This study was carried out to develop new zoysiagrass (Zoysia japonica Steud.) cultivar ‘Halla Green 2’ (Grant number: No. 118). To develop a zoysiagrass cultivar with dwarfism by using the mutation breeding method, the wild type control "Gosan" plants were irradiated using a 30 Gy gamma ray source in 2010. Dwarf mutants were selected from the mutated grasses in successive generations. Dwarf mutant lines were identified and a new zoysiagrass variety Halla Green 2 was developed. The plant height of Halla Green 2 was 3.4 and 1.8 times lower than that of Gosan and Zenith, respectively. This cultivar has dwarf characteristics such as shorter sheath, shorter leaf blade, shorter flag leaf, and shorter third internode of stolon compared to those of Gosan and Zenith. Additionally, the sheaths and leaf blades color of Gosan, Zenith and Halla Green 2 were all light green, whereas their stolons were purple, yellow-green and yellow green, respectively. Trichomes(hairs) were visible on both adaxial and abaxial surfaces of the Gosan leaves, whereas only on the adaxial side of the Zenith and Halla Green 2 leaves. The Halla Green 2 grass showed distinguishable morphological traits compared to those of wild type Gosan and Zenith.

To develop a dwarf turfgrass (Zoysia japonica) cultivar with artificial mutation-induced breeding method, the wild type control "Gosan" plants were exposed to a 30 Gy gamma ray source in 2010. The mutant lines showing short height were selected from successive generations. One of the resulting dwarf lines obtained was registered under the cultivar name of “Halla Green 1” (2016). The dwarf phenotype of the Halla Green 1 includes a reduction of the height by 4.5-fold, an increase in leaf and third internode lengths by about 6- and 2.3-fold, respectively, compared to the Gosan, and approximately 2.4-, 3.8-, and 1.5-fold relative to the Zenith, respectively. In addition, the Halla Green 1 had a sheath of darker green coloring compared to the light green Gosan and Zenith. The leaf blades of Gosan, Zenith and Halla Green 1 were all light green, whereas their stolons were purple, yellow-green and light purple, respectively. Trichomes presented on both adaxial and abaxial surfaces of the Gosan’s leaves, and only on the adaxial side of the Zenith’s leaves, but none on the Halla Green 1 leaves. The Halla Green 1 exhibited sufficiently distinct morphological traits when compared with the wild type Gosan and Zenith that the dwarf phenotype enhances its commercial viability.

Zoysiagrass are damaged by fungi diseases such as large patch, dollar spot, pythium blight and brown patch. Large patch is one of the major diseases caused by Rhizoctonia solani AG2-2 on zoysiagrass fields e.g. golf courses. Plant chitinases have been known PR (Pathogen related)-protein. In this study, we isolated two chitinase genes (Zjchi1 and Zjchi2) from zoysiagrass. Antifungal activity analysis revealed that Zjchi2 protein inhibited mycelium extension of fungi. A further study, we cloned 5` upstream region from two chitinase genes for investigating transcription regulatory mechanism that inducing of two chitinase genes dependent R. solani. -818 bp and -799 of upstream region from Zjchi1 and Zjchi2 successfully isolated using in vitro LA (Long and Accurate) PCR system. And then, we generated promoter-GUS reporter constructs with deletion construct based on W-boxes. Constructs were introduced into Arabidopsis thaliana by Agrobacterium-mediated transformation for stable expression of GUS reporter gene.

With the purpose of improving ginsenoside production in Korean wild ginseng (Panax ginseng Meyer) mutant adventitious root lines, a synthetic gene encoding squalene synthase (PgSS2) was placed under the control of 35S promoter and transferred to Panax ginseng. Embryogenic callus obtained from ginseng adventitious root lines were transformed by infection with A. tumefaciens strain EHA105 containing the PgSS2 gene. Ten phosphinothricin-resistant plants were generated on selection medium, and the transgene integration and expression in these plants were confirmed by PAT test strip, RT-PCR and Southern hybridization. Ginsenoside analysis by HPLC revealed that the total contents of the 8 ginsenoside types (Rg1, Re, Rf, Rh1, Rb1, Rc, Rb2, Rd) in transgenic adventitious root lines were about 1.6-fold higher than that of the mutant control line (MCL1). This transformation method may facilitate the improvement of Panax ginseng in terms of the accumulation levels of ginsenoside.