1) of laccase and 12.5 mM TEMPO. The activated Sepharose was used for immobilization of trypsin as model protein. Highest degree of immobilization was obtained at pH 10.5 but the activity yield was only 31% of that loaded on the gel. The yield of gel bound trypsin activity was increased to 76% (corresponding to about 43 U g(-1) Sepharose) when the immobilization was performed in the presence of trypsin inhibitor, benzamidine. The... (More)
- Cross-linked Sepharose beads were treated with laccase-TEMPO system for oxidation of the primary alcohol groups on the sugar moieties. Optimal activation conditions using Trametes versicolor laccase were at pH 5 and 22 degrees C, giving an aldehyde content of 55 mu mol g(-1) Sepharose with 28 units g(-1) of laccase and 12.5 mM TEMPO. The activated Sepharose was used for immobilization of trypsin as model protein. Highest degree of immobilization was obtained at pH 10.5 but the activity yield was only 31% of that loaded on the gel. The yield of gel bound trypsin activity was increased to 76% (corresponding to about 43 U g(-1) Sepharose) when the immobilization was performed in the presence of trypsin inhibitor, benzamidine. The immobilization yields were comparable to that obtained on the matrix activated using sodium periodate (containing 72 mu mol aldehyde per g Sepharose). Recycling and storage of the immobilized trypsin preparations showed high stability of the enzyme bound to laccase-TEMPO activated gel. (C) 2010 Elsevier B.V. All rights reserved. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/1877978
- author
- Mendoza, Laura LU ; Mamo, Gashaw LU ; Flores, Ninoska ; Gimenez, Alberto and Hatti-Kaul, Rajni LU
- organization
- publishing date
- 2011
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- Laccase mediator system, Trametes versicolor, Cross-linked Sepharose, Periodate activation, Trypsin
- in
- Journal of Molecular Catalysis B: Enzymatic
- volume
- 68
- issue
- 3-4
- pages
- 270 - 274
- publisher
- Elsevier
- external identifiers
-
- wos:000287114900008
- scopus:78651385759
- ISSN
- 1873-3158
- DOI
- 10.1016/j.molcatb.2010.11.016
- language
- English
- LU publication?
- yes
- id
- a2951951-b008-4d55-80e2-9328818960dc (old id 1877978)
- date added to LUP
- 2016-04-01 11:03:15
- date last changed
- 2022-01-26 04:59:36
@article{a2951951-b008-4d55-80e2-9328818960dc,
abstract = {{Cross-linked Sepharose beads were treated with laccase-TEMPO system for oxidation of the primary alcohol groups on the sugar moieties. Optimal activation conditions using Trametes versicolor laccase were at pH 5 and 22 degrees C, giving an aldehyde content of 55 mu mol g(-1) Sepharose with 28 units g(-1) of laccase and 12.5 mM TEMPO. The activated Sepharose was used for immobilization of trypsin as model protein. Highest degree of immobilization was obtained at pH 10.5 but the activity yield was only 31% of that loaded on the gel. The yield of gel bound trypsin activity was increased to 76% (corresponding to about 43 U g(-1) Sepharose) when the immobilization was performed in the presence of trypsin inhibitor, benzamidine. The immobilization yields were comparable to that obtained on the matrix activated using sodium periodate (containing 72 mu mol aldehyde per g Sepharose). Recycling and storage of the immobilized trypsin preparations showed high stability of the enzyme bound to laccase-TEMPO activated gel. (C) 2010 Elsevier B.V. All rights reserved.}},
author = {{Mendoza, Laura and Mamo, Gashaw and Flores, Ninoska and Gimenez, Alberto and Hatti-Kaul, Rajni}},
issn = {{1873-3158}},
keywords = {{Laccase mediator system; Trametes versicolor; Cross-linked Sepharose; Periodate activation; Trypsin}},
language = {{eng}},
number = {{3-4}},
pages = {{270--274}},
publisher = {{Elsevier}},
series = {{Journal of Molecular Catalysis B: Enzymatic}},
title = {{Laccase mediator system for activation of agarose gel: Application for immobilization of proteins}},
url = {{http://dx.doi.org/10.1016/j.molcatb.2010.11.016}},
doi = {{10.1016/j.molcatb.2010.11.016}},
volume = {{68}},
year = {{2011}},
}