Encapsulation of tannase for the hydrolysis of tea tannins

Citation
Dk. Boadi et Rj. Neufeld, Encapsulation of tannase for the hydrolysis of tea tannins, ENZYME MICR, 28(7-8), 2001, pp. 590-595
Citations number
8
Categorie Soggetti
Biotecnology & Applied Microbiology",Microbiology
Journal title
ENZYME AND MICROBIAL TECHNOLOGY
ISSN journal
01410229 → ACNP
Volume
28
Issue
7-8
Year of publication
2001
Pages
590 - 595
Database
ISI
SICI code
0141-0229(20010507)28:7-8<590:EOTFTH>2.0.ZU;2-W
Abstract
Tannase was encapsulated in alginate, chitosan. carrageenan or pectin gel m atrices, and in the case of alginate coated with high or low molecular weig ht chitosan to reduce enzyme release. Cross-linking with glutaraldehyde als o improved enzyme retention. Activate enzyme preparations were obtained, al though carrageenan gels were unstable in tea, Tannase activity was evaluate d by reduction in centrifugable flocculated) tea solids, and a reduction in tea cream measured turbidimetrically after removal of flocculated solids. Tannin interactions with the polysaccharide gels increased the level of cen trifugable solids (flocculent) in the tea. An optimum bead formulation cons isted of an alginate core, coated with chitosan and cross-linked with gluta raldehyde. Both core and coating materials contained active enzyme. Beads w ere prepared in a single step procedure involving extrusion of alginate/tan nase solution into a hardening bath containing tannase-loaded, chitosan sol ution. Tannase retained hydrolytic activity through three successive batch cycles, for 3 total period of 39h processing, and tea cream was visibily; r emoved by treatment with the immobilized tannase. Activity remained stable during 1-month bend storage under refrigeration. (C) 2001 Elsevier Science Inc. All rights reserved.