수종의 식물병원균(흰비단병균, 균핵병균, 좀검은균 핵병균)이 생산하는 가수분해산소(Cellulase Cx, Invertase, , Xylanase, PMG, PG, Phosphatase, Protease)를 균계체내의 효소 및 배양여액내의 효소와 균핵내의 효소(좀검은균핵병균은 제외)로 나누어 그의 생산량과 pH에 따른 활성의 변화를 검토한 결과를 요약하면 다음과 같다. 1. 배양 10일후의 Cx활성은 균핵병균이 다른 균에 비하여 활성이 높았고 흰비단병균과 균핵병균은 산성측(pH 3.0 부근)에서, 좀검은균핵병균은 중성측(pH6.0 부근)에서 활성이 높았다. 2. 흰비단병균의 Invertase는 다른균에 비하여 약 20배정도 높은 활성을 보였고 3균주 모드 배양여액과 균계체간에 효소활성의 차가 인정되지 않았다. 3. Xylanase의 활성은 3균주 모두 균계체, 균핵 및 배양여액에 따라 또 pH에 따라 아주 다양한 변화를 나타냈고 균핵내에서 활성이 높았다. 4. 의 활성은 공시균중 좀검은균핵병균의 균계체, 배양여액이 가장 높았다. (약 12.0ug/min) 흰비단병균과 균핵병균ㅇ서는 균계체나 균핵에서 보다 배양여액에서 높았는데 활성최적pH는 균계체, 균핵 모두 pH 6.2였으나 배양여액에서는 흰비단 병균과 균핵병균이 pH3.0이었는데 반해 좀검은균핵병균은 pH6.2였다. 5. PMG의 활성은 공시균 모두 배양여액에서 높았고 균계체에서는 균핵병균과 좀검은균핵병균이 높았으며 활성최적 pH는 균에 따라 또는 측정부분에 따라 다양하게 나타났다. 6. PG의 활성은 흰비단 병균과 균핵병균의 균계체에서 각각 9,1ug/min. 9.5ug/min으로서 가장 높았고 활성최적 pH는 흰비단병균이 pH4.5부근 균핵병균이 pH.3.0부근이었다. 7. 흰비단병균과 균핵병균의 Phosphatase는 산성측(최적 pH3.5)에서 활성이 높았고 좀검은 균핵 병균은 산성, 중성, 알카리측에서 각각 Peak가 나타났으나 최적 pH는 9.5였다. 8. 공시균주 모두 Protease는 pH 10.0에서 최고활성을 나타냈고 특히 좀검은균핵 병균의 배양여액내 효소활성이 높았다.

Sclerotinia sclerotiorum(Lib.) de Bary의 상치, 오이 및 유채의 3균주에 대하여 PDA를 기본부지로하여 광선이 이들의 균핵형성에 미치는 영향을 연구하였다. 광원으로서는 주광색 형광등을 사용하였다. 그 결과를 요약하면 다음과 같다. 1) 계속광처리에서 광도 480Lux까지는 광도가 증가함에 따라 증가했지만 성숙균핵의 건물중은 이와는 반대로 감소하였다. 그리고 800 Lux 처리에서는 균핵시원체의 유기가 크게 억제되었고 성숙균핵은 거의 형성되지 않았다. 2) 5000Lux의 고광도라 하더라도 48시의 단시간처리는 균핵시원체수 및 성숙균핵수를 증가시켰다. 그러나 성숙균핵의 건물중은 160 Lux에서만 다소 증가하는 경향이 있었다. 3) 광 shock 즉 1분간치의 계속광 48시간까지의 160 Lux, 500Lux 처리는 모두 균핵형성수와 건물중을 증가시켰는데 균핵형성수와 건물중을 증가시켰는데 균핵형성수는 500Lux에서 균핵건물중은 160Lux에서 더 높았다.

Background : Sclerotinia rot, caused by a fungus Sclerotinia sclerotiorum, is one of the serious and unpredictable yield losses in perilla (Perilla frutescens) leaf production in Korea. Screening disease resistant genetic resources is necessary to develop disease-resistant cultivars and conduct related research. Methods and Results : A Total of 150 perilla accessions, including 123 Korean landraces and 27 cultivars developed in Korea, were evaluated for resistance to Sclerotinia rot (Sclerotinia sclerotiorum) using detached leaf inoculation technique. Sclerotinia sclerotiorum isolate KACC40457 was inoculated at the seedling stage (five to six leaves). For detached leaf method, a mycelial plug was placed fungus-side down on the main leaf vain and incubated at 22 ± 1℃ on moistened paper towel in a plastic box. Three Korean landraces, including IT117036, IT117106, and IT117110, and cultivar IT229431 showed 100% of resistance ratio (no. of plants showed below 1 ㎝ of lesion size/total evaluated plants × 100). Seven accessions including five landraces, IT117080, IT117107, IT117048, 117042, 117029, and two cultivaers, IT276225 and IT213781, showed high level of resistance that is higher than 80% of resistance ratio Conclusion : 11 accessions which showed strong and moderate level of resistance to Sclerotinia rot could be possibly used by breeders, farmers, and researchers to produce new disease resistant cultivars and use them commercially. However, research related to the exploration of appropriate materials (accessions) for breeding cultivars with good quality, high functional components, high consumer acceptability, etc. should be continued, considering pathogenicity test was conducted in young stage.

To develop environment-friendly agricultural products with anti-microbial activity against Sclerotinia sclerotiorum as a pathogen of sclerotium disease, Aristolochia tagala Champ. was extracted by methanol and its extract was fractionated into several solvent fractions. The chloroform fraction, which showed the highest antimicrobial activity, was separated by column chromatography and obtained forty three subfractions. The forty three fractions were searched the anti-fungal activities by bioassay. The most active No. 26 subfraction was analyzed by GC-MS. Each mass spectra, corresponding to each peak of chromatogram, was compared to MS database of Wiley library. As a result, 2,4-di-tetra-butyl-phenol, 2-mono-palmitin, 1-mono-stearin were profiled as maine compounds in No. 26 subfraction. Bioassay using commercial 1-mono-stearin to test for the anti-microbial activity conformed the antimicrobial active compound. In conclusion, 1-mono-stearin identified from Aristolochia tagala Champ. was antimicrobial chemical against Sclerotinia sclerotiorum.

To develop environment-friendly agricultural products with anti-microbial activity against Sclerotinia sclerotiorum as a pathogen of sclerotium disease, Usnea longissima was extracted by methanol and its extract was fractionated into several solvent fractions. The chloroform fraction, which showed the highest antimicrobial activity, was separated by silica gel-column chromatography and obtained into nine group subfractions. The nine group fractions were searched the antifungal activities by bioassay. The most active No. 3 subfraction was analyzed by GC-MS. Each mass spectra, corresponding to each peak of chromatogram, was compared to database of Wiley library. As a result, Usnic acid was identified as main compounds. In conclusion, Usnic acid isolated from Usnea longissima was antimicrobial chemical against Sclerotinia sclerotiorum as a pathogen of sclerotium disease.