• Korean Journal of Food Science and Technology
• /
• v.37 no.5
• /
• pp.833-837
• /
• 2005

Antioxidative activities of pine, oak, and lily pollen extracts were evaluated based on 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical-scavenging ability and inhibition of lipid peroxidation in animal tissues. Each pollen was extracted with 50% ethanol, 100% ethanol or water. DPPH radical-scavenging capacity of 50% ethanol extract ($EC_{50}$ 40.0 mg/mL) of pine pollen was higher than those of water (46.8 mg/mL) and 100% ethanol (131.2 mg/mL) extracts of pollen. Fifty percent ethanol (3,2 mg/mL) was also better than 100% ethanol (4.5 mg/mL) and water (8.3 mg/mL) for extraction of oak pollen. For preparation of lily pollen extracts, 100% ethanol was most effective (14.0 mg/mL), followed by water (18.8 mg/mL) and 50% ethanol (24.0 mg/mL). Oak pollen showed higher DPPH radical-scavenging activity than others. Lipid peroxidation in rat brain homogenate induced by ascorbate-Fe3+-EDTA and rat kidney homogenate were inhibited by water extracts of all pollens in dose-dependent manner. Extracts of oak and lily pollen showed higher lipid peroxidation inhibition than pine pollen extract. Polyphenol content was highest in oak pollen extract $(32.5{\pm}0.7\;{\mu}g/mg\;pollen)$, followed by lily extract $(25.9{\pm}1.4\;{\mu}g/mg\;pollen)$ and pine extract $(9.3{\pm}0.7\;{\mu}g/mg\;pollen)$.

• KSBB Journal
• /
• v.14 no.4
• /
• pp.445-451
• /
• 1999

Glutathione production was carried out using mixed cells of E. coli TG1/pDG7 $\alpha$ and bakers yeast in an Aerated Slurry Bioreactor. Glutathione-producing enzymes were stable for 34 hours, yielding 4.6 mM glutathione in suspension reaction. Glutahione production with high density mixed cells was studied as a function of flow rate in an Aereated Slurry Bioreactor. Glutathione concentration was higher than that in suspension reaction for 32 hours at the substrate feeding rate of 5.2 mL/hr with cell recycle in continuous Aerated Slurry Bioreactor. It was for 42 hours at 2.6 mL/hr and 22 hours at 5.2 mL/hr without cell recycle. Glutahione productivity was 25.7 mg/g wet $cell{\cdot}hr$ at the substrate feeding rate of 10.4 mL/hr with cell recycle, but 5.28 mg/g wet $cell{\cdot}hr$ at 5.2 mL/hr and 1.65 mg/g wet $cell{\cdot}hr$ at 2.6 mL/hr without cell recycle. Effective production time increased from 25 to 45 hours, by using a surfactant, tween 80. As a purfing gas, nitrogen was tested instead of air to avoid a possible oxidizing effect on glutathione-producing enzymes, resulting in the increase of effective production time to 40 hours.

• Korean Journal of Microbiology
• /
• v.38 no.4
• /
• pp.312-317
• /
• 2002

Erythritol is of interest as a low calorie sweetner. Penicillium sp. KJ8l was screened for erythritol producer in nature. The effect of culture conditions on erythritol production by Penicillium sp. KJ81 was examined. This strain produced about 12 g/l erythritol and a small amout of glycerol. Erythritol was not produced from mannitol, arabinose, sorbitol, and xylose but from glucose, sucrose, fructose, mannose, lactose, maltose, and galactose. This strain was able to produce erythritol in a medium containing 60% sucrose but demonstrated the highest productivity of erythritol in a 30% sucrose medium. The highest yield in Penicillium sp. KJ8l was obtained when 0.5% ammonium sulfate was added to the medium containing 30% sucrose and 0.5% yeast extract. Penicillium sp. KJ81 produced 28.2 g/l erythritol when this strain was cultured in the medium containing 30% sucrose, 0.5% yeast extract, 0.5%$(NH_{4})_{2}SO_{4}$ 0.1% $KH_{2}PO_{4}$ and 0.01% $MgCl_{2}$ under the condition of 1 vvm aeration and 200 rpm agitation at $37^{\circ}C$ for 10 days in 5ι jar fermentor.

• Korean Journal of Clinical Laboratory Science
• /
• v.52 no.4
• /
• pp.372-380
• /
• 2020

In this study, the sterilization ability of S. aureus and P. aeruginosa was evaluated using a plasma generator with a flexible electrode structure. Both strains were prepared at a concentration of 1.5×106 CFU/mL and inoculated and spread evenly on two medium plates. The medium were kept at a distance of 3 cm and 9 cm from the plasma generator and were plasma discharged from 30 sec to 10 minutes. The growth of colonies on the media, were subsequently compared with the control group. The mean colonies of S. aureus formed at a 3 cm distance were 9.2×102 (log value 2.96) CFU/mL for the 5 min discharge period and 8.0×10 (1.90) CFU/mL for the 10 min discharge period. When the medium was exposed for 5 min and 10 min at a 9 cm distance, the mean colonies of S. aureus formed were 2.16×103 (3.33) and 2.4×102 (2.38) CFU/mL, respectively. The medium containing P. aeruginosa kept at a 3 cm distance and exposed to 3, 5, 10-minute discharge, did not form any colonies. When kept at a 9 cm distance for 3 minutes, 6.0×102 (2.78) CFU/mL mean colonies were formed but no colonies were formed at exposure periods of 5 and 10 minutes. This enhanced sterilization effect was confirmed in experiments of S. aureus and P. aeruginosa using TiO2.

• Journal of Bio-Environment Control
• /
• v.22 no.3
• /
• pp.241-247
• /
• 2013

For in vitro minimal-growth conservation of S. sarmentosum, the in vitro shoots with 10 mm length were cultured on Murashige and Skoog's media (MS) containing different levels of agar (0.8, 1.2, 1.6, 2%), Gelrite (0.4, 0.6, 0.8, 1%), ABA (0, 5, 10, $20mg{\cdot}L^{-1}$), and sucrose (2, 3, 6, and 9%) without subculture at $4^{\circ}C$ and $25^{\circ}C$. All media were supplemented with $0.2mg{\cdot}L^{-1}$ BA, agar and Gelrite media, with 5% sucrose, sucrose media, with 1.2% agar, and ABA media, with 5% sucrose and 1.2% agar, respectively. In vitro minimal-growth conservation in room-temperature ($25^{\circ}C$) was effective in the media containing with $10mg{\cdot}L^{-1}$ ABA or 1.6% agar, and the healthy plantlets could be preserved for 10 months without subculture. After 12 months at $4^{\circ}C$, survival rate was 100% in all media. The in vitro minimal-growth conservation in low temperature ($4^{\circ}C$) was effective in the media containing with $10mg{\cdot}L^{-1}$ ABA or 6% sucrose, and the healthy plantlets could be preserved over 18 months without subculture. Especially, long-term conservation using minimal growth of S. sarmentosum was much more efficient in the medium containing high level sucrose at $4^{\circ}C$ compared to others.

• Molecules and Cells
• /
• v.23 no.2
• /
• pp.161-169
• /
• 2007

We identified two alternatively spliced variants of the peroxisomal targeting signal 1 (PTS1) receptor protein Pex5ps in monocot (rice, wheat, and barley) but not in dicot (Arabidopsis and tobacco) plants. We characterized the molecular and functional differences between the rice (Oryza sativa) Pex5 splicing variants OsPex5pL and OsPex5pS. There is only a single-copy of OsPEX5 in the rice genome and RT-PCR analysis points to alternative splicing of the transcripts. Putative light-responsive cis-elements were identified in the 5' region flanking OsPEX5L and Northern blot analysis demonstrated that this region affected light-dependent expression of OsPEX5 transcription. Using the pex5-deficient yeast mutant Scpex5, we showed that OsPex5pL and OsPex5pS are able to restore translocation of a model PTS1 protein (GFP-SKL) into peroxisomes. OsPex5pL and OsPex5pS formed homo-complexes via specific interaction domains, and interacted with each other and OsPex14p to form hetero-complexes. Although overexpression of OsPex5pL in the Arabidopsis pex5 mutant (Atpex5) rescued the mutant phenotype, overexpression of OsPex5pS only resulted in partial recovery.

• ALGAE
• /
• v.23 no.1
• /
• pp.31-52
• /
• 2008

This study analyzes characteristics of phytoplankton communities around Wolseong nuclear power plant by selecting 16 stations from July 2006 to June 2007 and understands the influences on standing crops and chlorophyll a of phytoplankton by passing through the cooling water system. The total species number is 283, among which diatoms is 208 occupying 73.5% of total taxa. The mean of total standing crops is 469,380-3,704,114 cells L-1. It is the highest in April 2007 because blooming of Chaetoceros socialis occurs during this period. The mean standing crops of microplankton and nanoplankton are average 129,666-3,392,640 cells L-1 and 240,943-650,505 cells L-1 respectively, which occupy 54.01% and 46.54% of total standing crops. The mean concentrations of total chlorophyll a is 0.64-5.39 μg L-1. The mean concentrations of chlorophyll a of microplankton, nanoplankton and picoplankton are 1.33 μg L-1, 0.21 μg L-1 and 0.49 μg L-1 respectively. Dominant species around Wolseong neclear power plant during this study are Chaetoceros debilis, Chaetoceros socialis, Leptocylindrus danicus, Pseudo-nitzschia fraudulenta, P. subfraudulenta and Thalassiosira decipiens. Fluctuation rates of standing crops and chlorophyll a concentrations of phytoplankton passing through the cooling water system are 22.80% and 50.48% respectively. Decrease of standing crops and chlorophyll a concentrations of phytoplankton means that community structure of phytoplnakton may change at the discharge areas.

• Journal of Environmental Impact Assessment
• /
• v.11 no.1
• /
• pp.1-12
• /
• 2002

중부지방 3백만 주민의 상수원으로 이용되는 대청호는 부영양화가 심화되어 적절한 수질관리가 없으면 상수원수의 최저등급인 3급수를 만족할 수 없는 상태에 이르고 있다. 그래서 2002년 1월에 금강수계 물관리 및 주민지원 등에 관한 법률이 제정되었는 바, 오염총량제와 수변구역의 지정을 통한 수질보전 등을 주요한 내용으로 포함하고 있다. 오염총량제를 실천하기 위해서는 대청호의 환경용량을 추정하는 것이 필수 불가결하다. 환경용량의 추정은 장래 대청호 수질영향권역에서 개발사업이 이뤄질 때 환경영향평가 특히 누적영향평가를 위해 필요하다. 대청호의 환경용량을 추정하기 위해 오염부하량과 유량의 변화가 대청호의 총질소와 총인농도에 미치는 영향을 WASF5모형으로 분석하였다. 총질소 부하량이 50%증가한다고 가정했을때 갈수기. 명수기, 홍수기에 각각 0.14-0.29 mg/l, 0.12-0.16 mg/l and 0.03-0.05 mg/l 정도의 농도 변화가 예측되었다. 총질소 부하량이 지금의 반이하로 감소하더라도 총질소농도 5급수기준 (1.0-1.5 mg/l)을 달성할 수가 없다. 대청호의 환경용량을 상수원수 3급수기준으로 산정한다면, 그것은 현재의 총질소 부하량의 반보다 훨씬 적다고 추정할 수 있으며 따라서 총질소 부하량은 지금의 반이하로 줄어들어야 할 것이다. 총인 부하량이 50%증가한다고 가정했을 때 갈수기, 평수기, 홍수기에 각각 0.005-0.011 mg/l, 0.004-0.006 mg/l and 0.001-0.002 mg/l 정도의 농도 변화가 예측되었다. 총인 부하량이 지금의 반이하로 감소하더라도 총인 농도 4급수기준 (0.05-0.1 mg/l)을 간신히 달성할 수 있다. 따라서 대청호의 환경용량은 지금의 총인 부하량의 반정도로 추정할 수 있으며 총인 부하량은 지금의 반이하로 줄어들어야 할 것이다. 오염부하량을 줄이기 위한 방안을 정오염원과 비정오염원으로 나눠 제시하였고 오염총량제 실현방안을 제시하였다.

• Journal of Plant Biotechnology
• /
• v.49 no.4
• /
• pp.325-330
• /
• 2022

In this study, a plant tissue culture system was established for Atractylodes spp., an economically valuable medicinal crop in Korea that has low domestic production and is increasingly imported. In particular, Atractylodes ovata was treated with four types of cytokinins, 6-benzylaminopurine (BA), zeatin, kinetin, and thidiazuron (TDZ), in two different concentrations (0.5 and 1.0 mg/L). Among the four types of cytokinins, the BA treatment was effective for the shoot and root growth of A. ovata. Both the 0.5 mg/L and 1.0 mg/L concentrations of BA showed similar results; however, the 1.0 mg/L concentration of BA was more effective in promoting shoot and root growth. The treatments showed that the TDZ treatment was not effective for the shoot and root growth, except for the number of shoots and the fresh weight (FW) of the root; therefore, it was unsuitable for this species. In this study, we established a mass production system of A. ovata. Our results showed that direct in vitro regeneration may make a significant contribution to improving the cultivation of the medicinal plant A. ovata.

• Journal of the Korean Chemical Society
• /
• v.38 no.11
• /
• pp.808-818
• /
• 1994

The neutral compounds [$MCl_3L_2$(MeCN)] (M = Mo, V: L = $PPh_3$, 1/2 phda) have been prepared from the reaction of starting material $MCl_z$ (M = Mo; z = 5, M = V; z = 3) with N,P-donating ligands in acetonitrile solution. Addition of $AgClO_4$ to these neutral monomeric compounds in acetone solution were produced [$MCl_3-_nL_2(MeCN)(S)_n$]$(ClO_4)_n$ (n = 1, 2 : s = solvent). Finally treatment of bivalent cationic compound and neutral compound was formed chloride bridged dinuclear complex $[(MeCN)(L)_2ClM({\mu}-Cl)_2M'Cl(L)_2(MeCN)](ClO_4)_2$ and treatment of univalent cationic compound with half equivalent pyrazine to pyrazine bridged complex $[(MeCN)(L)_2Cl_2M({\mu}-pyz)M'Cl_2(L)_2(MeCN)](ClO_4)_2$. These complexes are characterized by elemental analysis, $^1H$, $^{13}C$ NMR, IR, Far-IR and UV-Vis spectroscopy.