All kinds of crops including foods, feeds and turf grasses are damaged frequently by various environmental stresses such as drought, salt, cold, and high temperature, which cause the loss of agronomic productivity. Plants cannot escape from environmental stresses. Thus, plants were evolving in the direction of overcoming environmental stresses. Some genes such as ARF, AB13, NAC, HSF, WRKY respond to environmental stresses have been reported in plants. The genes play a role in stress responses pathway of plants, the transcription factor in response to environmental stress. Typically OsWRKY76 increased the low temperature resistance, AtWRKY28 been reported to be related to the environmental stress. Zoysiagrass (Zoysia japonica Steud.) is used primarily useful for the garden or the golf course. But WRKY, environmental stress-related gene, is unknown in zoysiagrass. Here, we report the analyzing of WRKY genes and response by cold, dehydration and senescence stresses in zoysiagrass. Three WRKY gene (ZjWRKY3, ZjWRKY5, ZjWRKY7) cloning from zoysiagrass. It was transformed in arabidopsis and zoysiagrass. It will be a function analysis.

The effect of osmotic condition on β-glucuronidase (GUS) transient expression was evaluated in microspore-derived embryos of wheat. Microspore explants were treated on medium containing various mannitol concentrations prior to and post bombardment with plasmid DNA pAHC25 containing uidA gene controlled by maize ubiquitin 1 (UBI1) promoter. GUS expression in the bombarded explants was examined by histochemical and fluorometric assays. Increased GUS expression was observed with mannitol treatment when compared to untreated explants. The histochemical study showed that the number of blue (GUS) foci were the highest in the bombarded explants treated with 0.6 M mannitol medium. The fluorometric assay of bombarded explants also proved 3.5-fold increase in GUS activity with 0.6 M mannitol treatment when compared to without mannitol treatment. These results indicate that 0.6 M mannitol is beneficial for improving transformation efficiency of wheat microspore-derived embryos or embryogenic calli through biolistic transformation.