• 한국염색가공학회지
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• 제10권1호
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• pp.20-24
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• 1998

Oligomeric extracts of poly(ethylene terephthalate-co-ethylene isophthalate)s [(PET/EI] are analyzed by high performance liquid chromatography(HPLC) and nuclear magnetic resonance spectroscopy (NMR). Existence of separated peaks for small cyclics of trimer and tetramer gives the existence of structural isomeric forms. NMR confirms that cyclization of PET/EI occurs more easily at the site of isophthaloyl unit.

• 한국섬유공학회:학술대회논문집
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• 한국섬유공학회 2001년도 가을 학술발표회 논문집
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• pp.247-250
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• 2001

2, 3-Dicyanopyrazine derivatives have been synthesized by condensation of diaminomaleonitrile(DAMN) and a -diketone compounds. Diaminomaleohitrile (DAMN) is well known as a tetramer of hydrogen cyanide and a useful compound in the chemical industry not on]y as a starting material for synthesis of various heterocyclic compounds but also as an intermediate for synthesis of glycine, adenine, guanine et al. (omitted)

• IMMUNE NETWORK
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• 제4권1호
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• pp.53-59
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• 2004

Background: Minor histocompatibility HY antigen, as a transplantation antigen, has been known to cause graft rejection in MHC (major histocompatibility complex) matched donor-recipient. The aim of our study is to investigate the role of male antigen (HY) disparity on MHC matched pancreatic islet transplantation and to examine the mechanism of the immune reaction. Methods: Pancreatic islets were isolated and purified by collagen digestion followed by Ficoll gradient. The isolated islets of male C57BL6/J were transplanted underneath the kidney capsule of syngeneic female mice rendered diabetic with streptozotocine. Blood glucose was monitored for the rejection of engrafted islets. After certain period of time, tail to flank skin transplantation was performed either on mouse transplanted with HY mismatched islets or on sham treated mouse. The rejection was monitored by scoring gross pathology of the engrafted skin. Results: HY mismatched islets survived more than 300 days in 14 out of 15 mice. The acceptance of second party graft (male B6 islets) and the rejection of third party graft (male BALB/c islets) in these mice suggested the tolerance to islets with HY disparity. B6 Skin with HY disparity was rejected on day $25{\pm}7$. However, HY mismatched skin transplanted on the mice tolerated to HY mismatched islets survived more than 240 days. Tetramer staining in these mice indicated the CTL recognizing MHC Db/Uty was not deleted or anergized. Conclusion: The islet transplantation across HY disparity induced tolerance to HY antigen in C57BL6 mouse, which in turn induced tolerance to HY mismatched skin, which otherwise would be rejected within 25 days. The MHC tetramer staining suggested the underlying mechanisms would not be clonal deletion or anergy.

• 한국염색가공학회지
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• 제14권6호
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• pp.305-312
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• 2002

In order to give a silk-like touch to PET fabrics, the PET fabrics were treated with NaOH alkaline solution in various conditions. In alkaline treatment, the liquor flow type pilot weight reduction apparatus with magnetostrictive ultrasonic transducer was used for the study. The effects of ultrasonic application, treatment time and temperature at NaOH 4% and 6"A solution on the decomposition rate of PET fabrics. From the results of the decomposition rate of PET fabrics, the qualitative and quantitative analysis of oligomer after decomposition of PET fabrics carried out by the HPLC. On the other hand, the surface pore characteristics of decomposition PET fabrics measured by porosimetery. The pore characteristics on the surface of treated PET fiber depended on the decomposition rate and did not depend on the ultrasonic cavitation. The pore diameter of alkaline untreated PET fiber were 15A and those of treated PET fibers were 5~6$\AA$ at the maximum pore volume. The average pore sizes of fiber before and after treatment were 141 h and 160h, respectively. Total amount of oligomer of the untreated PET fibers were 1.70wt% and 67.7% of total oligomer occupied with PET cyclic trimer and PET cyclic tetramer. Total amount of oligomer of fiber with 26.9% and 48.0% of weight loss without ultrasonic application were 1.78wt% and 1.79wt%, respectively. Also total amount oligomer of fibers which were reduced 27.7% and 48.2% of weight loss with ultrasonic application were 1.74wt%. This result showed that the removal rate of oligomer in the process of alkaline hydrolysis with ultrasonic higher than that of without ultrasonic application.tion.

• 한국식품영양학회지
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• 제14권6호
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• pp.579-584
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• 2001

Chitosna을 Bacillus pumilus BN-262 유래의 chitosanase로 처리하여 trimer, tetramer, pentamer가 전체 올리고당 중 64.3%에 달하는 비교적 저분자의 chitooligosaccharides로 구성된 LMW-chitooligosaccha-rides를 얻었으며, chitosan을 Trichoderma viride 유래의 cellulase로 처리하여 중합도7이상의 것이 전체 올리고당 중 49.3%에 달하는 상대적으로 분자량이 큰 chitooligosaccharides로 구성된 HMW-chitooligosac-charides를 얻었다. 제조된 chitooligosaccharides의 항균성과 콜로니 형성 저해 활성을 측정하였다. LMW chitooligosaccharides의 Bacillus cereus, Bacillus subtilis, Candida albicans, Escherichia coli, Escherichia coli O157:H7, Lactobacillus plantarum, Listeria mo-nocytogenes, Pseudomonas aeruginosa, Salmonella enteritidis, Salmonella typhimurium, Staphylococcus aureus, Streptococcus mutans에 대한 MIC(최소저해농도)는 각각 1.5%, 1.5%, above 2.0%, 1.5%, 1.5%, below 0.5%, 2.0%, 1.5%, above 2.0%. 1.0%, 1.5%, 1.0%였으며, HMW-chitooligosaccharides의 Bacillus cereus, Bacillus subtilis, Candida albicans, Esche-richia coli, Escherichia coli O157 : H7, Lactobacillus plantarum, Listeria monocytogenes, Pseudomonas aeruginosa, Salmonella enteritidis, Samlmonella typhimurium, Staphylococcus aureus, Streptococcus mutans에 대한 MIC는 각각 1.0%, 1.0%, 2.0% 이상, 1.0%, 1.0%, 0.25% 이하, 1.0%, 1.0%, 2.0%, 1.0%, 1.0%, 0.5%였다.

• 한국미생물·생명공학회지
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• 제18권3호
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• pp.268-272
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• 1990

Zymomonas mobilis의 알코올 탈수소 효소 유전자가 클로닝된 대장균 형질전환체의 세포 추출물로부터 알코올 탈수소 효소를 분리정제하였다. 형질전환된 Escherichia coli(pADS93)가 생산하는 Z.mobilis 유전자 유래의 알코올 탈수소 효소는 분자량이 40,000인 동일한 4개의 subunits로 구성된 tetramer임이 밝혀졌으며 이것은 Z.mobilis의 세포 추출물로부터 분리한 알코올 탈수소 효소와 동일하였다. 이 효소의 정반응(ethanol 산화)은 pH의 영향을 많이 받으며 pH는 10.0이었고 역반응(acetaldehyde 환원)에서는 최적의 pH가 7.5-8.5 이었지만 pH에 따라 크게 영향을 받지는 않았다.

• The Korean Journal of Physiology and Pharmacology
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• 제5권5호
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• pp.367-371
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• 2001

The chromosome 7-linked long QT syndrome (LQT2) is caused by mutations in the human ether-a- go-go-related gene (HERG) that encodes the rapidly activating delayed rectifier $K^+$ current, $I_{Kr},$ in cardiac myocytes. Different types of mutations have been identified in various locations of HERG channel. One of the mechanisms for the loss of normal channel function is due to membrane trafficking of channel protein. The decreased channel function in some deletion mutants appears to be due to loss of coupling with wild type HERG to form the functional channel as the tetramer. Most of missense mutants with few exceptions could interact with wild type HERG to form functional tetramer and caused dominant negative suppression with co-injection with wild type HERG showing variable effects on current amplitude, voltage dependence, and kinetics of activation and inactivation. Two missense mutants at pore regions of HERG found in Japanese LQT2 (A614V and V630L) showed accentuated inward rectification due to a negative shift in steady-state inactivation and fast inactivation. One mutation in S4 region (R534C) produced a negative shift in current activation, indicating the S4 serving as the voltage sensor and accelerated deactivation. The C-terminus mutation, S818L, could not express the current by mutant alone and did not show dominant negative suppression with co-injection of equal amount of wild type cRNA. Co-injection of excess amount of mutant with wild type produced dominant negative suppression with a shift in voltage dependent activation. Therefore, multiple mechanisms are involved in different mutations and functional abnormality in LQT2. Further characterization with the interactions between various mutants in HERG and the regulatory subunits of the channels (MiRP1 and minK) is to be clarified.

• Journal of Microbiology and Biotechnology
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• 제15권2호
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• pp.274-280
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• 2005

A chitinase was purified from the culture supernatant of Paenibacillus illinoisensis KJA-424 by protein precipitation, DEAE-Sephadex anion-exchange chromatography, and Sephadex G-150 gel filtration. The molecular weight of the purified chitinase was 54 kDa on SDS-PAGE and activity staining. Optimal pH and temperature were pH 5.0 and 60$^{circ}$C, the presence of 10 ruM Ag$^{+}$ and Hg$^{2+}$ inhibited the activity by $92.1/%$ and $97.7/%$, and the K$_{m}$ and V$_{max}$ values were 1.12 mg chitin mrl and 1.48$\mu$mol GlcNAc min$^{-1}$, respectively. The enzyme hydrolyzed tetramer to dimer, pentamer to dimer and trimer, and hexamer to dimer, trimer and tetramer, indicating an endo-splitting mechanism. The chitinase had no hydrolytic activity toward dimer and trimer. The chitinase inhibited the mycelial growth of Rhizoctonia solani, suggesting an antifungal property.

• 대한전자공학회논문지SD
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• 제39권8호
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• pp.17-23
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• 2002

전자빔 증착 장비를 이용하여 SrS:CuCl TFEL 소자를 제작한 후, 발광특성을 조사하였다. 형광체 모체는 SrS 분말을 사용하였고, 발광중심체로는 CuCl 분말을 0.05 ~ 0.6 at% 범위에서 첨가하였다. 증착 온도 500℃, 전자빔 전류 20 ~ 40 mA 및 증착율 5 ~ 10 /sec의 조건에서 형광층 두께를 6000 으로 증착시켰다. CuCl 농도가 낮을 때에는 monomer, dimer, trimer 및 tetramer 발광센터에 의한 청색 발광을 확인할 수 있었으나 휘도가 낮았다. CuCl 농도가 높을 때에는 dimer와 trimer 발광센터에 의한 밝은 녹청색 빛을 방출하였다. 최적의 발광특성은 CuCl 농도를 0.2 at% 첨가한 SrS:CuCl TFEL 소자에서 관찰되었으며, 문턱전압, 휘도(L/sub 40/), 효율(η/sub 20/) 및 CIE 색좌표는 각각 55 V, 728 cd/㎡, 0.49 lm/W 및 (0.21, 0.33)을 나타내었다.

• KSBB Journal
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• 제24권2호
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• pp.170-176
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• 2009

한국산 장류콩 종자로부터 최종적으로 Sephadex G-100상에서 분리한 lectin의 분자량, 적혈구 응집력, 온도, 열 안정성, 및 pH의 생화학적 특성을 조사하였다. 분리된 lectin을 SDS-PAGE한 결과, 분자량이 32 kDa와 22 kDa인 2개의 band가 나타났으며, Native PAGE에 의해서 108 kDa의 tetramer임을 알 수 있었다. Lectin은 trypsin을 처리한 사람의 A, B, AB, O 혈액과 쥐 혈액에서 혈구응집 반응이 일어나지 않았으나 토끼에서는 응집 반응이 일어났으며, trypsin을 처리하지 않은 모든 혈액에서는 응집반응이 일어나지 않았다. 이 lectin은 최적온도가 20-$50^{\circ}C$이며, 10-$60^{\circ}C$ 에서 열 안정성을 보였다. 최적 pH는 7.2로서 6.2 이하와 8.0 이상에서는 활성이 상설되었다.