Background : Recently, there is an urgent demand for development of new varieties with enhanced resistance to various biotic/abiotic stresses. One generation of ginseng is four years, so it takes a long time to breed. To increase the efficiency of the ginseng breeding and save time and effort, it is necessary to build a ginseng core collection. This study examined the major growth characteristics of genetic sources for the establishment of core collection. Methods and Results : As plant materials, 187 ginseng lines collected in 2003 were used in this study. Ginseng Seeds were harvested at the end of July 2014, sown in mid-November, and cultivated in 2015 for one year in the field and then transplanted into the main field in 2016. All phenotypes including agronomic characteristics, seed yield, and physiological response to biotic/abiotic stresses were investigated according to the ginseng GAP and UPOV guidelines. The stem colors of the collected ginseng germplasm were classified as the five classes; light green, green, light purple, purple and dark purple, but most of them were purple or dark purple. The locations of distribution of anthocyanin coloration in stem were classified into the four classes; proximal end, proximal end and petiole part, the entire stem and the stem with purple not revealed, but most of them were petiole part or the entire stem. The shapes of leaflet were classified the four classes; the long elliptic, elliptic, slender type, and spatulate type. Most of surveyed lines were elliptic type. When the leaflet of ginseng was laterally cut, the shape was classified into the three types; concave type, plane type and convex type. Most of surveyed lines were red berry color. Conclusion : The genetic pool of ginseng is known to be narrow. The results of this study showed similar characteristics among the ginseng fields collected. In the future, we will carry out the survey about quantitative characteristics and correlations of ginseng genetic resources for establishment of Korean ginseng core collection.

Background : Endophytes are generally regarded as beneficial microorganisms that live in plant tissues without disease symptoms. The endophytic species may differ depending on the plant age, the sampled time, the plant genotype, and the tissue. Although numerous endophytes have been identified from various plants, little is known about the endophytic bacteria of Panax quinquefolius, a useful herb plant. Therefore, the aim of this study is to investigate diversity and distribution of endophytic bacteria from 2-years-old to 6-years-old P. quinquefolius and to evaluate antimicrobial activity of isolates. Methods and Results : Initially, 2-years-old to 6-years-old plants were collected and sterilized with 70% ethanol and sodium hypochlorite, subsequently we prepared individual suspensions which were mixed with sample and sterile distilled water. A total of 88 single colonies were obtained from the LB agar plates spreading suspension. Using 16S rDNA sequencing, the taxonomic status of the isolates were determined consequently 42 species were identified. The 42 species were classified into 4 phylum; Proteobacteria (64%), Firmicute (27%), Actinobacteria (8%), and Bacteroidetes (1%). Based on age, the isolates of 5-years-old plant showed highest diversity. Moreover, Actinomycetales, Bacillales, and Pseudomonadales were equally dispersed as predominant orders in 5-years-old plant. The antagonistic activities of isolates against a phytopathogen, Pseudomonas syringae pv. tomato DC3000 : GFP (Pst : GFP) were performed using dual culture assays. We measured antibacterial activity by quantifying fluorescence of Pst:GFP which representing pathogen growth. As a result, 36 isolates inhibited growth of Pst:GFP. Interestingly, all species belonging Pseudomonas in this study showed strong antibacterial activity against Pst : GFP. Conclusion : These results improve our understanding of the structure and diversity of the endophytic bacteria of P. quinquefolius. Furthermore, we suggest that bacterial endophytes with antimicrobial activity might have useful as materials for biocontrol agents.

Background : Ginseng (Panax ginseng C. A. Meyer) is a precious herb plant belonging to Araliaceae family especially in Asia and it has been cultivated more than a thousand years as a traditional medicine. Due to their pharmacological efficacy, old ginseng plants are traded high price, however, there are no crucial criteria to determine the ginseng age. To prevent illegal transactions, we assessed the telomere of ginseng roots based on modifications of the assays reported previously. Methods and Results : It is known that telomere length of ginseng root is shorter upon organismal aging. In this study, to support the determination of ginseng age, we modified and investigated methods through telomere analysis. Firstly, we examined the southern blot analysis whether telomere length depends on ginseng age. Based on previous study, we measured telomerase activity that is correlate with age. Furthermore, telomeric DNA was quantified by fluorescence in situ hybridization (FISH) to corroborate telomere shortening. The older ginseng root was shown short telomere length to compare with younger ginseng roots. Also enzyme activity of telomerase and amount of telomeric DNA represented decrease patterns upon age. Conclusion : Taken together, it is help to determine the age of ginseng through various methods using telomere because the results shown to positive correlation between telomeric characteristics and age for ginseng.

Background : The P. ginseng breeding line G07006, was selected for salt tolerance through salinity screening of mature leaves at the NIHHS of the RDA in 2014-2016. However, it is difficult to maintain a genetically stable breeding line of cross-pollinating crop in the field. Therefore molecular marker required to identify and maintain breeding line G07006. Methods and Results : DNA was extracted following the CTAB DNA extraction protocol (Doyle and Doyle, 1987) with modifications. A pair-end (PE) library was constructed and sequenced using an Illumina MiSeq platform by Lab Genomics, Inc. (Seongnam, Korea). Approximately 4.0 Gb of sequencing data were obtained, and de novo assembled by a CLC genome assembler(v. beta 4.6, CLC Inc., Rarhus, Denmark). The complete chloroplast(CP) genome size is 156,356 bp, including two inverted repeats (IRs) of 52,060 bp, separated by the large single-copy (LSC 86,174 bp) and small single-copy (SSC 18,122 bp) regions. This CP genome encodes 114 unigenes (80 protein-coding genes, four rRNA genes, and 30 tRNA genes), in which 18 are duplicated in the IR regions. Conclusion : This complete chloroplast DNA sequence will provide conducive to discriminate line G070006 (salt-tolerant) and further enhancing genetic improvement program of this important medical plant.