• Microbiology and Biotechnology Letters
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• v.19 no.3
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• pp.248-252
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• 1991

- Mutation process and substrate induction of 7i-ichoderma viride cellobiohydrolase were investigated by immunological techniques. Since mutants of Trichodemza uiride such as QM9123, QM9414, TKO41 and MCG77 produced immunologically same cellobiohydrolase, it may be that the mutation be occurred in the reguratory gene rather than in the structural gene of cellobiohydrolase. a-Cellulose and Solka Floc were found to be the best inducer for the production of cellobiohydrolase in Trichodemza viride culture compared to low molecular weight inducer such as carboxylmethyl cellulose and cellobiose.

• Applied Chemistry for Engineering
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• v.4 no.1
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• pp.188-195
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• 1993

Polyelectrolyte complexes and graft copolymers as biomaterials were synthesized from the water soluble cellulose derivatives. Polyelectrolyte complexes have been prepared from carboxymethyl cellulose (CMC) and gelatin. Graft copolymers(Mc-g-AA) were synthesized by grafting acrylic acid (AA) onto methyl cellulose(MC). (Mc-g-AA) and gelatin polyelectrolyte complexes were also prepared. The optimum conditions of each sample were investigated after chemical crosslinking or heat treatment. The preliminary results show that these materials might be interesting for biomedical applications.

• Mycobiology
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• v.35 no.1
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• pp.21-24
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• 2007

To evaluate which dye is effective in a plate assay for detecting extracellular cellulase activity produced by fungi, four chromogenic dyes including remazol brilliant blue, phenol red, congo red, and tryphan blue, were compared using chromagepic media. For the comparison, 19 fungal species belonging to three phyla, ascomycota, basidiomycota, and zygomycota were inoculated onto yeast nitrogen-based media containing different carbon substrates such as cellulose (carboxylmethyl and avicel types) and cellobiose labeled with each of the four dyes. Overall, the formation of clear zone on agar media resulting from the degradation of the substrates by the enzymes secreted from the test fungi was most apparent with media containing congo red. The detection frequency of cellulase activity was also most high on congo red-supplemented media. The results of this study showed that congo red is better dye than other three dyes in, a plate assay for, fungal enzyme detection.

• The Korean Journal of Mycology
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• v.39 no.2
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• pp.126-130
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• 2011

In the course of search for multifunctional microbial inoculants, three Bacillus strains (BS11-1,BS11-2,BS11-3) with biological control and biofertilizing effects were selected. In this study, their ability for solubilization of insoluble phosphate, production of indole-3-acetic acid (IAA), siderophore, and hydrolytic enzymes, and antagonism against phytopathogenic fungi were estimated. All strains produced IAA and siderophore depending on culture time and produced a visible clear zone on agar plate containing 0.5% carboxylmethyl cellulose as a carbon source. Also, these strains exhibited antifungal activities against phytopathogenic fungi, Botrytis cinerea, Cylindrocarpon destructans, Fusarium oxysporum, Rhizoctonia solani, and Phytophthora capsici.

• Journal of Life Science
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• v.25 no.6
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• pp.680-685
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• 2015

Previously, cellulase and xylanase producing microorganism, Bacillus subtilis NC1, was isolated from soil. Based on the 16S rRNA gene sequence and API 50 CHL test the strain was identified as Bacillus subtilis, and named as B. subtilis NC1. We cloned and sequenced the genes for cellulase and xylanase. Plus, the deduced amino acid sequences from the genes of cellulase and xylanase were determined and were also identified as glycosyl hydrolases family (GH) 5 and 30, respectively. In this study to optimize the medium parameters for cellulase production by B. subtilis NC1 the RSM (response surface methodology) based on CCD (central composite design) model was performed. Three factors, tryptone, yeast extract, and NaCl, for N or C source were investigated. The cellulase activity was measured with a carboxylmethyl cellulose (CMC) plate and the 3,5-dinitrosalicylic acid (DNS) methods. The coefficient of determination (R²) for the model was 0.960, and the probability value (p=0.0001) of the regression model was highly significant. Based on the RSM, the optimum conditions for cellulase production by B. subtilis NC1 were predicted to be tryptone of 2.5%, yeast extract of 0.5%, and NaCl of 1.0%. Through the model verification, cellulase activity of Bacillus subtilis NC1 increased from 0.5 to 0.62 U/ml (24%) compared to the original medium.