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Micropropagation of Atractylodes macrocephala Koidz. by Axillary Bud Culture
Mei Lan Jin(김미란),Yeon Bok Kim(김연복),Chinreddy Subramanyam Reddy(친레디 서부라만얌 레디),Jin Tae Jeong(정진태),Sang Hoon Lee(이상훈),Sung Cheol Koo(구성철),Mok Her(허목),Jae Ki Chang(장재기),Woo Moon Lee(이우문) 한국약용작물학회 2017 한국약용작물학회 학술대회논문집 Vol.2017 No.2
Mei Lan Jin,김청아,이상훈,허목,구성철,한종원,이우문 한국약용작물학회 2018 한국약용작물학술대회 발표집 Vol.2018 No.10
Background : Ligusticum chuanxiong Hort is a perennial herb of the Umbelliferae family and an important traditional oriental medicinal plant. The compounds contained in L. chuanxiong can be divided into five kinds, essential oil, alkaloids, phenolic acids, phthalide lactones, and other constituents. These compounds have cardiovascular and cerebrovascular effects, antioxidants, neuroprotection, anti-fibrinolytic, antidotes, anti-inflammatory and antitumor activities. In this study, we anticipated to establish the in vitro propagation system of L. chuanxiong, which is a high economic value as medicinal herb, by plant tissue culture to solve the problem of root stocks contamination. Methods and Results : The whole study was carried out in the department of Herbal crop research, Eumseong, RDA. In this study, L. chuanxiong nodes was used as an explant and it was surface sterilized by 2% sodium hypochlorite for 1 minutes, then washed with ddH2O several times. Further the surface sterilized nodes were placed on MS basal media. Multiple shoots were induced on MS, SH, WPM media with 0.1 - 2 ㎎/ℓ auxin (NAA, IBA) and cytokine (BA). In this study we obtained 4.6 multi-shoots per an explant, and growth of the shoot was also favorable in the presence of 1.0 ㎎/ℓ BA. Subsequent transfer of these regenerated shoots on 1/2 MS media resulted in root formation. The rooted plantlets were able to grow in soil after 3 weeks of acclimatization. Conclusion : The optimal conditions for in vitro propagation of L. chuanxiong were established through this experiment.
Mei Lan Jin,김청아,이상훈,허목,구성철,한종원,이우문 한국약용작물학회 2018 한국약용작물학술대회 발표집 Vol.2018 No.10
Background : Adenophora triphylla var japonica is a perennial herb that belongs to Campanulaceae. Radix Adenophorae is a dried rhizome of A. triphylla and same genus plant. It has contains chemicals such as cycloartenyl acetate, lupenone, β-sitosterol, taraxerone, octacosanoic acid, and praeruptorin A. Radix Adenophorae considered to be effective regulating humoral and cellular immunity, antimutation, restraining adenocarcinoma cell, strengthening cardiac function, allaying a fever, and easing pain and cough. In this study, we tried to establish a mass production system of A. triphylla which has high economic value as a medicinal herb by plant tissue culture in order to cultivate standard varieties. Methods and Results : In this study, A. triphylla internode was used as a explant and it was surface sterilized by 1% sodium hypochlorite for 5 minutes, consequently several times washed with ddH2O. Further it was placed in to MS medium including with axillary bud. The 1/2MS, B5, SH was used in this research. And the plant growth regulator of 0.1 - 2 ㎎/ℓ auxins (NAA, IBA) and cytokines (BA) were used respectively to achieve multiple shoots. The whole study was carried out in the department of Herbal crop research, Eumseong, RDA. Conclusion : In this study we obtained, 6.2 multi-shoots per an explant, and the shoot growth was also favorable in the presence of 1.0 ㎎/ℓ BA and 1.0 ㎎/ℓ IBA.
2015년 인삼재배지에서의 인삼뿌리썩음병원균의 분리동정 및 토양밀도검정
Mei Lan Jin,Kyeon Hun Park,Sung Woo Lee,Dong Yun Hyun,Seung Ho Lee 한국약용작물학회 2016 한국약용작물학술대회 발표집 Vol.2016 No.10
Background : Ginseng (Panax ginseng C.A. Meyer) is one of the most important medicinal plants in Korea, but its yields are often reduced by a variety of root pathogens. The root rot of ginseng is a destructive soil-borne disease caused by Cylindrocarpon destructans (teleomorph: Ilyonectria radicicola). To monitor contamination with C. destructans in ginseng harvested in 2015 were sampled from 57 different growing fields. The spore number of C. destructans was quantified by use of a specific primers and selective media (radicicol) in soils of ginseng fields. Methods and Results : The ginseng samples were surface-sterilized and placed on potato dextrose agar plates for 7 day incubation at 20℃. Emerging fungal colonies were counted primarily based on colony and conidia morphology. Further species level identification was confirmed by ITS rDNA sequencing. For quantification of the soil-borne C. destructans, the genomic DNA was extracted from the soil using a NucleoSpin soil kit (MN, Germany). Density of C. destructans was determined by species specific real time PCR (qPCR). The qPCR was completed by running a melting curve analysis. Conclusion : The C. destructans associated with root rot disease of ginseng were detected in more than 60% in pyeongtaek-1, pochenon-1, jecheon-1, chungju-1 and jinan-4. As results of the study, the correlation between pathogen density and identification clearly clarified in the soil.