Production of D-glucose dehydrogenase for the determination of D-glucose
The optimum conditions for D-glucose dehydrogenase production from Bacillus thuringiensis M15 were investigated in flask cultures. Various concentrations of carbon and nitrogen sources including the culture conditions were studied for the enzyme production. The highest enzyme yield was obtained from...
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th-cmuir.6653943832-71952014-08-30T03:51:41Z Production of D-glucose dehydrogenase for the determination of D-glucose Boontim N. Yoshimune K. Lumyong S. Moriguchi M. The optimum conditions for D-glucose dehydrogenase production from Bacillus thuringiensis M15 were investigated in flask cultures. Various concentrations of carbon and nitrogen sources including the culture conditions were studied for the enzyme production. The highest enzyme yield was obtained from 100 ml of cultivation medium containing (w/v) 0.12% trehalose, 0.25% ammonium chloride, 0.1% KH2PO4, 0.1% K2HPO4, 0.01% MgSO4·7H2O and 0.02% yeast extract, pH 6.5. The suitable culture condition at 30°C was shaking speed at 100 rev min -1 for 2 days. The highest enzyme activity and specific activity in flask culture were 3 mU ml-1 and 6 mU mg-1, respectively. At the final optimization step, the enzyme total unit was higher than the beginning step about 4 times. The maximum enzyme activity in a jar fermentor which obtained from 21 h cultivation was 1.27 mU ml-1. 2014-08-30T03:51:41Z 2014-08-30T03:51:41Z 2004 Article 15904261 http://www.scopus.com/inward/record.url?eid=2-s2.0-1842843877&partnerID=40&md5=93f98e018c1df981b1c12d1adb62ce74 http://cmuir.cmu.ac.th/handle/6653943832/7195 English |
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The optimum conditions for D-glucose dehydrogenase production from Bacillus thuringiensis M15 were investigated in flask cultures. Various concentrations of carbon and nitrogen sources including the culture conditions were studied for the enzyme production. The highest enzyme yield was obtained from 100 ml of cultivation medium containing (w/v) 0.12% trehalose, 0.25% ammonium chloride, 0.1% KH2PO4, 0.1% K2HPO4, 0.01% MgSO4·7H2O and 0.02% yeast extract, pH 6.5. The suitable culture condition at 30°C was shaking speed at 100 rev min -1 for 2 days. The highest enzyme activity and specific activity in flask culture were 3 mU ml-1 and 6 mU mg-1, respectively. At the final optimization step, the enzyme total unit was higher than the beginning step about 4 times. The maximum enzyme activity in a jar fermentor which obtained from 21 h cultivation was 1.27 mU ml-1. |
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Article |
author |
Boontim N. Yoshimune K. Lumyong S. Moriguchi M. |
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Boontim N. Yoshimune K. Lumyong S. Moriguchi M. Production of D-glucose dehydrogenase for the determination of D-glucose |
author_facet |
Boontim N. Yoshimune K. Lumyong S. Moriguchi M. |
author_sort |
Boontim N. |
title |
Production of D-glucose dehydrogenase for the determination of D-glucose |
title_short |
Production of D-glucose dehydrogenase for the determination of D-glucose |
title_full |
Production of D-glucose dehydrogenase for the determination of D-glucose |
title_fullStr |
Production of D-glucose dehydrogenase for the determination of D-glucose |
title_full_unstemmed |
Production of D-glucose dehydrogenase for the determination of D-glucose |
title_sort |
production of d-glucose dehydrogenase for the determination of d-glucose |
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2014 |
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http://www.scopus.com/inward/record.url?eid=2-s2.0-1842843877&partnerID=40&md5=93f98e018c1df981b1c12d1adb62ce74 http://cmuir.cmu.ac.th/handle/6653943832/7195 |
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