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Studies on some Enzymes from Germinating oil and Cereal Seeds

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dc.contributor.advisor Huque, Entazul M.
dc.contributor.author Sana, Niranjan Kumar
dc.date.accessioned 2022-09-20T07:25:17Z
dc.date.available 2022-09-20T07:25:17Z
dc.date.issued 2004
dc.identifier.uri http://rulrepository.ru.ac.bd/handle/123456789/876
dc.description This Thesis is Submitted to the Department of Biochemistry and Molecular Biology, University of Rajshahi, Rajshahi, Bangladesh for The Degree of Doctor of Philosophy (PhD) en_US
dc.description.abstract Degradation of three varieties of Brassica and wheat seed storage substances at different periods of germination have been studied to have a comparative data on their chemical composition. Free sugar contents of the three varieties of Brassica and wheat seeds differ slightly. Wheat seeds contain a little higher amount of free sugar than that of Brassica seeds. Reducing sugar contents also vary in Brassica and wheat seeds. During germination, the degradation of free sugar and reducing sugar in Brassica seeds is faster than in wheat seeds. Wheat seeds contain a larger amount of starch than that of Brassica seeds. Among the three varieties of wheat seeds, Akbar variety has the highest percentage of starch. The starch contents of both seeds decrease gradually dming germination. Total protein and water-􀀷oluble protein content of the three varieties of Brassica seeds is slightly higher than that of wheat seeds. During germination, protein depletion starts after initial imbibition, and is completed in between 96 to 120 hours. Brassica seeds contain a significant amounts of lipid. Among Brassica seeds, napus variety contains the highest amount of lipid, followed by campestries and jtmcia varieties. Lipid degradation starts after 24 hours of ( germination and is completed within 72 to 96 hours. The results suggest that degradation of seed reserve nutrients accelerate the development of seedling growth during germination. Lipid degrading enzyme lipase was identified in germinating Brassica napus L. The enzyme was purified to homogeneity by solvent extraction, followed by Sephadex G- 75, DEAE and CM-cellulose ion exchange chromatography. The enzyme was purified to 68 fold with the final specific activity of 39-mmol min·1 mg·1 at 37°C using olive oil as a substrate. --------- en_US
dc.language.iso en en_US
dc.publisher University of Rajshahi en_US
dc.relation.ispartofseries ;D2405
dc.subject Seeds en_US
dc.subject Cereal Seeds en_US
dc.subject Germinating oil en_US
dc.subject Biochemistry and Molecular Biology en_US
dc.title Studies on some Enzymes from Germinating oil and Cereal Seeds en_US
dc.type Thesis en_US


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