Immobilization of invertase on carboxymethylcellulose prepared from nata de coco for the inversion of sucrose

Nata de coco, the cellulose produced by Acetobacter aceti with coconut water as substrate, was used as starting material in the synthesis of carboxymethylcellulose after treatment with NaOH and monochloroacetic acid. The product, referred to as carboxymethyl-“nata”(CMN), had a degree of substitution...

Full description

Saved in:
Bibliographic Details
Main Authors: Fundador, Erwin Oliver V., Sabularse, V. C., Revilleza, M. A. J. R.
Format: text
Published: Animo Repository 2003
Subjects:
Online Access:https://animorepository.dlsu.edu.ph/faculty_research/5521
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: De La Salle University
id oai:animorepository.dlsu.edu.ph:faculty_research-6406
record_format eprints
spelling oai:animorepository.dlsu.edu.ph:faculty_research-64062022-05-04T01:48:15Z Immobilization of invertase on carboxymethylcellulose prepared from nata de coco for the inversion of sucrose Fundador, Erwin Oliver V. Sabularse, V. C. Revilleza, M. A. J. R. Nata de coco, the cellulose produced by Acetobacter aceti with coconut water as substrate, was used as starting material in the synthesis of carboxymethylcellulose after treatment with NaOH and monochloroacetic acid. The product, referred to as carboxymethyl-“nata”(CMN), had a degree of substitution of 0.76, a higher value than those previously reported. This was used in the immobilization of invertase via ionic interaction and adsorptive forces, which produced a viscous colloidal suspension. Agar was incorporated to facilitate pellet formation. Interactions between the agar and the CMN-invertase may have resulted from ionic interactions as well as H-bonding. The immobilized enzyme retained 71% of its initial activity and exhibited optimum pH of 4.5 and an optimum temperature of 55 C. It was more sensitive to pH and temperature changes. The Michaelis constant, Km, was 107.43 mM for the immobilized enzyme, and 71.42 mM for the free enzyme. The Vmax values were 89.28 µmole min-1 and 82.64 µmole min for the free and immobilized enzyme, respectively. Statistical analyses showed that V values did not vary significantly. The higher K of the immobilized enzyme may be attributed to diffusional effects, steric hindrance and conformational modifications of the enzyme. The immobilized enzyme has potential for further applications because of its stability with storage, repeated and continuous use. 2003-01-01T08:00:00Z text https://animorepository.dlsu.edu.ph/faculty_research/5521 Faculty Research Work Animo Repository Invertase Sugar—Inversion Acetobacter Chemistry
institution De La Salle University
building De La Salle University Library
continent Asia
country Philippines
Philippines
content_provider De La Salle University Library
collection DLSU Institutional Repository
topic Invertase
Sugar—Inversion
Acetobacter
Chemistry
spellingShingle Invertase
Sugar—Inversion
Acetobacter
Chemistry
Fundador, Erwin Oliver V.
Sabularse, V. C.
Revilleza, M. A. J. R.
Immobilization of invertase on carboxymethylcellulose prepared from nata de coco for the inversion of sucrose
description Nata de coco, the cellulose produced by Acetobacter aceti with coconut water as substrate, was used as starting material in the synthesis of carboxymethylcellulose after treatment with NaOH and monochloroacetic acid. The product, referred to as carboxymethyl-“nata”(CMN), had a degree of substitution of 0.76, a higher value than those previously reported. This was used in the immobilization of invertase via ionic interaction and adsorptive forces, which produced a viscous colloidal suspension. Agar was incorporated to facilitate pellet formation. Interactions between the agar and the CMN-invertase may have resulted from ionic interactions as well as H-bonding. The immobilized enzyme retained 71% of its initial activity and exhibited optimum pH of 4.5 and an optimum temperature of 55 C. It was more sensitive to pH and temperature changes. The Michaelis constant, Km, was 107.43 mM for the immobilized enzyme, and 71.42 mM for the free enzyme. The Vmax values were 89.28 µmole min-1 and 82.64 µmole min for the free and immobilized enzyme, respectively. Statistical analyses showed that V values did not vary significantly. The higher K of the immobilized enzyme may be attributed to diffusional effects, steric hindrance and conformational modifications of the enzyme. The immobilized enzyme has potential for further applications because of its stability with storage, repeated and continuous use.
format text
author Fundador, Erwin Oliver V.
Sabularse, V. C.
Revilleza, M. A. J. R.
author_facet Fundador, Erwin Oliver V.
Sabularse, V. C.
Revilleza, M. A. J. R.
author_sort Fundador, Erwin Oliver V.
title Immobilization of invertase on carboxymethylcellulose prepared from nata de coco for the inversion of sucrose
title_short Immobilization of invertase on carboxymethylcellulose prepared from nata de coco for the inversion of sucrose
title_full Immobilization of invertase on carboxymethylcellulose prepared from nata de coco for the inversion of sucrose
title_fullStr Immobilization of invertase on carboxymethylcellulose prepared from nata de coco for the inversion of sucrose
title_full_unstemmed Immobilization of invertase on carboxymethylcellulose prepared from nata de coco for the inversion of sucrose
title_sort immobilization of invertase on carboxymethylcellulose prepared from nata de coco for the inversion of sucrose
publisher Animo Repository
publishDate 2003
url https://animorepository.dlsu.edu.ph/faculty_research/5521
_version_ 1767196349571268608