In this study, the antioxidative activity of Jeolpyun containing S. glauca (Bunge) Bunge powder (2%, 4%, 6%, and 8%) and extract (2%, 4%, 6%, and 8%) was evaluated based on the total polyphenol contents, electron-donating ability, scavenging of superoxide anion radical, and decomposition of hydrogen peroxide. Total polyphenol contents of Jeolpyun containing 8% S. glauca (Bunge) Bunge powder were the highest with a value of 2,280±0.00 μg GAE/mL. It was observed that total polyphenol content exhibited a significant relation with concentrations at p<0.05. The electron-donating ability of Jeolpyun containing 8% S. glauca (Bunge) Bunge extract was the highest with a value of 83.93±0.69%. The electron-donating abilities revealed significant differences between concentrations (p<0.05). The superoxide radical scavenging ability of the blank was 0.01523±0.00068 and Jeolpyun containing 6% S. glauca (Bunge) Bunge powder was the highest with a value of 0.00977±0.00842. The hydrogen peroxide decomposing ability of Jeolpyun containing 0% S. glauca (Bunge) Bunge powder was －0.00377±0.0049; 8% S. glauca (Bunge) Bunge powder revealed the highest decomposing ability of －0.0476±0.0234. Hydrogen peroxide decomposing abilities revealed significant differences between concentrations (p<0.05). Jeolpyun containing S. glauca (Bunge) Bunge powder and extract demonstrated improved antioxidative activities.

In this study, S. glauca (Bunge) Bunge extract was testified total polyphenol contents, electron donating ability on DPPH, and scavenging ability of superoxide anion radical and hydrogen peroxide. Total polyphenol contents of S. glauca (Bunge) Bunge extract were 7,053.30±915.93 μg GAE/mL. In the fractions, fraction by ethanol was the highest content of 10,973.30±1,000.24 μg GAE/mL. Fractions of ethyl acetate and water were 2,386.70±166.53 μg GAE/mL, 2,413.30±41.63 μg GAE/mL respectively. It was shown that total content of polyphenol according to solvent was significant relation at p<0.05. In the experiment of the electron donating ability, 70% ethanol extract and methylene chloride fraction were －246.15±24.17%, －254.01± 16.54% respectively. In case of ethyl acetate fraction, it was the highest electron donating ability to DPPH radical, 39.06±0.34%, and then water fraction of 36.71±5.55%, ethanol fraction of 29.77±2.57%, gradually. Electron donating abilities revealed significant difference (p<0.05) between the solvents. The superoxide radical scavenging ability of standard material was 0.029±0.0011; 70% ethanol extract of 0.022±0.00052, methylene chloride fraction of 0.027±0.00031, ethyl acetate fraction of 0.024±0.0011, ethanol fraction of 0.021±0.00024 and water fraction of 0.024±0.00019. Hydrogen peroxide scavenging ability of 70% ethanol extract was －0.0029±0.00040 and the others were as follow; methylene chloride fraction (－0.0042±0.00058), ethyl acetate fraction (－0.003± 0.0041), ethanol fraction (－0.0029±0.0015) and water fraction (－0.0028±0.00090).

생대추가 신소득 작목으로 부각되면서 재배지가 확대되고 있으나 우리나라 장마기와 최근 이상기후로 인해 대추 수분·수정 및 착과에 문제 가 발생하고 있는 실정이다. 이에 생대추 재배를 위해 도입된 비가림하우스에서 서양종 꿀벌과 서양뒤영벌을 이용하여 화분매개곤충의 활동 특성 과 착과 효율에 어떠한 영향을 미치는지 구명하고자 본 시험을 수행하였다. 대추 복조 품종을 대상으로 비가림하우스에 망실을 씌워 서양종 꿀벌 과 서양뒤영벌을 2016년 6월 1일부터 7월 25일까지 약 55일정도 방사하였다. 서양종 꿀벌은 주로 오후에 활동이 많았으나 서양뒤영벌의 활동은 시간에 관계없이 다소 균일하였다. 대추 신초 가지의 착과율을 조사한 결과 방화곤충을 차단한 무처리 5.5% 대비 서양종 꿀벌은 10.2%, 서양뒤 영벌은 8.9%로 대추 비가림하우스내 화분매개곤충 활용시 착과량 증진으로 농가 소득증대에 기여할 것으로 생각된다.

In this study, the sensory and mechanical characteristics of white bread containing different levels of Korean and Chinese sansa powder were evaluated. Korean sansa was smaller and more reddish than that of Chinese sansa. Sansa powder contained ursolic acid, citric acids, and flavonoids, which have antioxidative effects. Contents of total flavonoids in Korean and Chinese sansa powder were 217.67±7.64 mg/100 g and 127.67±7.85 mg/100 g, respectively. The mechanical and sensory characteristics of bread added with different levels (0, 2, 4, and 6%) of Korean and Chinese sansa powder were evaluated. Lightness of crust and crumb of bread containing Korean sansa powder decreased as the level of Korean sansa powder increased, whereas they increased as the level of Chinese sansa powder increased. Mechanical texture parameters such as hardness and gumminess increased as the level of Korean and Chinese of sansa powder increased. In a sensory evaluation, control, bread containing 2 or 4% Korean sansa powder, and bread containing 2% Chinese sansa powder showed higher overall acceptability than the others. In conclusion, these results indicate that the recommended substitution level for sansa powder in bread is 2 or 4% Korean sansa powder and 2% Chinese sansa powder.

Extraction of Sedum sarmentosum Bunge by super critical carbon dioxide was operated under 40-50℃and 200-250 atm, thus, yield of extraction was very low as 4 wt%. Rats were administrated with the extract orally once a day for succesive 6 days, followed by treatment with carbon tetrachloride (CCl4) on the sixth day. The activities of aminotransferase, alkaline phosphatase, γ-glutamyl transpeptidase, lactate dehydrogenase and contents of triglyceride, total cholesterol in the extract-pretreated rats were decreased compared to the CCl4controled rats, whereas content of HDL-cholesterol was increased. Especially content of hepatic malondialdehyde (MDA) and atherogenic index (AI) were decreased and HTR was increased in the extract-pretreated rats, and reduced peroxidative liver damage in the CCl4-induced hepatotoxicity rats. In addition, activities of hepatic superoxide dismutase, catalase, glutathione peroxidase in the extract-pretreated rats were significantly decreased compared to the CCl4 controled rats, but the content of glutathione was significantly increased. These results suggest that extract of Sedum sarmentosum Bunge has hepatoprotective effect in the CCl4-intoxicated rats.

Background : The isoflavonoids, triterpene and polysaccharides were know as major components in Astragalus membranaceus Bunge. Especially, isoflavonoids are classified as ononin, calycosin-glucoside of glycon binding and formononetin, calycosin of aglycone binding. In this study, we performed fermentation by a lot of microorganisms which were derived foods. Methods and Results : The A. membranaceus was extracted with 50% Ethanol and it was concentrated using rotary evaporator. In order to change in isoflavonoids, we fermented the A. membranaceus extracts with microorganisms which have β-glucosidase activity. we chose 20 microorganisms using esculin agar method and three strains with the highest activity of β -glucosidase were identified by pNP assay. The extracts of A. membranaceus were fermented during 3 days in sterilized distilled water, as 1 Brix and 3 Brix. The isoflavonoids of fermented extract, respectively days 0, 1, 2 and 3, were analyzed using High Pressure Liquid Chromatography (HPLC). In addition, the fermented A. membranaceus extracts was investigated about whitening effect using tyrosinase and radical scavenging activity by 1,1-diphenyl-2-picrylhydrazyl radical (DPPH). As a result of β-glucosidase activity by pNP assay, we selected two strains, Pediococcus pentosaceus (KACC 81017BP), Saccharomyces cerevisiae (KACC 83014BP). On the third day of fermentation of S. cerevisiae, isoflavone aglycone was the highest. The calycosin-glucoside and ononin in fermented A. membranaceus extract were reduced, calycosin and formononetin was increased compared to control. Also, we confirmed higher activity than control in tyrosinase inhibition rate on the third day of fermentation, as 78.38% and lower IC50 value of radical scavenging activity as 584.68 ㎍/㎖. Conclusion : From the above results, we may suggest that A. membranaceus aboveground parts might have useful as a safe material for functional food and pharmaceutics.

Background : The major components in Astragalus membranaceus are isoflavonoids, triterpene and polysaccharides. Also, isoflavonoids was composed to aglycon and glucoside derivatives. In this study, we performed fermentation process (enzyme treatment) and steam processing (high temperature and pressure) to increase aglycon such as formononetin and calycosin. Methods and Results : The steam processing was performed at a lot of conditions, such as temperature (80, 100, 120℃) and time (30, 60 and 120 min). Fermentation processing carried out by A. membranaceus extract fermented with microorganisms which have high β -glucosidase activity (selection by esculin agar method) for detached glucose from isoflavonoids, converted to algycon. The isoflavonoids were analyzed using high pressure liquid chromatography (HPLC) in fermentation product of A. membranaceu extract by treated with steam processing at various conditions. As a result of β-glucosidase activity by pNP assay, we selected three strains, Pediococcus pentosaceus, Weissella cibaria and Saccharomyces cerevisiae. Isoflavone aglycon was the highest in fermentation product by S. cerevisiae for 3 days, but change of isoflavonoids was not observed in steam processing. The calycosin-glucoside and ononin were reduced in fermentation product of A. membranaceus extract, whereas calycosin and formononetin was increased. Conclusion : This results showed that isoflavone glycoside converted to isoflavone aglycon in A. membranaceus by fermentation process, it seems to be available for industrial use.

Background : Anemarrhena asphodeloides Bunge is herbaceous perennial plant used for medicine with tuber root. This experiment was conducted to establish proper drying method of Anemarrhena asphodeloides for GAP post-harvest management manual. Methods and Results : Anemarrhena asphodeloides radix was cut in 3mm thickness after washing. Drying methods were air curing, sun drying, and hot-air drying (45℃, 50℃, 55℃, 60℃). Dry matter ratio (DMR) and moisture content (MC) were checked for every 12 hours for air curing and sun drying and checked for every 2 hours for hot-air drying. In 6 hours hot air drying at 45℃ and 50℃, DMR and MC were 39.9%, 38.4% and 13.5%, 12.8% respectively. In 4 hours hot air drying at 60℃, DMR and MC were 38.0% and 13.6% respectively. In air curing and sun drying for 4 days, DMR and MC were 37.0%, 37.6% and 12.3%, 13.1% respectively. Color value according to drying methods was higher as 74.57 in ℓ value under 50℃ hot air drying and lower as 65.35 under air-curing. a value was higher as 3.50 under air-curing and lower as 0.47 under 50℃ hot air drying. Conclusion : In 6 hours hot air drying at 50℃, MC was 12.8% and color value was higher as 74.57 in ℓ value and lower as 0.47and 22.59 in a value and b value respectively. This result showed that hot air drying for 6 hours at 50℃ was more proper for Anemarrhena asphodeloides radix drying.

To evaluate the protective effect of Ajuga multiflora BUNGE (AMB) extract on the toxicity of lead acetate (LA), environmental pollutant, cell viability was measured by XTT assay using cultured NIH3T3 fibroblasts. And also, the effect of antioxidant, butylated hydroxytoluene (BHT) on LA-induced cytotoxicity was analysed. For the protective effect of AMB extract on LA-induced cytotoxicity, NIH3T3 fibroblasts were pretreated with 80 or 90 μg/mL of AMB extract for 2 hours before the treatment of LA. And also, the antioxidative effects of AMB extract against LA-induced cytotoxicity were assessed by DPPH-radical scavenging activity, superoxide dismutase (SOD)-like activity and inhibitory activity of lipid peroxidation (LP). In this study, LA significantly decreased cell viability dose-dependently compared with control, and then XTT50 value was determined at 46.1 μM of LA. In the effect of BHT against LA-induced cytotoxicity, it effectively prevented toxic effect of LA by the significant increase of cell viability. In the protective effect of AMB extract on LA-induced cytotoxicity, it significantly increased cell viability which was decreased by LA-induced cytotoxicity, and also it showed the antioxidative effects such as DPPH-radical scavenging activity, SOD-like activity and inhibitory activity of LP. From these results, it is suggested that the cytotoxicity of LA is involved in oxidative stress, and AMB extract effectively prevented the cytotoxicity induced by LA via an antioxidative effect. Conclusively, the natural substance such as AMB extract may be alternative resources for the prevention or treatment of diseases related with oxidative stress.

Background: This study were performed to determine the effect of root pruning of Zizyphus jujuba var. inermis (Bunge) Rehder. Root cutting inhibit vegetative growth and promote reproductive growth as temporarily reducing growth, net assimilation, water potential of leaf and cytokinin level. Methods and Results: The root pruning was treated of the root cutting widths 50, and 80㎝ and the root cutting depths 10, and 20㎝. The amount of root pruning and the number of suckers were the highest in the root-pruning treatment at a width of 50㎝ and a depth of 20㎝. The blooming time was from June 18 to 20, and no difference was observed in the blooming time among the rootpruning treatments. The number of flowers was rather higher in the root-pruning treatment at a width of 50㎝ and a depth of 20㎝ and at a width of 80㎝ and a depth of 20㎝. The percentage of fruit setting was higher in the plants whose roots were pruned at a depth of 20㎝ than in the untreated plants. The fruit size, fruit weight, and sugar content showed no difference among the root-pruning treatments. Conclusions: The results showed that percentage of fruit setting increased with root pruning, while no difference was observed in the growth and fruit quality of plants.

Salvia miltiorrhiza has been used for treating heart and liver disease. In the present study, the influences of temperature on photosynthetical capacity of S. miltiorrhiza under controlled cultivation environment using growth chamber were investigated because of providing information about growth and secondary metabolite synthesis. And effect of harvesting time on growth properties and constituents such as salvianolic acid B, cryptotanshinone, tanshinone I, tanshinone IIA were evaluated. Maximum photosynthesis rate (5.102 μmol CO2/m2/s) and net apparent quantum yield (0.147 μmol CO2/m2/s), stomatal conductance (0.035 mmol/m2/s) and water use efficiency (7.108 μmol CO2/mmol H2O) was highest at 20℃. Results of chlorophyll fluorescence showed that elevated temperature had contributed to reduce a quantum yield and electron flux in photosystem. This result demonstrated that favorable temperature condition was determined at 20℃. Contents of salvianolic acid B, cryptotanshinone, tanshinone I and tanshinone IIA was highest in root sample harvested at 20 March, whereas growth and yield of S. miltiorrhiza had no significant differences with harvesting time. Therefore, this study shows that temperature play an important role in photosynthetic activity and harvesting time have influence upon accumulation of constituents in root of S. miltiorrhiza.

본 연구는 국내산 단삼을 활용하여 amylase계, cellulase 계, pectinase계 및 protease계 효소제를 이용한 저온 추출법 에 따른 단삼 추출물의 이화학적 품질 변화를 조사하였다. 단삼 추출물의 수율, pH, 당도 및 색도 변화는 amylase계 효소를 이용하여 60℃, 4시간 처리구에서 58.3%, pH 6.04, 5.97°Brix와 65.06(L) 및 35.13(b)로 가장 높게 나타났으며, a값은 protease계 효소를 이용하여 60℃에서 처리구에서 14.88로 붉은색을 나타내었다. 효소제를 이용한 단삼 추출 물의 항산화능은 추출농도 55 ppm에서 DPPH 및 ABTs 소거능 84.25 및 74.11%로 amylase계 효소를 이용하여 6 0℃, 4시간 처리구에서 가장 높은 소거능을 나타내었다. 총 페놀성 화합물 함량은 60℃효소 처리구간들에서 비교적 높은 함량을 나타내었다. 단삼 추출물의 salvianolic acid B 함량은 60℃에서 4시간, amylase계 효소구에서 3,002 mg%로 가장 높은 함량을 나타내었으며, cryptotanshinone 함량은 60℃ 4시간 amylase 및 protease계 효소 처리구에서 3.8 mg%으로 가장 높게 나타났으며, tanshinon Ⅰ함량은 60℃ 4시간 protease계 효소구에서 14.2 mg%으로 가장 높게 나타났다. 이상의 결과로 amylase계 효소를 이용하여 단삼 의 저온 효소 추출시 단삼 추출물의 지표성분의 안정적 추출이 가능한 바, 기능성 소재로서 대량생산을 통한 산업 적 이용이 가능할 것으로 판단되며, 효소제를 이용한 저온 효소추출법은 천연물의 다양한 원료에 접목시킬 수 있을 것으로 생각된다.

Background : This study examined the effect of harvesting time on the growth, yield characteristics, and major beneficial components in Salvia miltiorrhiza. Methods and Results : Although plant height, stem diameter and branch length were not affected by harvesting time, the number of stems was highest when harvested in mid October. There were no differences in root length and thickness, however, the rhizome was thicker when it was harvested at the end of October or early November than when it was harvested in early and mid October. The dried root weight also showed a similar pattern. However, there was a statistically significant increase to 408 ㎏ (16%) in the rhizome weight when in late October and a rise to 455 ㎏ (29%) when harvested in early November. Harvest time had little effect on the content of the major component of S. miltiorrhiza. For example, salvianolic acid content rose from 9.42 to 9.64% with later harvest times, and tanshinone ΠA content was tended to be slightly more increased in mid October which S. miltiorrhiza has 0.22% tanshinon ΠA than in early October. Conclusions : According to these results, the optimum harvest time for S. miltiorrhiza is early November when plant or major component yields are hightest. There were no significant harvest time effects on the major beneficial components.