• 제목/요약/키워드: Monokaryotic strains

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Extracellular Enzyme Activities of the Monokaryotic Strains Generated from Basidiospores of Shiitake Mushroom

  • Kwon, Hyuk-Woo;Back, In-Joung;Ko, Han-Gyu;You, Chang-Hyun;Kim, Seong-Hwan
    • Mycobiology
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    • 제36권1호
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    • pp.74-76
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    • 2008
  • To obtain basic information on the biochemical property of basidiospores of shiitake mushroom (Lentinula edodes), the ability of producing extracellular enzyme was assessed using a chromogenic plate-based assay. For the aim, amylase, avicelase, $\beta$-glucosidase, CM-cellulase, pectinase, proteinase, and xylanase were tested against monokaryotic strains generated from forty basidiospores of two different parental dikaryotic strains of shiitake mushroom, Sanjo-101Ho and Sanjo-108Ho. These two parental strains showed different degree of extracellular enzyme activity. No identical patterns of the degree of enzyme activity were observed between monokaryotic strains and parental strains of the two shiitake cultivars. The degree of extracellular enzyme activity also varied among monokaryotic strains of the two shiitake cultivars. Our results showed that dikaryotic parental strains of shiitake mushroom produce monokaryotic basidiospores having very diverse biochemical properties.

Isolation and Characterization of Monokaryotic Strains of Lentinula edodes Showing Higher Fruiting Rate and Better Fruiting Body Production

  • Ha, Byeong-Suk;Kim, Sinil;Ro, Hyeon-Su
    • Mycobiology
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    • 제43권1호
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    • pp.24-30
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    • 2015
  • The effects of monokaryotic strains on fruiting body formation of Lentinula edodes were examined through mating and cultivation of the mated dikaryotic mycelia in sawdust medium. To accomplish this, monokaryotic strains of L. edodes were isolated from basidiospores of the commercial dikaryotic strains, Chamaram (Cham) and Sanjo701 (SJ701). A total of 703 matings (538 self-matings and 165 outcrosses) were performed, which generated 133 self-mates and 84 outcross mates. The mating rate was 25% and 50% for self-mating and outcross, respectively. The bipolarity of the outcross indicated the multi-allelic nature of the mating type genes. The mating was only dependent on the A mating type locus, while the B locus showed no effect, implying that the B locus is multi-allelic. Next, 145 selected dikaryotic mates were cultivated in sawdust medium. The self-mated dikaryotic progenies showed 51.3% and 69.5% fruiting rates for Cham and SJ701, respectively, while the fruiting rate of the outcross mates was 63.2%. The dikaryotic mates generated by mating with one of the monokaryotic strains, including A20, B2, E1, and E3, showed good fruiting performance and tended to yield high fruiting body production, while many of the monokaryotic strains failed to form fruiting bodies. Overall, these findings suggest that certain monokaryotic strains have traits enabling better mating and fruiting.

Genetic and Biochemical Characterization of Monokaryotic Progeny Strains of Button Mushroom (Agaricus bisporus)

  • Kwon, Hyuk Woo;Choi, Min Ah;Yun, Yeo Hong;Oh, Youn-Lee;Kong, Won-Sik;Kim, Seong Hwan
    • Mycobiology
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    • 제43권1호
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    • pp.81-86
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    • 2015
  • To promote the selection of promising monokaryotic strains of button mushroom (Agaricus bisporus) during breeding, 61 progeny strains derived from basidiospores of two different lines of dikaryotic parental strains, ASI1038 and ASI1346, were analyzed by nucleotide sequencing of the intergenic spacer I (IGS I) region in their rDNA and by extracellular enzyme assays. Nineteen different sizes of IGS I, which ranged from 1,301 to 1,348 bp, were present among twenty ASI1346-derived progeny strains, while 15 different sizes of IGS I, which ranged from 700 to 1,347 bp, were present among twenty ASI1038-derived progeny strains. Phylogenetic analysis of the IGS sequences revealed that different clades were present in both the ASI10388- and ASI1346-derived progeny strains. Plating assays of seven kinds of extracellular enzymes (${\beta}$-glucosidase, avicelase, CM-cellulase, amylase, pectinase, xylanase, and protease) also revealed apparent variation in the ability to produce extracellular enzymes among the 40 tested progeny strains from both parental A. bisporus strains. Overall, this study demonstrates that characterization of IGS I regions and extracellular enzymes is useful for the assessment of the substrate-degrading ability and heterogenicity of A. bisporus monokaryotic strains.

Nucleus-Selective Expression of Laccase Genes in the Dikaryotic Strain of Lentinula edodes

  • Ha, Byeongsuk;Lee, Sieun;Kim, Sinil;Kim, Minseek;Moon, Yoon Jung;Song, Yelin;Ro, Hyeon-Su
    • Mycobiology
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    • 제45권4호
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    • pp.379-384
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    • 2017
  • In mating of Lentinula edodes, dikaryotic strains generated from certain monokaryotic strains such as the B2 used in this study tend to show better quality of fruiting bodies regardless of the mated monokaryotic strains. Unlike B2, dikaryotic strains generated from B16 generally show low yields, with deformed or underdeveloped fruiting bodies. This indicates that the two nuclei in the cytoplasm do not contribute equally to the physiology of dikaryotic L. edodes, suggesting an expression bias in the allelic genes of the two nuclei. To understand the role of each nucleus in dikaryotic strains, we investigated single nucleotide polymorphisms (SNPs) in laccase genes of monokaryotic strains to reveal nuclear origin of the expressed mRNAs in dikaryotic strain. We performed reverse transcription PCR (RT-PCR) analysis using total RNAs extracted from dikaryotic strains (A5B2, A18B2, and A2B16) as well as from compatible monokaryotic strains (A5, A18, and B2 for A5B2 and A18B2; A2 and B16 for A2B16). RT-PCR results revealed that Lcc1, Lcc2, Lcc4, Lcc7, and Lcc10 were the mainly expressed laccase genes in the L. edodes genome. To determine the nuclear origin of these laccase genes, the genomic DNA sequences in monokaryotic strains were analyzed, thereby revealing five SNPs in Lcc4 and two in Lcc7. Subsequent sequence analysis of laccase mRNAs expressed in dikaryotic strains revealed that these were almost exclusively expressed from B2-originated nuclei in A5B2 and A18B2 whereas B16 nucleus did not contribute to laccase expression in A2B16 strain. This suggests that B2 nucleus dominates the expression of allelic genes, thereby governing the physiology of dikaryons.

Genotyping of Agaricus bisporus Strains by PCR Fingerprints

  • Min, KyongJin;Oh, YounLee;Kang, HeeWan
    • 한국균학회소식:학술대회논문집
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    • 한국균학회 2014년도 추계학술대회 및 정기총회
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    • pp.41-41
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    • 2014
  • Agaricus bisporus, commonly known as the button mushroom, is the most widely cultivated species of edible fungi. Low frequency of recombination ratio and homokaryotic or monokaryotic spore on meiotic basidia form obstacles for breeding programs. Since the first hybrid varieties for white button mushrooms were released in Europe, new varieties released afterwards were either identical of very similar to these first hybrids on morphologies. Therefore, different DNA markers have been used to define unique varieties of A. bisporus strains. Aim of this study is to assess the genetic diversity of different A. bisporus strains in Korea. Twelve UFP (Universal fungal primer, JK BioTech. Ltd), 12 simple sequence repeat (ISSR) and 30 SSR primers were used to assess genetic diversity of monokaryotic and dikaryotic Agaricus bisporus strains including other 19 Agaricus spp. Of them, four UFP, four SSR primers, $(GA)_8T$, $(AG)_8YC$, $(GA)_8C$ and $(CTC)_6$ and seven SSR markers produced PCR polymorphic bands between the Agaricus species or within A. bisporus strains. PCR polymorphic bands were inputted for UPGMA cluster analysis. Forty five strains of A. bisporus are genetically clustered into 6 groups, showing coefficient similarity from 0.75 to 0.9 among them. In addition, genetic variations of monokaryotic and dikaryotic Agaricus bisporus strains were partially detected by PCR technologies of this study. The varieties, Saea, saedo, Saejeong and Saeyeon that have recently been developed in Korea were involved in the same group with closely genetic relationship of coefficient similarity over 0.96, whereas, other strains were genetically related to A. bisporus strains that were introduced from USA, Eroupe and Chinese.

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톱밥재배용 표고 품종의 단핵균사체와 2핵균사체의 한천과 톱밥배지에서의 균사생장 (Mycelial Growth of Monokaryotic and Dikaryotic Strains of Lentinula edodes Cultivars for Sawdust Cultivation on the Agar and Sawdust Culture media)

  • 김민경;김성태;김소라;김은지;진미경;이용국;서건식
    • 현장농수산연구지
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    • 제19권1호
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    • pp.83-90
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    • 2017
  • 표고 육종 소재를 개발하기 위하여 톱밥봉지재배용 품종의 2핵균사체와 단핵균사체를 한천배지와 톱밥배지에서 배양적 특성을 조사하였다. 품종은 산조 701호, 산조 705호, 참아람, 추제 2호를 사용하였다. 공시 표고 품종의 균사생장은 산조 705호를 제외한 품종 모두 PDA에서 가장 양호하였으나 산조 705호는 MCM에서의 균사 생장이 가장 양호하였다. 품종에 관계없이 표고 균사는 MEA에서 가장 안정적인 균사생장을 보였다. 톱밥배지에서 공시균주의 균사생장은 품종 간의 큰 차이는 보이지 않았으나 산조 701호와 705호보다 약 10%정도 빠르게 생장하는 것으로 나타났다. 산조701호와 참아람의 단핵균사체는 2핵 균사체보다 균사생장이 저조하였다. 2핵균사체는 참아람이 산조 701호보다 균사생장이 양호하였으나 단핵균사체는 전체적으로는 산조 701호가 참아람보다 균사생장이 양호하였다. 선발된 단핵 균사체는 균사생장이 매우 다양하고, 형성된 균총의 형태도 매우 다양하여 유전적으로 매우 다양한 단핵 균사체가 선발된 것으로 추정할 수 있고, 이들 단핵 균사체는 교배육종을 위한 좋은 육종 소재로 기대된다.

발색반응 분석법을 이용한 표고 교배균주의 세포외효소 분비 능력 평가 (Assessment of the Ability of Extracellular Enzyme Production in Hybrid Strains of Lentinula edodes by Chromogenic Reaction-based Plate Assay)

  • 권혁우;김준영;고한규;박흥수;김성환
    • 한국균학회지
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    • 제39권2호
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    • pp.99-104
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    • 2011
  • 표고버섯의 육종은 두 개의 다른 모균주에 의한 교배와 버섯생산에 좋은 형질을 지닌 교잡균주의 선발이 요구된다. 본 연구에서는 서로 다른 두 계통의 표고 모균주에서 유래한 단핵균주와 이들 단핵균주간의 교배로부터 만들어진 교잡균주에 대하여 발색반응 배지를 이용하여 세포외 분해효소의 분비능력 정도를 비교하여 생화학적 특성이 우수한 균주를 선발할 가능성에 대하여 조사하였다. 모균주로부터 유래한 단핵균주들 간에 ${\beta}$-glucosidase, avicelase, CM-cellulase, amylase, pectinase, xylanase, protease의 분비능력에 차이가 있음을 확인하였다. 교잡균주에 있어서도 단핵균주의 조합에 따라 효소 분비능력이 달라지는 것을 볼 수 있었다. 이에 따라 발색반응배지를 이용한 세포외효소 평가법이 표고의 육종과정 중에 생성되는 교잡균주들의 평가에 활용 할 수 있을 것으로 사료된다.

Mating Relationship between the parent and the mutant strains in Pleurotus ostreatus

  • Lee, Byung-Joo;Lee, Mi-Ae;Kim, Yong-Gyun;Lee, Kwang-Won;Lim, Yong-Pyo;Lee, Byung-Eui;Song, Ho-Yeon
    • 한국버섯학회지
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    • 제10권3호
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    • pp.101-108
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    • 2012
  • Pleurotus ostreatus 'Miso' is a mutant strain showing white color in pileus from the known parent strain 'Wonhyeong 1'. Shape and several other characters also vary with culture conditions. Mating experiments were performed to understand interstrain mating relationship using monokaryons of the parent and the mutant strains. All monokaryons were grown from single spores isolated from freshly collected fruit bodies. Pairings were performed in 90 mm petri dishes on PDA. They were allowed to grow at 25 until two fronts of the advancing mycelia met and developed a conspicuous contact zone. The contact zone and the outer edges of paired colonies on each plate were examined for clamp connections. The parent and the mutant resulted in tetrapolar incompatibility in intrastrain crosses. In interstrain crosses, each monokaryotic tester strain of the parent strain was out-crossed to monokaryotic tester strains of the mutant. As a result of these crosses it was found that both strains share the same A and B incompatibility factors yielding 25% compatibility.

표고에서의 RNA 바이러스 수직감염 (Vertical Transmission of RNA Mycoviruses in Lentinula edodes)

  • 김은진;박미정;김민준;정연석;장영선;가강현
    • 한국균학회지
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    • 제50권4호
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    • pp.263-274
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    • 2022
  • 표고는 중요한 상업용 버섯이며, 표고에서의 바이러스 감염에 대한 여러 보고가 있었다. 톱밥 재배 품종인 산백향(NIFoS 2778)과 태향고(NIFoS 4317)에 대한 바이러스 검출 결과, 이들이 2개의 mycoviruses (LeV-HKB 및 LeNSRV1)에 감염되어 있음을 확인하였다. 각 품종의 자실체에서 분리된 담자포자에서 유래한 80개의 단핵균사에서 바이러스 감염을 조사한 결과, 대부분의 단 핵균사들이 바이러스에 감염되어 있었으며, LeV-HKB와 LeNSRV1의 수직감염률에 차이가 있었다. LeV-HKB가 LeNSRV1 보다 높은 수직감염률을 나타낸 것이다. 따라서 mycovirus의 수직 감염 기작이 바이러스 종에 따라 다른 것으로 보인다. 다음으로, 담자포자 유래 단핵균사들의 생장속도를 조사하여 바이러스 감염과 생장속도의 상관관계를 조사하였다. 바이러스 감염과 균사 생장속도 사이에 통계적으로 유의한 상관관계가 없었지만, 감염된 바이러스의 종류가 늘어날수록 생장속도가 감소하는 경향을 확인하였다. 본 연구는 mycovirus의 수직 감염 기작을 이해하는 데 기여하고, 바이러스에 감염되지 않은 단핵균사를 이용한 무바이러스 품종 개발을 촉진하는 데 기여할 수 있을 있을 것 기대된다.

Occurrence of dsRNA Mycovirus (LeV-FMRI0339) in the Edible Mushroom Lentinula edodes and Meiotic Stability of LeV-FMRI0339 among Monokaryotic Progeny

  • Kim, Jung-Mi;Yun, Suk-Hyun;Park, Seung-Moon;Ko, Han-Gyu;Kim, Dae-Hyuk
    • The Plant Pathology Journal
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    • 제29권4호
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    • pp.460-464
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    • 2013
  • dsRNA was found in malformed cultures of Lentinula edodes strain FMRI0339, one of the three most popular sawdust cultivated commercial strains of shiitake, and was also found in healthy-looking fruiting bodies and actively growing mycelia. Cloning of the partial genome of the dsRNA revealed the presence of the RdRp sequence of a novel L. edodes mycovirus (LeV), and sequence comparison of the cloned amplicon showed identical sequences sequence to known RNA-dependent RNA polymerase genes of LeV found in strain HKA. The meiotic stability of dsRNA was examined by measuring the ratio of the presence of dsRNA among sexual monokaryotic progeny. More than 40% of the monokaryotic progeny still contained the dsRNA, indicating the persistence of dsRNA during sexual reproduction. Comparing the mycelia growth of monokaryotic progeny suggested that there appeared to be a tendency toward a lower frequency of virus incidence in actively growing progeny.