본 연구에서는 시설재배와 토경(매립) 복령의 성분 분석 및 생리활성 비교를 위해 연구하였다. 일반성분 분석 결과 산소가 45~46%로 가장 많이 포함하고 있었으며 다음으로 39~41%의 탄소, 6.06~6.1% 수소, 0.21~0.22% 질소로 나타났다. 그리고 시험을 실시한 복령 모두에서 황 성분은 발견되지 않았다. 시설 및 토경 재배 복령을 ICP 분석법으로 11종의 무기질을 분석한 결과 S, Fe, Mg, Zn의 함유량은 1년차, 2년차 모두 토경 재배 복령이 시설 재배 복령보다 많았으며 특히 Fe와 Zn의 함유량은 각각 약 3.1~4.9배, 3.6~3.9배 높았다. 50% 에탄올 복령 추출물의 DPPH와 ABTS radical 소거활성과 FRAP 방법을 실행하여 항산화 효과를 알아보았다. 복령 추출물 10 mg/ml의 농도에서 시설 및 토경 재배 복령의 DPPH IC50 값은 1년산 시설 재배(8.601mg/mL), 1년산 토경 재배(12.85mg/mL), 2년산 시설 재배(1.23mg/mL), 2년산 토경 재배(1.18 mg/mL)로 나타났으며 ABTS IC50값은 1년산 시설 재배(15.85mg/mL), 1년산 토경 재배(14.59 mg/mL), 2년산 시설 재배(3.9 mg/mL), 2년산 토경 재배(14.92 mg/mL)로 계산되었다. 연구에 사용한 복령의 항산화 활성은 농도 의존적인 증가를 보였고 2년산 시설 재배 복령이 가장 높은 항산화 활성을 나타냈다. FE-SEM을 이용하여 복령 입자의 초미세구조를 관찰한 결과 샘플간의 뚜렷한 차이점은 발견되지 않았다.

This work aimed to discriminate the geographical origins of Domestic and Chinese Wolfiporia extensa. subjected to of oxygen (45.32 to 48.07%), carbon (38.09 to 40.12%), hydrogen (6.05 to 6.78%), and nitrogen (0.16 to 0.23%). Antioxidant activity was examined by DPPH free radical scavenging activity. According to the results of the experiment, no significant differences were found between domestic (IC50, 7.25 mg/ml) and Chinese (IC50, 8.35 mg/ml) Poria cocos wolf. However, as determined by the inorganic mineral contents were significantly different between domestic and Chinese W. extensa. The amount of potassium in domestic and Chinese W. extensa was 47.60 ± 8.78% and 33.14 ± 17.27%, respectively. The results of this study suggested that the analysis of inorganic components by ED-XRF should be useful for origin identification of Poria cocos wolf.

This study is carried out to compare ingredients and antioxidant activity of Bokryeong, Poria cocos wolf, cultivated in the landfill and facility. Comparisons of the composition of the landfill and facility Bokryeong were conducted in the first and second year. As a result, there was no statistically significant difference in all four components (oxygen, carbon, hydrogen, nitrogen). In the second year, GC-MS analysis was carried out using the extracts containing ginseng epidermis, using the samples taken from the Gangwon-do area in the first year and the second year. As a result, 1,3-Dihydroxyacetone dimer, 2-Furancarboxaldehyde, and Acetaldehyde were detected in the landfill Bokryeong. 2-Furancarboxaldehyde and Acetaldehyde contents were higher in facility Bokryeng. In biological activity assay, The anti-inflammatory of the landfill Bokryeng and facility Bokryeng were compared by using Raw 267.4 cell lines. As a result, it was confirmed that both of them had anti-inflammatory, but no difference was found.

The aim of the study was carried out to investigate a single oral toxicity of a 50% ethanol extract derived from fruiting body of Poria cocus (PCE) using male and female SD rats. Groups consisted of five male and female rats were treated with a single dose of the test substance intragastrically at 0, 5, 50, 300 and 2,000 mg/kg, respectively. Animals were monitored for the mortality and changes in the body weight, clinical signs and gross observation during the 14 days after dosing, upon necropsy. As the results, we could not find any mortality. Compared with the control group, significant weight change was not observed in the experimental group. Also there was no difference in water and food consumption or gross pathological findings at terminal sacrifice among the groups of rat treated with different doses of the test substance. The results suggested that the approximate lethal dose of ACM in both female and male rats were considered as over 5000 mg/kg.

In order to examine the hypolipidemic and hepatic steatosis preventing activities, we investigated mechanism of Auricularia auricula-judae 70% ethanol extract (AAE) in vivo and in vitro. Normal diet (ND) and high fat diet (HFD) with or without 0.1% (w/w), 0.3% (w/w) and 1% (w/w) AAE were given to male C57BL/6 mice. Plasma lipids and liver enzymes were measured and tissue sections of liver were examined. Further mechanistic studies in mouse 3T3-L1 adipocytes were performed in vitro by verifying triglyceride, glycerol, GPDH (glycerol-3-phosphate dehydrogenase) activity and mRNA expression of adipogenic and lipogenic genes using RT-PCR amplification. Body weight and adipose tissue mass were significantly reduced in ND and (HFD plus AAE) fed mice compared to HFD mice. These findings suggest that AAE may reduce the risk of hepatic steatosis by modulating plasma lipids via the regulation of adipogenic/lipogenic transcriptional factors. AAE may have interesting applications to improve plasma lipids and liver enzymes (A part of results have been published in Int J Med Mushrooms).

This study was carried out to determine the basic mycelial culture conditions for Poria cocos growth. According to colony diameter and mycelial density, suitable media for mycelial growth were Malt yeast extract, Potato dextrose agar, Yeast extract agar, and Yeast malt agar. The optimum temperature for mycelial growth was between 25 and 35oC, and the optimum pH value was between 4 and 7. Carbon and nitrogen sources were fructose and yeast extract. The optimum C/N ratio was about 10 to 1 with 2% glucose. Other minor components for optimal growth were thiamine-HCl and nicotinamide as vitamins, acetic and lactic acid as organic acids, and MgSO4·7H2O and FeSO4·7H2O as mineral salts. Wolfiporia cocos is a well-known traditional medicine in China, Japan, Korea, and other Asian countries owing to its numerous therapeutic properties. With the aim to determine the morphology and genetic characteristics of W. cocosten strains of W. cocos were cultivated in vitro, and subsequently, rapid amplification of polymorphic DNA was performed. To the best of our knowledge, this is the first study to examine the morphology of fruit bodies of W. cocos in Korea. W. cocos were cultured on PDA agar at different temperatures (12, 16, 20, 24, and 28oC) under 12-hour light (600 Lux) / 12-hour dark photoperiod condition for 1 month. Appearance of fruit body was the highest at 28°C condition in all the strains investigated. Honeycomb-like structure on sclerotia was observed in Andong 01, Andong 02, Andong 03, KFRI 1104, KFRI 1105, KFRI 1106, KFRI 1107, KFRI 1108, and ASI 13007 strains. The KFRI 1103 strain formed cosmos petal-like structure on sclerotia. The average size of basidiospores was recorded as 7.55 μm in height and 3.35 μ in width. This study was carried out to discriminate the geographical origin from Korea and Chinese Wolfiporia extensa. By proximate composition analysis, both were identified as similar, showed oxygen was 45.32-48.07%, carbon was 38.09-40.12%, hydrogen was 6.05~6.78% and nitrogen was 0.16-0.23%. Antioxidant activity was examined by DPPH free radical scavenging activity. No significant differences were found as well for the antioxidant activity between Korean and Chinese product. However, the contents of inorganic components ED-XRF (X-Ray Fluorescence Spectrometer) were significant different in Chinese and domestic W. extensa. The Potassium and iron in Chinese and domestic W. extensa were 47.60±8.78% and 14.5±3.86% as well as 33.14±17.27% and 9.13±4.83%, respectively. From the above resuls, the analysis of inorganic components by ED-XRF may be used for discrimination of the geographical origin of W. extensa.

Wolfiporia cocos is a well-known traditional medicine in China, Japan, Korea, and other Asian countries owing to its numerous therapeutic properties. With the aim to determine the morphology and genetic characteristics of W. cocosten strains of W. cocos were cultivated in vitro, and subsequently, rapid amplification of polymorphic DNA was performed. To the best of our knowledge, this is the first study to examine the morphology of fruit bodies of W. cocos in Korea. W. cocos were cultured on PDA agar at different temperatures (12, 16, 20, 24, and 28oC) under 12-hour light (600 Lux) / 12-hour dark photoperiod condition for 1 month. Appearance of fruit body was the highest at 28°C condition in all the strains investigated. Honeycomb-like structure on sclerotia was observed in Andong 01, Andong 02, Andong 03, KFRI 1104, KFRI 1105, KFRI 1106, KFRI 1107, KFRI 1108, and ASI 13007 strains of . The KFRI 1103 strain formed cosmos petal-like structure on sclerotia. The average size of basidiospores was recorded as 7.55 μm in height and 3.35 μ in width.

This study aimed to discriminate the geographical origins of domestic and chinese Wolfiporia extensa. They were subjected to oxygen (45.32 to 48.07%), carbon (38.09 to 40.12%), hydrogen (6.05 to 6.78%), and nitrogen (0.16 to 0.23%). Antioxidant activity was examined by DPPH free radical scavenging activity. According to the results of the experiment, no significant differences were found between domestic (IC50, 7.25 mg/ml) and Chinese (IC50, 8.35 mg/ml) W. extensa. However, as determined by the inorganic mineral contents were significantly different between domestic and Chinese W. extensa. The amount of potassium in domestic and Chinese W. extensa was and 33.14 ± 17.27%, 47.60 ± 8.78%, respectively. The results of this study suggested that the analysis of inorganic components by ED-XRF should be useful for origin identification of W. extensa

This study was carried out to determine the basic mycelial culture conditions for Poria cocos growth. According to colony diameter and mycelial density, suitable media for mycelial growth were Malt yeast extract, Potato dextrose agar, Yeast extract agar, and Yeast malt agar. The optimum temperature for mycelial growth was between 25 and 35oC, and the optimum pH value was between 4 and 7. Carbon and nitrogen sources were fructose and yeast extract. The optimum C/N ratio was about 10 to 1 with 2% glucose. Other minor components for optimal growth were thiamine-HCl and nicotinamide as vitamins, acetic and lactic acid as organic acids, and MgSO4·7H2O and FeSO4·7H2O as mineral salts.

Auricularia auricula-judae is an edible mushroom, which is known as wood ear, free ear, black ear mushroom, and free jelly fish. This study was carried out to obtain the basic information for mycelial culture conditions of Auricularia auriculajudae. According to colony diameter and mycelial density, the media for suitable mycelial growth were PDA and MCM. The optimum temperature for mycelial growth was 25~30oC. Carbon and nitrogen sources were mannose and malt extract, respectively. The optimum C/N ratio was in the range of 10 to 1 with 2% glucose. Other minor components for the optimal growth were thiamine-HCl and biotin as vitamins, succinic acid and lactic acid as organic acids, and MgSO4·7H2O and KH2PO4 as mineral salts.

To determine the optimal media 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℃. 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℃ for 5 days. Our results will be useful to researchers who aim to study extracellular enzyme activity in Ganoderma lucidum

Ganoderma applantaum belonged to Polyporaceae of Basidiomycetes and has been known as one of the popular medicinal mushrooms due to high antitumor and anti-diabetes activity. This study was carried out to obtain the basic information for mycelial culture conditions of Ganoderma applantaum. According to colony diameter and mycelial density, the media for suitable mycelial growth of them were shown in PDA and MEA. The optimum temperature for mycelial growth was 25~30℃The colonies are white, flocculose and underside of the plates is whitish to cream. Carbon and nitrogen sources were mannose and malt extract, respectively. The optimum C/N ratio was 10:1 to 5:1with 2% glucose concentration, vitamin was thiamine- HCl, organic acid was succinic acid, and mineral salt was MgSO4ㆍ7H2O. Present experiments were conducted to determine the possibility of artificial culture with sawdusts of G. applantaum. The pH value which was 6.0 of oak sawdust and6.4 of ricebran. Mycelial density on oak sawdust of G.applantaum spp. was higher than Ganoderma lucidium (a control). Wt. of dried fruiting body (g) of G. applantaum. (origin culture: GBEA-01, strain name: SamJung(三淨)) showed that 16.0 g on oak sawdust bottle cultivation (850㎖), 7.8 g on oak sawdust and G. lucidum. This present study was undertaken to investigate comparative anti-tumor activity of water extracts of G. lucidum ASI 7125 (GLE), G. applantaum SamJung (GAE) in vitro. The anti-tumor activity in the present study was evaluated by sulforhodamine B (SRB) and microtetrazolium (MTT) assay in terms of cell survival level. The results showed that DW, GLE and GAE inhibited proliferation showing both tumor cells.

A series of activated carbons were prepared from coconut shells and coal-tar pitch binder by physical activation with steam in this study. The effect of variable processes such as activation temperature, activation time and ratio of mixing was investigated for optimizing those preparation parameters. The activation processes were carried out continuously. The nitrogen adsorption isotherms at 77 K on pellet-shaped activated carbons show the same trend of Type I by IUPAC classification. The average pore sizes were about 19-21a. The specific surface areas (SBET) of pellet typed ACs increased with increasing the activation temperature and time. Specific surface area of AC treated for 90 min at temperature 900℃ was 1082 m2/g. The methylene blue numbers continuously increased with increasing the activation temperature and time. On the other hand, iodine numbers highly increased till activation time of 60 min, but the rate of increase of iodine numbers decreased after that time. This indicates that new micropores were created and the existing micropores turned into mesopores and macropores because of increased reactivity of carbon surface and H2O.