• 제목/요약/키워드: Cultivated mushrooms

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Historical Record of Mushroom Research and Industry in Korea

  • Yoo, Young Bok;Oh, Youn Lee;Shin, Pyung Gyun;Jang, Kab Yeul;Sung, Gi-Ho;Kong, Won-Sik
    • 한국균학회소식:학술대회논문집
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    • 한국균학회 2014년도 춘계학술대회 및 임시총회
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    • pp.13-13
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    • 2014
  • Two kinds of mushrooms, Gumji (金芝; Ganoderma) and Soji, were described in old book of Samguksagi (History of the three kingdoms; B.C 57~A.D 668; written by Bu Sik Kim in 1145) in Korea-dynasty. Many kinds of mushrooms were also described in more than 17 kinds of old books during Chosun-dynasty (1392~1910) in Korea. Nowadays, mushroom cultivation has been increased through out the world last decade years. Production of mushrooms has also been increased 10-20% and many varieties have been cultivated. Similar trends were also observed in Korea. Approximately two hundred commercial strains of 37 species in mushrooms were developed and distributed to cultivators. Somatic hybrid variety of oyster mushroom 'Wonhyeong-neutari' were developed by protoplast fusion, and distributed to grower in 1989. The fruiting body yield index of somatic hybrids of Pleurotus ranged between 27 and 155 compared to parental values of 100 and 138. In addition, more diverse mushroom varieties such as Phellinus baumi, Auricularia spp., Pleurotus ferulae, Hericium erinaceus, Hypsizigus marmoreus, Grifola frondosa, Agrocybe aegerita and Pleurotus cornucopiae have been attempted to cultivate in small scale cultivation. Production of mushrooms as food was 190,111 metric tons valued at 800 billion Korean Won (one trillion won if include mushroom factory products; 1dollar = 1,040 Won) in 2011. Major cultivated species are Pleurotus ostreatus, Pleurotus eryngii, Flammulina velutipes, Lentinula edodes, Agaricus bisporus, and Ganoderma lucidum, which cover 90% of total production. Since mushroom export was initiated from 1960 to 1980, the export and import of mushrooms have been increased in Korea. Technology developed for liquid spawn production and automatic cultivation systems lead to the reduction of the production cost resulting in the increasement of mushroom export. However some species were imported because of high production cost for these mushrooms requiring the effective cultivation methods. Developing of effective post-harvest system will be also directly related to mushroom export. In academic area, RDA scientists have been conducting mushroom genome projects. One of the main results is the whole genome sequencing of Flammulina velutipes for molecular breeding. An electrophoretic karyotype of of F. velutipes was obtained using CHEF with 7 chromosomes, with a total genome size of approximately 26.7 Mb. The mususcript of the genome of F. velutipes was published in PLOS ONE this year. For medicinal mushrooms, we have been conducting the genome research on Cordyceps and its related species for developing functional foods using this mushroom. In 2013, Korea Food and Drug Administraion (KFDA) approved Cordyceps mushroom for its value as an immune booster.

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버섯에서 분리한 형광성 Pseudomonas spp. 의 ITS I 영역 분석에 의한 계통 분류 (Phylogeneitc Analysis of Fluorescent Pseudomonas spp. Isolated from the Cultivated Mushrooms on the Basis of ITS I Region)

  • 고승주;고승주;강희완;전명숙;류진창
    • 한국식물병리학회지
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    • 제14권4호
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    • pp.350-357
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    • 1998
  • A total of 12 strains of fluorescent Pseudomonas isolated from the cultivated mushrooms such as Agaricus bisporus and Pleurotus ostreatus were collected. They consisted of pathogenic Pseudomonas spp. and epiphytic Pseudomonas spp. of the cultivated mushroom. To analyze the phylogenetic relationship of these strains, ITS I region, the 16S-23S intergenic spacer region in the ribosomal RNA (rRNA) operon, was cloned and sequenced. The spacer regions of these strains were 495∼527 nucleotides in length and contained the genes encoding isoleucine-tRNA (tRNAIle) and alanine-tRNA (tRNAAla). The reciprocal homologies of each ITS I sequence among these strains were in the range of 84.2%∼98.8%. According to the analysis of ITS I sequences, the fluorescent Pseudomonas spp. were phylogenetically classified into three clusters. Cluster I consisted of Pseudomonas fluorescens, P. tolaasii, P. gingeri’, and P.‘reactans’(WLRO). Cluster II comprised Pseudomonas fluorescens biovar C and F. Cluster III composed P. agarici. Cluster I and II could be classified into P. fluorescens complex. P. agarici formed an independent taxon clearly separable from P. florescens complex.

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인공재배 버섯에 병을 일으키는 Pseudomonas속 병원세균에 관한 연구 2. 버섯 세균성 갈색점무늬병의 병원세균 Pseudomonas tolaasii와 White Line 형성균의 세균학적 특성 (Studies on the Pathogenic Pseudomonas Causing Bacterial Diseases of Cultivated Mushrooms in Korea 2. Bacteriological Characteristics of tolaasii Causing Mushroom Brown Blotch and White Line Reacting Organisms)

  • 김종완;권순익;강희진
    • 한국식물병리학회지
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    • 제11권4호
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    • pp.353-360
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    • 1995
  • Tests were performed on 232 bacterial strains (71 strains of Pseudomonas tolaasii and 161 white line reacting organisms, WLRO) isolated from cultivated mushrooms. As results, P. tolaasii was divided into 5 groups on the basis of the phenotypical characteristics for the strains, and group 3 was the major one including 48 (62%) out of the total 71 strains. WLRO were classified into 23 groups, and group 10 was the major group (65 strains, 30% of the total WLRO tested). A white line was well formed at 22$^{\circ}C$ and at 4 mm distance between P. tolaasii and WLRO colonies in their dual culture on Pseudomonas agar F medium within 36-hr incubation, but not formed at $25^{\circ}C$ even for 72-hr incubation. The morphological, cultural and biological properties of P. tolaasii group 3, and the main group of WLRO, group 10, were different only in the light of pathogenicity. Also group 2 of P. tolaasii had the characteristics similar to group 24 of WLRO which was pathogenic to cultivated mushrooms, suggesting the P. tollaasiii and WLRO strains may be the same species although their white line forming ability and pathogenicity were more or less different from one another. Subculture of the strains in P. tolaasii group 1 induced the variation of their pathogenicity, white line forming ability and utilization of sodium benzoate and sodium tartrate, and thus it can be inferred that they were converted to strains having the characteristics of group 3 or WLRO groups.

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한약박에서 재배한 느타리버섯의 성장 및 저장 중 품질 특성의 비교 (The Comparison of Growth and Quality Characteristics during the Storage of Pleurotus ostreatus Cultivated in the Remnants of Medicinal Herb Extracts)

  • 전중호;고병섭;김주호;남상필;엄영란;홍상미;황학수;박선민
    • 한국식품영양과학회지
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    • 제38권2호
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    • pp.211-216
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    • 2009
  • 일반적으로 폐기 처분하거나 비료로 재활용하는 한약을 추출하고 남는 한약박을 발효하여 영양분으로 첨가하는 팰릿 대신 폐면과 섞어 균상배지로 사용하여 느타리버섯을 재배할 때 수확량과 저장성에 대한 연구를 하였다. 또한, 한약박은 불특정 한약재들이 섞여 있으므로 이로 인해 문제가 나타날 수도 있으므로 한약박의 성분이 느타리버섯으로 전이되는지 여부를 조사하였다. 한약박 70%나 100%에서 느타리버섯을 재배할 때 질병이 생겨 고사되는 버섯의 수도 적었고, 성장속도도 빨라서 수확량도 많았다. 폐면과 펠릿을 이용한 대조군과 한약박을 배지에서 재배한 처리군들의 HPLC chromatogram에 차이를 전혀 나타내지 않았고 지표물질로 사용한 glycyrrhizin이 전혀 검출되지 않았다. 즉, 한약박의 성분 자체가 그대로 전이되지는 않았고, 한약박에 함유된 성분을 영양소로 이용하여 버섯의 품질을 향상시켰다. 한약박을 70%나 100%를 사용한 배지에서 재배된 느타리버섯의 저장성이 향상되어 저장기간 동안 중량 감소가 가장 적었고, 갓과 자루의 경도의 저하도 가장 적었다. 그러나 외관의 품질을 나타내 주는 색도의 변화는 배지 종류에 영향이 적었다. 결론적으로 한약박을 70% 이상을 배지로 사용하였을 때 한약성분의 직접적인 전이는 없어서 버섯의 상품성을 저하시키지 않았으며 성장률이 빠르며 수확률도 많았고, 조직이 치밀하여 저장성도 향상시켰다. 그러므로 한약박을 느타리버섯뿐만 아니라 여러 종류의 버섯 재배에 활용하는 것이 필요하겠다.

한국산 느타리 버섯류 (Pleurotus sp.)의 휘발성 향기성분 (Volatile Components of Oyster Mushrooms (Pleurotus sp.) Cultivated in Korea)

  • 정순택;홍재식
    • 한국균학회지
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    • 제19권4호
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    • pp.299-305
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    • 1991
  • Simultaneous distillation-extration method에 의해 4종의 국내에서 인공재배되고 있는 느타리 버섯류 (Pleurotus sp)로부터 휘발성 향기성분을 분리한 다음 GC-MS 및 GC에 의한 표준품과의 머무름 시간 비교에 의해 성분을 확인 하였다. 확인된 54종의 휘발성 화합물중 저온성 느타리 (Pleurotus ostreatus ASI 201)에서는 1-octen-3-ol, 3-octanone, 3-octanol등이, 원형 느타리 (Pleurotus florida--ostreatus-ostreatus)에서는 1-octen-3-ol, n-hexanol, 3-octanone, 3-octanol, phenol등이, 애느타리 (Pleurotus ostreatus)에서는 1-octen-3-ol, n-pentanal, n-hexanol, n-pentanol, 3-octanone, 3-octanol, 1,5-octadien-3-one등이었다. 특히 확인된 성분중에는 탄소수가 8개인 alcohol 및 carbonyl화합물이 많았으며 전체 향기성분에 대한 $C_8$화합물의 비율은 각각 56.60%, 72.46%, 54.84%, 35.85%이었다.

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Current prospects of mushroom production and industrial growth in India

  • Raman, Jegadeesh;Lee, Seul-Ki;Im, Ji-Hoon;Oh, Min-Ji;Oh, Youn-Lee;Jang, Kab-Yeul
    • 한국버섯학회지
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    • 제16권4호
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    • pp.239-249
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    • 2018
  • The global mushroom industry has grown rapidly in recent years in terms of beneficial effects, market value, and demand. India has a wide range of agro-climatic conditions and is largely an agricultural country with a cultivated area of about 4.37 %, generating about 620 million tons of agro waste annually. Mushroom cultivation not only helps recycle agro wastes, but also fills the nutritional gap prevalent among a large population of India. Recently, government industrial policy and creative innovation has promoted research and other endeavors aiming towards the cultivation of mushrooms. Mushroom cultivation in India was initiated in Solan, in the mid-sixties. Mushroom cultivation has been successful in temperate regions of the Himalayas, the Western Ghats, and the hills of northeast India. Recently, many unemployed people have begun to adopt mushroom cultivation as a means of self-employment. It is high time that Indian mushroom cultivators and consumers became aware of the nutritional and medicinal values of cultivated and wild species of mushrooms. The total mushroom production in India between 2010 and 2017 was approximately 0.13 million tons, accounting for a 4.3% increase in the average growth rate of mushrooms per annum. In particular, the total production of white button mushrooms is the highest, with a share of about 73% of total mushroom production. In this review article, we have analyzed the current scenario of the Indian mushroom industry and its contribution to the economic growth of the country.

야생버섯에서 분리한 미기록종 버섯기생균 Sepedonium laevigatum 보고 (Unrecorded mycoparasitic fungus Sepedonium laevigatum isolated from wild mushrooms in South Korea)

  • 오승윤
    • 한국버섯학회지
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    • 제20권4호
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    • pp.249-253
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    • 2022
  • 버섯기생균은 버섯을 기주로 살아가면서 병을 일으킬 수 있는 진균이다. 야생버섯의 버섯기생균이 재배종에 병을 일으키는 병원균이 될 수 있다는 점에서 야생버섯의 버섯기생균 다양성을 연구하는 것은 버섯 산업에 중요하다. 그러나 국내에서는 야생버섯의 기생균 다양성에 관한 연구가 많지 않다. 본 연구에서는 버섯 다양성 조사 과정 중 발견한 버섯기생균을 분리하여 분자계통분석과 형태적 특성 조사를 통해 분석하였다. 그 결과 분리된 균주가 미기록종인 Sepedonium laevigatum 종으로 동정되었으므로, 이 균주의 배양적 특성과 미세구조의 특성을 조사하여 기재하였다.

동남아 수출을 위한 느타리류 완성형배지의 최적 조건 및 운송 온도 (Selection of optimum conditions and distribution temperature of complete substrates of Pleurotus species for export to Southeast Asia)

  • 오민지;임지훈;오연이;장갑열;김민식;강현민
    • 한국버섯학회지
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    • 제20권4호
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    • pp.258-262
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    • 2022
  • 동남아 지역에서 한국산 버섯에 대한 선호도가 높기 때문에 신선버섯 형태가 아닌 현지에서 바로 생육하여 유통 할 수 있는 완성형배지 형태의 수출을 확대하고자 안전한 유통조건을 선발하였다. 일반느타리(Pleurotus ostreatus) '솔타리' 품종과 여름 느타리(P. sajor-caju) '삼복' 품종으로 1 kg 완성형배지를 제조하여 배양정도와 저장온도에 따라 10일 간 저장 후 버섯을 생육하였다. 70% 배양된 배지를 5~10℃에서 저장한 경우, 생육일수가 빨랐고 버섯 발생이 균일하고 안정적이었다. 0℃와 15℃로 설정된 컨테이너를 이용하여 베트남으로 실제 수출하여 달랏 지역에서 재배한 결과, 높은 온도에서 운송된 경우 생육일수가 1~2일 단축되었고, '솔타리'의 경우 수확량이 약 10% 증수되었다. 또한, '삼복'의 경우 수확량은 비슷하였으나 자실체 품질이 매우 우수하여 상품성이 좋았다.

In Vitro Experiment to Evaluate 137Cs Dissolution in the Digestion Process of Mushrooms

  • Nishiono, Kanoko;Yamanishi, Hirokuni
    • Journal of Radiation Protection and Research
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    • 제45권4호
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    • pp.154-162
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    • 2020
  • Background: Several studies have reported that wild mushrooms contain high amounts of radioactive cesium (137Cs). After the Fukushima Daiichi Nuclear Power Plant Accident, a significantly high concentration of 137Cs has been detected in wild mushrooms, and their consumption may be the cause of the chronic internal exposure of local consumers to radioactivity. Therefore, an accurate evaluation of the internal radioactivity resulting from mushroom ingestion is needed. Materials and Methods: The 137Cs elution rate through the cooking and digestion stages was evaluated using in vitro experiments. The edible mushroom Pleurotus djamor was taken as a sample for the experiments. The mushrooms were cultivated onto solid media containing 137Cs. We evaluated the internal dose based on the actual conditions using the elution rate data. For various cooking methods, the results were compared with those of other wild edible mushrooms. Results and Discussion: From the elution experiment through cooking, we proved that 25%-55% of the 137Cs in the mushrooms was released during soaking, boiling, or frying. The results of a simulated digestion experiment after cooking revealed that almost all the 137Cs in the ingested mushrooms eluted in the digestive juice, regardless of the cooking method. The committed effective dose was reduced by 20%-75% when considering the dissolution through the cooking process. Conclusion: We found that cooking lowers 137Cs concentration in mushrooms, therefore reducing the amount of radioactivity intake. Besides, since there were differences between mushroom types, we demonstrated that the internal exposure dose should be evaluated in detail considering the release of 137Cs during the cooking stages.

Identification of Medicinal Mushroom Species Based on Nuclear Large Subunit rDNA Sequences

  • Lee Ji Seon;Lim Mi Ok;Cho Kyoung Yeh;Cho Jung Hee;Chang Seung Yeup;Nam Doo Hyun
    • Journal of Microbiology
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    • 제44권1호
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    • pp.29-34
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    • 2006
  • The purpose of this study was to develop molecular identification method for medical mushrooms and their preparations based on the nucleotide sequences of nuclear large subunit (LSD) rDNA. Four specimens were collected of each of the three representative medicinal mushrooms used in Korea: Ganoderma Incidum, Coriolus versicolor, and Fomes fomentarius. Fungal material used in these experiments included two different mycelial cultures and two different fruiting bodies from wild or cultivated mushrooms. The genomic DNA of mushrooms were extracted and 3 nuclear LSU rDNA fragments were amplified: set 1 for the 1.1-kb DNA fragment in the upstream region, set 2 for the 1.2-kb fragment in the middle, and set 3 for the 1.3-kb fragment downstream. The amplified gene products of nuclear large subunit rDNA from 3 different mushrooms were cloned into E. coli vector and subjected to nucleotide sequence determination. The sequence thus determined revealed that the gene sequences of the same medicinal mushroom species were more than $99.48\%$ homologous, and the consensus sequences of 3 different medicinal mushrooms were more than $97.80\%$ homologous. Restriction analysis revealed no useful restriction sites for 6-bp recognition enzymes for distinguishing the 3 sequences from one another, but some distinctive restriction patterns were recognized by the 4-bp recognition enzymes AccII and HhaI. This analysis was also confirmed by PCR-RFLP experiments on medicinal mushrooms.