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장진성,배강국,김우곤,김선재,국일현,김성청,Jang, Jin-Seong,Bae, Gang-Guk,Kim, U-Gon,Kim, Seon-Jae,Guk, Il-Hyeon,Kim, Seong-Cheong 대한기계학회 2000 大韓機械學會論文集A Vol.24 No.2
Residual stress induced in U-bending and tube-to-tubesheet joint processes of PWR's row-1 heat exchanger tube was measured by X-ray method and Hole-Drilling Method(HDM). Compressive residual stresses(-) at the extrados surface were induced in U-bending, and its maximum value reached -319 MPa in axial direction at the position of $\psi$ = $0^{\circ}$. Tensile residual stresses(+) of $\sigma_{zz}$ = 45 MPa and $\sigma_{\theta\theta}$ = 25 MPa were introduced in the intrados surface at the position of $\psi$ = $0^{\circ}$. Maximum tensile residual stress of 170 MPa was measured at the flank side at the position of $\psi$ = $90^{\circ}$, i.e., at apex region. It was observed that higher stress gradient was generated at the irregular transition regions (ITR). The trend of residual stress induced by U bending process of the tubes was found to be related with the change of ovality. The residual stress induced by the explosive joint method was found to be lower than that by the mechanical roll method. The gradient of residual stress along the expanded tube was highest at the transition region (TR), and the residual stress in circumferential direction was found to be higher than the residual stress in axial direction.
크롬계 탄화물의 분포와 형태가 니켈계 합금 600의 염기응력부식에 미치는 영향
김선재,최종호,성진경,김우곤,박순동,이창규,정용환,국일현,Kim, Seon-Jae,Choe, Jong-Ho,Seong, Jin-Gyeong,Kim, U-Gon,Park, Sun-Dong,Lee, Chang-Gyu,Jeong, Yong-Hwan,Guk, Il-Hyeon 한국재료학회 1998 한국재료학회지 Vol.8 No.8
32$0^{\circ}C$, 40%NaOH 용액의 autoclave에서 약 300wppm의 탄소를 함유하고 있는 15Cr-9Fe-balanced Ni 합금 판상시편에 대해 응력부식 저항성을 조사하였다. 부식시편은 $700^{\circ}C$, 100시간 동안의 열처리로 합금내부에 석출될 수 있는 가능한 한 많은 양의 크롬계 탄화물을 석출시킨 후, 다시 재용해에 의해 크롬계 탄화물의 형태를 조절하는 $800^{\circ}C$-$950^{\circ}C$범위의 최종열처리를 시행하고 급냉시킨 다음 U-자형으로 응력을 가하여 준비되었다. 최종열처리 온도가 올라감에 따라 시편들의 입계응력부식균열(IGSCC ) 전파속도는 $900^{\circ}C$까지는 거의 직선적으로 증가하다가 $950^{\circ}C$에서는 $700^{\circ}C$에서 얻은 값보다도 더 낮게 감소하였다. 즉, 크롬계 탄화물이 재용해되어 그 밀도가 감소함에 따라 IGSCC저항성이 감소하다가 완전히 재용해된 $950^{\circ}C$ 열처리 조건에서 오히겨 가장 큰 IGSCC 저항성을 나타내었다. 이와같은 최조열처리 온도에 따른 니켈계 합금 600의 부식거동은 입계에 존재하는 크롬계탄화물의 형태변화 때문이 아니라 입계에서 탄소-크롬계 탄화물-크롬간의 상평형에 의해 이루어지는 탄소의 입계편석량이 크롬계탄화물이 존재할 때에는 열처리 온도에 따라 증가하다가 그것이 완전히 재용해 되었을 때 가장 낮아지기 때문인 것으로 생각된다.
Kim, Seong U,Jo, Eun-Jung,Noh, Yuseon,Mun, Hyoyoung,Ahn, Young-Deok,Kim, Min-Gon American Chemical Society 2018 ANALYTICAL CHEMISTRY - Vol.90 No.17
<P>Bacterial infections are common causes of morbidity and mortality worldwide; therefore, environmental contamination by bacterial pathogens represents a global public health concern. Consequently, a selective, rapid, sensitive, and in-field detection platform for detecting significant bacterial contamination is required to ensure hygiene and protect public health. Here, we developed a fast and simple platform for the selective and sensitive detection of bacteria by measuring adenosine triphosphate (ATP) bioluminescence following targeted photothermal lysis mediated by antibody-conjugated gold nanorods. This method employed both targeted photothermal lysis of bacteria by near-infrared (NIR) irradiation and highly selective detection of the lysed bacteria via ATP bioluminescence within 36 min (incubation, 30 min; NIR irradiation, 6 min). The use of the proposed method allowed limits of detection in pure solution of 12.7, 70.7, and 5.9 CFU for <I>Escherichia coli</I> O157:H7, <I>Salmonella typhimurium</I>, and <I>Listeria monocytogenes</I>, respectively. Additionally, bacteria were successfully detected on artificially inoculated plastic cutting boards. Furthermore, this method was highly specific, without cross-reaction among pathogenic bacteria. We believe that the proposed method has significant potential as an on-site diagnostic tool for applications associated with public health and environmental pollution monitoring.</P> [FIG OMISSION]</BR>
U G Kim,Soon Jae Kwon,Yiming Wang,Sang Gon Kim,Kyu Young Kang,Sun Tae Kim 한국육종학회 2012 한국육종학회 심포지엄 Vol.2012 No.07
Here, we first demonstrate that identification of rice brown spot disease fungus (Cochliobolus miyabeanus, C. miyabeanus) proteins is possible in infected tissues using in planta apoplastic proteome with non-destructive tissues. In planta apoplastic proteins from rice leaves inoculated with C. miyabeanus, CM2 (compatible race), were isolated by vacuum infiltration with CaCl2/Na-acetateextractionbuffer, separated by SDS-PAGE, and identified by MudPIT. Of the 529 proteins that were identified by MudPIT, a large proportion (490) was from the rice. Numerous carbohydrate metabolic process (48), oxidation and reduction (44), response to oxidative stress (20%) were identified and confirmed their expression at RNA levels using microarray. Bioinformatic analysis showed that 176 and 39 of these proteins have a signal peptide in rice and rice brown spot fungus, respectively, using Signal P. The large proportion of proteins interestingly identified from the in planta apoplast were involved inprotease, hydrophobin, and host cell wall hydrolysis (Xylanase, beta-glucosidase) derived from pathogen. Thus, we suggest that in planta rice apoplastic secretome will be an important clue to understand the rice-rice brown spot fungus interactions.
Kim, Seong U.,Batule, Bhagwan S.,Mun, Hyoyoung,Byun, Ju-Young,Shim, Won-Bo,Kim, Min-Gon The Royal Society of Chemistry 2018 The Analyst Vol.143 No.3
<P>We have developed a novel strategy for the colorimetric detection of PCR products by utilizing a target-specific primer modified at the 5′-end with an anti-DNAzyme sequence. A single-stranded DNAzyme sequence folds into a G-quadruplex structure with hemin and shows strong peroxidase activity. When the complementary strand binds to the DNAzyme sequence, it blocks the formation of the G-quadraduplex structure and loses its peroxidase activity. In the presence of the target gene, PCR amplification proceeds, and anti-DNAzyme sequence modified primers present in the reaction mixture form a double strand through primer extension. Therefore, it does not block the DNAzyme sequence. Further, a colorimetric signal is generated by the addition of 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonate) (ABTS) and H2O2 at the end of the reaction. We have successfully detected a single copy of the HIV type 1 <I>gag</I> gene in buffer and 10 copies in human serum. The strategy developed could be used to detect DNA and RNA in complex biological samples by simple primer designing that includes DNAzyme and a DNA extended primer.</P>
Kim, Seong U.,Jo, Eun-Jung,Mun, Hyoyoung,Noh, Yuseon,Kim, Min-Gon American Chemical Society 2018 Journal of agricultural and food chemistry Vol.66 No.19
<P>Here, we report an enhanced colorimetric method using enzymatic amplification with nitroblue tetrazolium (NBT)/5-bromo-4-chloro-3-indolyl phosphate (BCIP) precipitation for the ultrasensitive detection of <I>Escherichia coli</I> O157:H7 through immunomagnetic separation-selective filtration. Biotinylated anti-<I>E. coli</I> O157:H7 antibody and streptavidin-alkaline phosphatase were conjugated to the surface of magnetic nanoparticles, and <I>E. coli</I> O157:H7-conjugates complexes remained on the membrane filter surface. The resultant light brown spots on the membrane filter were amplified with NBT/BCIP solution to yield enzyme-catalyzed precipitation, which increased with an increasing <I>E. coli</I> O157:H7 concentration. <I>E. coli</I> O157:H7 was detected in pure samples with limits of detection of 10 and 6.998 colony-forming units (CFU)/mL through visual observation and measurement of optical density, respectively. The proposed method was applied to a lettuce sample inoculated with selective <I>E. coli</I> O157:H7, which was detected within 55 min without cross-reactivity to non-target bacteria. This enhanced colorimetric method has potential for on-site detection of food contaminants and environmental pollutants.</P> [FIG OMISSION]</BR>
Kim, Seong U.,Batule, Bhagwan S.,Mun, Hyoyoung,Shim, Won-Bo,Kim, Min-Gon Elsevier 2018 FOOD CONTROL Vol.84 No.-
<P><B>Abstract</B></P> <P> <I>Salmonella enterica</I> is one of the most encountered causative pathogens of food-borne illnesses. Outbreaks of such diseases are commonly associated with the consumption of fresh fruits and vegetables. In this study, we report a simple colorimetric strategy for the detection of <I>S. enterica</I> Serovar Typhimurium in fresh-cut lettuce leaves based on polymerase chain reaction (PCR) products generated by gene-specific primers integrated with the horseradish peroxidase-mimicking DNAzyme (HRPzyme). The HRPzyme sequence was integrated at the 5′ end of the forward and reverse primers specific to 16S rRNA of <I>S. enterica</I> Typhimurium. At the end of the PCR reaction, unamplified HRPzyme-integrated primers were folded into G-quadruplex structure in the presence of hemin and then, they catalyzed the oxidation of 2,2′-azinobis (3-ethylbenzothiazolinesulfonic acid) (ABTS) with H<SUB>2</SUB>O<SUB>2</SUB>. The intensity of oxidized ABTS colorimetric signal was linearly and inversely related to <I>S. enterica</I> Typhimurium concentration. The latter relationship demonstrated diagnostic potential of this rapid, simple, highly sensitive, and selective colorimetric platform for <I>S. enterica</I> Typhimurium detection.</P> <P><B>Highlights</B></P> <P> <UL> <LI> One pot and two-step HRPzyme-integrated PCR-based colorimetric detection strategy. </LI> <LI> HRPzyme sequence integrated with forward and reverse primers employed as a signaling probe. </LI> <LI> Highly sensitive and selective detection method of Salmonella upto single cfu mL<SUP>−1</SUP>. </LI> <LI> Successfully employed to detect Salmonella on the lettuce leaves sample. </LI> </UL> </P> <P><B>Graphical abstract</B></P> <P>[DISPLAY OMISSION]</P>
Kim, Hyuk Min,Lee, Hong Jun,Lee, Man Young,Kim, Seung U.,Kim, Byung Gon The Korean Society for Brain and Neural Science 2010 Experimental Neurobiology Vol.19 No.2
<P>The molecular microenvironment of the injured spinal cord does not support survival and differentiation of either grafted or endogenous NSCs, restricting the effectiveness of the NSC-based cell replacement strategy. Studying the biology of NSCs in <I>in vivo</I> usually requires a considerable amount of time and cost, and the complexity of the <I>in vivo</I> system makes it difficult to identify individual environmental factors. The present study sought to establish the organotypic spinal cord slice culture that closely mimics the <I>in vivo</I> environment. The cultured spinal cord slices preserved the cytoarchitecture consisting of neurons in the gray matter and interspersed glial cells. The majority of focally applied exogenous NSCs survived up to 4 weeks. Pre-exposure of the cultured slices to a hypoxic chamber markedly reduced the survival of seeded NSCs on the slices. Differentiation into mature neurons was severely limited in this co-culture system. Endogenous neural progenitor cells were marked by BrdU incorporation, and applying an inflammatory cytokine IL-1β significantly increased the extent of endogenous neural progenitors with the oligodendrocytic lineage. The present study shows that the organotypic spinal cord slice culture can be properly utilized to study molecular factors from the post-injury microenvironment affecting NSCs in the injured spinal cord.</P>
Ho-166 부착풍선도자를 이용한 방사선 조사의 돼지 관상동맥 스텐트 재협착 예방 효과
김원 ( Kim Won ),정명호 ( Jeong Myeong Ho ),박옥영 ( Park Og Yeong ),정우곤 ( Jeong U Gon ),박우석 ( Park U Seog ),김주한 ( Kim Ju Han ),안영근 ( An Yeong Geun ),조정관 ( Jo Jeong Gwan ),박종춘 ( Park Jong Chun ),강정채 ( Kang Je 한국지질동맥경화학회 ( 구 한국지질학회 ) 2002 韓國脂質學會誌 Vol.12 No.1
배경 : 국내에서 개발된 방사선 동위원소 Holmium-166 (166Ho)은 주로 베타선을 방출하며, 166Ho을 부착한 풍선도자를 이용하여 돼지 관상동맥 재협착 모형에서 풍선확장술 후 신생내막 증식을 전신적 부작용 없이 안전하고 효과적으로 억제하였음을 보고한 바 있다. 본 연구에서는 돼지 관상동맥 스텐트 재협착 모형에서 스텐트 시술 후 신생내막 증식에 의한 재협착 병변을 166Ho 부착 풍선도자를 이용하여 치료하여 그 효과를 관찰하고자 하였다. 방법