생장조절물질과 광도가 국화 경정배양에 미치는 영향 을 조사하였다. 다신초(multiple shoots) 형성은 국화 경 정을 MS배지에 kinetin 2.0mg · L-1와 NAA 0.2mg · L-1 첨가된 배지에 배양하였을 때 촉진되었으며, 형성된 다 신초는 MS배지에 kinetin 2.0mg · L-1와 NAA 0.02 mg · L-1 첨가된 배지에 배양하였을 때 생육이 촉진되었 다. 한편, 국화 경정을 NAA 0.2mg·L-1와 BA 1.0mg · L- 1가 첨가된 배지에 배양하였을 경우에는 절편체당 신초 형성 수가 6.9개로 가장 많았으나 형성된 신초의 대부분 이 유리질화 되었다. 기내에서 국화묘의 생장은 광도 100 μmol · m-2 · s-1 PPFD에서 신초의 길이와 엽록소 함량이 가장 높았다.

To understand molecular mechanisms underlying adaptation of plant cells to saline stress and stress memory, we developed Arabidopsis callus suspension-cultured cells adapted to high salt. Adapted cells to high salt exhibited enhanced tolerance compared to control cells. Moreover, the salt tolerance of adapted cells was stably maintained even after the stress is relieved, indicating that the salt tolerance of adapted cells was memorized. Salt-adapted and stress memorized cells were densely aggregated and formed multi-layered cell lump. Cell morphology analysis using transmission electron microscopy indicated that cell wall thickness of salt-adapted cells was significantly induced compared to control cells. In order to characterize metabolic responses of plant cells during adaptation to high salt stress as well as stress memory, we compared metabolic profiles of salt-adapted and stress-memorized cells with control cells by using NMR spectroscopy. A principle component analysis showed clear metabolic discrimination among control, salt-adapted and stress-memorized cells. Compared with control cells, metabolites related to shikimate metabolism such as tyrosine, and flavonol glycosides, which are related to protective mechanism of plant against stresses were largely up-regulated in adapted cell lines. Moreover, coniferin, a precursor of lignin, was more abundant in salt-adapted cells than control cells. The results provide new insight into metabolic level mechanisms of plant adaptation to saline stress as well as stress memory.

To identify novel signaling components involved in regulation of plant responses to phosphate (Pi) starvation, we screened an Arabidopsis T-DNA activation tagging library for mutants with altered Pi-starvation responses. Here, we report the identification and characterization of novel activation-tagged mutant involved in Pi starvation signaling in Arabidopsis. The hpd (hypersensitive to Pi deficiency) mutant exhibits enhanced phosphate uptake and altered root architectural change under Pi starvation compared to wild type. Expression analysis of auxin-responsive DR5::GUS reporter gene in hpd mutant indicated that both auxin biosynthesis and auxin translocation under Pi starvation are suppressed in hpd mutant plants. Impaired auxin translocation in roots of hpd mutant was attributable to abnormal root architecture changes in Pi starvation conditions. Mis-regulation of auxin translocation in hpd mutant was further confirmed by analysis of expression patterns of auxin efflux carrier proteins, PIN-FORMED (PIN) 1, 2, and 3 fused with GFP. Not only expression levels but also expression domains of PIN proteins were altered in hpd mutant in response to Pi starvation. Molecular genetic analysis of hpd mutant revealed that the mutant phenotype is caused by the lesion in ENHANCED SILENCING PHENOTYPE4 (ESP4) gene whose function is proposed in mRNA 3’-end processing. The results propose that mRNA processing plays crucial roles in Pi homeostasis as well as developmental reprograming in response to Pi deprivation in Arabidopsis.

In order to determine the optimum harvest time for the seed production of inbreds and hybrids in silage corn, the ears of sib-pollinated 'KS5', 'KS7rhm', and 'Ga209' and cross-pollinated 'KS5' ~times 'KS6' (Suwon19), 'KS7 rhm' ~times 'KSl17' (Suwonok), and 'Ga209' ~times 'DB544'(Kwanganok) were harvested at the one-week intervals from 4 to 10 weeks after silking. The optimum harvest time for the seed production for 'KS5', 'KS5' ~times 'KS6', 'KS7 rhm', and 'KS7rhm' ~times 'KS117' was 7 weeks after silking considering both emergence rate and plumule growth in cold test. Although earlier harvested seeds showed similar germination rate as the seeds harvested at the optimum time at 25~circC , their emergence rate were lower in cold test. Seed weight and α -amylase activity of earlier harvested seeds were lower compared to those of seeds harvested at the optimum time, while leakage of total sugars and electrolytes were higher. However, the later harvested seeds showed lower germination rates at 25~circC and emergence rates in cold test probably due to the lower α -amylase activity although they showed increased seed weight and reduced leakage of total sugars and electrolytes. In contrast, the emergence rate of 'Ga209' and 'Ga209' ~times 'DB544' in cold test increased up to 10 weeks after silking probably due to the increased seed weight and α -amylase activity and reduced sugar and electrolyte leakages during the germination. The cross-pollinated F1 hybrid seeds showed higher germination and emergence rates at 25~circC and in cold test, and higher plumule growth and α -amylase activity compared to those of sib-pollinated inbreds.