• 폴리머
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• 제32권2호
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• pp.138-142
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• 2008

분자 날인 기술은 표적 분자에 대해 높은 선택도를 갖는 합성 재료를 제조하기 위한 효과적인 방법이다. 본 연구에서는 주형 분자로 테오필린(theophylline)을, 가교제로 폴리에스터-아크릴레이트 수지를 사용하여 UV 중합을 통해 분자 날인 고분자(MIP)를 합성하였다. 기능성 단량체 종류가 MIP의 성능에 미치는 영향을 알아보기 위해, 메타크릴산(mathacrylic acid), 아크릴산(acrylic acid), 그리고 아크릴 아미드(acrylic amide)를 기능성 단량체로 각각 사용하여 MIP를 합성하였다. MIP는 비날인 고분자(NIP)보다 테오필린에 대해 훨씬 더 높은 재결합 능력을 보였다. 메타크릴산을 사용하여 합성한 MIP는 가장 높은 재결합 능력을 보였다. MIP의 선택도는 테오필린과 분자구조가 유사한 카페인(caffeine) 용액을 사용하여 조사하였다. 클로로포름보다 극성인 증류수를 용매로 사용하였을 경우 MIP의 테오필린 재결합 성능은 감소하였다.

• Journal of Microbiology and Biotechnology
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• 제18권8호
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• pp.1377-1385
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• 2008

The uracil-sensing domain in archaeal family B-type DNA polymerases recognizes pro-mutagenic uracils in the DNA template, leading to stalling of DNA polymerases. Here, we describe our new findings regarding the molecular, mechanism underpinning the stalling of polymerases. We observed that two successive deaminated bases were required to stall TNA1 and KOD1 DNA polymerases, whereas a single deaminated base was enough for stalling Pfu DNA polymerase, in spite of the virtually identical uracil-sensing domains. TNA1 and KOD1 DNA polymerases have a much higher extension rate than Pfu DNA polymerase; decreasing the extension rate resulted in stalling by TNA1 and KOD1 DNA polymerases at a single deaminated base. These results strongly suggest that these polymerases require two factors to stop DNA polymerization at a single deaminated base: the presence of the uracil-sensing domain and a relatively slow extension rate.

• 대한수의학회지
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• 제38권3호
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• pp.565-573
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• 1998

To study the specific tools for the diagnosis of Newcastle disease virus (NDV) in chicken, polymerase chain reaction (PCR) and its presumable conditions were evaluated for the detection of hemagglutinin-neuraminidase (HN) gene of NDV RNA. For these purposes, Kyojeongwon strain of the NDV was propagated in allantoic cavity of SPF embryonating chicken eggs, and viral RNA was extracted from fractionated virus after the allantoic fluids were ultracentrifuged with sucrose gradient. The first-strand cDNA was then made for the HN gene of NDV RNA by reverse transcription at $42^{\circ}C$ for 1 hour using specific primer complementary to the HN gene. The single-stranded cDNA was used as template in the PCR of the HN-DNA, and various conditions of the PCR were evaluated to set up method for the specific detection of the HN-DNA. The PCR conditions promising for the detection of HN gene consist of preheating at $94^{\circ}C$, 5 min, 30 cycles of denaturation at $94^{\circ}C$, 1 min, annealing at $55^{\circ}C$, 1 min and polymerization at $72^{\circ}C$, 2 min, and a cycle of extension at $72^{\circ}C$, 5 min. when NDVs of allantoic fluids without fractionation were applied to the above PCR condition, the HN genes were detected effectively not only from Kyojeongwon but from other velogenic strains such as Herts and a field isolate.