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Optimal Medium Conditions for the Detection of Cellulolytic Activity in Ganoderma lucidum

  • Jo, Woo-Sik (Department of Agricultural Environment, Gyeongbuk Agricultural Technology Administration) ;
  • Bae, Soon-Hwa (Department of Agricultural Environment, Gyeongbuk Agricultural Technology Administration) ;
  • Cho, Doo-Hyun (Department of Agricultural Environment, Gyeongbuk Agricultural Technology Administration) ;
  • Park, So-Deuk (Department of Agricultural Environment, Gyeongbuk Agricultural Technology Administration) ;
  • Yoo, Young-Bok (Mushroom Research Division Department of Herbal Crop Research National Inst. of Horicultural & Herbal Science, RDA) ;
  • Park, Seung-Chun (College of Veterinary Medicine, Kyeongbuk National University)
  • Published : 2009.12.31

Abstract

To determine the optimal medium conditions for the detection of the cellulolytic activity in Ganoderma lucidum, we varied three media conditions: dye reagent, pH, and temperature. First, we evaluated the use of four dyes, Congo Red, Phenol Red, Remazol Brilliant Blue, and Trypan Blue. To observe the effect of pH on the chromogenic reaction, we also made and tested various media spanning acidic and alkaline pHs, ranging from 4.5 to 8.0. Furthermore, in order to research the effect of temperature on the clear zone and the fungus growing zone, we tested temperatures ranging from 15 to $35{^{\circ}C}$. On the whole, the best protocol called for Ganoderma lucidum transfer onto media containing Congo red with pH adjusted to 7.0, followed by incubation at $25{^{\circ}C}$ for 5 days. Our results will be useful to researchers who aim to study extracellular enzyme activity in Ganoderma lucidum.

Keywords

References

  1. Abraham, L., Hoffman, B., Gao, Y. and Breuil, C. 1998. Action of Ophiostoma piceae proteinase and lipase on wood nutrients. Can. J. Microbiol. 44:698-701 https://doi.org/10.1139/cjm-44-7-698
  2. Castro, G. R., Ferrero, M. A., Mendez, B. S. and Sineriz, F. 1993. Screening and selection of bacteria with high amylolytic activity. Acta Biotechnol. 13:197-201 https://doi.org/10.1002/abio.370130220
  3. Hashimoto, K. 1972. Biochemical studies on the mushroom. Toyo Shokuhin Kenkyusho Kenkyu Hokukusho 10:163
  4. Hejgaard, J. and Gibbons, G. C. 1979. Screening for alpha-amylase in cereals: improved gel-diffusion assay a dye-labelelled starch substrate. Carlsberg Res. Commun. 44:21-25 https://doi.org/10.1007/BF02910868
  5. Hong, J. S., Uhm, T. B., Jung, G. T. and Lee, K. B. 1984. Studies on the enzymes produced by Pleurotus sojor-caju. Kor. J. Mycol. 12:59-64
  6. Hyun, M. W., Yoon, J. H., Park, W. H. and Kim, S. H. 2006. Detection of cellulolytic activity in ophiostoma and leptographium species by chromogenic reaction. Mycobiology 34:108-110 https://doi.org/10.4489/MYCO.2006.34.2.108
  7. Kim, H. W. and Kim, B. K. 1999. Biomedical triterpenoids of Ganoderma lucidum (Curt.: Fr.) P. Karst. (Aphyllophoromycetideae). Int. J. Med. Mushrooms 1:121-138 https://doi.org/10.1615/IntJMedMushrooms.v1.i2.20
  8. Park, W. H., Kim, T. H. and Ro, I. H. 1986. Studies on enzymes of the higher fungi of Korea (II): Identification of cellulolytic enzyme in Lenzites betulina. Kor. J. Mycol. 14:225-229
  9. Shin, D. S., Lee, H. H., Lim, K. P., Cho, N. S. and Cho, B. M. 1991. Chemistry of Forest Product, pp. 121-122. Haeng Mun Sa, Seoul
  10. Yoon, J. H., Park, J. E., Suh, D. Y., Hong, S. B., Ko, S. J. and Kim, S. H. 2007. Comparison of dyes for easy detection of extracellular cellulases in fungi. Mycobiology 35:21-24 https://doi.org/10.4489/MYCO.2007.35.1.021

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