M. Puri et al., STUDIES ON THE APPLICABILITY OF ALGINATE-ENTRAPPED NARINGINASE FOR THE DEBITTERING OF KINNOW JUICE, Enzyme and microbial technology, 18(4), 1996, pp. 281-285
Screening of matrices for the immobilization of naringinase demonstrat
ed that 2% sodium alginate was an optimal matrix. Upon immobilization,
30 U of naringinase gave 82% naringin hydrolysis in 3 h, broadening o
f pH optima has attributed desirable flexibility for debittering kinno
w juice of varying pHs, and temperature profiles indicated on improved
thermostability which could be handy during the reduction in cost of
debittering. Alginate permitted attainment of equilibrium readily with
no hindrance in the inflow of naringin and the outflow of naringenin/
prunin, and adequate mechanical stability, cumulatively indicating the
feasibility of its commercial exploitation. The application of kineti
c parameters optimized with pure naringin to kinnow juice resulted in
60% debittering. It suggested the desirability of ultrafiltration to m
inimize product inhibition in order to maximize naringin hydrolysis, a
nd subsequent fortification by the permeate at the end of debittering
to formulate sweetened kinnow juice with nourishing and natural charac
teristics. Efforts to change over from the batch process to a continuo
us column process are underway.