• 한국작물학회:학술대회논문집
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• 한국작물학회 2006년도 한국약용작물학회 공동춘계학술발표회
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• pp.226-227
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• 2006

• The Plant Pathology Journal
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• 제27권2호
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• pp.183-186
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• 2011

During the summer of 2005, specimens of soybean cultivars (Daepung, Daewon, Hwanggeum and Taegwang) showing frogeye leaf spot (FLS) were obtained from various areas in Korea. Eight isolates identified as Cercospora sojina were inoculated on the adaxial leaf surfaces of 63 Korean soybean cultivars; the disease responses to each isolate were evaluated 14 days and 21 days after inoculation. Based on the disease responses (resistant or susceptible) of the cultivars by the isolates, a set of cultivars (Anpeong, Bogwang, Cheongdu No. 1, Cheongja No. 3, Dachae, Daemang, Jangwon, Namhae, Sowon, Taegwang) were selected and inoculated with seven isolates for further testing pathogenic variance. Interestingly, 6 out of 7 tested C. sojina isolates revealed differential ability in infecting different soybean cultivars. This result may indicate the possibility of new race occurrence or pathogenic variation; this also presents evidence for prevalent FLS occurrence during humid and hot weather in Korea.

• 식물병연구
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• 제21권3호
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• pp.243-249
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• 2015

점무늬병은 콩에서 최대 50% 정도의 수량감소가 보고된 병으로 최근 한국 콩 재배포장에서 큰 문제로 대두되고 있어 최근 6년간의 보급 품종을 대상으로 콩 점무늬병에 대한 저항성 검정을 실시하였다. 표준화된 검정방법을 적용하기 위해 가장 효과적인 포자 형성 배지 조건을 탐색하고 저항성 검정 평가 기준을 확립하였다. 포자형성은 $25^{\circ}C$, 12시간 광 조건과 암 조건에서 V8 juice를 이용한 배지의 포자 형성이 가장 효과적임을 알 수 있었다. 접종은 $10^5spores/ml$로 준비하여, 제 5 복엽 완전전개기인 V6 stage까지 키운 건강한 콩 식물체에 실시하였고 병 반응은 28일 동안 관찰하였다. 그 결과 대풍은 8개 균주 모두 저항성을 보였고, 신팔달2호는 7개 균주에, 연풍, 청아는 6개 균주에 저항성을 보였다. 반면에 황금, 태광, 대원, 천상, 신화 등은 평가한 8개 균주에 모두 감수성 반응을 나타내었다. 콩 점무늬병에 대한 저항성 품종을 육종하기 위해 표준화되고 정밀화된 저항성 검정방법과 판정 체계를 갖추는 것은 매우 중요하며 이 방법은 차후 포장 저항성 검정에도 적용할 수 있을 것이라 기대한다.

• Journal of Crop Science and Biotechnology
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• 제11권2호
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• pp.91-100
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• 2008

Melting curve analysis of fluorescently labeled DNA fragments is used extensively for genotyping single nucleotide polymorphism(SNP). Here, we evaluated a SNP genotyping method by melting curve analysis with the two probe chemistries in a 384-well plate format on a Roche LightCycler 480. The HybProbe chemistry is based on the fluorescence resonance energy transfer(FRET) and the SimpleProbe chemistry uses a terminal self-quenching fluorophore. We evaluated FRET HybProbes and SimpleProbes for two SNP sites closely linked to two quantitative trait loci(QTL) for southern root-knot nematode resistance. These probes were used to genotype the two parents and 94 $F_2$ plants from the cross of PI 96354$\times$Bossier. The SNP genotypes of all samples determined by the LightCycler software agreed with previously determined SSR genotypes and the SNP genotypes determined on a Luminex 100 flow cytometry instrument. Multiplexed HybProbes for the two SNPs showed a 98.4% success rate and 100% concordance between repeats two of the same 96 DNA samples. Also, we developed a HybProbe assay for the Rcs3 gene conditioning broad resistance to the frogeye leaf spot(FLS) disease. The LightCycler 480 provides rapid PCR on 384-well plate and allows simultaneous amplification and analysis in approximately 2 hours without any additional steps after amplification. This allowed for a reduction of the potential contamination of PCR products, simplicity, and enablement of a streamlined workflow. The melting curve analysis on the LightCycler 480 provided high-throughput and rapid SNP genotyping and appears highly effective for marker-assisted selection in soybean.