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HY-SPLIT 모형을 이용한 오염물질의 장거리 이동 추적
전의찬,우정헌 東新大學校 1996 論文集 Vol.8 No.-
Due to the rapid economic development for the last 20 years, Asian countries' fuel consumption has doubled twice every twelve years. Also, serious environmental problems, especially air pollution, have followed rapid urbanization and development in Northeast Asia, where Korea is located. The pattern of long range transport of air pollutants was investigated in the Northeast Asia region. The focus of this study was the impact of air pollutants from China on the air quality of Korea. From the meteorological data from the 1st to the 5th of January 1995, the backward and forward trajectories were calculated using the Hybrid model 'HY-SPLIT', and the contributions of air pollutants from cities of China to the air quality in Korea were analyzed. It was concluded that the air pollutants from China could have a great influence on the air quality in Korea. The trajectories showed that the air pollutants from Beijing and Jinan, Shandong Province, the most heavily industrialized areas in China, could be influenced strongly to the air quality in Korea.
Woo, Eui-Jeon,Lee, Seungjae,Cha, Hyunju,Park, Jong-Tae,Yoon, Sei-Mee,Song, Hyung-Nam,Park, Kwan-Hwa American Society for Biochemistry and Molecular Bi 2008 The Journal of biological chemistry Vol.283 No.42
<P>TreX is an archaeal glycogen-debranching enzyme that exists in two oligomeric states in solution, as a dimer and tetramer. Unlike its homologs, TreX from Sulfolobus solfataricus shows dual activities for alpha-1,4-transferase and alpha-1,6-glucosidase. To understand this bifunctional mechanism, we determined the crystal structure of TreX in complex with an acarbose ligand. The acarbose intermediate was covalently bound to Asp(363), occupying subsites -1 to -3. Although generally similar to the monomeric structure of isoamylase, TreX exhibits two different active-site configurations depending on its oligomeric state. The N terminus of one subunit is located at the active site of the other molecule, resulting in a reshaping of the active site in the tetramer. This is accompanied by a large shift in the 'flexible loop' (amino acids 399-416), creating connected holes inside the tetramer. Mutations in the N-terminal region result in a sharp increase in alpha-1,4-transferase activity and a reduced level of alpha-1,6-glucosidase activity. On the basis of geometrical analysis of the active site and mutational study, we suggest that the structural lid (acids 99-97) at the active site generated by the tetramerization is closely associated with the bifunctionality and in particular with the alpha-1,4-transferase activity. These results provide a structural basis for the modulation of activities upon TreX oligomerization that may represent a common mode of action for other glycogen-debranching enzymes in higher organisms.</P>
초분광센서를 활용한 이산화질소 농도 추정식에 관한 연구
전의익(Eui-Ik Jeon),박진우(Jin-Woo Park),임성하(Seong-Ha Lim),김동우(Dong-Woo Kim),유재진(Jae-Jin Yu),손승우(Seung-Woo Son),전형진(Hyung-Jin Jeon),윤정호(Jeong-Ho Yoon) 한국산학기술학회 2019 한국산학기술학회논문지 Vol.20 No.6
국내 산업단지에서 배출되는 대기오염물질의 모니터링을 위해 굴뚝원격감시시스템이 운영되고 있으나 대상 시설이 한정적이어서, 시스템이 설치되지 않은 시설은 단속 요원이 직접 모니터링 및 단속을 수행하고 있다. 그래서 효율적인 산업단지에서 배출되는 대기오염물질의 모니터링을 위해 다양한 센서를 활용한 연구들이 수행되고 있다. 이에 따라 본 연구에서는 초분광센서로 측정할 수 있는 분광복사량을 활용하여 대기오염물질 중 이산화질소의 농도를 추정할 수 있는 공식을 개발하고 검증하였다. 농도 추정식 개발을 위해 다양한 농도의 이산화질소를 대상으로 태양천정각, 관측천정각, 상대방위각을 다르게 하여 분광복사량을 관측하였다. 관측된 분광복사량에서 특정 파장 간의 값의 차이를 흡수 깊이로 하였으며, 흡수 깊이와 이산화질소 농도와의 관계를 이용하여 농도 추정식을 개발하였다. 그리고 개발된 농도 추정식들의 검증을 위해 이산화질소와 아황산가스가 혼합된 가스를 대상으로 측정한 분광복사량을 이용하였다. 그 결과, 추정식의 형태에 따라 결정 계수와 RMSE가 0.71~0.88, 72~323 ppm으로 나타났으며, 지수 형태의 농도 추정식의 결정 계수가 가장 높게 나타났다. 추정식의 형태에 따라 농도의 변화에 따른 추정 농도의 정확도가 일정하지 않지만, 향후 농도 추정식의 고도화가 이루어진다면 초분광 센서를 활용하여 산업단지 배출되는 이산화질소의 모니터링에 사용 가능할 것으로 판단된다. The CleanSYS(Clean SYStem) is operated to monitor air pollutants emitted from specific industrial complexes in Korea. So the industrial complexes without the system are directly monitored by the control officers. For efficient monitoring, studies using various sensors have been conducted to monitor air pollutants emitted from industrial complex. In this study, hyperspectral sensors were used to model and verify the equations for estimating the concentration of NO2(nitrogen dioxide) in air pollutants emitted. For development of the equations, spectral radiance were observed for NO₂ at various concentrations with different SZA(Solar Zenith Angle), VZA(Viewing Zenith Angle), and RAA(Relative Azimuth Angle). From the observed spectral radiance, the calculated value of the difference between the values of the specific wavelengths was taken as an absorption depth, and the equations were developed using the relationship between the depth and the NO₂ concentration. The spectral radiance mixed gas of NO₂ and SO₂(sulfur dioxide) was used to verify the equations. As a result, the R2(coefficient of determination) and RMSE(Root Mean Square Error) were different from 0.71~0.88 and 72~323 ppm according to the form of the equation, and R<SUP>2</SUP> of the exponential form was the highest among the equations. Depending on the type of the equations, the accuracy of the estimated concentration with varying concentrations is not constant. However, if the equations are advanced in the future, hyperspectral sensors can be used to monitor the NO₂ emitted from the industrial complex.
Jeon, Jae-Won,Park, Bum-Chan,Jung, Joon-Goo,Jang, Young-Soon,Shin, Eui-Cheol,Park, Young Woo The Korean Association of Immunobiologists 2013 Immune Network Vol.13 No.4
The $PrP^C$ is expressed in many types of immune cells including monocytes and macrophages, however, its function in immune regulation remains to be elucidated. In the present study, we examined a role for $PrP^C$ in regulation of monocyte function. Specifically, the effect of a soluble form of $PrP^C$ was studied in human monocytes. A recombinant fusion protein of soluble human $PrP^C$ fused with the Fc portion of human IgG1 (designated as soluble $PrP^C$-Fc) bound to the cell surface of monocytes, induced differentiation to macrophage-like cells, and enhanced adherence and phagocytic activity. In addition, soluble $PrP^C$-Fc stimulated monocytes to produce pro-inflammatory cytokines such as $TNF-{\alpha}$, $IL-1{\beta}$, and IL-6. Both ERK and $NF-{\kappa}B$ signaling pathways were activated in soluble $PrP^C$-treated monocytes, and inhibitors of either pathway abrogated monocyte adherence and cytokine production. Taken together, we conclude that soluble $PrP^C$-Fc enhanced adherence, phagocytosis, and cytokine production of monocytes via activation of the ERK and $NF-{\kappa}B$ signaling pathways.
Jeon, Hong Jin,Woo, Jong-Min,Lee, Seung-Hwan,Kim, Eui-Joong,Chung, Seockhoon,Ha, Jee Hyun,Fava, Maurizio,Mischoulon, David,Kim, Ji-Hae,Heo, Jung-Yoon,Yu, Bum-Hee by Lippincott Williams Wilkins. 2014 JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY Vol.34 No.2
ABSTRACT: Although many patients with major depressive disorder (MDD) complain of neurocognitive impairment, the effects of antidepressant medications on neurocognitive functions remain unclear. This study compares neurocognitive effects of tianeptine and escitalopram in MDD. Patients with MDD (N = 164) were randomly assigned in a 1:1 ratio to either tianeptine (37.5 mg/d) or escitalopram (10 mg/d) for 12 weeks. Outcome measures included clinical improvement, subjective cognitive impairment on memory and concentration, the Mini–Mental State Examination, the Continuous Performance Test, the Verbal Learning Test, and the Raven Progressive Matrices, assessed every 4 weeks. After 12 weeks, the tianeptine group showed significant improvement in commission errors (P = 0.002), verbal immediate memory (P < 0.0001), Mini–Mental State Examination (P < 0.0001), delayed memory (P < 0.0001), and reasoning ability (P = 0.0010), whereas the escitalopram group improved in delayed memory and reasoning ability but not in the other measures. Both groups significantly improved in subjective cognitive impairment in memory (P < 0.0001) and concentration (P < 0.0001). Mixed effects model repeated measures analyses revealed that the tianeptine group had a significant improvement in scores of commission errors (F = 6.64, P = 0.011) and verbal immediate memory (F = 4.39, P = 0.038) from baseline to 12 weeks, compared with the escitalopram group, after controlling for age, sex, education years, baseline scores, and changes of depression severity. The treatment of MDD with tianeptine led to more improvements in neurocognitive functions, especially in commission errors and verbal immediate memory, compared with escitalopram, after controlling for changes in depression severity. Both drugs improved subjective cognitive impairment of memory and concentration.
( Woo Soo Jeong ),( Yu-ri Kim ),( Seong-jin Hong ),( Su-jeong Choi ),( Ji-ho Choi ),( Shin-young Park ),( Eui-jeon Woo ),( Young Min Kim ),( Bo-ram Park ) 한국미생물 · 생명공학회 2019 Journal of microbiology and biotechnology Vol.29 No.12
Isomaltooligosaccharides (IMOs) have good prebiotic effects, and long IMOs (LIMOs) with a degree of polymerization (DP) of 7 or above show improved effects. However, they are not yet commercially available, and require costly enzymes and processes for production. The Nterminal region of the thermostable Thermoanaerobacter thermocopriae cycloisomaltooligosaccharide glucanotransferase (TtCITase) shows cyclic isomaltooligosaccharide (CI)-producing activity owing to a catalytic domain of glycoside hydrolase (GH) family 66 and carbohydrate-binding module (CBM) 35. In the present study, we elucidated the activity of the C-terminal region of TtCITase (TtCITase-C; Met740-Phe1,559), including a CBM35-like region and the GH family 15 domain. The domain was successfully cloned, expressed, and purified as a single protein with a molecular mass of 115 kDa. TtCITase-C exhibited optimal activity at 40°C and pH 5.5, and retained 100% activity at pH 5.5 after 18-h incubation. TtCITase-C synthesized α-1,6 glucosyl products with over seven degrees of polymerization (DP) by an α-1,6 glucosyl transfer reaction from maltopentaose, isomaltopentaose, or commercialized maltodextrins as substrates. These results indicate that TtCITase-C could be used for the production of α-1,6 glucosyl oligosaccharides with over DP7 (LIMOs) in a more cost-effective manner, without requiring cyclodextran.
Senescence is accelerated through donor cell specificity in cloned pigs.
Jeon, Hyun Yong,Jeong, Yeon Woo,Kim, Yeon Wook,Jeong, Yeon Ik,Hossein, Shamim M,Yang, Hyun,Hyun, Sang Hwan,Jeung, Eui-Bae,Hwang, Woo Suk D.A. Spandidos 2012 International journal of molecular medicine Vol.30 No.2
<P>Animals cloned by somatic cell nuclear transfer (SCNT) sometimes have abnormalities that result in large offspring syndrome or early death during gestation due to respiratory and metabolic defects. We cloned pigs using two sources of donor cells and observed phenotypic anomalies in three pigs cloned from one type of cell, s-pig fetal fibroblasts. These animals had many wrinkles on their faces and bodies and looked older than age-matched normal pigs. We performed the present study to examine whether the wrinkled phenotype in the cloned pigs was due to senescence, a genetic problem with donor specificity, or epigenetic problems with reprogramming. To address this issue, we investigated biomarkers of senescence, including telomere length and the expression of senescence-associated β-galactosidase (SA-β-gal), glyceraldehyde phosphate dehydrogenase (GAPDH) and β-actin. We also assessed the methylation status of euchromatic PRE-1 repetitive sequences and centromeric satellite DNA, and measured the mRNA levels of six imprinted genes, Copg2, Mest, Igf2R, GNAS, SNRPN and Ube3a. The telomeres of the wrinkled cloned pigs were much shorter than those of the normal cloned pigs and age-matched normal pigs. In the wrinkled cloned pigs, SA-β-gal activity was detected and GAPDH and β-actin were repressed. The mRNA levels of Mest, GNAS and Ube3a were reduced in the wrinkled cloned pigs, although there was no difference between the normal cloned pigs and normal controls. This gene expression analysis indicates that the wrinkled abnormality of our pigs originates from genetic abnormalities in the donor cells used for SCNT.</P>