• Mycobiology
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• 제43권3호
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• pp.297-302
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• 2015

Two white rot fungi, Ceriporia sp. ZLY-2010 (CER) and Stereum hirsutum (STH) were used as biocatalysts for the biotransformation of (-)-${\alpha}$-pinene. After 96 hr, CER converted the bicyclic monoterpene hydrocarbon (-)-${\alpha}$-pinene into ${\alpha}$-terpineol (yield, 0.05 g/L), a monocyclic monoterpene alcohol, in addition to, other minor products. Using STH, verbenone was identified as the major biotransformed product, and minor products were myrtenol, camphor, and isopinocarveol. We did not observe any inhibitory effects of substrate or transformed products on mycelial growth of the fungi. The activities of fungal manganese-dependent peroxidase and laccase were monitored for 15 days to determine the enzymatic pathways related to the biotransformation of (-)-${\alpha}$-pinene. We concluded that a complex of enzymes, including intra- and extracellular enzymes, were involved in terpenoid biotransformation by white rot fungi.

• 한국균학회지
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• 제40권2호
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• pp.98-103
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• 2012

본 연구에서는 백색부후균 중 줄버섯, 단색털구름버섯, 산느타리 및 유관버섯 등의 균사체를 이용하여 congo red, amaranth, orange G 및 methylene blue 등의 합성염료 탈색에 관한 실험을 수행하였다. 실험 결과 줄버섯과 단색털구름버섯은 congo red가 함유된 고체와 액체배지에서 이들 염료를 93~95% 탈색하였으며 amaranth는 약 80%, orange G는 62~70% 탈색시키는 것으로 나타났으나 유관버섯에 의한 3종류의 염료 탈색율은 30% 내외로 매우 낮았다. congo red, amaranth 및 orange G 등 각각의 염료가 첨가된 배지에서의 염료 탈색율은 이들 배지에서 배양한 균사체의 생장과 상관관계가 있는 것으로 나타났다. 그러나 모든 공시 균주는 methylene blue가 함유된 고체와 액체배지에서 methylene blue를 효과적으로 탈색하지 못하는 것으로 나타났다. 공시된 백색부후균의 액체 배지에서의 리그닌 분해효소 생산을 탐색하기 위해 1%의 나프탈렌이 첨가된 PDB 배지에 공시균을 10일 간 배양 후 효소의 종류와 양을 분석한 결과 모든 공시균은 laccase, lignin peroxidase 그리고 manganese peroxidase 등의 효소를 생산하는 것으로 확인되었으며 공시균주 중 줄버섯이 리그닌 분해 효소의 생산이 가장 왕성한 것으로 나타났다.

• Journal of Microbiology and Biotechnology
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• 제10권3호
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• pp.344-348
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• 2000

Abstract The removal percentage (94%) of 100 ppm of pyrene in a shaken culture of white rot fungus, Irpex lacteus, was much higher than that in a static culture (37.9%). Over 90% of the pyrene disappeared with I. lacteus grown at $15-27^{\circ}C$, yet less than 50% was removed at $37^{\circ}C$. The transformation rates of pyrene ($4.5-5.0{\;}\mu\textrm{g}/ml/day$) were not very different among cultures with 5- 30% inoculum sizes, and over 90% of the 100 ppm pyrene was removed in every case during 20 days of incubation. The biodegradation of pyrene by I. lacteus was confirmed by measuring the $CO_2$ evolved from the mineralization of the added pyrene. The activity of lignin peroxidase (LiP), which is known to be involved in the biodegradation by white rot fungi, was high between 8 to 12 days of incubation. Although manganese peroxidase activity was demonstrated during the same period as LiP, its activity was quite low, and no laccase activity was detected. Even though the activity patterns of ligninolytic enzymes did not coincide with the pyrene removal, this study shows that I. lacteus has a high biodegrading capability and can be a candidate for the bioremediation of polycyclic aromatic hydrocarbon contaminants.inants.

• 한국미생물·생명공학회지
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• 제27권6호
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• pp.500-508
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• 1999

Several white-rot fungi collected from the mountains of Korea were evaluated for their ability to decolorize azo, polymeric, and reactive dyes. Strains CJ-105, CJ-212 and CJ-315, identified as Trametes sp., Pleurotus sp. and Fomes sp., respectively, showed higher potential for decolorization of those dyes in either solid or liquid media. For Trametes sp. CJ-105, 100ppm of Remazol Brilliant blue R and 500ppm of Acid Red 264 were completely decolorized after 2 days under liquid culture. The dominating ligninolytic enzyme existing in the culture broth was laccase (E.C. 1.10.3.2). Also, Pleurotus sp. CJ-212 and Fomes sp. CJ-315 showed similar patterns in decolorization of Remazol Brilliant Blue R and Acid Red 264. The extent of decolorization of the dyes in liquid culture was found to be proportional to the activities of the ligninolytic of decolorization of the dyes in liquid culture was found to be proportional to the activities of the ligninolytic enzymes produced by each strain. In addition to that Trametes sp. CJ-105 was highly effective in degradation of polycyclic aromatic hydrocarbons and pentachlorophenol by the activity of the ligninolytic enzymes produced. In this study, we found that white-rot fungi, Trametes sp. CJ-105(KFCC 10941), Pleurotus sp. CJ-212(KFCC 10943) and Fomes sp. CJ-315(KFCC 10942), were effective in decolorizing a wide range of structurally different synthetic dyes, as well as some chemical compounds which are known to be hardly degradable.

• Journal of Microbiology and Biotechnology
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• 제17권7호
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• pp.1147-1151
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• 2007

Biodegradation of endocrine-disrupting bisphenol A was investigated with several white rot fungi (Irpex lacteus, Trametes versicolor, Ganoderma lucidum, Polyporellus brumalis, Pleurotus eryngii, Schizophyllum commune) isolated in Korea and two transformants of T. versicolor (strains MrP 1 and MrP 13). I. lacteus degraded 99.4% of 50 mg/l bisphenol A in 3 h incubation and 100% in 12 h incubation. which was the highest degradation rate among the fungal strains tested. T. versicolor degraded 98.2% of 50 mg/l bisphenol A in 12 h incubation. Unexpectedly, the transformant of the Mn-repressed peroxidase gene of T. versicolor, strain MrP 1, degraded 76.5% of 50 mg/l bisphenol A in 12 h incubation, which was a lower degradation rate than wild-type T. versicolor. The removal of bisphenol A by I. lacteus occurred mainly by biodegradation rather than adsorption. Optimum carbon sources for biodegradation of bisphenol A by I. lacteus were glucose and starch, and optimum nitrogen sources were yeast extract and tryptone in a minimal salts medium; however, bisphenol A degradation was higher in nutrient-rich YMG medium than that in a minimal salts medium. The initial degradation of endocrine disruptors was accompanied by the activities of manganese peroxidase and laccase in the culture of I. lacteus.

• The Plant Pathology Journal
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• 제24권1호
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• pp.8-16
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• 2008

Aurofusarin is a polyketide pigment produced by some Fusarium species. The PKS12 and GIP1 genes, which encode a putative type I polyketide synthase (PKS) and a fungal laccase, respectively, are known to be required for aurofusarin biosynthesis in Gibberella zeae (anamorph: Fusarium graminearum). The ten additional genes, which are located within a 30 kb region of PKS12 and GIP1 and regulated by a putative transcription factor (GIP2), organize the aurofusarin biosynthetic cluster. To determine if they are essential for aurofusarin production in G. zeae, we have employed targeted gene deletion, complementation, and chemical analyses. GIP7, which encodes O-methyltransferase, is confirmed to be required for the conversion of norrubrofusarin to rubrofusarin, an intermediate of aurofusarin. GIP1-, GIP3-, and GIP8-deleted strains accumulated rubrofusarin, indicating those gene products are essential enzymes for the conversion of rubrofusarin to aurofusarin. Based on the phenotypic changes in the gene deletion strains examined, we propose a possible pathway for aurofusarin biosynthesis in G. zeae. Our results would provide important information for better understanding of naphthoquinone biosynthesis in other fdarnentous fungi as well as the aurofusarin biosynthesis in G. zeae.

• 생약학회지
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• 제31권3호
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• pp.345-350
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• 2000

From the heartwood of Rhus verniciflua, four known flavonoids (1-4) were isolated along with an unknown one (5). Compounds 1-4 were identified to be garbanzol, sulfuretin, fisetin and fustin by NMR data. NMR data of 1-4 were fully assigned by the aids of 2D-NMR spectra. Among these compounds, only sulfuretin had significant cytotoxic and antioxidant ability at high concentrations. In addition, it seems likely that the 5-hydroxy-lacking flavonoids could not influence on the activity of laccase with cofactor of cupric cation, which catalyzes oxidative coupling reaction, in this plant.

• 한국버섯학회지
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• 제11권2호
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• pp.87-91
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• 2013

느타리 버섯 No. 42균주를 5가지 배지에서 연구한 결과, 리그닌 분해효소인 Lac와 MnP는 생산되었으나 LiP는 생산되지 않았다. 실험한 본 균주의 경우 리그닌 분해효소인 Lac와 MnP의 생산에 밀기울이 관여하는 것을 확인 할 수 있었다. 액체배지에서는 GPYW에서 Lac(2.4 U/ml)와 MnP(3.6 U/ml)가 최대 생산됨을 알 수 있었으며 고체배지에서는 WMW에서 MnP(4.0 U/ml)가 최대 생산되었으며 W에서는 Lac(11.0 U/ml)가 최대 생산되었다.

• 한국환경농학회지
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• 제21권4호
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• pp.261-268
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• 2002

Monochlorophenol인 2-, 3- 및 4-chlorophenol에 대해서 D. concentrica, T. versicolor, P. ostreatus 3균주를 이용하여 저항성, 분해능, 분해산물 등을 비교 분석하였다. T. versicolor는 monochlorophenol의 종류 및 농도의 증가에 따라 전혀 영향을 받지 않고 균사 생장이 이뤄지며, D. concentrica는 3-, 4-chlorophenol에서 100 mg/L 이상으로 농도가 증가하면 균사 생장이 느려져 제한을 받고 있는 것으로 나타났다. P. ostreatus는 두 균주와 달리 대조구 자체의 생장이 14일 정도로 상당히 느렸으나 2-, 3-chlorophenol을 첨가했을 때 오히려 1$\sim$2일 정도씩 생장이 촉진되는 결과를 나타냈다. 2-Chloro- phenol 이나 3-chlorophenol에서는 P. ostreatus가 제일 우수한 분해능을 보였으며 4-chlorophenol의 경우는 T. versicolor가 2균주에 비하여 월등하게 우수하게 나타나 균주에 따른 mono- chlorophenol의 분해능에 있어서 차이가 있고, 염소의 치환 위치에 따라 ortho나 meta 보다는 para 위치에 염소가 치환된 4-chlorophenol이 D. concentrica나 P. ostreatus의 경우 분해가 느린 것으로 나타났다. 그러나 T. versicolor는 2-, 3- 및 4-chlorophenol의 저항성 시험에서 균사 생장이 제한을 받지 않고 우수한 생장력을 갖고 있는 것처럼 분해능 시험에 있어서도 우수하였다. 균주별로 pH와 균사량은 P. ostreatus > T. versicolor > D. concentrica 순으로 높았으며, 균주내에서 배양일수별로 pH의 변이는 유동적이었고 균사량은 조금씩 증가하였으나 뚜렷한 차이는 없었다. 즉, 2-, 3- 또는 4-chlorophenol의 목질분해균을 이용한 분해에 있어서 pH 및 균사량은 monochlorophenol의 분해능과는 상관관계가 낮은 것으로 나타났다. T. versicolor와 P. ostreatus의 경우는 높은 laccase의 유도 효과를 나타내면서 monochlorophenol의 분해에 영향을 주는 것으로 생각된다. Monochlorophenol의 분해산물로는 1,3,5-trihydroxyl benzene, 1-ethyl-1-hydroxyl poltane, 2-pro-penoicacid, methylmalonic acid, 2-methyl-4-keto-pentan-2-ol 등과 지방산의 일종인 tetradecanoic acid, hexadecane, hept-adecanoic acid, octadecanoic acid 등이 확인되었다.

• Applied Biological Chemistry
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• 제38권6호
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• pp.490-495
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• 1995

Cellulomonas sp. KL-6 균주가 생산하는 cellulase 중 CMCase나 FPase는 세포외로 다량 분비되나 ${\beta}-glucosidase$는 cell bound form으로 존재하여 배양액에서의 생산은 극히 미약하였다. CMCase와 FPase는 배양 5일째에, ${\beta}-glucosidase$는 배양 4일째에 각각 최대생산을 나타내었다. $CaCO_3(0.1%)$가 첨가된 효소생산 최적조건에서 CMCase는 $82\;unit/m{\ell}$를, FPase는 $80\;unit/m{\ell}$를 그리고 ${\beta}-glucosidase$는 $1.2\;unit/m{\ell}$를 각각 생산하였고 이는 기본배지에서 보다 $60{\sim}70%$의 생산증가를 가져왔다. KL-6 균주는 lignase와 laccase의 생산은 없었다.