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Gi‑Su Ham,Young‑Kyun Kim,Young Sang Na,Kee‑Ahn Lee 대한금속·재료학회 2021 METALS AND MATERIALS International Vol.27 No.1
This study investigated the effect of Ti addition on microstructure and high-temperature oxidation property of AlCoCrFeNihigh-entropy alloy. Ti content was controlled at 0 at% and 1 at%. The two alloys were found to have BCC single phase, andthe average grain sizes of Ti0.0 and Ti1.0 were 47.3 μm and 49.7 μm, respectively, showing similarity. The EDS mappingof the inside of grains found that both alloys were characterized to be divided into Al-Ni element rich region and Cr–Feelement rich region. As a result of high-temperature oxidation test at 1100 °C, oxidation weight gains were measured atTi0.0: 0.75 mg/cm2 and Ti1.0: 0.17 mg/cm2, respectively. The results indicate that Ti addition largely improved high temperatureoxidation resistance of AlCoCrFeNi HEA. Ti1.0 alloy, in particular, showed remarkably more excellent 1100 °Chigh-temperature oxidation resistance than other previously reported major ones such as NiCrAl and FeCrAl. In the surfaceand cross-section observations after oxidation tests, both alloys were found to have Al2O3oxides mostly. While the Ti0.0material was observed to have Al2O3spallation macroscopically, the Ti1.0 alloy showed Al2O3spallation only in some localareas. In addition, a unique result was found in AlCoCrFeNiTix(x=0,1) alloy that BCC → FCC phase transformation was accelerated,and FCC phase layer was formed in the surficial area where Al element had been depleted due to high-temperatureoxidation. Moreover, as Ti was added, the thickness of FCC layer induced by high-temperature oxidation decreased. Basedon the results, it was also discussed on how to improve the high-temperature oxidation resistance of AlCoCrFeNiTixHEA.
Lee, Gi Woo,Lee, Sang Kuk Elsevier 2009 Chemical physics letters Vol.470 No.1
<P><B>Graphical abstract</B></P><P>Spectroscopic identification of jet-cooled <I>p</I>-fluoro-α-methylbenzyl radical in corona discharge.</P><ce:figure></ce:figure> <P><B>Abstract</B></P><P>We report the first spectroscopic identification of the <I>p</I>-fluoro-α-methylbenzyl radical in the gas phase. Precursor <I>p</I>-fluoro-ethylbenzene seeded in a large amount of carrier gas was electrically discharged to produce the benzyl-type radicals in a corona excited supersonic expansion using a pinhole-type glass nozzle, from which the vibronic emission spectrum was recorded in the visible region. From an analysis of the spectrum observed, we identified spectroscopically the formation of the <I>p</I>-fluoro-α-methylbenzyl, in which the energy of the D<SUB>1</SUB>→D<SUB>0</SUB> electronic transition and a few vibrational mode frequencies in the ground electronic state were determined by comparison with those from an <I>ab initio</I> calculation and with those from the known data of the precursor.</P>
Lee Hyun Gi,Park Jin-Ki,Kim Sung-Woo,Ko Eun-Mi,Kim Byoung-Ju,Jo Su-Jin,Byun Sung-June,Yang Boh-Suk,Chang Won-Kyong,Lee Hoon-Taek,Lee Poong-Yeon The Korean Society of Animal Reproduction 2006 Reproductive & developmental biology Vol.30 No.2
This study was conducted to examine the effect of IRES controlled reporter gene on screening and production of recombinant human erythropoietin (EPO) proteins from cultured CHO cells. The cDNA was cloned for EPO from human liver cDNA Using site-directed mutagenesis, we generated recombinant human EPO (rhEPO) with two additional N-glycosylations (Novel erythropoiesis-stimulating protein: NESP). Wild type hEPO and NESP were cloned into expression vectors with GFP reporter gene under regulatory control of CMV promoter and IRES so that the vectors could express both rhEPO and GFP. The expression vectors were transfected to cultured CHO-K1 cells. Under microscopy, expression of GFP was visible. Using supernatant of the culture, ELISA assay, immunocytochemistry and in vitro assay using EPO dependant cell line were performed to estimate biological activity to compare the production characteristics (secretion levels, etc.) between rhEPO and NESP. The activity of NESP protein, obtained by mutagenesis, was described and compared with its rhEPO counterpart produced under same conditions. Although NESP had less secretion level in CHO cell line, the biological activity of NESP was greater than that of rhEPO. These results are consistent with previous researches. We also demonstrated that rhEPO and GFP proteins expressed simultaneously from transfected CHO cell line. Therefore we conclude that use of GFP reporter gene under IRES control could be used to screen and produce rhEPO in cultured CHO cells.
Development of transgenic rice lines expressing the human lactoferrin gene
Lee, Jin-Hyoung,Kim, Il-Gi,Kim, Hyo-Sung,Shin, Kong-Sik,Suh, Seok-Cheol,Kweon, Soon-Jong,Rhim, Seong-Lyul The Korean Society of Plant Biotechnology 2010 식물생명공학회지 Vol.37 No.4
Lactoferrin is an 80-kDa iron-binding glycoprotein that is found in high concentrations in human milk. Human lactoferrin (hLF) has several beneficial biological activities including immune system modulation and antimicrobial activity. In the present study, we devolved a method of hLF expression through introducing the hLF gene construct into Oriza sativa cv. Nakdong using the Agrobacterium-mediated transformation system. The expression of the hLF gene under the control of the rice glutelin promoter was detected in the seeds of transgenic rice plants. Transformed rice plants were selected on media containing herbicide(DL-phosphinothricin) and the integration of hLF cDNA was confirmed by Southern blot analysis. The expression of the full length hLF protein from the grains of transgenic rice plants was verified by Western blot analysis. The lactoferrin expression levels in the transformed rice grains determined by enzyme-linked immunosorbant assay accounted for approximately 1.5% of total soluble protein. Taken together, these data indicate that rice grains expressing hLF can be directly incorporated into infant formula and baby food.
Study on the Reproductive Function in Transgenic Pig Harboring Human Erythropoietin (hEPO) Gene
Lee, Hyun-Gi,Lee, Hwi-Cheul,Chung, Hak-Jae,Hwang, In-Sul,Choi, Myoung-Seob,Byun, Sung-June,Lee, Seung-Hoon,Kim, Min-Ji,Woo, Jae-Seok,Chang, Won-Kyong,Lee, Poong-Yeon,Lee, Hoon-Taek,Park, Jin-Ki The Korean Society of Animal Reproduction 2008 Reproductive & developmental biology Vol.32 No.2
Our previous study showed that transgenic (TG) pigs harboring human EPO (hEPO) gene have been shown to have reproductive disorders, including low pregnancy rates, irregular estrus cycle and low little size. To investigate these reasons, we assessed estrus behavior (standing response) and plasma $17{\beta}$-estradiol ($E_2$) level, which partly reflect reproductive function, during the estrus cycles after synchronization and superovulation by hormone treatments. Then, we analysed blood composition and expression of hEPO gene in TG pigs. Pigs were injected with PG600. After 10 days, pigs were fed with Regumate porcine for 6 days. Blood samples were collected from jugular vein. Analysis of blood composition and $E_2$ level were measured by Hemavet 950 and $E_2$ ELISA kit, respectively. And, the expression of hEPO gene in reproductive organs was quantitated by real-time RT-PCR. The percentage of estrus behavior in TG was significantly decreased. Hematocrit (HCT), hemoglobin (Hb) concentration and red blood cell (RBC) number were significantly higher in TG than wild type (WT). On the other hand, high expression of hEPO gene in TG was observed in the mammary gland as well as in the uterus. Moreover, plasma $E_2$ level was significantly higher in TG than WT. These results suggest that nonspecific expression of hEPO gene in the other organs of TG may affect blood composition and plasma $E_2$ level, thereby causing reproductive disorders.