• 한국지반환경공학회 논문집
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• 제12권10호
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• pp.23-28
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• 2011

본 연구에서는 생계면활성제, SWA 1503, Triton X-100 및 SDS를 포함하는 다양한 계면활성제의 토양에 대한 흡착 특성을 조사하였다. 프로인드리히 흡착 등온 모델이 계면활성제의 실험 결과를 가장 잘 설명하는 것으로 나타났다. 실험결과 점토 함량의 증가에 따라 계면활성제의 토양에 대한 흡착량이 증가하였다. 이와 같은 결과는 점토가 모래에 비해 표면적이 넓어 점토의 토양표면과 공극에 계면활성제의 흡착이 많이 이루어지는 것에 기인한다. 시간에 따른 흡착실험의 경우 biosurfactant > SWA 1503 > Triton X-100 > SDS 순으로 흡착량이 높은 것으로 나타났다.

• 한국동물생명공학회지
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• 제36권4호
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• pp.253-260
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• 2021

Organ transplantation is currently the most fundamental treatment for organ failure, but there is a shortage of organ supply compared to those in need. Regenerative medicine has recently developed a decellularization technique that overcomes the limitations of conventional organ transplantation and attempts to reconstruct damaged tissues or organs to their normal state. Several decellularization methods have been suggested. In this experiment, the decellularization methods were used to find effective decellularization methods for humanlike porcine placenta. The optimal conditions for decellular support are low DNA content and high glycos amino glycans (GAGs) and collagen content. In order to satisfy this condition, SDS and Triton X-100 and SDS + Triton X-100 were used as the detergent used for decellularization in this experiment. The contents were compared according to the decellularization time (0, 12, 24, 48 and 72 hours), and the concentrations of SDS (0.2, 0.5, 0.7 and 1.0%) were mixed in 1.0% Triton X-100 to analyze the contents. When decellularized using SDS and Triton X-100, respectively, it was confirmed that the contents of DNA and GAGs were opposite to each other. And decellularization treatment for 24 hours at 0.5% SDS was able to obtain an effective decellular support. If decellularization studies of various detergents can be obtained an effective decellular support, and furthermore, cell culture experiments can confirm the effect on the cells.

• Asian-Australasian Journal of Animal Sciences
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• 제21권3호
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• pp.358-363
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• 2008

The intracytoplasmic sperm injection (ICSI) procedure has recently been utilized to produce transgenic animals and may serve as an alternative to the conventional pronuclear microinjection in species such as pigs whose ooplasm is opaque and pronuclei are often invisible. In this study, the effects of sperm membrane disruption and electrical activation of oocytes on in vitro development and expression of transgene green fluorescent protein (GFP) in ICSI embryos were tested to refine this recently developed procedure. Prior to ICSI, sperm heads were treated with Triton X-100+NaCl or Triton X-100+NaCl+NaOH, to disrupt membrane to be permeable to exogenous DNA, and incubated with linearized pEGFP-N1 vector. To induce activation of oocytes, a single DC pulse of 1.3 kV/cm was applied to oocytes for $30{\mu}sec$. After ICSI was performed with the aid of a micromanipulator, in vitro development of embryos and GFP expression were monitored. The chemical treatment to disrupt sperm membrane did not affect the developmental competence of embryos. 40 to 60% of oocytes were cleaved after injection of sperm heads with disrupted membrane, whereas 48.6% (34/70) were cleaved without chemical treatment. Regardless of electrical stimulation to induce activation, oocytes were cleaved after ICSI, reflecting that, despite sperm membrane disruption, the perinuclear soluble sperm factor known to mediate oocyte activation remained intact. After development to the 4-cell stage, 11.8 (2/17, Triton X-100+NaCl+NaOH) to 58.8% (10/17, Triton X-100+NaCl) of embryos expressed GFP. The expression of GFP beyond the stage of embryonic genome activation (4-cell stage in the pig) indicates that the exogenous DNA might have been integrated into the porcine genome. When sperm heads were co-incubated with exogenous DNA following the treatment of Triton X-100+NaCl, GFP expression was observed in high percentage (58.8%) of embryos, suggesting that transgenic pigs may efficiently be produced using ICSI.

• 한국미생물·생명공학회지
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• 제17권1호
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• pp.29-34
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• 1989

고도 카드뮴 내성 효모, Hansenula anomala B-7 의 intact cell에 의한 카드뮴의 세포내 축적에 미치는 계면활성제의 영향를 검토하고, Triton X-100의 존재하에서의 카드뮴 축적에 미치는 제인자 등을 검토했다. 카드뮴의 축적은 0.1% Triton X-100과 Aerosol OT에 의하여 약 40% 이상 증가되었다. 카드뮴 이온에 대한 Km값은 0.247mM로 계산되었다. 카드뮴의 축적 최적 pH는 pH7.0에서 pH10.0 사이였으며, 최적온도는 4$0^{\circ}C$였다. 카드뮴의 최적 축적은 정치보다 진탕하므로 약 3배 증가되었으며, 진탕속도는 영향을 미치지 않았다. 카드뮴과 아연 이온을 공존시키므로 카드뮴의 축적이 아연 이온에 의하여 저해되었다.

• Korean Chemical Engineering Research
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• 제53권4호
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• pp.524-529
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• 2015

본 논문에서는 저온활성 protease의 생산을 최적화하기 위하여 극지 미생물인 Enterobacteriaceae sp. PAMC 25617의 반응표면분석법을 이용한 배지의 최적화를 수행하였다. One-factor-at-a-time 방법을 이용하여 yeast extract, TritonX-100이 protease의 생산에 영향을 미치는 주요인자인 것을 확인하였다. 물리적인 환경 요인으로 pH를 추가하여 반응표면분석 방법을 이용한 최대 protease 생산 농도를 갖는 각 인자들의 농도를 확인한 결과 5 g/L peptone, 3 g/L malt extract, 10 g/L $C_6H_{12}O_6$, 6.690 g/L yeast extract, 0.018 g/L TritonX-100의 농도에 pH 6.777의 조건에서 미생물을 배양하였을 경우, 최대 10.049 U/L의 protease가 생산될 수 있는 것으로 예측되었다. 실제 배양 결과 8.03 U/L의 protease가 얻어졌으며, 최적화 이전의 생산농도와 비교하여 150% 이상의 증가를 이루었다. 결과적으로 배지최적화를 통한 protease 생산량의 증가에 반응표면분석법의 적용이 유용하다는 것을 확인할 수 있는다. 이러한 결과로부터, 배지 최적화를 이용한 극지 미생물 유래 cold-adapted protease 생산량의 증가가 여러 산업 분야에서 유용하게 이용될 수 있을 것으로 생각된다.

• 한국미생물·생명공학회지
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• 제24권6호
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• pp.712-716
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• 1996

The effects of non-ionic surfactants (Triton X-100 and Tween 80) on cloned glucoamylase production and secretion in recombinant Saccharomyces cerevisiae culture were studied. Even though the extracellular glucoamylase activity was increased by addition of Tween 80 due to the increase of the cell mass, Tween 80 did not play a role in the increase of glucoamylase secretion. On the addition of Triton X-100 addition, the secretion efficiency was increased while the cell growth was inhibited. Triton X-100 was added to the culture broth after 24 hr of culture to minimize the inhibition of the cell growth, and consequently the glucoamylase activity in the culture broth was increased by 12%.

• 미생물학회지
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• 제24권4호
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• pp.370-376
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• 1986

From the outer membrane portion of Gram-negative Klebsiella pneumoniae, the activity of 2-furaldehyde dehydrogenase depending upon beta-nicotinamide adenine dinucleotide was detected. Cytoplasmic membrane was preferentially extracted from crude membrane with $Mg^{2+}$ and Triton X-100, and then outer membrane was collected by ultracentrifugation. The crude enzyme was obtained by solubilization of outer membrane with lysozyme, ethylene diamine tetraacetate and Triton X-100. Thereafter 2-furaldehyde dehydrogenase was partially purified through column chromatography on QAE-Sephadex Q-50 and Sephadex G-150 and the enzyme activity was analyzed by means of high performance liquid chromatography. The optimal pH for the activity of the enzyme was about 9.5 and the optimal temperature was about $85^{\circ}C$. The partially purified enzyme retained tis activity at $85^{\circ}C$ for 5 hours. The optimal concentration of Triton X-100 for the activity of the enzyme was about 1.5% in the reaction mixture.

• 멤브레인
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• 제22권3호
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• pp.224-233
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• 2012

기체분리용 분리막의 투과성능을 향상시키기 위해 비이온성 첨가제로 Triton X-100을 사용하여 건습식 상분리법에 의하여 polysulfone 중공사 막을 제조하였으며, 첨가제에 따른 기체투과 거동의 변화를 관찰하였다. 또한 에어갭, 고분자의 농도, 도프탱크 온도와 같은 다양한 방사 조건을 조절하여 그 영향을 관찰하였다. 제조된 중공사 막은 전자주사현미경(SEM)과 bubble flow meter를 통해 각각 모폴로지와 기체투과 특성에 대한 평가를 실시하였다. SEM 분석을 통해 Triton X-100이 첨가된 막은 다양한 에어갭에서도 매끄러운 외부 스킨층을 가지는 것을 확인하였다. 중공사 막의 거대기공은 에어갭이 4에서 90 cm로 증가함에 따라 더욱 발달하며, 높은 투과도를 나타내는 것을 확인하였다. 또한 상대적으로 낮은 고분자 농도(30 wt% polysulfone)와 높은 첨가제 농도(15 wt% Triton X-100) 조건에서 높은 투과도를 나타내었다. 도프 탱크 온도를 조절하였을 때, $100^{\circ}C$에서 제조된 막은 첨가제와 용매의 휘발로 인해 낮은 투과특성을 나타냈다.

• 대한화학회지
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• 제41권6호
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• pp.284-291
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• 1997

양이온성 계면활성제인 Cetylpyridinium Chloride(CPC)와 비이온성 계면활성제인 Triton X-100(TX-100)의 혼합계면활성제가 n-알코올(메탄올, 에탄올, 1-프로판올, 1-부탄올 및 1-펜탄올) 수용액에서 나타내는 임계미셀농도값($CMC^*$)을 25$^{\circ}C$에서 UV 분광광도법으로 측정하였다. 이들 $CMC^*$ 값들로부터 여러 가지 열역학 함수값들을 유사상태분리모델(pseudo-phase separation model)을 이용한 식에 의해 계산하였으며 그 값들을 상호 비교하였다. 그 결과 n-알코올들을 첨가한 CPC/TX-100 혼합계면활성제의 미셀화는 비이상적 혼합미셀모델과 잘 일치하였으며, 이상적 혼합미셀모델과는 음의 벗어남을 보였다.

• Journal of Photoscience
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• 제9권2호
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• pp.293-295
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• 2002

The structural stability of bacteriorhodopsin (bR) solubilized by Triton X-100 (TX-100) was studied by measuring the denaturation kinetics in the dark and under illumination, and compared with the structural stability of bR solubilized by octyl-${\beta}$-glucoside (OG). In the dark, bR solubilized by TX- 100 was more stable than bR solubilized by OG. Under illumination, bR solubilized by TX-100 showed light-induced denaturation in the same manner as bR solubilized by OG. These results in the dark well correlated with the experimental results of the visible CD band. Although solubilized bR in the TX-100 concentration range of 2-50 mM showed almost identical positive CD band and did not denature in the dark at 35$^{\circ}$C, the kinetic constant of the photobleaching increased with the increase of TX-100 concentration. These results suggested that photo-intermediates of solubilized bR are destabilized by TX-100 micelles.