dc.description.abstract |
The purpose of this study was to determine the
effect of high pressure steaming pretreatment followed by
alkali treatment to make the lignocellulose waste material
susceptible to enzymatic attack. The Mangifera indlca saw
dust was subjected at high presure steaming C350 + 15 psi)
for 30 min. followed by alkali treatment at room temperature
in attempt to improve extent of digestibility and both
methods of treatment found to be ideal. The saw dust waste,
mainly consists of approximately cellulose <53 - 58%),
hemicellulose C18 - 21%) and lignln C18 - 22%) . The ternary
complex cellulose-lignln hemicellulose, was broken and the
hemicellulose and lignln components were rendered easily
extractable with water and dilute sodium hydroxide solution
at room temperature, respectively. The X-ray diffraction
pattern before and after the pretreatment showed a marked
decrease in the ordered crystalline structure of the
cellulose fibre in the raw material. Trlchoderma viride 1060
and Aspergillus wentii Pt. 2804 were found to be suitable
culture for production of maximum amount of cellulase and
/?-glucosidase in 13 days at 30 G. Lignln free saw dust was
nearly as good a substrate for production of extracellular
cellulase and f?-glucosidase by T. vlrlde and A. wentii, as
pure cellulose where as, untreated saw dust found to be the
poor substrate due to the presence of admixtures binding the
cellulose. The equl proportion of ^-glucosidase and
Ill
cellulase, hydrolysed cellulose to about 80% in 48 h whereas,
only with cellulase, 54.6% hydrolysis of cellulose was
possible. The addition of ^3-glucosidase found to be an
important step, both in terms of maximum saccharification and
less incubation period. The pH 4.8 was an optimum because
below and above this pH, there was and sharp decline in
maximum percent saccharification. Similarly the temperature
also played an important role in the hydrolysis of cellulose
o
and 50 G found to be ideal temperature. The glucose obtained
from the cellulose found to be an cheap and exceUent
substrate for single cell protein and citric acid production. |
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