Beet armyworm, Spodoptera exigua are difficult to control using chemical insecticides because of the development of insecticide resistance. For eco-friendly beet armyworm managements, various control agents are required. Entomopathogenic fungus is one of promise control agents as an alternative to chemcal control agent. We conducted bioassays with entomopathogenic fungi to select high virulence isolate to larva of beet armyworm. The bioassay was used 150 entomopathogenic fungal isolates which were isolated from soil samples of nine provinces by insect-bait method using Galleria mellonella and Tenebrio molitor. . Three isolates, Metarhizium spp. FT83, FT89 and FT90 had high virulence as 84.6%, 100% and 100%, respectively, against S. exigua. The medial lethal time(LT50) of conidia of three isolates was 5.01, 2.99 and 2.92days respectively.

Bemisia tabaci, sweetpotato whitefly, has been recognized one of the most destructive insect pests worldwide because of increased resistance to some insecticide groups requiring alternative strategies for its control. We conducted a study of the influence of relative humidity, temperature and different developmental stages on the susceptibility of sweetpotato whitefly to conidia of Isaria javanica isolate, which had been reported high virulence against Q biotype of B. tabaci. The mortality of tobacco whitefly was low at low constant relative humidities, but was high when kept high humidity for first 24 hours and transferred to low humidity. The Isaria isolate had wide range of temperature (15℃ to 35℃) to control sweetpotato whitefly. The isolate has virulence to the egg and all developmental stages of nymph of B. tabaci. These results indicated that the isolate had good control effects at various environmental conditions and is an excellent candidate to develop a microbial pesticide to control sweetpotato whitefly.

Sweetpotato whitefly (Bemisia tabaci), especially Q biotype, has been recognized one of the most destructive insect pests worldwide because of increased resistance to some insecticide groups requiring alternative strategies for its control. We studied the conidia production of entomopathogenic fungus Isaria javanica Pf04, which had been reported high virulence isolate against Q biotype of B. tabaci, using grain. Brown rice was most suitable for conidia mass production of the isolate of I. javanica. Conidia was produced high at 25 ~ 27.5℃. The isolate produced more spores when conidia suspension directly inoculated onto media than two-phase fermentation. When concentration of inoculum was high spore production was high, but increasing rate of conidia production was highest at low inoculum concentration (1×105 conidia/ml) as 6,700 times increase compared with 20 times increase at high inoculum concentration (1×108 conidia/ml). These results indicated that the isolate can produce more conidia with cheap agricultural product and can develop as a microbial pesticide to control sweetpotato whitefly.

To collect entomopathogenic fungi we sampled soils from two different cultural types of farm which are conducting conventional culture and organic culture, and non-crop land. Forty-seven soil samples were collected from 9 provinces. Among them, 7 samples were collected from non-crop land, 6 samples were from organic farm and 34 samples were from conventional culture farm. Insect-bait method using Galleria mellonella and agar plating method were conducted to collect entomopathogenic fungi. Collection of entomopathogenic fungi using insect-bait method was highest in non-crop land as 7.1 mycotic cadavers per soil sample followed by organic farm with 3.6 and conventional farm with 3.3. Result from agar plating method showed the highest colony forming unit (cfu) was in organic farm followed by non-crop land, but cfu in conventional cultivating farm was a half compared with the non-crop land.

The influenza virus is an important respiratory risk affecting humans, and effective treatments are needed. Some oriental medicines are currently applied for treatment of common colds as well as influenza infection. Previous studies have reported that the therapeutic properties of MA-128 are effective for treatment of psoriasis antiasthmatic and atopic dermatitis. In this study, we investigated the therapeutic properties of the novel herbal medicine, MA-128, for treatment of influenza virus infection by oral administration. MA-128 is an active natural biological compound from herbal-marine origin. The results showed that oral administration of MA-128 in mice could confer a survival benefit against Type A influenza virus infection. Daily oral administration of MA-128 resulted in delayed death in infected mice for three days against mouse adapted H3N2 (A/Philippines/2/82). However, it protected more than 60% of mice from lethal infection of 2009 pandemic H1N1 (A/Korea/CJ01/2009) influenza virus. In addition, lung viral titers were significantly reduced at seven days post infection (~100 times) compared with mock-treated mice and viruses were cleared at 9 dpi only in the MA-128 treated groups. This study demonstrated the potential of the novel herbal medicine, MA-128, as an herbal remedy against influenza A viruses.

The objective of this study was to determine the effect of macrophages on growth of human colon cancer cells. The results showed that co-culture of colon cancer cells with macrophages inhibited the growth of colon cancer cells (HCT116 and SW620) depending on the number of macrophages, RAW 264.7 cells, and activated THP-1 cells accompanied by down regulation of pSTAT3 in cancer cells. We also found that expression and release of cancer cell growth inhibitory cytokines, IL-1 receptor antagonist (IL-1ra) and IL-10, was increased in macrophages. Blocking of the STAT3 pathway with specific inhibitor and siRNA of STAT3 abolished the growth of colon cancer cells and expression of IL-1ra and IL-10. In addition, neutralization of IL-1ra and IL-10 with antibodies resulted in reversal of macrophage-induced inhibition of cancer cell growth. These data showed that IL-1ra and IL-10 released from macrophages inhibit growth of colon cancer cells through inhibition of the STAT3 pathway.

Field sequential 액정 디스플레이(FSLCD)는 컬러필터를 사용하지 않아 높은 투과율 특성을 보이고 광 원으로 LED를 사용함으로써 색재현성이 매우 우수하다. 하지만 FSLCD(60Hz 구동)를 실현하기 위해서는 액정의 응답속도가 5ms이하로 고속응답 특성을 보여야 한다. 따라서 본 논문에서는 고속응답 ECB(electrically controlled birefringence) 셀의 최적 구조를 연구하여 5ms 이하의 응답시간을 얻었다. 그리고 ECB 모드에서 높은 구동전압과 시야각을 개선하기 위해 필름 보상을 연구하였다. 판상형 액정필름(discotic film)과 TAC(triacetyl cellulose) 필름의 위상차 값을 최적화함으로써 구동전압을 5V로 낮추고 상하좌우에서 160° 이상(CR>10:1)의 시야각을 실현하였다.

Backgoound : This study was conducted to serve as a basis for the selection of superior lines by analyzing the content of antioxidant component and antioxidant activity in Schisandra chinensis Collections Methods and Results : In order to examine antioxidant component and antioxidant activity, 154 species of Schisandra chinensis from whole country were used. Antioxidant component was investigated by total flavonoid content and total phenolic content and antioxidant activity was evaluated by DPPH radical scavenging activity and ABTS radical scavenging activity. As a result, the total amounts of flavonoids was highest in SC-20 with 5.03 ㎎/g. However the content of polyphenols showed highest in SC-22 with 2.76 ㎎/g. In addition antioxidant activity results were also relatively high in SC-22. The IC50 value was 548 ㎍/㎖ in DPPH radical scavenging and 640 ㎍/㎖. in ABTS+ radical scavenging. Conclusion : As demand for high income crop has increased, new cultivar breeding is required to produce high quality Schisandra chinensis From this study, analyses of antioxidant component and antioxidant activity in collection can be used for new Schisandra chinensis breeding. Especially SC-22 can be superior lines with high antioxidant component and antioxidant activity.

In order to determine the short-term impact induced by chloride ionic, CaCl2 was used to study the chloride ionic effects of salinity on substrate and growth of Dracacena braunii grown in ornamental hydro-culture. A distilled water (control) was enriched with 10, 20, 50, 100, and 150 g･L -1 of CaCl2, respectively. Before planting, acidity and electronic conductivity values remarkably increased with increasing concentration of CaCl2. However, 4 weeks after planting, acidity values decreased to a slightly acidic pH, while there were not significant differences among electronic conductivity values obtained. Number of root, fresh weight, and total chlorophyll content were significantly decreased in response to CaCl2 concentration in comparison with control, whereas dry weight, water content, and color of stem were no significant effect of CaCl2 concentration less than 20 g･L -1 . These results showed that initial CaCl2 concentrations above 20 g･L -1 is considered to be the threshold value that will sustain the Dracacena braunii in the growth condition and above which plant growth will be retarded.

Background : Tooth vitality is reflected by the health of dental pulp. Schisandrin C is a natural compound extracted from the fruit of Schisandra chinensis which has anti-inflammatory and anti-oxidant properties. The role of Schisandrin C on human dental pulp cells (HDPCs) has not been studied yet. This study examined the properties of Schisandrin C as an anti-inflammatory and anti-oxidant compound, and whether its characteristics promote mitochondrial biogenesis in HDPCs. Methods and Results : HDPCs were extracted from fresh third molars and cultured. Reactive oxidative stress (ROS) and nitric oxide (NO) formation were analyzed by a Muse cell analyzer. Western blotting and gelatin zymography were used to identify the presence of anti-oxidants, as well as inflammatory and mitochondrial biogenesis. Confocal microscopy was used for the detection of mitochondrial activity. Schisandrin C inhibited lipopolysaccharide (LPS)-stimulated inflammatory molecules; intracellular adhesion molecule-1 (ICAM-1), vascular cell adhesion molecule-1 (VCAM-1), matrix metalloproteinase-2 and -9 (MMP-2/9), NO production, ROS formation and the mitogen-activated protein (MAPK) pathway through minimizing the nuclear factor kappa B (NF-kB) translocation. Schisandrin C increased the expression of superoxide dismutase (SOD) enzymes as well as heme oxygenase-1 (HO-1) and peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC-1a) through the phosphorylated-protein kinase B (p-AKT) and nuclear factor erythroid 2-related factor-2 (Nrf-2) pathways. The anti-inflammatory and anti-oxidant properties of Schisandrin C promoted mitochondrial biogenesis. Conclusions : These results suggest that Schisandrin C may be used as an anti-inflammatory compound to reduce oral inflammation such as pulpitis.