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dc.contributor.authorNahar, Kazi Sumaita
dc.date.accessioned2022-12-19T09:29:21Z
dc.date.available2022-12-19T09:29:21Z
dc.date.issued2018
dc.identifier.urihttp://hdl.handle.net/123456789/156
dc.description.abstractIn the present study, alpha amylase was produced from Bacillus amyloliquefaciens in optimized condition by submerged fermentation technique. Biochemical tests were performed to identify the bacteria. The enzyme was extracted and purified by ammonium sulphate precipitation. Amylase activity and specific activity of the purified amylase was found to be 10 U/ml/min and 0.89 U/mg/min respectively. The enzyme was further purified by dialysis and size exclusion chromatography. The 16s rRNA gene was extracted from the bacteria and sent for sequencing to identify the strain. The result of the sequence analysis of the gene will be used to design primer and clone the amylase gene to over express the enzyme for industrial use in textile industry.en_US
dc.description.sponsorshipSubmitted by: Kazi Sumaita Nahar Advisor: Prof. A. K. M. Moniruzzaman Mollahen_US
dc.language.isoen_USen_US
dc.publisherAsian University for Women, Chittagong, Bangladeshen_US
dc.subjectAlpha amylase, B. amyloliquefaciens, amylase activity, purification, 16s rRNA gene, cloning, textile industryen_US
dc.titleExtraction and Purification of Alpha Amylase from Bacillus amyloliquefaciens and Identification of the Strain by 16s rRNA Gene Sequencingen_US
dc.typeThesisen_US


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