• Proceedings of the Microbiological Society of Korea Conference
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• 2005.05a
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• pp.186.1-186
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• 2005

• Mycobiology
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• v.45 no.2
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• pp.119-122
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• 2017

Herein, nuruks derived from non-glutinous and glutinous rice inoculated with Aspergillus oryzae N159-1 (having high alpha-amylase and beta-glucosidase activities) were used to produce Korean alcoholic beverages. The resultant beverages had enhanced fruity (ethyl caproate and isoamyl alcohol) and rose (2-phenethyl acetate and phenethyl alcohol) flavors and high taste scores.

• Proceedings of the Zoological Society Korea Conference
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• 1998.10b
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• pp.182.2-182
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• 1998

No Abstract, See Full Text

• Proceedings of the Korean Society for Applied Microbiology Conference
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• 1986.12a
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• pp.528.1-528
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• 1986

Cellulose utilising hybrids between Cellulomonas fimi and Bacillus pumilus were isolated after PEG mediated protoplast fusion. 33% (w/v) PEG #6, 000 and 50mM $Ca^{++}$were optimum concentration. The intergeneric fusion frequency was 3.2$\times$10$^{-7}$ xtracellular CMCase and $\beta$-glucosidase activities were detected from one hydrid unlike only CMCase was detected from Cellulomonas fimi.

• Proceedings of the PSK Conference
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• 2003.04a
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• pp.224.2-225
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• 2003

Ginsenoside, major components of ginseng have been reported to show various biological activities including an increase of cholesterol metabolism. stimulation of serum protein synthesis, immunomodulatory effects. To explain these pharmacological actions, it is thought that ginseng saponins should be metabolized by human intestinal bacteria after they are orally administered. (omitted)

• 한국약용작물학회:학술대회논문집
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• 2007.11a
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• pp.318.1-318.1
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• 2007

• Proceedings of the Korean Society of Life Science Conference
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• 2006.09a
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• pp.78.2-78.2
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• 2006

• Proceedings of the Korean Society of Applied Entomolohy Conference
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• 2003.10a
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• pp.104-104
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• 2003

• Korean Journal of Microbiology
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• v.26 no.1
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• pp.6-12
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• 1988

Cellobiase ($\beta$-glucosidase) is an enzyme of the cellulase system in cellulolytic microor-ganisms. The chromosomal DNA fragment which include cellobiase gene of Cellulomonas biazotea was cloned in Eschericia coli via plasmid pBR 322 vector. Restriction enzyme Sal I was used to obtain adequate size of fragments from C. biazotea. chromosomal DNA. The transformant of E. coli HB101 with recombinant plasmid pBG101 showed cellobiase activity, which is not ordinary in E. coli HB101. The enzyme activity of the transformant was as of 20% lower than that of C. biazotea.

• Proceedings of the PSK Conference
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• 2001.04a
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• pp.180.1-180.1
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• 2001