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Optimization of recovery of esterase from Serratia marcescens using combination of the solvent impregnated resin and aqueous two-phase extraction techniques


Citation

Abdul Aziz, Nur Fazrin Husna and Abbasiliasi, Sahar and Ariff, Arbakariya and Hui, Suan Ng and John Chi, Wei Lan and Ahmad, Rosma and Joo, Shun Tan (2018) Optimization of recovery of esterase from Serratia marcescens using combination of the solvent impregnated resin and aqueous two-phase extraction techniques. Separation Science and Technology, 53 (18). 2952 - 2960. ISSN 0149-6395; ESSN:1520-5754

Abstract

The performance of tunable aqueous polymer phase impregnated resins (TAPPIR) which is the combination of the solvent impregnated resin principle and an aqueous two-phase system for the separation of esterase from Serratia marcescens was evaluated in this study. Different molecular weight of polyethylene glycol (PEG) (2000, 4000 and 6000) at concentration ranging from 5% to 20% (w/w) and potassium citrate were used to construct the aqueous phase in TAPPIR technology. Optimum composition of PEG and salt for esterase partitioning was determined using response surface methodology. The optimum condition for the purification of esterase was impregnation of 25% (w/w) of PEG 2000 into 4 mm porous glass beads and extraction of esterase using 15% (w/w) potassium citrate at pH 8 containing 12% (w/w) crude loading with the addition of 4% (w/w) NaCl. Esterase from S. marcescens was successfully purified by the TAPPIR technology up to 5.32 of purification factor with a yield of 75.98%.


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Additional Metadata

Item Type: Article
Divisions: Faculty of Biotechnology and Biomolecular Sciences
Halal Products Research Institute
DOI Number: https://doi.org/10.1080/01496395.2018.1497653
Publisher: Taylor & Francis
Keywords: Esterase; Tunable aqueous polymer-phase impregnated resins; Polyethylene glycol; Purification
Depositing User: Mr. Sazali Mohamad
Date Deposited: 27 Nov 2019 03:49
Last Modified: 27 Nov 2019 03:49
Altmetrics: http://www.altmetric.com/details.php?domain=psasir.upm.edu.my&doi=/10.1080/01496395.2018.1497653
URI: http://psasir.upm.edu.my/id/eprint/75166
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