• Title/Summary/Keyword: PolA

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Optimization for nonlinear systems via block pulse transformation

  • Ahn, Doo-Soo;Park, Jun-Hun;Kim, Jong-Boo;Lee, Seung;Go, Young-Ki
    • 제어로봇시스템학회:학술대회논문집
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    • 1990.10b
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    • pp.969-973
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    • 1990
  • This paper presents a method of suboptimal control for nonlinear systems via block pulse transformation. The adaptive optimal control scheme proposed by J.P. Matuszewski is introduced to minimize the performance index. Nonlinear systems are controlled using the obtained optimal control via block pulse transformation. The proposed method is simple and computationally advantageous. Viablity of the this method is established with simulation results for the van der Pol equation for comparision with other methods.

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Development of a User-friendly continuous-system (사용자 편의성을 고려한 연속체계 모의실험 언어의 개발)

  • 민경하
    • Journal of the Korea Society for Simulation
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    • v.2 no.1
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    • pp.78-90
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    • 1993
  • 기존의 모의 실험언어를 이용해서 연속 체계를 모의 실험하는 것을 사용자가 언어에서 요구하는 형태로 모델을 형성해야 하는 어려움이 따른다. 따라서 본 연구에서는 사용자에게 최대한 편의성을 제공하는 연속체계 모의 실험언어인 PCSL (Postech Continuous -system Simulation Language)를 개발하였다. PCSL은 주어진 대상을 모델링한 미분방정식과 그것을 푸는데 필요한 여러 가지 제약 사항으로 이루어진 간단한 프로그램을 입력으로 받아 자동으로 모의 실험을 수행함으로서 사용자의 노력이 최소화하게 된다. PCSL 처리 시스템의 구성은 주어진 모델을 C 프로그램으로 변형하는 변환기, 모의 실험 알고리즘을 구현한 C 프로그램을 생성하는 생성기, 모의 실험을 수행하는 실행기, 사용자 인터페이스 등으로 되어있다. 구현 예로는 먼저 선형 상미분방정식의 예로 mass-damper-spring system, 비선형 상미분방정식의 예로 van der Pol 방정식, 연립 상미분방정식의 예로는 mixing tank problem 등을 보였다.

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BISTRO: Magnetic Fields in Serpens Main

  • Kwon, Woojin
    • The Bulletin of The Korean Astronomical Society
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    • v.44 no.1
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    • pp.41.2-41.2
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    • 2019
  • The B-fields In STar-forming Region Observations (BISTRO 1 and 2) is a large program of the James Clerk Maxwell Telescope (JCMT) using SCUBA-2 and POL-2, starting in 2016. We aim to study the roles of magnetic fields in star formation by observing 32 fields of nearby low-mass and high-mass star forming regions. The angular resolution and the wavelength provided by JCMT (14 arcsecond at 850 micrometer) are ideal to investigate the intermediate scales of magnetic fields (1000-20000 au) associated in cold dense cores and filaments. We report the current status of this project and discuss the magnetic fields of the Serpens Main molecular cloud in which several filaments with various physical properties have been identified.

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Neuropeptide Regulation of Signaling and Behavior in the BNST

  • Kash, Thomas L.;Pleil, Kristen E.;Marcinkiewcz, Catherine A.;Lowery-Gionta, Emily G.;Crowley, Nicole;Mazzone, Christopher;Sugam, Jonathan;Hardaway, J. Andrew;McElligott, Zoe A.
    • Molecules and Cells
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    • v.38 no.1
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    • pp.1-13
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    • 2015
  • Recent technical developments have transformed how neuroscientists can probe brain function. What was once thought to be difficult and perhaps impossible, stimulating a single set of long range inputs among many, is now relatively straight-forward using optogenetic approaches. This has provided an avalanche of data demonstrating causal roles for circuits in a variety of behaviors. However, despite the critical role that neuropeptide signaling plays in the regulation of behavior and physiology of the brain, there have been remarkably few studies demonstrating how peptide release is causally linked to behaviors. This is likely due to both the different time scale by which peptides act on and the modulatory nature of their actions. For example, while glutamate release can effectively transmit information between synapses in milliseconds, peptide release is potentially slower [See the excellent review by Van Den Pol on the time scales and mechanisms of release (van den Pol, 2012)] and it can only tune the existing signals via modulation. And while there have been some studies exploring mechanisms of release, it is still not as clearly known what is required for efficient peptide release. Furthermore, this analysis could be complicated by the fact that there are multiple peptides released, some of which may act in contrast. Despite these limitations, there are a number of groups making progress in this area. The goal of this review is to explore the role of peptide signaling in one specific structure, the bed nucleus of the stria terminalis, that has proven to be a fertile ground for peptide action.

Influence of substituted phenylcarbamoyl group on the fungicidal activites of a new 5,6-dihydro-2-trifluoromethyl-1,4-oxathiincarboxanilide derivatives (새로운 5,6-dihydro-2-trifluoromethyl-1,4-oxathiincarboxanilide 유도체의 항균활성에 미치는 치환-phenylcarbamoyl group의 영향)

  • Sung, Nack-Do;Yu, Seong-Jae;Nam, Kee-Dal;Chang, Kee-Hyuk;Hahn, Hoh-Gyu
    • The Korean Journal of Pesticide Science
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    • v.2 no.3
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    • pp.64-69
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    • 1998
  • New thirty derivatives of 5,6-dihydro-2-trifluoromethyl-1,4-oxathiin carboxanilide as substrate(S) were synthesized and their fungicidal activities in vivo against rice sheath blight(Rhizoctonia solani) and wheat leaf rust(Puccinia recondita) were examined. The structure activity relationships(SAR) between the activities($pI_{50}$) and a physicochemical parameters of substituents(X) at the phenylcarbamoyl group were analyzed using the adaptive regression analysis method. The 3-methoxy, 11, 3-isopropyloxy, 13 and 3-isopropyl substituent, 25 as X on the phenylcarbamoyl group exhibited the most highest fungicidal activity against the two fungi. The fungicidal potency of the (S) against Puccinia recondita was higher than Rhizoctonia solani. In case of Rhizoctonia solani, the molecular hydrophobicity(${\pi}>0$) and resonance effect(R<0) by meta-alkyl substitutents with electron donating were important factors in determining fungicidal activity. And the HOMO energy(HOMO>0), ABSQ, sum of absolute values of the atomic charges on each atom and specific polarizability(Sp.Pol<0) of (S) were significantly influential towards fungicidal activity against Puccinia recondita.. The interaction between (S) and receptor agonist from the based on SAR studies proceeds through charge-control reaction, and conditions to show higher activity has been also discussed.

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Gene Cloning and Expression of Thermostable DNA Polymerase from Thermus thermophilus HJ6 (Thermus thermophilus HJ6 유래 내열성 DNA Polymerase의 유전자 클로닝 및 발현)

  • Seo, Min-Ho;Kim, Bu-Kyoung;Kwak, Pyung-Hwa;Kim, Han-Woo;Kim, Yeon-Hee;Nam, Soo-Wan;Jeon, Sung-Jong
    • Microbiology and Biotechnology Letters
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    • v.37 no.1
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    • pp.17-23
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    • 2009
  • The gene encoding Thermus thermophilus HJ6 DNA polymerase (Tod) was cloned and sequenced. The open reading frame (ORF) of the Tod gene was composed of 2,505 nucleotides and encoded a protein (843 amino acids) with a predicted molecular weight of 93,795 Da. The deduced amino acid sequence of Tod showed 98% and 86% identities to the Thermus thermophilus HB8 DNA pol and Thermus aquaticus DNA pol, respectively, The Tod gene was expressed under the control of the bacteriophage $\lambda$ promoters PR and PL on the expression vector pJLA503 in Escherichia coli strain BL21 (DE3) codon plus. The expressed enzyme was purified by heat treatment, $HiTrap^{TM}$ Q column, and $HiPrep^{TM}$ Sephacryl S-200 HR 26/60 column chromatographies. The optimal temperature and pH for DNA polymerase activity were found to be $75{\sim}80^{\circ}C$ and 9.0, respectively. The optimal concentrations of $Mg^{2+}$ and $Mn^{2+}$ were 2.5 mM and 1 mM, respectively. The enzyme activity was activated by divalent cations, and was inhibited by monovalent cations. The result of the PCR experiment with Tod DNA polymerase indicates that this enzyme might be useful in DNA amplification and PCR-based applications.

A yeast Chromosomal Gene that Induces Defective Interfering Particles of L-A dsRNA Virus in $ski^-$ Host Cells ($ski^-$ 기주 세포에서 L-A dsRNA 바이러스의 defective interfering particle을 유도하는 효모 유전자)

  • 이현숙
    • Korean Journal of Microbiology
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    • v.29 no.2
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    • pp.75-79
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    • 1991
  • The yeast L-A virus (4.6 kb dsRNA genome) encodes the major coat protein and a "gag-pol" fusion minor coat protein that separately encapsidate itself and $M_{1}$, a 1.8 kb dsRNA satellite virus encoding a secreted protein toxin (the killer toxin). The teast chromosomal SKI genes prevent viral cytopathology by lowering the virus copy number. Thus, $ski^{-}$ mutants are ts and cs for growth. We transformed a ski2-2 virus-infested mutant with a yeast bank in a high copy cloning vector and selected the rare healthy transformants for analysis. One type of transformant segregated M-O L-A-O cells with high frequency. Elimination of the DNA clone from the ski2-2 strain eliminated this phinotype and introduction of the DNA clone recovered from such transformants into the parent ski2-2 strain, or into ski3 or ski6 mutants gave the same phenotype. This killer-curing phenotype was due to the curing of the helper L-A dsRNA virus. The 6.5 kb insert only had this activity when carried on a high copy vector and in $ski^{-}$ cells (not in $SKI^{+}$ cells). This 6.5 kb insert acts as a mutagen on L-A dsRNA producing a high rate of deletion mutations.mutations.

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Effect of Benzo[a]pyrene on Genes Related to the Cell Cycle and Cytochrome P450 of Saccharomyces cerevisiae

  • Lee, Hyun-Joo;Gu, Man-Bock
    • Journal of Microbiology and Biotechnology
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    • v.13 no.4
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    • pp.624-627
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    • 2003
  • Benzo[a]pyrene (B[a]P) is an environmental pollutant that has been implicated in carcinogenesis. Saccharomyces cerevisiae was treated with B[a]P, and the responses of its cytochrome P450 (CYP) enzyme and DNA-damage checkpoint genes were examined through gene expression profiles using a reverse transcription polymerase chain reaction (RT-PCR). The DNA-damage checkpoint genes tested were the chk1 and pds1 genes, involved in a metaphase arrest, the swi6 gene targeted by G1 arrest, the pol2 gene related to S phase arrest, and the cln2 gene encoding a cyclin protein, all of which are based on rad9 and rad24. Among these genes, no noticeable effect was found when the cells were exposed to various concentrations of B[a]P. However, the transcriptional activity of CYP51 was significantly different when the cells were exposed to B[a]P. Accordingly, the present results indicate that cytochrome P450 plays a more significant role than DNA-damage checkpoint genes in the response of S. cerevisiae to B[a]P.