• 한국버섯학회지
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• 제9권1호
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• pp.17-21
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• 2011

다향(CM061202)은 충청남도농업기술원에서 양송이 신품종 육성을 위해 갈색종에서 161개의 담자포자 균주를 분리하여 선발된 계통중의 하나로 705호와 생산력을 비교한 결과 수량, 균사생장 및 품질특성이 우수하여 신품종으로 선정되었으며 그 특성은 다음과 같다. 다향 균사를 퇴비추출버섯 완전배지(CE/MCM)에 접종하여 $25^{\circ}C$ 온도에서 15일 배양시 균사생장 길이는 63mm로 705호(38mm)에 비해 양호하였다. 볏짚을 이용한 균상 재배시 다향의 생육 온도는$15{\sim}19^{\circ}C$로 705호($15{\sim}17^{\circ}C$)에 비해 $2^{\circ}C$ 높았다. 다향의 갓 색깔은 갈색이고, 초발이소요일수는 30일로 705호(29일) 보다 1일 느렸다. 수량성은 $49.1kg/3.3m^2$으로 705호($35.8kg/3.3m^2$)보다 37% 증수되었다. 다향의 개체중은 16.0g으로 705호(14.0g)보다 무거웠으며, 갓의 두께와 직경이 705호 보다 두꺼웠다. 또한 다향은 705호에 비해 대의 길이가 짧고, 굵을 뿐만 아니라 경도, 탄력성 등 물리성이 양호하였다.

• 한국버섯학회지
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• 제5권2호
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• pp.86-90
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• 2007

느타리버섯의 품종 다양화를 위해 단핵균주교잡에 의해 육성된 적단느타리버섯의 주요특성은 다음과 같다. 가. 균사생장적온은 $26{\sim}30^{\circ}C$이고 버섯발생 및 생육온도는 $18{\sim}23^{\circ}C$이었다. 나. 갓의 형태는 깊은깔대기형이며 다발형이고, 대는 가늘고 짧은형이며 갓, 대 모두 분홍색을 나타내었다. 다. 병재배시 배양일수는 $20^{\circ}C$에서 20일, 초발이소요일수는 $18{\sim}20^{\circ}C$재배조건에서 4일이며 생육일수는 4일이 소요되었다. 봉지재배에서는 균배양일수는 22일, 초발이 소요일수는 6일, 생육일수는 5일정도 소요되었다. 라. 버섯의 균일성에 있어서 갓색과 갓형태의 이형개체 발생은 없었고, 균사생장량 및 종균배양기간에서도 지역간 균일한 결과를 나타내었다. 마. 농가실증시험 결과 유효개체수는 850cc병재배시는 31.5개이며, 2kg 봉지재배시 47개체수를 얻었으며 수량은 병재배시 134.5g, 봉지재배시 350.0g의 수량을 얻었다.

• 한국버섯학회지
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• 제15권1호
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• pp.25-30
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• 2017

팽이버섯의 다수성 신품종 개발을 위하여, 단포자 교잡에 의해 육성된 신품종 '백승'의 주요 특성은 다음과 같다. '백승'의 원균배양 적정배지는 MEA(Malt Extract Agar) 배지이며 균사생육 적정온도는 $25^{\circ}C$였다. 자실체 발생 적정온도는 $14^{\circ}C$, 자실체 생육온도는 $7^{\circ}C$로 기존품종과 동일하였다. 초발이는 $11{\pm}1$일 소요되었으며 생육일수는 $14{\pm}1$일 이었다. '백승' 수확적기의 자실체는 갓의 직경이 $11.3{\pm}0.4mm$, 대의 길이가 $89.2{\pm}7.1mm$이며 수량은 850 ml 병당 $153.7{\pm}12.5g$이었으며, '우리1호'의 수확적기의 자실체는 갓의 직경이 $10.7{\pm}1.0mm$, 대의 길이가 $91.3{\pm}20.8mm$, 수량은 $139.8{\pm}17.8g$이었다. 갓은 백색 반구형이며 대는 백색으로 굵고 곧으며 길이는 중간으로 다발성이며 품질과 수량이 우수하였다. 유전적 유연관계로 표현하기보다는 '백승'은 대조구와 다른 DNA 밴드 양상을 보였다.

• The Plant Pathology Journal
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• 제29권1호
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• pp.31-41
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• 2013

The presence of Citrus tristeza virus (CTV) has previously been reported in citrus growing regions of Turkey. All serologically and biologically characterized isolates including I$\breve{g}$d${\i}$r, which was the first identified CTV isolates from Turkey, were considered mild isolates. In this study, molecular characteristics of the I d r isolate were determined by different methods. Analysis of the I$\breve{g}$d${\i}$r isolate by western blot and BD-RT-PCR assays showed the presence of MCA13 epitope, predominantly found in severe isolates, in the I$\breve{g}$d${\i}$r isolate revealing that it contains a severe component. For further characterization, the coat protein (CP) and the RNA-depen-dent RNA polymerase (RdRp) genes representing the 3' and 5' half of CTV genome, respectively, were amplified from dsRNA by RT-PCR. Both genes were cloned separately and two clones for each gene were sequenced. Comparisons of nucleotide and deduced amino acid sequences showed that while two CP gene sequences were identical, two RdRp clones showed only 90% and 91% sequence identity in their nucleotide and amino acid sequences, respectively, suggesting a mixed infection with different strains. Phylogenetic analyses of the CP and RdRp genes of I$\breve{g}$d${\i}$r isolate with previously characterized CTV isolates from different citrus growing regions showed that the CP gene was clustered with NZRB-TH30, a resistance breaking isolate from New Zealand, clearly showing the presence of severe component. Furthermore, two different clones of the RdRp gene were clustered separately with different CTV isolates with a diverse biological activity. While the RdRp-1 was clustered with T30 and T385, two well-characterized mild isolates from Florida and Spain, respectively, the RdRp-2 was most closely related to NZRB-G90 and NZRB-TH30, two well-characterized resistance breaking and stem pitting (SP) isolates from New Zealand confirming the mixed infection. These results clearly demonstrated that the I$\breve{g}$d${\i}$r isolate, which was previously described as biologically a mild isolate, actually contains a mixture of mild and severe strains.

• Clinical and Experimental Reproductive Medicine
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• 제31권3호
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• pp.155-168
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• 2004

Objective: Melatonin, which is secreted by pineal gland play an important role in the regulation of ovarian function via seasonal rhythm and sleep in most mammals. It also has a role in the protection of cells by removing toxic oxygen free radicals brought about by metabolism. In the present study, effects of melatonin on the mouse oocyte maturation were examined using two different culture conditions provided with 5% or 21% oxygen concentration. Material and Method: Immature mouse oocytes were obtained from the ovarian follicles of $3{\sim}4$ weeks old ICR strain mice intraperitoneally injected with 5 I.U. PMSG 44 hour before. Under stereomicroscope, morphologically healthy oocytes with distinct germinal vesicle (GV) were liberated from the graafian follicles and collected using mouth-controlled micropipette. They were then cultured for 17 hour at $37^{circ}C$, 5% $CO_2$ and 21% $O_2$ (95% air) or 5% $CO_2$, 5% $O_2$ and 90% $N_2$. New modified Hank's balanced salt solution (New MHBS) was used as a culture medium throughout the experiments. Effects of melatonin were examined at a concentration of $0.0001{\mu}M$, $0.01{\mu}M$ or $1.0{\mu}M$. For the prevention of spontaneous maturation of immature oocytes during culture, dibutyryl cyclic AMP (dbcAMP) and/or hypoxanthine were included in the medium. Results: Under 21% oxygen condition, oocytes cultured in the presence of $0.01{\mu}M$ melatonin showed a significantly higher maturation rates, in terms of germinal vesicle breakdown (95.0% vs 89.0%) and polar body formation (88.1% vs 75.4%), compared to those cultured with $0.0001{\mu}M$ or $1.0{\mu}M$ melatonin. However, no difference was observed in oocytes cultured under 5% oxygen whether they were treated with melatonin or not. In the presence of $0.01{\mu}M$ melatonin, oocytes either cultured under 21% or 5% oxygen exhibited no difference in the polar body formation (85.6% vs 86.7%). However, in the absence of melatonin, oocytes cultured under 21% oxygen exhibited lower polar body formation (74.7%). When oocytes were cultured in the presence of dbcAMP alone or with varying concentrations of melatonin, those treated with both compounds always showed better maturation, i.e., germinal vesicle breakdown and polar body formation, compared to those cultured with dbcAMP alone. At the same concentration of melatonin, however, oocytes exposed to 21% oxygen showed poor maturation than those to 5% oxygen. Similar results were obtained from the experiments using hypoxanthine instead of dbcAMP. Conclusion: Based upon these results, it is suggested that melatonin could enhance the meiotic maturation of mouse oocytes under 21% oxygen concentration, and release oocytes from the meiotic arrest by dbcAMP or hypoxanthine regardless of the concentration of oxygen, probably via the removal of oxygen free radicals.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2009년도 제38회 동계학술대회 초록집
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• pp.362-362
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• 2010

Today, vast attention has been paid to periodic arrays of nanostructures due to their potential for applications such as memory with huge storage density. Such application requires large-scale fabrication of well ordered nano-sized structures. One of the most widely used methods for the ordered nanostructures is lithography. This top-down process, however, has the limit to reduce size. Here the promising alternative is the self-organization of ordered nano-sized structures such as large scale 2d carbon-induced reconstructions on W(110). In the present study, we report on the first well-resolved atomic resolution STM studies of the well-known R($15{\times}3$) and R($15{\times}12$) carbon induced reconstruction of the W(110). From the atomic image of R($15{\times}3$) for different values of tunneling gap resistance, we can tell there are no missing atoms in unit cells of R($15{\times}3$) and some atomic displacements are substantial from the clean W(110), even though not all the imaged position of atoms correspond to tungsten, but may include those of carbon. We are considering two cases; First case is related to lattice deformation, or top layer of W(110) is deformed in the process of relief of strain caused by random inserting of carbon atoms possibly in the interstitial position. In the second case, R($15{\times}3$) unit cell results from a coincidence lattice between clean W(110) substrate and tungsten carbide overlayer which has rectangular atomic arrangement and giving R($15{\times}3$) coincidence lattice. beta-W2C showing rectangular unit cell should be a candidate. Further, we report on new reconstructions. Unlike the well-known R($15{\times}12$) consisting of two parts, two inner structures between two "Backbone" structures. The new reconstruction, which we found for the first time, contains more parts between the "Backbone"s. Sometimes we can observe the reconstruction consists of only inner parts without "Backbone" parts. Thus, the observed reconstruction can be built by constructing of two types of "Lego"-like block. Moreover, the rectangle shape of "Backbone" transform to parallelogram-like shape over time, the so-called wavy-R($15{\times}12$). Adsorption of hydrogen can be the reason for this transformation.

• 식물조직배양학회지
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• 제25권3호
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• pp.207-217
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• 1998

한국에서 자생한 자연산 tumor 조직과 근권토양으로부터 형질전환율이 높은 hypervirulent Agrobacterium spp를 분리하기 위해서 Salix, Diospyros, Populus 및 Malus에서 형성된 tumor 조직과 근권토양을 채취하괴 Schroth 선택배지와 New and Kerr 배지를 이용하여 78 균주의 colony를 특성에 따라 분리하였다. 이중에서 48 균주가 당근 disc에서 tumor를 형성하였으며 tumor를 형성한 균주중 형성시기가 빠르며 크기가 커 hypervirulent 균주로 생각되는 A. tumefaciens SP101을 biotype 1, 그리고 A. tumefaciens SM042를 biotype 2로 동정하였다. 토양중에서 선발한 A. tumefaciens SM042와 disarmed A. tumefaciens PC2760에 kanamycin 저항성 유전자를 함유하고 있는 binary vector pGA643을 도입하여 conjugant인 A. tumefaciens SM643과 A. tumefaciens PC643을 kanamycin과 tetracycline이 함유된 최소배지에서 획득하였다. 연초의 형질전환을 위해서 conjugant Agrobacterium과 연초조직을 동시배양 후 2,4-D와 kanamycin이 함유된 선발배지에 치상하여 형질전환을 유도한 결과 A. tumefaciens SM643이 A. tumefaciens PC643보다 더 많은 캘러스가 형성되었다. 그러나 A. tumefaciens PC643을 사용한 형질전환 캘러스는 대부분 friable한 캘러스로 유도되었으며 정상적으로 식물체로 생장하였으나 A. tumefaciens SM643을 사용한 캘러스는 매우 딱딱하며 둥그런 형태의 캘러스와 friable한 캘러스가 혼재한 상태로 생장하였으며, 이중에서 friable한 캘러스는 정상적인 shoot가 형성되었으나 딱딱한 캘러스로 유도된 형질전환체는 식물체로 형성되지 않고 반구형 미색의 전형적인 tumor 캘러스로 생장하였다. 한편 형질전환시 캘러스를 유도하지 않고 직접 shoot를 형성시킨 결과 disarmed Ti-plasmid를 사용하지 않고 wild-type Ti-plasmid를 사용해도 정상적인 형질전환체를 획득할 수 있었다.

• 한국균학회지
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• 제49권3호
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• pp.405-412
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• 2021

복령은 한국, 일본, 중국을 포함한 동북아시아 지역에서 사용되어 왔던 중요한 약용버섯이다. 복령은내부색깔을기준으로적복령과백복령으로구분하며, 일반적으로 백복령이 농가에서 재배되고 있다. 본 연구에서는 2가지 재배 복령과 3가지 야생 복령을 이용하여 이원교배를 통해 만들어진 균주로부터 톱밥배지에서 균핵을 형성하는 균주를 선발하려고 하였다. 단포자는 PDA 배지에서 만들어진 복령의 자실체로부터 분리하였다. 분리된 교잡균주 338개 중 39개가 소나무 톱밥배지에서 3개월 동안 배양하는 과정에서 백색 또는 황색의 균핵을 형성하였다. 톱밥배지를 이용한 균핵 형성 균주의 선발은 매우 간단하고 쉬운 방법이며 본 논문에서 처음으로 제시하는 것이다. 그리고 선발된 균주는 향후 새로운 품종을 개발하고자 야외실험을 시도할 계획이다.

• Journal of Microbiology and Biotechnology
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• 제33권1호
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• pp.83-95
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• 2023

These days, bacterial detection methods have some limitations in sensitivity, specificity, and multiple detection. To overcome these, novel detection and identification method is necessary to be developed. Recently, NGS panel method has been suggested to screen, detect, and even identify specific foodborne pathogens in one reaction. In this study, new NGS panel primer sets were developed to target 13 specific virulence factor genes from five types of pathogenic Escherichia coli, Listeria monocytogenes, and Salmonella enterica serovar Typhimurium, respectively. Evaluation of the primer sets using singleplex PCR, crosscheck PCR and multiplex PCR revealed high specificity and selectivity without interference of primers or genomic DNAs. Subsequent NGS panel analysis with six artificially contaminated food samples using those primer sets showed that all target genes were multi-detected in one reaction at 10⁸-10⁵ CFU of target strains. However, a few false-positive results were shown at 10⁶-10⁵ CFU. To validate this NGS panel analysis, three sets of qPCR analyses were independently performed with the same contaminated food samples, showing the similar specificity and selectivity for detection and identification. While this NGS panel still has some issues for detection and identification of specific foodborne pathogens, it has much more advantages, especially multiple detection and identification in one reaction, and it could be improved by further optimized NGS panel primer sets and even by application of a new real-time NGS sequencing technology. Therefore, this study suggests the efficiency and usability of NGS panel for rapid determination of origin strain in various foodborne outbreaks in one reaction.

• 한국버섯학회지
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• 제21권4호
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• pp.241-246
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• 2023

본 연구는 농촌진흥청에서 육성한 백승과 국외 수집자원(KMCC02260)을 모본으로 하여 단핵균주를 분리 후 mon-mon교잡을 통해 '백운' 품종을 육성하였다. 균사배양 특성은 25℃에서 두 품종의 균사생장이 가장 좋았으며 15, 25℃에서 백운의 균사생장 속도가 대조품종보다 더 빨랐으며 배지별 시험에서도 모든 배지에서 백운의 균사생장이 우수하였다. 톱밥 병에 접종 후 균사 배양기간은 백운이 2일, 초발이일수도 1일 더 빨라 전체적인 생육기간을 단축시켰으며 수량은 228.0±10.9 g/병(850 ml)으로 대조품종 대비 8.3% 증수하였다. 백운의 형태적인 특성은 갓이 크고 대가 굵으며 갓이 순백색이었다. 대치배양과 유전적 다형성 검정 결과, 백운이 두 모본과 대조품종과 유전적으로 다르다는 것을 확인하였다.