Background : Lentinula edodes contain a variety of biosurgical substances and a large amount of beta-glucan, which is known for immune-boosting effects. L. edodes was cultivated in nation wide of Korea. And, almost farmhouse using imported strains from Japan and China. Therefore, this study was conducted to prove the excellence of domestic strains to replace imported strains. Methods and Results : In this study, beta-glucan content, which is a unique immune component of domestic and imported strains, was compared to the native immune component of domestic L. edodes strains and imported L. edodes strains. In this test, the Korean strains such as Baekwahyang, Sanjo303ho, Suhyanggo, Cheonbaekgo, and the imported L. edodes strains is Mori290, Moriyujiro. The analysis results are as followings. The proximate compositions were ranged 3.74 - 5.50% in ash, 15.22 - 25.84% in crude protein, 0.93 - 1.43% in crude fat, 6.95 - 9.89% in crude fiber of Korean L. edodes strains and imported L. edodes strains, respectively. Major minerals of Korean L. edodes strains and imported L. edodes strains were potassium (684 - 904.05 ㎎%), calcium (0.46 - 0.65 ㎎%), sodium (8.77 - 11.01 ㎎%), magnesium (30.45 - 33.93 ㎎%). The content of beta-glucan from Korean L. edodes strains and imported L. edodes strains were ranged from 35.69% to 38.68%. Conclusion : As the results of chemical analysis were showed the no difference between Korean L. edodes strains and imported L. edodes strains. These results are meaning that the Korean L. edodes strains quality of the components is not inferior to imported strains. We expected that the Korean L. edodes strains could replace imported L. edodes strains.

Background : Lentinus edodes are highly utilized as food and medicine, and are known to be suitable for preventing diabetes, high blood pressure and arteriosclerosis. L. edodes were known for prevent obesity metabolisms. Also, present consumers persue the healthy and thin condition. Our research perpose is determined the prevent obesity using L. edodes extracts. Methods and Results : The effect on adipocyte differentiation and the accumulation of fat in the L. edodes extract on 3T3-L1 cell preadipocyte and cell toxicity were tested. We measurement to evaluate the inhibition effects of L. edodes extracts on the growth of 3T3-L1 cell adipocytes. The tested cells were treated with L. edodes extracts by ethanolic extracts (concetrations at 10, 50, 100 ㎍/㎖) and hot water extracts (temperature at 50℃, 60℃, 70℃, 80℃, 90℃), respectively. Cell toxicity did not affect the growth of cells growth in hot water extracts. Intracellular lipid accumulation was measured by Oil red O method. The inhibitory effect on 3T3-L1 cell by treatment different ethanolic extract concentrations and temperature of hot-waters. The optimal inhibitory conditions of lipid accumulation by ethanoic extracts and hot water extracts were determined the 32.5% ethanol extracts and 33.3% 50℃ hot water extracts. Conclusion : The results of this study showed that L. edodes extracts had an potentials for reduce lipid accumulation activities. Further more we will examine about the mechanisms of anti obesity activities from L. edodes extracts. This results provides that the basis for antiobesity foods or medicines using Lentinus edodes extracts.

Background : Lentinula edodes (Shiitake mushroom) is a common edible mushroom with a number of potential therapeutic and nutritional applications. However, the growth of Lentinula edodes were classified in accordance with nutrients have no differences in seemingly. The growth characteristics of L. edodes were difficult to find out influenced about between oak and medium. Quantitative real-time polymerase chain reaction (qRT-PCR) is a powerful tool to analyze the mechanisms underlying the biosynthetic pathways of these substances. Methods and Results : A gene encoding amylase AMY was successfully isolated from the L. edodes using RT-PCR. The putative amino acid sequence encoded by AMY showed the highest the homology with the sequence of glycoside hydrolase family 13. We compared the amylase activity and levels of gene expression in L. edodes grown on different breeding materials (oak, and medium), strains from oak (Chunbaegko, and Mori 290), and strains from medium (Tanong, and Carrefour), respectively. Quantitative reverse transcription PCR utilizing pairs of primers specific for AMY gene expression shows that the expression of AMY was induced polysaccharide, and increased during the process of fruiting body formation in L. edodes by medium compositions. Conclusion : This result indicates that amylase may play an important role of growth in morphogenesis of medium condition growth mushroom. The present work will contribute to RT-PCR studies in L. edodes.

Background: Hair loss related syndromes are increasing due to environmental pollution and stress. Hair care products are mainly prepared by mixing chemicals and natural extracts, such as those obtained from medicinal plants. The purpose of this study was to investigate the effects of 70% ethanol extracts from the flowers of Calendula officinalis, fruit body of Phellinus linteus, and the whole plant of Houttuynia cordata on the growth of CCD-986 cells, hair follicle dermal papilla cells (HFDPC), and 3T3-L1 cells. Methods and Results: All sample extracts at all concentrations, except for that from P. linteus fruit body at 500㎍/㎖, were cytotoxic to CCD-986 cells. However, none of the sample extracts were cytotoxic to HFDPC. The lipid differentiation of 3T3-L1 cells regulates hair regeneration via secretion of platelet derived growth factor. The 70% ethanol extract of H. cordata whole plant promoted hair growth. Adipogenesis rate significantly increased in a treatment concentration-dependent manner. Conclusions: These results suggest that 70% ethanol extracts of C. officinalis flower, P. linteus fruit body and H. cordata could be used for the development of hair care products.