Overproduction of Bioethanol From Cellulosic Wastes
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Abstract
One of the most attractive lignocellulosic feedstock for the production of
newlinebioethanol is the rice straw because of its cheaper and most abundantly found in
newlinenature. Adding to it, it has high cellulose content that can be hydrolyzed into sugars
newlineupon fermentation. The presence of lignin in the raw material makes it inferior in the
newlineprocess of conversion of rice straw to bioethanol. Thus, selection of a suitable
newlinepretreatment method that is cost-effective and which takes less time needs to be
newlinedeveloped. Also, enzymatic hydrolysis is an essential step for degrading rice straw
newlineinto fermentable sugars. Currently, for industrial bioethanol production, reseachers
newlineare depending on the commercial enzymes that are quite expensive. Development of
newlineinexpensive enzymes that can improve the parameters of hydrolysis is quite
newlinenecessary. Finally, the heart in bioethanol production is the fermentation and
newlinemicroorganisms such as yeasts are able to produce bioethanol in industrial scale. For
newlinethis purpose, isolation of potential yeasts strains for obtaining maximum bioethanol
newlineyield is required.
newlineHence, in the present piece of work, we have isolated yeast species and
newlinebased on biochemical, morphological and molecular analysis, the potential isolates
newlinewere identified as Saccharomyces cerevisiae and Hanseniaspora guilliermondii. The
newlineoptimum conditions for bioethanol production were also investigated. The
newlineincubation time of 72 h was found to be best for bioethanol production by the best
newlineisolate and maintaining the temperature and pH at 30°C and 4.5 respectively was
newlinefound optimum. Physical treatment by grinding and milling followed by 4% NaOH
newlinealkali treatment was found to be the best pretreatment technique and was
newlineinvestigated by the FTIR, XRD and SEM analysis. Another fungus isolates which
newlinewas identified as Aspergillus flavus was checked for its hydrolysis efficiency and
newlinewas found the ability to produce cellulose enzyme. However, use of commercial
newlineenzymes was found to be more efficient. The extracted bioethanol was analysed by
newlinethe
newline1
newlineH NMR and
newline13
newlineC which confirms the presence of bioethanol. Strain
newlineimprovement was done by mutagenesis which involves exposing the
newlinemicroorganisms to UV rays and chemical mutagens such as EtBr and EMS. The
newlinebioethanol yield of the wild strain (21.77%) was compared with that of the mutant
newlinestrain (24.29%) which was achieved on treatment with EMS. Also, treatment with
newlineEtBr also resulted in giving higher bioethanol yield but was found that not all the
newlinemutants produced higher yields. Thus, searching for a favorable strain for improving
newlinebioethanol production is in dire need.
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