Background : Ginseng root rot caused by soil-borne pathogens, Cylindrocarpon destructans and Fusarium solani, is a major factors of replanting failure in ginseng cultivation. Some of the phenolic compounds detected in the soil of commercially cultivated American ginseng could inhibit the seed germination and seedling growth of American ginseng. Our study is to investigate the causes of replanting failure of ginseng by overhead flooding treatment and soil incorporation of ginseng fine root in soil infected with root rot pathogens. Methods and Results : To make soil occurring continuous cropping injury, 2-year-old ginseng infected with Cylindrocarpon destructans replanted in soil cultivated ginseng for 5 years. Treatment are as follows: 1) control, 2) water of 2ℓ was irrigate infected soil of 20ℓ, 3) ginseng fine root of 20g was mixed with infected soil of 20ℓ. Soil pH was increased, while other inorganic components were significantly reduced by overhead flooding treatment. Soil incorporation of ginseng fine root decreased soil pH, but increased EC, NO3, P2O5 and K, meanwhile, did not affected changes in organic matter, calcium, magnesium, sodium. Irrigation treatment in soil occurring replanted failure promoted distinctly above-ground growth of ginseng, and inhibited the occurrence of root rot because inorganic nutrient like NO3, P2O5 and K were decreased to optimal levels, and the density of soil pathogens could be reduced. Growth of ginseng was not inhibited, while root rot was promoted by soil incorporation of ginseng fine root. Conclusion : Irrigation treatment was effective in promoting the growth of ginseng and inhibited root rot distinctly. Ginseng fine root remaining in the soil after ginseng harvest did not affect the above-ground growth of ginseng, while promoted the occurrence of root rot.

The SS (Bacillus subtilis 10%), WS (Microbial extract 70%), and DS (Sulfur 78%) agents were selected by mycelial growth inhibitory effect test against kiwifruit soft rot pathogen (B. dothidea) with 11 kinds of environment-friendly agricultural materials on PDA medium for 10 days. They showed at 94.2%, 65.2%, 58.9%, respectively. The control value of WS and SS agents were better than DS in storage experiment. It was effective SS and WS single application, DS-WS and WS-SS alternate application in the field trial.

Pink Rot on melon and White Stain Symptom on grape are caused by Trichothecium roseum, one of the most important diseases of grape and melon. These diseases have been occurred in national-wide in Korea and causes irreversible damage on the grape and the melon at harvest season. This research presents the evaluation of the capacity of Bacillus subtillis HK2 to protect both melon and grape against T. reseum and establishes its role as a biocontrol agent. In this study, we isolated a Bacillus strain HK2 from rhizosphere soil, identified it as Bacillus subtillis by 16S rRNA analysis and demonstrated its antifungal activity against T. roseum. Under I-plate assay it was observed that the effect of hyphal growth inhibition was not due to production of volatile compounds. The optimum culture condition of HK2 was found at 30℃ and initial pH of 7.0. Application of HK2 culture suspension reduced 90.2% of white stain symptom on grape as compared to control, resulting in greater protection to grape against T. roseum infestation. Butanol extract of HK2 culture purified using flash column chromatography. The antifungal material was a polar substance as it showed antifungal activity in polar elute. Therefore, our results indicated a clear potential of B. subtilis HK2 to be used for biocontrol of Pink rot in melon and white stain symptom on grape caused by T. roseum.

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.

Fusarium crown root rot (FCRR) is a severe fungal disease caused by Fusarium oxysporum f. sp. radicis-lycopersici (FORL) in tomato. Resistance to FORL is conferred by single dominant locus Frl on chromosome 9, but its precise genomic location is not clearly determined. In this study, detailed location of Frl was assessed by using a set of molecular markers physically anchored on Chr.9 and F2 and RIL population derived from FORL-resistant inbred AV107-4 (S.lycopersicum) x susceptible L3708 (S. pimpinellifolium). Bioassay of the two populations with a FORL strain isolated from Korea resulted in single dominant heritance of the resistance. Two SCAR and 11 CAPS markers encompassing 3.6Mb~72Mb of Chr.9 were developed from the Tomato-EXPEN 2000 map and SolCAP SNP-array analysis. These markers were genotyped on 345 F2 plants. A high level of cosegregation with the resistance were observed for 5 markers which were mapped at a large physical interval of 5.1Mb (T1212) to 46.4Mb (SSR237), indicating that genetic recombination was highly suppressed in this region. Cosegregation of these markers with Frl was confirmed by using 126 RILs. The results implied that, in contrast with the previously reported long arm, Frl is present on a pericentromeric region of short arm of Chr. 9, in which crossing-over is severely suppressed. The marker set was further tested on 12 FORL-resistance or susceptibility commercial cultivars. Unlike the biparental populations, frequent linkage break was observed for T1212 and D4 in commercial cultivars. T1212 and D4 showed 50% and 100% match with the phenotype, respectively. D4, a CAPS, was converted to a high resolution melting (HRM) marker and tested on 55 breeding lines from private seed companies (Fig.3). All breeding lines showed the HRM genotype for resistance allele, indicating that D4 can be useful for selecting FORL-resistance tomato plants.

본 연구는 수박 과실썩음병의 원인균인 A. avenae subsp. citrulli에 대해 항균활성을 갖는 친환경 유기농자재를 개발할 목적으로 오배자(S. chinensis)를 대상으로 수행되었다. 오배자를 MeOH로 추출하여 용매분획을 하였고, 용매분획 중에서 가장 강한 활성을 나타낸 hexane fraction을 column chromatography로 분리하여 활성이 강한 분획들을 GC-MS로 분석하였다. GC chromatogram 상의 주요 peak에 해당하는 mass spectrum과 Wiley library를 비교하여 profiling한 결과, 지방산인 myristic acid, palmitic acid와 3-n-pentadecylphenol이 주요 물질로 검출되었다. 이들 검출 화합물의 항균활성을 검정하기 위하여 표준품을 사용하여 bioassay한 결과, myristic acid와 3-n-pentadecylphenol 화합물이 강한 활성을 보였다. 따라서 오배자로부터 분리한 myristic acid와 3-n-pentadecylphenol 화합물이 항균 활성물질인 것을 구명하였다.

To study the effect of crop rotation on the control of ginseng root rot, growth characteristics and root rot ratioof 2-year-old ginseng was investigated after the crops of 18 species were cultured for one year in soil contaminated by thepathogen of root rot. Fusarium solani and Cylindrocarpon destructans were detected by 53.2% and 37.7%, respectively, frominfected root of 4-year-old ginseng cultivated in soil occurring the injury by continuous cropping. Content of NO3, Na, andP2O5 were distinctly changed, while content of pH, Ca, and Mg were slightly changed when whole plant of crops cultured forone year were buried in the ground. All of EC, NO3, P2O5, and K were distinctly increased in soil cultured sudangrass, pea-nut, soybean, sunnhemp, and pepper. All of EC, NO3, P2O5, and K among inorganic component showed negative effect onthe growth of ginseng when they were excessively applied on soil. The growth of ginseng was promoted in soil cultivatedperilla, sweet potato, sudangrass, and welsh onion, while suppressed in Hwanggi (Astragalus mongholicus), Deodeok(Codonopsis lanceolata) Doraji (Platycodon grandiflorum), Gamcho (Glycyrrhiza uralensis), Soybean. All of chicory, lettuce,radish, sunnhemp, and welsh onion had effective on the inhibition of ginseng root rot, while legume such as soybean,Hwanggi, Gamcho, peanut promoted the incidence of root rot. Though there were no significant correlation, NO3 showedpositive correlation, and Na showed negative correlation with the incidence of root rot.

본 연구는 전작물 재배에 따른 마늘 흑색썩음균핵병 피해 경감 효과를 평가하기 위해 2년간 수행되었다. 콩 참깨 호박 네마장황, 대파를 전작물로 재배하였으며, 대조구로 휴경처리구와 병원균 무접종구를 두었다. 전적물 재배 후 마을을 파종하고 재배하면서, 흑색썩음균핵병 이병주율과 수량을 조사하였다. 2013년 흑색썩음균핵병은 병원균 무접종구, 콩, 네마장황처리구에서 가장 낮았으며, 호박처리구에서 가장 높았다. 2014년에는 네마장황, 콩, 대파처리구에서 흑색썩음균핵병 이병주율이 낮았으며, 호박처리구에서 가장 높았다. 처리구 별 마늘의 수량은 2013년에는 콩, 네마장황, 대파 처리구에서 가장 높았고 호박처리구에서 가장 적었으며, 2014년에는 콩, 네마장황, 대파처리구에서 높았고, 호박처리구에서 가장 적어 이병주율과 유사한 경향을 보였다. 이상의 결과를 토대로 콩-마늘과 네마장황-마늘재배체계가 흑색썩음균핵병을 억제하기 위한 윤작체계가 될 수 있을 것으로 생각되었다.

To control the disease of root rot in ginseng nursery, inorganic sulfur solution of 0.1%, 1.0%, and 2.0% were irrigated by amount of 10ℓ per 3.3m2 before sowing. On the last ten days of July, Fusarium solani and F. oxysporum were similarly detected by 44.8% and 43.8%, respectively, while Cylindrocarpon destructans was low detected by 4.4% in the diseased seedling. The more sulfur's concentration was increased, the more soil pH was decreased. Soil pH was decreased from 5.87 to 4.59 by the irrigation of sulfur solution of 1.0%. The more sulfur's concentration was increased, the more electrical conductivity (EC) of soil was increased. EC was increased from 0.27 dS/m to 1.28 dS/m by the irrigation of sulfur solution of 1.0%. Irrigation of sulfur solution was effective on the inhibition of damping-off caused by Rhizoctonia solani in ginseng seedling. Control value for damping-off by the irrigation of sulfur solution of 1.0% and 2.0% were 75.7%, and 78.5%, respectively. Growth of leaf was inhibited by the irrigation of sulfur solution of 2.0%. Root weight per 3.3m2 showed the peak in sulfur solution of 1.0%, while survived-root ratio and root weight per plant were decreased in the level of 2.0%. Survived-root ratio of seedling in sulfur solution of 1.0% was distinctly increased by 4.7 times compare to the control, but control value for root rot was relatively low as 49.2%. Mycelium growth of C. destructans, F. solani, and R. solani were distinctly inhibited by the increase of sulfur's concentration in vitro culture using PDA medium.