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In relation to this article, we declare that there is no conflict of interest.
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Received December 5, 2008
Accepted January 25, 2009
articles This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Cost-cutting of nitrogen source for economical production of cellulolytic enzymes by Trichoderma inhamatum KSJ1

Department of Civil, Earth and Environmental Engineering, Chonnam National University, Korea
seongjun@jnu.ac.kr
Korean Journal of Chemical Engineering, July 2009, 26(4), 1070-1074(5), 10.1007/s11814-009-0178-7
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Abstract

For saccharifying food wastes, cellulolytic enzymes were produced using Trichoderma inhamatum KSJ1 in modified Mandel’s medium. In a previous study, 0.1% bacto peptone in Mandel’s medium was established as the best organic nitrogen source for the production of cellulolytic enzymes using strain KSJ1. However, economically, peptone was too expensive. Therefore, soybean, yeast and Chunggookjang (fermented soybean paste) were substituted for peptone in this research. Also, yeast or ground soybean hydrolyzed by sulfuric acid or from a culture broth of Bacillus alcalophilus, a strain producing protease, was added to the medium as the nitrogen source to the production of cellulolytic enzyme. In the cultivation using 0.5% yeast hydrolyzed with a culture solution of B. alcalophilus as the nitrogen source, the activities of FPase and amylase were 0.20 and 2.17 U/mL in a 100 mL flask, compared to 0.35 and 1.24 U/mL with the 0.1% peptone as control, respectively. In a 10 L jar fermenter, the activities of FPase and amylase were improved to 0.40 and 4.82 U/mL in the cultivation, respectively, using 0.5% yeast hydrolyzed with the culture broth, compared with 0.38 and 3.79 U/mL, respectively, for the 0.1% peptone as control. Therefore, hydrolyzed yeast was established as an available nitrogen source for the industrial scale production of cellulolytic enzymes by strain KSJ1, resulting in a 52.3% cost reduction in the production of cellulolytic enzyme by substitution of the expensive nitrogen sources.

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