• 한국버섯학회지
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• 제5권1호
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• pp.29-33
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• 2007

버섯산업의 활성화자료 제공과 버섯의 가정내 재배 학생들의 과학탐구용으로 사용키위해서 일반 가정주택의 실내에서 버섯류 재배가능성 검토의 일환으로 수행한 실험의 결과를 요약하면 다음과 같다. 가. 가정내 각실별 온 습도 측정결과는 세면실에서 64~72%, 온도 $20.2{\sim}26.0^{\circ}C$로 상대적으로 거실, 부엌등 타실보다 버섯생육에 유리한 조건을 나타내었다 (1999. 4. 25~7. 25). 나. 느타리버섯 상자재배에서 세면실의 경우 초발이소요 일수는 3일, 수량은 2,060g, 회수율은 90%였다. 다. 느타리버섯 봉지볏짚재배에서 세면실의 경우 초발이 소요일수는 2일, 수량은 90g, 회수율은 153%였다. 라. 느타리버섯 봉지톱밥재배에서 세면실의 경우 초발이 소요일수는 4일, 수량은 770g, 회수율은 89%였다. 마. 영지버섯 봉지톱밥재배에서 세면실의 경우 초발이소요일수는 11일, 수량은 172g, 회수율은 16%, 중량감소율은 61%로 나타났다. 바. 본시험에서 수행한 4처리 모두 거실, 침실, 부엌에 비해 세면실에서의 생산된 버섯의 수량이 우수하였다. 사. 본 실험의 결과를 일부 기술하여 "내손으로 재배하는 가정버섯 효능과 활용법"이란 제목의 책자를 공동저술하였다 (장 등, 2003).

• 한국균학회지
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• 제15권4호
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• pp.260-267
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• 1987

영지추출물이 효모의 증식과 생리에 미치는 영향을 검토하기 위하여 영지의 용매별 추출물을 0, 0.1, 0.5, 1.0%되게 첨가한 Henneberg 액체배지에 S. cerevisiae를 접종하고, 5일간 발효$(30^{\circ}C)$과정중 균체생산, Alcohol 발효, $CO_2$ 발생 등을 조사하였다. 1. 발효과정중 72시간후 효모 세포수는 증류수추출물(Dw) 1.0% 첨가구>에탄올추출물(Et) 1.0% 첨가구>증류수추출물(Dw) 0.5% 첨가구>에탄올추출물(Et) 0.5%첨가구>증류수추출물(Dw) 0.1% 첨가구>에탄올추출물(Et) 0.1% 첨가구>대조구의 순이고 특히 1.0%구는 대조구보다 5.3배 많았다. 2, 건조균체량은 각 시험구 모두 대조구보다 많았고, Dw 1.0%구와 Et 1.0%구는 120시간 발효 후 대조구에 비해 약 1.7배였다. 3. 알코올 발효과정중 알코올 함량은 영지추출물의 첨가량이 증가함에 따라 많아졌다. 4. 발효과정중 효모의 단위 시간당 $CO_2$ 발생 속도는 영지추출물을 증량할수록 대조구보다 빠르다.

• 한국식품영양과학회지
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• 제19권2호
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• pp.180-186
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• 1990

For the investigation of the effects of G. lucidum on prevention and attention of hypercholeste-rolemia and atherosclerosis dietary hypercholesterolemic rats were fed with 2.0g% G. lucidum extracts for 4 weeks. And then concentrations of total cholesterol triglyceride phospholipid in serum and liver and those of HDL-cholesterol lipid peroxide glucose in serum were analyzed. Concentration of total cholesterol in serum was the lowest in the control group(basal diet+ wa-ter) and HDL-cholesterol in serum were significantly higher in groups of control 2(hyperchole-sterolemic ratslongrightarrowbasal+water) and 4(hypercholesterolemic ratslongrightarrowbasal+G.l. extract) The concentration of triglyceride in serum were signficantly lower in groups 4 and 5(hypercholeste-rolemic ratslongrightarrowcholesterol+G. l. extract) than in the control group. Phospholipid content in serum were not significantly different among all groups. Ttal cholesterol in liver was significa-ntly higher in hypercholesterolemic rats than in the control group and triglyceride concentration were signficantly higher in groups of 3(hypercholesterolemic ratslongrightarrowcholesterol+water) and 5 than others. Phospholipid in liver was significantly higher in group 3 than in the control group but groups of 4 and 5 were lower. As for lipid peroxide in serum was the lowest in group 4 and glucose concentration was lowest in group 5 than in other groups.

• Korean Journal of Acupuncture
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• 제29권2호
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• pp.271-289
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• 2012

Objectives : Ganoderma lucidum(Ganoderma or lingzhi, 靈芝) is a well-known oriental medical mushroom containing many bioactive compounds. The possible mechanisms involved in its effects on cancer cells remain to be elucidated. In the present study, the anti-proliferative and apoptotic activities of the G. lucidum ethanol extract(GEE), in AGS human gastric cancer cells were investigated. Methods : It was found that exposure of AGS cells to GEE resulted in the growth inhibition in a dose and time dependent manner as measured by trypan blue count and MTT assay. The anti-proliferative effect of GEE treatment in AGS cells was associated with morphological changes and formation of apoptotic bodies, and the flow cytometry analysis confirmed that GEE treatment increased the populations of apoptotic-sub G1 phase. Growth inhibition and apoptosis of AGS cells by GEE were connected with a concentration and time-dependent up-regulation of tumour necrosis factor-related apoptosis-inducing ligand(TRAIL) expression. Results : The levels of XIAP and survivin expression, members of IAP family proteins, were gradually down-regulated by GEE treatment. However other members of IAP family proteins such as cIAP-1 and cIAP-2 remained unchanged in GEE-treated AGS cells. GEE treatment also induced the proteolytic activation of caspase-3, caspase-8 and caspase-9 and a concomitant degradation of poly(ADP-ribose) polymerase(PARP) protein, a caspase-3 substrate protein. Additionally, GEE-induced apoptosis was associated with the inhibition of Akt activation in a concentration and time-dependent manner, and pre-treatment with LY294002, a phosphoinositide 3-kinase(PI3K)/Akt inhibitor, significantly increased GEE-induced growth inhibition and apoptosis. Conclusions : Therefore, G. lucidum has a strong potential as a therapeutic agent for preventing cancers such as gastric cancer cells.

• Journal of Microbiology and Biotechnology
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• 제17권7호
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• pp.1106-1112
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• 2007

This report provides the complete nucleotide sequences of the full-length cDNA encoding squalene synthase (SQS) and its genomic DNA sequence from a triterpene-producing fungus, Ganoderma lucidum. The cDNA of the squalene synthase (SQS) (GenBank Accession Number: DQ494674) was found to contain an open reading frame (ORF) of 1,404 bp encoding a 468-amino-acid polypeptide, whereas the SQS genomic DNA sequence (GenBank Accession Number: DQ494675) consisted of 1,984 bp and contained four exons and three introns. Only one gene copy was present in the G. lucidum genome. The deduced amino acid sequence of Ganoderma lucidum squalene synthase (GI-SQS) exhibited a high homology with other fungal squalene synthase genes and contained six conserved domains. A phylogenetic analysis revealed that G. lucidum SQS belonged to the fungi SQS group, and was more closely related to the SQS of U. maydis than to those of other fungi. A gene expression analysis showed that the expression level was relatively low in mycelia incubated for 12 days, increased after 14 to 20 days of incubation, and reached a relatively high level in the mushroom primordia. Functional complementation of GI-SQS in a SQS-deficient strain of Saccharomyces cerevisiae confirmed that the cloned cDNA encoded a squalene synthase.

• 한국균학회지
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• 제47권2호
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• pp.153-163
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• 2019

본 연구는 갯버들(Salix gracilistyla)의 화장품 소재로의 활용가능성을 판단하기 위해, 기존 일반적인 방법이 아닌 균사배양 방법을 통해 가능성을 확인하였고, 구체적으로는 대표적인 약용버섯인 불로초(Ganoderma lucidum) 균사의 배양을 통하여 그 효능을 확인하였다. 총 폴리페놀 및 플라보노이드 함량과 DPPH 라디칼소거능 분석결과에서는, 갯버들 추출물(SGE)이 불로초 균사배양 갯버들 추출물(GLSGE) 보다 높게 평가되었으나, 콜라게나제 활성 억제 평가에서는 불로초 균사배양 갯버들 추출물(GLSGE)이 갯버들 추출물(SGE)과 비교하여 상대적으로 낮게 평가되었다. 그럼에도 불구하고, 불로초 균사배양 갯버들 추출물(GLSGE)은 갯버들 추출물(SGE)을 처리한 경우보다, HDFn 세포의 생존율을 높은 수준으로 증가시켰으며, HDFn 세포의 제1형 프로콜라겐의 생합성 또한 매우 높은 수준으로 증가시키는 것이 확인되었다. 결과적으로 앞선 실험을 통해, 불로초 균사배양 갯버들 추출물이 항노화 활성을 가지는 기능성 화장품 소재로 활용 가능성이 있다고 사료되며, 기능성 소재의 효과를 더욱 증진시키기 위한 방안으로 불로초 균사의 배양이 효과적이라는 것을 의미한다.

• 한국식품영양과학회지
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• 제23권5호
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• pp.736-742
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• 1994

This study was designed to observe the effects of the mixed diets of edible mushrooms and vegetables oils on the lipid component and fatty acid composition in liver of the diet induced hydpercholesterolemic rats. Ten groups of male S.D. rats were fed a basal diet supplemented with 5% of one of three mushrooms(G.I, L.e, A.j) and 10% of one of three vegetable oils (olive ,safflower perilla) for three weeks. In liver, total cholesterol concentration was significantly low in group 3 (olive oil 10 % + L. edodes 5%) and 6 (safflower oil 10 % $_2$L. edodes 5%) , triglyceride concentration was low in groups 8 (perilla oil 10 % + g. lucidum 5%) and 9 (perilla oil 10% + L. edodes 5%) and phospholipid concentration was significantly low in groups 3, 5, (safflower oil 10 % + G.lucidum 5%), 6, 7 (safflower oil 10 % + A .judae 5%) 8, 9 and 10 (perilla oil 10% + a. judae 5%). in the fatty acid composition of total lipid inliver, monounsaturated fatty acid (MUFA) concentration s were high in groups 2 (olive oil 105 + g. lucidum 5%), 3, and 4 (olive oil 10% + A. judae 5%) and all the perilla oil groups, polyunsaturated fatty acid (PUFA) and linoleic aicd concentrations were signifciantly high in all the safflower oil groups. In the fatty acid composition of liver phospholipid , PUFA concentrations were ghih but MUFA concentrations were low. In the triglyceride component, MUFA were some more than saturated fatty acid (SFA) . In the cholesteryl ester component, MUFa concentrations were significantly high. In the fatty acid composition of liver lipid components, linholeic acid was high in the PUFA and so it was major fatty acid. Eicosapentaenoic acid (EPA) of phospholipid component in liver was significantly high.

• 한국미생물·생명공학회지
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• 제22권2호
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• pp.115-119
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• 1994

White mutant of Ganoderma lucidum(G4142) induced the non-basediocarpous basidiospores(NBB) from the aerial mycelia on agar media by the light illumination. Light was found to be necessary for NBB formation, but it also inhibited the growth of mycelium. The best sporulation was obtained at the periodic exposure of 16 hour light and 8 hour dark. Blue and yellow light were the most effective on sporulation, however, near UV and red light did not induce any spores. Effective light intensity for NBB bearing was about 1,000 lux as white light. Even after 16 days of culture, this strain did not form the pinhead nor chlamydospore. Optimum temperature for the mycelial growth and NBB formation were 30$\circ $C. Ganoderma lucidum G4142 exhibited the formation of stroma after five days of incubation at 30$\circ $C.

• 한국미생물·생명공학회지
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• 제28권4호
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• pp.209-213
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• 2000

The cultured mycelia of Ganoderma lucidum were extracted and the extract was separated into six fractions by organic solvent fractionation. The antihepatotoxic activity of all the fractions was evaluated by measuring activities of glutamic pyruvic transaminase (GPT) and glutamic oxaloacetic transaminase (GOT). Among the fractions tested, the high-polarity fractions such as aqueous and n-butanol fractions significantly reduced activities of GPT and GOT in CCl4- and galactosamine-intoxicated rat primary hepatocytes. When intracellular synthetic activities were measured by pulsing the rate primary cultured hepatocytes with [3H]-uridine and [3H]-leucine, activities of DNA, RNA and protein. When direct toxicities of the fractions were measured against human hepatoma(SK-Hep-1), the non-polarity fractions such as n-butanol and ethyl acetate fractions showed potent direct cytotoxicities even at the concentration of 1 $\mu\textrm{g}$/ml. These data showed that Ganoderma lucidum has hepatoprotective and hepatotoxic recovery principles in its mycelia.

• 한국약용작물학회지
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• 제25권1호
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• pp.29-36
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• 2017

Background: Ganoderma lucidum cultured on hulled barley was investigated as a potential natural source of antioxidants and anti-inflammatory agents. Methods and Results: The yields from Ganoderma lucidum cultured on hulled barley water and ethanol extract were 17.69% and 25.77%, respectively. The antioxidant activity of Ganoderma lucidum cultured on hulled barley extracts was confirmed by various methods including assayss of 2,2-diphenyl-1-picrylhydrazyl (DPPH), 2,2-azino-bis-(3-ethylbenzo thiazoline-6-sulfonic acid) (ABTS), nitrite radical scavenging, and $Fe^{3+}$ to $Fe^{2+}$ reducing power activity. The ethanol extract of Ganoderma lucidum cultured on hulled barley showed improved DPPH, ABTS and nitrite radical scavenging activity compared with the water extract. After treatment of RAW264.7 cells with Ganoderma lucidum cultured on hulled barley ethanol extracts, the cell viability compared with the control was 92.82%, even at a concentration of $3,000{\mu}g/m{\ell}$. The ethanol extract inhibited reactive oxygen species (ROS) generation in RAW264.7 cells stimulated with $H_2O_2$, even at low concentrations. In addition, the ethanol extract showed an inhibitory effects on the production of lipopolysaccharide-induced nitric oxide (NO) in RAW264.7 cells. Conclusions: This study suggests that the extract of Ganoderma lucidum cultured on hulled barley is a potential source of natural antioxidants and anti-inflammatory agents.