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Glycine betaine 엽면 처리가 토마토 유묘의 생육과 삼투조절물질 함량에 미치는 영향
강남준(Nam Jun Kang),권준국(Joon Kook Kwon),이재한(Jae Han Lee),박진면(Jin Myeon Park),이한철(Han Chul Rhee),최영하(Young Hah Choi) (사)한국생물환경조절학회 2006 생물환경조절학회지 Vol.15 No.4
토마토 유묘의 생육에 미치는 glycine betaine의 엽면처리 효과를 분석한 결과, 초장이나 건물중 등의 생육이 대조구인 증류수 처리에 비해 촉진되는 경향을 보였으며 25mM glycine betaine 처리가 가장 좋았다. 저온스트레스 하에서 삼투조절 역할을 하는 가용성 당과 proline의 축적량이 증류수 처리에 비해 glycine betaine 처리에서 낮은 경향을 보여 외부에서 엽면 처리한 glycine betaine이 삼투조절 역할을 한 것으로 판단되었으며 이러한 결과는 수용성 단백질과 유리 아미노산의 축적 양상에서도 잘 반영되었다. 이상의 결과로 보아 glycine betaine의 엽면 처리는 저온기 시설 토마토 재배 시 야간 저온정해를 극복할 수 있는 방법으로서 이용 가능성이 있을 것으로 사료된다. Effects of exogenously foliar applied glycine betaine (GB) on the growth and contents of osmolyte in tomato seedling was investigated. Plants treated with exogenous glycine betaine induced better biomass production and plant height during chilling stress than the untreated plants. The total soluble sugar contents in GB foliar-applied plants lower than that of untreated plants 28 days after foliar application. Total water soluble protein contents in GB foliar-applied plants did not change 28 days after chilling stress. In untreated plant, it decreased rapidly in the beginning of chilling stress. Proline contents in untreated plants rapidly increased by the beginning of chilling stress, and then slightly decreased during the next 3 weeks. However proline contents in GB foliar-applied plants did not change during the 28 days chilling stress period. The results suggest that foliar application of GB is a effect methods to increase the chilling tolerance of tomato seedlings in protected cultivation system at low temperature season.
Jong-Myeon Park,Shin-Nam Hong 한국물리학회 2016 THE JOURNAL OF THE KOREAN PHYSICAL SOCIETY Vol.68 No.2
Recently, many research has been conducted on the carbon-nanotube field-effect transistors (CNFETs) in expectation that the CNFETs could replace metal-oxide-semiconductor field-effect transistors (MOSFETs) in the sub-10-nm era. In consideration of both ballistic conduction and nonballistic conduction, including elastic scattering, optical phonon scattering, and acoustic phonon scattering, this paper presents the simulated dependence of the coaxially-gated single-walled semiconducting CNFET characteristics on the contact and the channel lengths. When the contact length was longer than 100 nm, the CNFETs showed a constant minimal value of the contact resistance. In this case, the saturated drain current was higher than that of CNFETs with a shorter contact length. When the channel was longer than 600 nm, the channel resistance was significantly increased due to acoustic phonon scattering. When the channel was shorter than 200 − 250 nm with optical scattering, acoustic scattering or all three scattering mechanisms taken into account, the contact resistance began to become larger than channel resistance.
Park, Jong-Myeon,Kim, Minseok S.,Moon, Hui-Sung,Yoo, Chang Eun,Park, Donghyun,Kim, Yeon Jeong,Han, Kyung-Yeon,Lee, June-Young,Oh, Jin Ho,Kim, Sun Soo,Park, Woong-Yang,Lee, Won-Yong,Huh, Nam American Chemical Society 2014 ANALYTICAL CHEMISTRY - Vol.86 No.8
<P>Full automation with high purity for circulating tumor cell (CTC) isolation has been regarded as a key goal to make CTC analysis a “bench-to-bedside” technology. Here, we have developed a novel centrifugal microfluidic platform that can isolate the rare cells from a large volume of whole blood. To isolate CTCs from whole blood, we introduce a disc device having the biggest sample capacity as well as manipulating blood cells for the first time. The fully automated disc platform could handle 5 mL of blood by designing the blood chamber having a triangular obstacle structure (TOS) with lateral direction. To guarantee high purity that enables molecular analysis with the rare cells, CTCs were bound to the microbeads covered with anti-EpCAM to discriminate density between CTCs and blood cells and the CTCs being heavier than blood cells were only settled under a density gradient medium (DGM) layer. To understand the movement of CTCs under centrifugal force, we performed computational fluid dynamics simulation and found that their major trajectories were the boundary walls of the DGM chamber, thereby optimizing the chamber design. After whole blood was inserted into the blood chamber of the disc platform, size- and density-amplified cancer cells were isolated within 78 min, with minimal contamination as much as approximately 12 leukocytes per milliliter. As a model of molecular analysis toward personalized cancer treatment, we performed epidermal growth factor receptor (EGFR) mutation analysis with HCC827 lung cancer cells and the isolated cells were then successfully detected for the mutation by PCR clamping and direct sequencing.</P><P><B>Graphic Abstract</B> <IMG SRC='http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/ancham/2014/ancham.2014.86.issue-8/ac403456t/production/images/medium/ac-2013-03456t_0008.gif'></P><P><A href='http://pubs.acs.org/doi/suppl/10.1021/ac403456t'>ACS Electronic Supporting Info</A></P>