Over-Stabilization of Chemically Modified and Cross-Linked Candida antarctica Lipase B Using Various Epoxides and Diepoxides

Candida antarctica lipase B, Cal-B, was (i) chemically modified with various epoxides, or (ii) cross-linked with various diepoxides in order to improve enzyme activity and thermal stability. Changed enzyme structure was confirmed by kinetic resolution of p-nitrophenol acetate with methanol and deter...

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Published in:Australian Journal of Chemistry
Main Authors: Miletic, Nemanja, Loos, Katja
Format: Article in Journal/Newspaper
Language:English
Published: CSIRO PUBLISHING 2009
Subjects:
Online Access:https://scidar.kg.ac.rs/handle/123456789/19835
https://doi.org/10.1071/CH09033
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spelling ftunivkragujevac:oai:https://scidar.kg.ac.rs:123456789/19835 2024-09-15T17:46:38+00:00 Over-Stabilization of Chemically Modified and Cross-Linked Candida antarctica Lipase B Using Various Epoxides and Diepoxides Miletic, Nemanja Loos, Katja 2009 application/pdf https://scidar.kg.ac.rs/handle/123456789/19835 https://doi.org/10.1071/CH09033 en eng CSIRO PUBLISHING Miletić, N., Loos, K. (2009): Over-stabilization of chemically modified and cross-linked Candida antarctica lipase B using various epoxides and diepoxides. Australian Journal of Chemistry, 62(8), 799-805. 0004-9425 https://scidar.kg.ac.rs/handle/123456789/19835 doi:10.1071/CH09033 000268955500007 info:eu-repo/semantics/openAccess Australian Journal of Chemistry Candida antarctica Lipase B Epoxides Diepoxides Michaelis–Menten article PublishedVersion 2009 ftunivkragujevac https://doi.org/10.1071/CH09033 2024-07-11T23:30:40Z Candida antarctica lipase B, Cal-B, was (i) chemically modified with various epoxides, or (ii) cross-linked with various diepoxides in order to improve enzyme activity and thermal stability. Changed enzyme structure was confirmed by kinetic resolution of p-nitrophenol acetate with methanol and determination of the kinetic parameters. Thermal stability measurements were carried out for each Cal-B derivative, proving that Cal-B modified with 1,2-epoxypropane and 1,2-epoxypentane, and cross-linked with 1,2,7,8-diepoxyoctane and 1,2,9,10-diepoxydecane showed higher stability than soluble enzyme. The influence of the length of the epoxide arm in the modification process, as well as the length of the spacer arm in the cross-linking process, on the final enzyme preparation properties was investigated. The amount of epoxides and diepoxides used for structural rearrangement played an important role in the derivatives’ characteristics. The influence of the precipitant used and the presence of additives, such as surfactant or crown-ether, during modification and cross-linking processes was also revealed. Published Article in Journal/Newspaper Antarc* Antarctica SCIDAR - A Digital Archive of the University of Kragujevac Australian Journal of Chemistry 62 8 799
institution Open Polar
collection SCIDAR - A Digital Archive of the University of Kragujevac
op_collection_id ftunivkragujevac
language English
topic Candida antarctica Lipase B
Epoxides
Diepoxides
Michaelis–Menten
spellingShingle Candida antarctica Lipase B
Epoxides
Diepoxides
Michaelis–Menten
Miletic, Nemanja
Loos, Katja
Over-Stabilization of Chemically Modified and Cross-Linked Candida antarctica Lipase B Using Various Epoxides and Diepoxides
topic_facet Candida antarctica Lipase B
Epoxides
Diepoxides
Michaelis–Menten
description Candida antarctica lipase B, Cal-B, was (i) chemically modified with various epoxides, or (ii) cross-linked with various diepoxides in order to improve enzyme activity and thermal stability. Changed enzyme structure was confirmed by kinetic resolution of p-nitrophenol acetate with methanol and determination of the kinetic parameters. Thermal stability measurements were carried out for each Cal-B derivative, proving that Cal-B modified with 1,2-epoxypropane and 1,2-epoxypentane, and cross-linked with 1,2,7,8-diepoxyoctane and 1,2,9,10-diepoxydecane showed higher stability than soluble enzyme. The influence of the length of the epoxide arm in the modification process, as well as the length of the spacer arm in the cross-linking process, on the final enzyme preparation properties was investigated. The amount of epoxides and diepoxides used for structural rearrangement played an important role in the derivatives’ characteristics. The influence of the precipitant used and the presence of additives, such as surfactant or crown-ether, during modification and cross-linking processes was also revealed. Published
format Article in Journal/Newspaper
author Miletic, Nemanja
Loos, Katja
author_facet Miletic, Nemanja
Loos, Katja
author_sort Miletic, Nemanja
title Over-Stabilization of Chemically Modified and Cross-Linked Candida antarctica Lipase B Using Various Epoxides and Diepoxides
title_short Over-Stabilization of Chemically Modified and Cross-Linked Candida antarctica Lipase B Using Various Epoxides and Diepoxides
title_full Over-Stabilization of Chemically Modified and Cross-Linked Candida antarctica Lipase B Using Various Epoxides and Diepoxides
title_fullStr Over-Stabilization of Chemically Modified and Cross-Linked Candida antarctica Lipase B Using Various Epoxides and Diepoxides
title_full_unstemmed Over-Stabilization of Chemically Modified and Cross-Linked Candida antarctica Lipase B Using Various Epoxides and Diepoxides
title_sort over-stabilization of chemically modified and cross-linked candida antarctica lipase b using various epoxides and diepoxides
publisher CSIRO PUBLISHING
publishDate 2009
url https://scidar.kg.ac.rs/handle/123456789/19835
https://doi.org/10.1071/CH09033
genre Antarc*
Antarctica
genre_facet Antarc*
Antarctica
op_source Australian Journal of Chemistry
op_relation Miletić, N., Loos, K. (2009): Over-stabilization of chemically modified and cross-linked Candida antarctica lipase B using various epoxides and diepoxides. Australian Journal of Chemistry, 62(8), 799-805.
0004-9425
https://scidar.kg.ac.rs/handle/123456789/19835
doi:10.1071/CH09033
000268955500007
op_rights info:eu-repo/semantics/openAccess
op_doi https://doi.org/10.1071/CH09033
container_title Australian Journal of Chemistry
container_volume 62
container_issue 8
container_start_page 799
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