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Xylooligosaccharides, as non-functional foods,
due to their unique properties like non cariogenicity,
reduction of pathogenic flora, increase of minerals
absorption, low caloric diet foods, etc. are gaining
importance in health care and pharmaceutical sectors.
In general these could be produced by degradative
and constructive pathways. Xylooligosaccharide
production using agroindustrial materials by green
chemical synthesis assumes importance in the present
biotechnological era. Hemicellulose, a cell wall
component of plant biomass, consists of non -cellulosic
polysaccharides, with xylan and mannan as its main
constituents. Enzymatic degradation of biomass leads to
production of different non-functional foods. In nature,
xylan can be first degraded to oligosaccharides and
finally to xylose by xylanase enzyme complex produced
by different microorganisms. Keeping this in view, in
the present study xylooligosaccharides production from
Birchwood xylan has been carried out by using xylanase
enzyme produced by various strains of bacteria and fungi
isolated from Indian Institute of Chemical Technology
campus soil samples. It was noticed that each xylanase
complex is unique in nature and produce the different
xylooligosaccharides initially which are further
catalyzed to simple sugars upon further continuation.
The time required for xylooligosaccharides differ with
the source of enzyme complex. The reducing sugar
analysis by DNS and chromatographic by TLC has
shown that among the different sources of xylanases
the fungal enzyme produces high amount of reducing
sugars mainly xylose than bacterial enzymes. The
reducing sugar concentration was increased with
increase of reaction time up to complete degradation of
xylan. Whereas the bacterial xylanases mainly produced
xylooligosaccharides in 10 hrs, after that concentration
of xylose increases.
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