• Title/Summary/Keyword: Merulius tremellosus

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Decolorization of a Dye by Immobilized Lignin Degrading Enzymes Generated from Transformants of Merulius tremellosus Fr. (아교버섯 형질전환체가 생산한 리그닌분해 고정화효소에 의한 염료 탈색)

  • Min, Dong-Suk;Ryu, Sun-Hwa;Kim, Myung-Kil;Choi, Hyoung-T.
    • Korean Journal of Microbiology
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    • v.48 no.3
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    • pp.225-227
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    • 2012
  • Lignin degrading enzymes from white rot fungi show broad substrate specificities, and therefore they can degrade variety of recalcitrant compounds. We have used three different protocols for the generation of immobilized laccase and manganese peroxidase crude enzymes from the genetically transformed strains of Merulius tremellosus Fr. These immobilized enzymes were used in the decolorization of Remazol Brilliant Blue R (RBBR), and they showed about 75% decolorization rates during the 48 h reactions. Although the decolorization efficiency decreased by 10-15% after a repeated use of the immobilized enzymes, these can be reused in various degrading reactions.

Taxonomic Investigations on Korean Higher Fungi ( I ) (한국산 고등균류의 분류학적 연구 ( I ))

  • Lim, Jeong-Han;Kim, Byong-Kak
    • Korean Journal of Pharmacognosy
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    • v.3 no.1
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    • pp.11-20
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    • 1972
  • To investigate the fungal flora in Korea, the basidiomycetes and other higher fungi were collected and examined. Five species Coriolus pinsitus, Hirshioporus fusco-violaceus, Hymenurhaete intricata, Merulius tremellosus, Steccherinum ochraceum, were newly added to the list of previously recorded Korean higher fungi, the total amounting to 386 species.

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Biodegradation of Endocrine-Disrupting Phthalates by Pleurotus ostreatus

  • Hwang, Soon-Seok;Choi, Hyoung-Tae;Song, Hong-Gyu
    • Journal of Microbiology and Biotechnology
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    • v.18 no.4
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    • pp.767-772
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    • 2008
  • Biodegradation of endocrine-disrupting phthalates [diethyl phthalate (DEP), dimethyl phthalate (DMP), butylbenzyl phthalate (BBP)] was investigated with 10 white rot fungi isolated in Korea. When the fungal mycelia were added together with 100 mg/l of phthalate into yeast extract-malt extract-glucose (YMG) medium, Pleurotus ostreatus, Irpex lacteus, Polyporus brumalis, Merulius tremellosus, Trametes versicolor, and T. versicolor MrP1 and MrP13 (transformant of the Mn-repressed peroxidase gene of T. versicolor) could remove almost all of the 3 kinds of phthalates within 12 days of incubation. When the phthalates were added to 5-day pregrown fungal cultures, most fungi except I. lacteus showed the increased removal of the phthalates compared with those of the non-pregrown cultures. In both culture conditions, p. ostreatus showed the highest degradation rates for the 3 phthalates tested. BBP was degraded with the highest rates among the 3 phthalates by all fungal strains. Only 14.9% of 100 mg/I BBP was degraded by the supernatant of P. ostreatus culture in YMG medium in 4 days of incubation, but the washed or homogenized mycelium of P. ostreatus could remove 100% of BBP within 2 days even in distilled water, indicating that the initial BBP biodegradation by P. ostreatus may be attributed to mycelium-associated enzymes rather than extracellular enzymes. The biodegradation rate of BBP by the immobilized cells of P. ostreatus was almost same as that in the suspended culture. The estrogenic activity of 100 mg/I DMP decreased during biodegradation by P. ostreatus.