Abstract:
Naringin is a major component found in all parts of citrus family trees and is responsible for
the bitter taste of their juices. Microorganisms that are associated with citrus family fruits appear to
have the ability to produce extracellular naringinase enzymes which can degrade the naringin
thereby reducing its bitterness. This study was aimed to isolate the naringinase producing bacteria
from bitter citrus fruit (Citrus medica) to debitter its juice and to identify the best naringinase
producing bacterium. Initially the naringinase producing strains were isolated from decayed bitter
citrus fruit and the soil where fruit is allowed to decay, using selective medium which was naringin
agar medium. Totally, seven strains were selected from the medium and out of which four strains
(BIC2, BIC3, BIC5 & BIC7) showed positive responses to qualitative naringinase assay and they
were selected for further studies. These selected bacterial strains were subjected to liquid
fermentation medium for 60 hours at 37ºC at 120 rpm and the produced crude enzyme was tested for
naringinase enzyme activity at pH 5 and 50 ºC for 10 minutes. Out of the four selected strains, the
strain BIC3 showed the best naringinase activity (1.225µmol/ml/min). Since the solid state
fermentation system provided natural habitat for bacteria, the naringinase activity was optimized
via solid state fermentation system using paddy husk as the support at 37ºC and pH 7 for 60 h. Based
on the morphological, microscopical and biochemical tests, the selected strain BIC3 was identified
-1 th
as Enterococcussp and the highest activity (302.54Ug Dry Matter) was obtained after 48 hours of
fermentation at 37ºC and at pH 7. Therefore Enterococcus sp. could be used to produce large scale
naringinase enzyme under solid state fermentation system using paddy husk as support, after the
optimization of the culture conditions.
