• 반도체디스플레이기술학회지
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• 제4권2호
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• pp.7-10
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• 2005

[ $SiO_{2}$ ] or SiON is usually deposited and annealed after formation of silicide in real transistor fabrication processes. Nickel silicide and nickel silicide with Co interlayer were annealed at 650$^{\circ}C$ for 30 min with silica top layer in this study to investigate its thermal stability. SEM, XPS, and FPP(four point probe) were employed for the investigation. Nickel silicide with Co interlayer showed improved thermal stability. Co interlayer seems to play a key role to the stability of nickel silicide.

• 약학회지
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• 제57권6호
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• pp.388-393
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• 2013

Previously, we have reported that lovastatin, an inhibitor of 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase, increased melanin synthesis through intracellular $Ca^{2+}$ release in B16 cells. In this study we investigated the possible involvement of nitric oxide (NO) in the mechanism of lovastatin-induced melanogenesis. Lovastatin elevated NO formation in a dose-dependent manner. Treatment with mevalonate, farnesyl pyrophosphate (FPP) and geranylgeranyl pyrophosphate (GGPP), precursors of cholesterol, did not significantly alter the lovastatin-induced NO production, suggesting that inhibition of cholesterol metabolism may not be involved in the mechanism of this action of lovastatin. Both NO formation and melanogenesis induced by lovastatin was significantly suppressed by treatment with $N^G$-nitro-L-arginine methyl ester (L-NAME) and 2-(4-carboxy-2-phenyl)-4,4,5,5-tetramethylinidazoline-1-oxyl-3-oxide (cPTIO), an inhibitor of NO synthase and a NO scavenger, respectively. The lovastatin-induced NO production was significantly affected not by EGTA, an extracellular $Ca^{2+}$ chelator, but by an intracellular $Ca^{2+}$ chelator (BAPTA/AM) and intracellular $Ca^{2+}$ release blockers (dantrolene and TMB-8). Taken together, these results suggest that lovastatin may induce melanogenesis through NO formation mediated by intracellular $Ca^{2+}$ release in B16 cells. These results further suggest that lovastatin may be a good candidate for the therapeutic application of various hypopigmentation disorders.

• 전력전자학회논문지
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• 제27권1호
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• pp.63-73
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• 2022

The differential power processor (DPP) system is used to prevent a decrease in the total power generation due to the partial shading of photovoltaic modules. Compared with traditional series strings and full power processing (FPP) converter solutions, the DPP converter system shows advantages in terms of modularization process, volume, and transformation losses. However, the system has a limitation in that the power generation process of differential power processors produces lower power under certain irradiation conditions. This paper proposes a structure and operating algorithm for differential power processing modules that can use a single power converter for multiple strings. The operational algorithm for the differential power regulators allows the maximum power generation to be maintained in comparison with conventional series-connected and differential power processing methods even under various partial shading conditions. The operation algorithm of the proposed DPP is verified by Matlab/Simulink simulations.

• 제어로봇시스템학회:학술대회논문집
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• 제어로봇시스템학회 2005년도 ICCAS
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• pp.1183-1188
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• 2005

In this paper, we propose a 3D automated measuring system which measures the mandibular movements and the reference plane of the jaw movements. In diagnosis and treatment of the malocclusions, it is necessary to estimate the mandibular movements and the reference plane of the jaw movements. The proposed system is configured with double stereo-cameras, PC, two moving pattern plates(MPPs), two fixed pattern plates(FPPs) and one orbital marker. The virtual pattern plate is applied to calculate the homogeneous transformation matrices which describe the coordinates systems of the FPP and MPP with respect to the world coordinates system. To estimate the parameters of the hinge axis, the Euler's theorem is applied. The hinge axis points are intersections between the FPPs and the hinge axis. The coordinates of a hinge axis point with respect to the MPP coordinates system are set up to fixed value. And then, the paths of the jaw movement can be calculated by applying the homogeneous transformation matrix to fixed hinge axis point. To examine the accuracy of the measurements, experiments of measuring the hinge axis points and floating paths of them are performed using the jaw motion simulator. As results, the measurement errors of the hinge axis points are within reasonable boundary, and the floating paths are very similar to the simulator's moving path.

• 약학회지
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• 제57권1호
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• pp.24-31
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• 2013

Although statins, inhibitors of 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase, have been shown to increase melanin synthesis, the exact mechanism of this action is not fully understood. In this study we investigated the possible involvement of intracellular $Ca^{2+}$ signal in the mechanism of stimulation of melanin synthesis induced by lovastatin in B16 cells. Lovastatin stimulated the production of melanin in a dose-dependent manner in the cells. Treatment with mevalonate, FPP and GGPP, precursors of cholesterol, did not significantly suppress the lovastatin-induced melanin production, suggesting that inhibition of cholesterol synthesis may not be involved in the mechanism of the action of lovastatin. In addition, lovastatin did not significantly alter the cAMP concentration and the stimulated production of melanin by lovastatin was not significantly changed by treatment with H89, a potent inhibitor of protein kinase A, which demonstrates that cAMP pathway may not be involved. However, lovastatin increased intracellular $Ca^{2+}$ concentration in a dose-related fashion. Treatment with EGTA, an extracellular $Ca^{2+}$ chelator did not significantly alter the lovastatin-induced intracellular $Ca^{2+}$ increase and melanin synthesis, whereas intracellular $Ca^{2+}$ reduction with BAPTA/AM and intracellular $Ca^{2+}$ release blockers (dantrolene and TMB-8) completely blunted these actions of lovastatin. Taken together, these results suggest that the intracellular $Ca^{2+}$ release may play an important role in the lovastatin-induced stimulation of melanin synthesis in B16 cells. These results further suggest that lovastatin may be useful for the treatment of hypopigmentation disorders, such as vitiligo.

• 한국축산식품학회지
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• 제30권3호
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• pp.466-471
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• 2010

본 시험은 육계 사료 내 발효 과일박 및 신선초박의 급여가 저장기간 중 계육의 지방산화도, 지방산 조성 및 콜레스테롤에 미치는 영향을 가능성을 알아보고자 시험을 실시하였다. 시험 처리는 무첨가구인 대조구(Control, C), 발효 사과박 1.0%(T1), 발효 배박 1.0%(T2), 발효 감귤박1.0%(T3) 및 발효 신선초박 1.0%(T4)로 처리구를 나누어 시험을 실시하였다. 시험 전 기간 동안 생산성에서는 대조구와 비교 시 발효 사과부산물 1.0% 첨가구에서 118%의 개선효과를 갖는 것으로 나타내었으며 처리구간 비교시에도 발효 사과 부산물 첨가구에서 가장 높게 나타났다. 발효 과일 부산물 및 신선초 부산물을 급여한 계육의 저장기간 중 지방산패도는 3일차까지는 차이가 없었으나 종료일인 7일차에 발효 감귤부산물에서 3.7 MDA mg/kg으로 다른 처리구와 비교 시 지방산화도에 대해 유의적인 개선효과가 나타났다(p<0.05). 하지만, 발효 신선초 부산물에서는 다른 처리구와 비교 시 개선효과가 나타나지 않는 것으로 나타나 본 실험에서는 발효 신선초 부산물이 저장 기간 중 지방산패도에 큰 영향을 하지 않는 것으로 나타났다. 계육 내 지방산 조성에서 전체 처리구간에 유의적인 차이는 나타내지는 않았다. 콜레스테롤 함량은 대조구에서 가장 높았으며 발효사과부산물 첨가구에서 가장 낮게 나타났다. 결과적으로 본 시험에서는 육계 사료 내발효 식물체 부산물의 첨가급여가 육계의 생산성에 대한 개선효과는 물론 혈액 및 계육 내 콜레스테롤 감소효과가 나타나 콜레스테롤 함량이 낮은 축산물 생산에 대한 충분한 가능성을 나타낸 결과라 할 수 있다. 하지만 현재까지 발효사료를 이용한 연구가 축산식품 이외의 산업에 국한된 점을 감안 할 때 축산분야 역시 이에 대한 다각적인 연구가 필요할 것으로 사료된다.

• BMB Reports
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• 제40권5호
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• pp.625-635
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• 2007

The enzyme squalene synthase (EC 2.5.1.21) catalyzes a reductive dimerization of two farnesyl diphosphate (FPP) molecules into squalene, a key precursor for the sterol and triterpene biosynthesis. A full-length cDNA encoding squalene synthase (designated as TcSqS) was isolated from Taxus cuspidata, a kind of important medicinal plants producing potent anti-cancer drug, taxol. The full-length cDNA of TcSqS was 1765 bp and contained a 1230 bp open reading frame (ORF) encoding a polypeptide of 409 amino acids. Bioinformatic analysis revealed that the deduced TcSqS protein had high similarity with other plant squalene synthases and a predicted crystal structure similar to other class I isoprenoid biosynthetic enzymes. Southern blot analysis revealed that there was one copy of TcSqS gene in the genome of T. cuspidata. Semi-quantitative RT-PCR analysis and northern blotting analysis showed that TcSqS expressed constitutively in all tested tissues, with the highest expression in roots. The promoter region of TcSqS was also isolated by genomic walking and analysis showed that several cis-acting elements were present in the promoter region. The results of treatment experiments by different signaling components including methyl-jasmonate, salicylic acid and gibberellin revealed that the TcSqS expression level of treated cells had a prominent diversity to that of control, which was consistent with the prediction results of TcSqS promoter region in the PlantCARE database.

• Journal of Microbiology and Biotechnology
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• 제15권4호
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• pp.880-886
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• 2005

Using carotenoid genes of Erwinia herbicola, metabolic engineering was carried out for lycopene production with the pAC-LYCO4 plasmid, which was composed of a chromosomal DNA fragment of E. herbicola containing the crtE, crtB, and crtI genes under the control of the tetracycline promoter and the ipi gene of Haematococcus pluvialis with the trc promoter. Plasmid pAC-LYCm4 was constructed for efficient expression of the four exogenous genes using a strong RBS sequence and the same tetracycline promoter. The optimized expression construct of pAC-LYCm4 increased Iycopene production three times as compared with pAC-LYCO4. pAC-LYCm5 containing ispA behind the four exogenous genes was constructed. There was no significant difference in Iycopene production and cell growth between pAC-LYCm4 and pAC-LYCm5. FPP synthase encoded by ispA was not rate-limiting for Iycopene production. Each gene of crtE, crtB, crtI, and ipi was overexpressed, using pBAD-crtE, pBAD-crtIB, and pBAD-ipiHPI, in addition to their expression from pAC-LYCm4. However, there was no increase oflycopene production with the additional overexpression of each exogenous gene. The four exogenous genes appeared to be not rate-limiting in cells harboring pAC-LYCm4. When pDdxs, pBAD24 containing dxs, was introduced into cells harboring lycopene synthetic plasmids, lycopene production of pAC-LYCO4, pAC-LYCm4, and pAC-LYCm5 was increased by 4.7-, 2.2-, and 2.2-fold, respectively. Lycopene production of pBAD-DXm4 containing crtE, crtB, crtI, ipi, and dxs was 5.2 mg/g dry cell weight with $0.2\%$ arabinose, which was 8.7-fold higher than that of the initial strain with pAC-LYC04. Therefore, the present study showed that proper regulation of a metabolically engineered pathway is important for Iycopene production.

• 대한조선학회논문집
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• 제41권6호
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• pp.120-125
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• 2004

There are very few numbers of 115K FPP (Fixed Pitch Propulsion) Tankers for the Baltic ice class IA because the minimum power requirement of FMA (Finish- Swedish Maritime Association) needs quite large engine power and the 40 m Beam is out of calculation range of FMA minimum power requirements. The shipyard has no choice except to increase the engine power to satisfy FMA minimum power requirement Rule. And the operation cost, efficiency of hullform and its building cost are not good from the ship owners' point of view To solve this problem, the experience of ice breaking tanker development and the ice tank test results were adopted. The main idea to reduce the ice resistance is by reducing waterline angle at design load waterline. The reason behind the main idea is to reduce the ice-clearing force. Two hull forms were developed to satisfy Baltic Ice class IA. Two ice tank tests and one towing tank test was performed at MARC (Kvaener-Masa Arctic Research Center) and SSMB (Samsung Ship Model Basin) facilities, respectively. The purpose of these tests was to verify the performance in ice and open water respectively The hull form 2 shows less speed loss compared to Hull form 1 in open water operation but hull form 2 shows very good ice clearing ability. finally the Hull Form 2 satisfying Baltic ice class IA. The merit of this hull form is to use the same engine capacity and no major design changes in hull form and other related designs But the hull structure has to be changed according to the ice class grade. The difference in two hull form development methods, ice model test methods and analysis methods of ice model test will be described in this paper.

• 생명과학회지
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• 제22권8호
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• pp.1024-1033
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• 2012

Kocuria gwangalliensis로부터 카로티노이드 생합성 경로의 첫 번째 단계 기질인 geranylgeranyl pyrophosphate (GGPP)를 생합성하는 GGPP synthase (CrtE)를 암호화하고 있는 crtE를 클로닝 하여 이를 KgGGPP로 명명하였다. 기존 세균에서 밝혀진 GGPP synthase의 아미노산 서열을 NCBI에서 검색하여 KgGGPP synthase의 아미노산 서열과 비교한 결과 Kocuria rhizophila와 59.6%의 상동성을 가지는 것을 확인하였다. crtE 유전자를 대장균에서 발현 시키기 위하여 pCcrtE 재조합 DNA를 구축하였고, 이를 대장균에서 발현시킨 결과 약 41 kDa의 재조합 단백질이 과발현 됨을 확인 할 수 있었으며, 이 단백질은 기존 세균에서 밝혀진 GGPP synthase와 유사한 분자량을 가지고 있다는 것을 알 수 있었다. CrtE 재조합 단백질의 활성을 분석하기 위하여 대장균 내에서 라이코펜의 생합성을 유도 하였다. 대장균의 경우 메발론산 경로를 통하여 FPP와 IPP를 생합성 하지만 crtE, crtB, crtI 유전자가 없기 때문에 라이코펜을 생합성 하지는 못한다. 대장균 내에서 라이코펜의 생합성을 위해서는 crtE, crtB, crtI 유전자의 발현이 필수적으로 요구되기 때문에 crtB, crtI 유전자의 경우는 P. haeundaensis에서 유래한 유전자를 이용하여 pRScrtBI 재조합 DNA를 구축하여 그 발현을 유도하였다. 상기 두 재조합 DNA를 대장균에서 공발현 시켰으며, HPLC 분석법을 이용하여 대장균 내에서 라이코펜의 생산 유무에 따른 KgGGPP synthase의 활성을 분석하였다.