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.