Influence of cholinium-based ionic liquids on the structural stability and activity of α-chymotrypsin. (27th October 2017)
- Record Type:
- Journal Article
- Title:
- Influence of cholinium-based ionic liquids on the structural stability and activity of α-chymotrypsin. (27th October 2017)
- Main Title:
- Influence of cholinium-based ionic liquids on the structural stability and activity of α-chymotrypsin
- Authors:
- Bisht, Meena
Venkatesu, Pannuru - Abstract:
- Abstract : Unanticipated high thermal stability and sustained activity of CT was found in the presence of [Ch][Ac], [Ch][Cl] and [Ch][Dhp], while [Ch][Cit] and [Ch][OH] act as strong destabilizers for the CT structure. Abstract : In recent years, the potential of α-chymotrypsin (CT) as biocatalysts has expanded new areas of its application ranging from pharmaceutical to chemical industries. However, attaining high thermal stability is one of the major challenges to the use of this enzyme in biocatalysis. In this regard, ionic liquids (ILs) have been used as promising media for the stabilization and preservation of proteins, enzymes, DNA and other biomolecules. In the present study, it was found that a series of cholinium-based ILs such as choline acetate ([Ch][Ac]), choline chloride ([Ch][Cl]), and choline dihydrogen phosphate ([Ch][Dhp]) stabilized the CT structure against thermal denaturation. The transition temperature ( T m ) of CT was increased from ∼48.9 °C (in the buffer) to 58 °C (in the ILs media). The enzymatic activity of CT in the presence of ILs was also monitored by using casein as the substrate. It was found that choline dihydrogen citrate ([Ch][Dhc]) and choline hydroxide ([Ch][OH]) dramatically decreased the enzyme activity. Both structural stability and enzymatic activity were retained in [Ch][Ac], [Ch][Cl] and [Ch][Dhp], indicating the suitability of these ILs as a high-temperature bio-catalytic reactor systems. Our results revealed that [Ch][Ac] is theAbstract : Unanticipated high thermal stability and sustained activity of CT was found in the presence of [Ch][Ac], [Ch][Cl] and [Ch][Dhp], while [Ch][Cit] and [Ch][OH] act as strong destabilizers for the CT structure. Abstract : In recent years, the potential of α-chymotrypsin (CT) as biocatalysts has expanded new areas of its application ranging from pharmaceutical to chemical industries. However, attaining high thermal stability is one of the major challenges to the use of this enzyme in biocatalysis. In this regard, ionic liquids (ILs) have been used as promising media for the stabilization and preservation of proteins, enzymes, DNA and other biomolecules. In the present study, it was found that a series of cholinium-based ILs such as choline acetate ([Ch][Ac]), choline chloride ([Ch][Cl]), and choline dihydrogen phosphate ([Ch][Dhp]) stabilized the CT structure against thermal denaturation. The transition temperature ( T m ) of CT was increased from ∼48.9 °C (in the buffer) to 58 °C (in the ILs media). The enzymatic activity of CT in the presence of ILs was also monitored by using casein as the substrate. It was found that choline dihydrogen citrate ([Ch][Dhc]) and choline hydroxide ([Ch][OH]) dramatically decreased the enzyme activity. Both structural stability and enzymatic activity were retained in [Ch][Ac], [Ch][Cl] and [Ch][Dhp], indicating the suitability of these ILs as a high-temperature bio-catalytic reactor systems. Our results revealed that [Ch][Ac] is the best stabilizer among all studied ILs for the native structure of CT, whereas [Ch][OH] is the strongest destabilizer for the CT structure. The outcome of our results can be helpful to overcome some of the major limitations found in the development of biocatalytic processes. … (more)
- Is Part Of:
- New journal of chemistry. Volume 41:Number 22(2017)
- Journal:
- New journal of chemistry
- Issue:
- Volume 41:Number 22(2017)
- Issue Display:
- Volume 41, Issue 22 (2017)
- Year:
- 2017
- Volume:
- 41
- Issue:
- 22
- Issue Sort Value:
- 2017-0041-0022-0000
- Page Start:
- 13902
- Page End:
- 13911
- Publication Date:
- 2017-10-27
- Subjects:
- Chemistry -- Periodicals
Chimie -- Périodiques
540 - Journal URLs:
- http://www.rsc.org/ ↗
http://www.rsc.org/is/journals/current/newjchem/njc.htm ↗ - DOI:
- 10.1039/c7nj03023a ↗
- Languages:
- English
- ISSNs:
- 1144-0546
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6084.319900
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 5329.xml