Immobilization of enzymes using non‐ionic colloidal liquid aphrons (CLAs): Activity kinetics, conformation, and energetics. Issue 5 (10th November 2015)
- Record Type:
- Journal Article
- Title:
- Immobilization of enzymes using non‐ionic colloidal liquid aphrons (CLAs): Activity kinetics, conformation, and energetics. Issue 5 (10th November 2015)
- Main Title:
- Immobilization of enzymes using non‐ionic colloidal liquid aphrons (CLAs): Activity kinetics, conformation, and energetics
- Authors:
- Ward, Keeran
Xi, Jingshu
Stuckey, David C. - Abstract:
- ABSTRACT: This study seeks to examine the ability of non‐ionic/non‐polar Colloidial Liquid Aphrons (CLAs) to preserve enzyme functionality upon immobilization and release. CLAs consisting of micron‐sized oil droplets surrounded by a thin aqueous layer stabilized by a mixture of surfactants, were formulated by direct addition (pre‐manufacture addition) using 1% Tween 80/mineral oil and 1% Tween 20 and the enzymes lipase, aprotinin and α‐chymotrypsin. The results of activity assays for both lipase and α‐chymotrypsin showed that kinetic activity increased upon immobilization by factors of 7 and 5.5, respectively, while aprotinin retained approximately 85% of its native activity. The conformation of the enzymes released through desorption showed no significant alterations compared to their native state. Changes in pH and temperature showed that optimum conditions did not change after immobilization, while analysis of activation energy for the immobilized enzyme showed an increase in activity at higher temperatures. Furthermore, the effect of bound water within the aphron structure allowed for some degree of enzyme hydration, and this hydration was needed for an active conformation with results showing a decrease in ΔH* for the immobilized system compared to its native counterpart. Biotechnol. Bioeng. 2016;113: 970–978. © 2015 Wiley Periodicals, Inc. Abstract : This article describes a novel immobilization technique utilizing non‐ionic Colloidal Liquid Aphrons. The techniqueABSTRACT: This study seeks to examine the ability of non‐ionic/non‐polar Colloidial Liquid Aphrons (CLAs) to preserve enzyme functionality upon immobilization and release. CLAs consisting of micron‐sized oil droplets surrounded by a thin aqueous layer stabilized by a mixture of surfactants, were formulated by direct addition (pre‐manufacture addition) using 1% Tween 80/mineral oil and 1% Tween 20 and the enzymes lipase, aprotinin and α‐chymotrypsin. The results of activity assays for both lipase and α‐chymotrypsin showed that kinetic activity increased upon immobilization by factors of 7 and 5.5, respectively, while aprotinin retained approximately 85% of its native activity. The conformation of the enzymes released through desorption showed no significant alterations compared to their native state. Changes in pH and temperature showed that optimum conditions did not change after immobilization, while analysis of activation energy for the immobilized enzyme showed an increase in activity at higher temperatures. Furthermore, the effect of bound water within the aphron structure allowed for some degree of enzyme hydration, and this hydration was needed for an active conformation with results showing a decrease in ΔH* for the immobilized system compared to its native counterpart. Biotechnol. Bioeng. 2016;113: 970–978. © 2015 Wiley Periodicals, Inc. Abstract : This article describes a novel immobilization technique utilizing non‐ionic Colloidal Liquid Aphrons. The technique employs the use of micron sized (5–20 μm) oil in water macroemulsions, stabilised by surfactants present in both phases with enzymes used as models for immobilization. Immobilization was achieved through surface adsorption, governed by hydrophobic interactions existing between enzyme and surfactant monomers as well as surface charge interactions between enzyme molecules. … (more)
- Is Part Of:
- Biotechnology and bioengineering. Volume 113:Issue 5(2016)
- Journal:
- Biotechnology and bioengineering
- Issue:
- Volume 113:Issue 5(2016)
- Issue Display:
- Volume 113, Issue 5 (2016)
- Year:
- 2016
- Volume:
- 113
- Issue:
- 5
- Issue Sort Value:
- 2016-0113-0005-0000
- Page Start:
- 970
- Page End:
- 978
- Publication Date:
- 2015-11-10
- Subjects:
- enzyme activity -- superactivity -- hydration -- thermodynamics -- CLA immobilization
Biotechnology -- Periodicals
Bioengineering -- Periodicals
660.6 - Journal URLs:
- http://onlinelibrary.wiley.com/doi/10.1002/bip.v101.5/issuetoc ↗
http://www.interscience.wiley.com ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/bit.25865 ↗
- Languages:
- English
- ISSNs:
- 0006-3592
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 2089.850000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 22.xml