• 한국식품위생안전성학회지
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• 제33권1호
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• pp.50-57
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• 2018

Salmonella는 전세계적으로 식중독을 유발하는 주요 원인 균으로서, 식중독을 유발하는 Salmonella를 신속하게 검출하는 방법은 식품 안전을 위한 중요한 도구이다. Real-time PCR은 식중독균을 검출하기 위한 신속검사법으로 널리 사용되어 왔다. 최근에는 NBS LabChip real-time PCR이라는 새로운 시스템이 칩타입으로 조작이 간편하며 초고속의 real-time PCR 시스템이라는 보고가 있었다. 본 연구에서는 살모넬라의 신속한 검출을 위하여 NBS LabChip real-time PCR에 기반하여 real-time PCR 반응 시간이 20분 이내인 검출법을 확인하고자 하였다. 프라이머와 프로브 설계를 위해 두 개의 타겟 유전자(invA, stn)가 선택되었으며, 특이도와 민감도(검출한계)를 평가함으로 개발된 검출법을 검증하고자 하였다. 본 연구에서는 특이도 검증을 위해 Salmonella 균주 42주와 Non-Salmonella 균주 21주를 포함하였으며, 본 방법으로 Salmonella 42주에 대해서만 정확하게 검출이 가능하였다. 검출한계는 살모넬라 genome DNA 기준으로 $10^1copies/{\mu}L$으며, 소시지에서는 4시간 증균 이후 접종균수로서 $10^1CFU/g$에서 $10^2CFU/g$까지 검출이 가능하였다. 본 연구에서 개발된 검출법은 신속한 식중독 원인조사에 활용될 수 있을 것으로 기대된다.

• 광물과 암석
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• 제35권4호
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• pp.507-520
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• 2022

지질과학 분야에서 암석의 생성 시기, 지각과 맨틀 진화연구의 기초자료로 활용되는 Sr 동위원소비는 열이온화 질량분석기(thermal ionization mass spectrometry, TIMS) 혹은 다검출기 유도결합 플라즈마 질량분석기(multi-collector plasma ionization mass spectrometry, MC-ICP-MS)와 같은 질량분석기를 이용하여 측정할 수 있다. 이 기술보고에서는, Sr 동위원소비 측정시, 원소의 불완전한 화학적 분리가 Sr 동위원소비의 참값 (true value)에 어떤 영향을 미치는지를 비교하였다. 실험에는 상업용 레진, NBS987(NIST SRM987) Sr 동위 원소 표준물질 그리고 일본지질조사소의 암석표준시료 JG1a, JB3, JA1를 이용하였다. 비교실험 결과, NBS987 Sr 동위원소 표준시료, 일본지질조사소의 암석표준시료 JG1a, JB3, JA1 모두 불완전한 분리에 의해 Rb이 남아있는 경우 ⁸⁷Sr/⁸⁶Sr의 측정값이 변하는 것이 명확하게 관찰된다. 이는 질량분석기 특히 MC-ICP-MS로 동위 원소비를 측정하고자 하는 경우, 동종동위원소의 간섭에 대한 보정에도 불구하고 측정값은 참값에서 벗어나므로 완전한 분리가 중요한 인자임을 지시해준다. 그러므로 MC-ICP-MS를 이용한 Sr 동위원소비 측정결과를 보고할 때는, 동종동위원소에 의한 영향을 판단할 수 있도록 Sr의 동위원소 전체의 측정강도와 더불어 ⁸⁵Rb의 측정강도도 함께 보고돼야 할 것이다.

• 대한치과교정학회지
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• 제45권3호
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• pp.130-135
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• 2015

Objective: In our previous study, glass-fiber-reinforced plastics (GFRPs) made from polycarbonate and glass fibers were prepared for esthetic orthodontic wires using pultrusion. These laboratory GFRP wires are more transparent than the commercially available nickel-titanium wire; however, an investigation of the color stability of GFRP during orthodontic treatment is needed. Accordingly, in the present study, the color stability of GFRP was assessed using colorimetry. Methods: Preparation of GFRP esthetic round wires (diameter: 0.45 mm [0.018 inch]) using pultrusion was described previously. Here, to investigate how the diameter of fiber reinforcement affects color stability, GFRPs were prepared by incorporating either $13-{\mu}m$ (GFRP-13) or $7-{\mu}m$ glass (GFRP-7) fibers. The color changes of GFRPs after 24 h, and following 1, 2, and 4 weeks of coffee immersion at $37^{\circ}C$, were measured by colorimetry. We evaluated the color stability of GFRPs by two evaluating units: the color difference (${\Delta}E^*$) and National Bureau of Standards (NBS). Results: After immersion, both GFRPs showed almost no visible color change. According to the colorimetry measurements, the ${\Delta}E^*$ values of GFRP-13 and GFRP-7 were 0.73-1.16, and 0.62-1.10, respectively. In accordance with NBS units, both GFRPs showed "slight" color changes. As a result, there were no significant differences in the ${\Delta}E^*$ values or NBS units for GFRP-13 or GFRP-7. Moreover, for both GFRPs, no significant differences were observed in any of the immersion periods. Conclusions: Our findings suggest that the GFRPs will maintain high color stability during orthodontic treatment, and are an attractive prospect as esthetic orthodontic wires.

• Bulletin of the Korean Chemical Society
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• 제23권12호
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• pp.1845-1847
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• 2002

• Journal of Photoscience
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• 제9권2호
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• pp.82-85
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• 2002

33kDa extrinsic protein, an important protein in oxygenic photosynthesis, was known to have no fixed configuration in solution. At 20$\^{C}$ and pH 6, 33kDa extrinsic protein showed changes of free energy of -14.6 kJ/mor$\^$-1/ and of standard volume of -120mL/mol, respectively, with increase of hydrostatic pressure, comparatively lower than for most proteins. NBS modification of Trp241 in 33kDa extrinsic protein dramatically changes the secondary protein structure, its affinity to photosystem II as well as photosynthetic oxygen evolution. The relationship between structural change and transport of oxygen, water and proton is deserved a further study.

• 한국통신학회논문지
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• 제21권6호
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• pp.1576-1586
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• 1996

The subject of this paper is the analysis of a Wire-TEM cell(W-TEM cell) which has an inner wire array rather than a metallic septum;its basic structure is similiar to a NBS TEM cell. To verify improved performances of this W-TEM cell as a standard EM field generator, well-known quasi-static approximations are employed and their resultant ingegral equations are numerically analyzed by moment method. Although the electric field strength of a W-TEM cell is 1.4 dB lower than tht of a NBS TEM cell, the uniformity of EM field patterns in a W-TEM cell is improved. It is also shown that the EM field distortions resulting from loading by the conditing objects under test(loading effects), are decreased considerably. This paper also deals with the investigations about relationship between the EM field distributions and the number of wire composing the inner conductor. Finally, the experimental analysis is performed on the practical model which is built on the basis of the design variables brought out by the theoretical andnumerical analysis.

• 대한유전성대사질환학회지
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• 제22권1호
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• pp.9-14
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• 2022

Glutaric aciduria type 1 (GA1; OMIM #231670) is a rare autosomal recessive inherited neurometabolic disorder caused by the deficiency of glutaryl-CoA dehydrogenase. Infantile-onset GA1 is the most common form characterized by striatal injury and progressive movement disorder, and it is often triggered by an acute encephalopathic crisis within the first three years of life. Once this crisis occurs, there is a high likelihood for ineffective or limited conventional interventions, neurological disorders, or even death. Therefore, early diagnosis and immediate preventive management, such as dietary therapy, is essential. In the past decades, newborn screening (NBS) by tandem mass spectrometry for GA1 has been largely introduced in many countries including Korea, and it has led to improvements in the neurological outcomes of patients with GA1. In this review, the clinical symptoms, natural histories, and outcomes before and after the introduction of NBS in patients are discussed.

• 암석학회지
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• 제10권3호
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• pp.157-171
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• 2001

다검출기 유도결합 플라즈마 질량분석기(Multi-Collector Inductively Coupled Plasma Mass Spectrometer; MC/ICP/MS; AXIOM MC 모델)를 이용한 Pb동위원소 분석 시 고려 사항인 Pb/Ti 비율, Pb농도 영향, 기질 원소 영향을 살펴보고, NBS 981 용액을 2001년 3월부터 8월까지 42번 측정하여 정확도 및 재현성 을 검토하였다. 그리고 암석, 청동기 및 퇴적물 시료의 Pb 동위원소를 분석하여 열 이온화 질량분석기(TIMS) 자료와 비교하였다. NBS 981 Pb 200 ng으로 동위원소 비율을 측정하였을 때 $^{206}$ $Pb^{204}$ , $Pb^{207}$ //$Pb^{204}$ , $Pb^{208}$ $Pb^{204}$ Pb 비율은 약 500 ppm(2sd), $^{/}$$207^{206}$ Pb 및 $Pb^{208}$ $Pb^{206}$Pb 비율은 100~200 ppm(2sd)의 재현성을 얻을 수 있었다. Pb등위원소 분석의 정확도 및 재현성 측면에서 최적 조건은 1) Pb/Tl농도 비가 10 이고 2) Pb농도가 100 ng/ml 이상이며 3) 질량 분별 효과는 지수 법칙에 따라 보정하고 이 때 사용된 Tl의 동위원소 비율($^{205}$ $Tl^{203}$ Tl)은 2.3887이며 질량 분별 인자는 측정된 $208^{Pb}$ $^{206}$ 및 $Pb^{205}$ $Tl^{203}$ Tl 비율로부터 경험적으로 구해진 Pb의 인자를 이용하는 것이었다. 시료 중의 기질 원소들(matrix elements)에 의한 Pb 동위원소 비율의 영향은 없는 것으로 판단되며, TIMS와 비교된 시료들에 대하여 Pb 등위원소들은 측정 오차 범위 내에서 잘 일치하였다. 즉, MC/ICP/MS에 의한 Pb 동위원소 분석은 시료 전처리 단계를 줄여도 WS와 유사한 정밀도를 얻을 수 있어 신속한 분석방법이라 할 수 있다.다.

• BMB Reports
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• 제32권3호
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• pp.294-298
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• 1999

Myo-inositol monophosphate phosphatase is a key enzyme in the phosphoinositide cell-signaling system. Incubation of myo-inositol monophosphate phosphatase from porcine brain with N-bromosuccinimide (NBS) resulted in a time-dependent loss of enzyme activity. The inactivation followed pseudo-first-order kinetics with the second-order rate constant of $3.8{\times}10^3\;M^{-1}min^{-1}$. The time course of the reaction was significantly affected by the substrate myo-inositol-1-phosphate, which afforded complete protection against the loss of catalytic activity. Spectrophotometric studies indicated that about one oxindole group per molecule of enzyme was formed following complete loss of enzymatic activity. It is suggested that the catalytic function of myo-inositol monophosphate phosphatase is modulated by the binding of NBS to a specific tryptophan residue at or near the substrate binding site of the enzyme.

• Journal of Microbiology and Biotechnology
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• 제17권1호
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• pp.130-137
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• 2007

A disease resistance related gene, MbR7, was identified in the wild apple species, Malus baccata. The MbR7 gene has a single open reading frame (ORF) of 3,288 nucleotides potentially encoding a 1,095-amino acid protein. Its deduced amino acid sequence resembles the N protein of tobacco and the NL27 gene of potato and has several motifs characteristic of a TIR-NBS-LRR R gene subclass. Ectopic expression of MbR7 in Arabidopsis enhanced the resistance against a virulent pathogen, Pseudomonas syringae pv. tomato DC3000. Microarray analysis confirmed the induction of defense-related gene expression in 35S::MbR7 heterologous Arabidopsis plants, indicating that the MbR7 gene likely activates a downstream resistance pathway without interaction with pathogens. Our results suggest that MbR7 can be a potential target gene in developing a new disease-resistant apple variety.