• 제목/요약/키워드: solvent pH

검색결과 898건 처리시간 0.029초

Organic Solvent and pH Induced Alteration of Product Specificity of CGTase

  • Park, Kyo-Sun;Oh, Hyun-Mi;Choe, Hui-Woog;Park, Chung-Ung;Lee, Kang-Min
    • Biotechnology and Bioprocess Engineering:BBE
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    • 제3권2호
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    • pp.78-81
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    • 1998
  • Cyclodextrin glucanotransferase [CGTase, E.C.2.4.1.19] is an extracellular enzyme, which catalyzes he formation of ${\alpha}$-, ${\beta}$-, ${\gamma}$- CDs from starch. Their proportions of formations depend on enzyme sources and reaction conditions. To understand what determines the product specificity of CGTases, we examined the alteration of product specificity of CGTase from Bacillus macerans by organic solvent sand pH. At acidic pH range less than pH 6 where the enzyme was unstable, the ratio of ${\alpha}$-/ ${\beta}$-CD production was increased 4 times more than that at neutral pH range. As we increased the concentration of 2-butanol, ${\alpha}$-/ ${\beta}$-CD ratio was proportionally increased but / ratio remained constant. The ${\alpha}$-/ ${\beta}$-CD ratio of products was increased in the reaction media which yielded low products.

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복분자 추출조건에 따른 페놀성 화합물의 특성변화 (Changes in Phenolic Compounds Properties of Rubi Fructus Extract Depending on Extraction Conditions)

  • 윤성란;정용진;이기동;권중호
    • 한국식품영양과학회지
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    • 제32권3호
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    • pp.338-345
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    • 2003
  • 복분자 추출에 따른 페놀성화합물의 특성변화를 조사하기 위하여 반응표면분석법으로 시료에 대한 용매비(5, 10, 15 mL/g), 에탄을 농도(20, 40, 60%) 및 추출시간(2, 4, 6 hr)을 달리하여 가용성 고형분 함량, 총 페놀성 화합물 함량, 전자 공여능, 항산화능 및 아질산염소거능의 변화를 모니터링 하였다. 가용성 고형분 함량, 총 페놀성 화합물 함량, 전자공여능 및 항산화능은 시료에 대한 용매비의 영향을 많이 받는 것으로 나타났다. 아질산염 소거능의 경우 pH 1.2 및 6.0에서는 에탄을 농도의 영향을 많이 받았으며, pH 3.0및 4.2에서는 추출시 간의 영 향을 많이 받는 것으로 나타났다. 가용성 고형분 함량에 있어서 최적 추출조건은 시료에 대한 용매비 14.16mL/g, 에탄을 농도 39.08% 및 추출시간 2.99 hr으로 나타났으며, 총페놀성 화합물 함량의 경우 시료에 대한 용매비 14.06mL/g, 에탄을 농도 35.51% 및 추출시간 3.15 hr으로 나타났다

pH-Sensitive Curdlan Acetate Microspheres를 이용한 Indomethacin의 방출 특성

  • 이창문;이영진;이기영;최춘순
    • 한국생물공학회:학술대회논문집
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    • 한국생물공학회 2003년도 생물공학의 동향(XII)
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    • pp.739-742
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    • 2003
  • 생분해성인 Curdlan을 이용하여 pH 의존성 약물 전달계 개발을 위한 실험을 수행한 결과, pH 1,4에서 약물 방출 보다 pH 7.4에서 약물 방출이 10배 이상 증가하였다. 이러한 결과로 curdlan acetate microsphere는 pH 의존성 약물 전달계로 유용하다고 판단된다.

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Bacillus sp. PY123 균주가 생성하는 수용성 황색수소의 부분 정제 및 그 안정성 (Partial Purification and Stability of a Water-soluble Yellow Pigment from Bacillus sp. PY123.)

  • 김지연;김광현;김병우;이광배
    • 환경위생공학
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    • 제14권4호
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    • pp.35-40
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    • 1999
  • For application of a yellow pigment as food additives, stability of a water-soluble yellow pigment from Bacillus sp. PY123 was investigated. The yellow pigment from Bacillus sp. PY123 was purified with pH treatment, activated carbon and silica gel column chromatography. The partial purified yellow pigment appeared only one spot on silica gel TLC after 12 evaporation and under irradiation of UV 253nm at dark room. Rf value of the pigment was measured at 0.04 and 0.12 with development of a solvent mixture (Butanol : Acetic acid : water = 4 :1:5) and a solvent mixture (Isopropanol : Ammonia : Water = 9 :1: 2), respectively, The partial purified pigment appeared a white fluorescence under UV365nm irradiation. The partial purified yellow pigment had a main peak and a minor peak on HPLC using 20mM phosphate buffer(pH 7.0) at 1ml/min flow rate. The partial purified pigment was stable at heat treatment, acidic pH, oxide-reductants and surfactants.

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Adsorption and Separation of U (VI), Co (II), and Dy (III) Metal Ions on Crown Synthetic Resin

  • Kim, Joon-Tae
    • 통합자연과학논문집
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    • 제10권1호
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    • pp.43-50
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    • 2017
  • Synthetic resins were combined 1-aza-12-crown-4 macrocyclic ligand with styrene divinylbenzene copolymer having 1%, 2%, 8%, and 16% crosslink by a substitution reaction. These synthetic resins were confirmed by chlorine content, elementary analysis, SEM, surface area, and IR-spectrum. As the results of the effects of pH, crosslink of synthetic resin, and dielectric constant of a solvent on metal ion adsorption for resin adsorbent, the metal ions showed high adsorption at pH 3 or over. Adsorption selectivity for the resin in ethanol solvent was the order of uranium ($UO_2{^{2+}}$) > cobalt ($Co^{2+}$) > dysprosium ($Dy^{3+}$) ion, adsorbability of the metal ion was the crosslink in order of 1%, 2%, 8%, and 16% and it was increased with the lower dielectric constant. In addition, theses metal ions could be separated in the column with 1% crosslink resin by using nitric acid (pH 2.0) as an eluent.

Synthesis and optimization of immunomodulating hydrogel for biomedical application

  • Muthuramalingam, Karthika;Park, Sanggyu;Cho, Moonjae
    • Journal of Applied Biological Chemistry
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    • 제61권4호
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    • pp.351-355
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    • 2018
  • Treatment towards wound healing, a complex and dynamic process, has been given a great deal of efforts in the last few decades. Focus has been imposed on developing wound dressings that meet the requirements for proper wound healing. In this study, hydrogel made from blends of poly (vinyl alcohol) and ${\beta}$-1,6-branched-${\beta}$-1,3-glucan (beta-glucan) were synthesized by modified solvent casting method for wound dressing application. Optimization of hydrogel composition and analysis of wound dressing parameters such as stability and fluid uptake capacity (in the presence of water, saline and different pH solutions) has been studied. The result indicated that the PVA/beta-glucan hydrogel hold its structural integrity even at alkaline pH (pH~9) and upholds fluids four times of its original weight. Thus, the developed hydrogel is expected to be a promising candidate as wound dressing.

Electroosmosis in skin during iontophoresis: effect of pH, current density and ionic strength

  • Kim, Su-Youn;Kang, Rae-Young;Kim, Hye-Ji;Roh, Kyung-Eun;Oh, Seaung-Youl
    • 대한약학회:학술대회논문집
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    • 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.1
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    • pp.294.1-294.1
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    • 2003
  • At pH 7.4 (physiological pH), skin is permselective to cations, due to the net negative charge of the current passing channels (pores) in skin. This causes the convective solvent flow (electroosmotic flow) from anode to cathodal direction. In this work, we have investigated several factors (pH. current density and ionic strength) that can affect the electroosmotic flow. (omitted)

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크레졸-물 용매펄프화의 탈리그닌에 관한 초미세구조적 분석 (Utrastructural Analysis of the Delignification Behaviour in P-Cresol-Water Solvent Pulping)

  • 김창근;조병묵
    • Journal of the Korean Wood Science and Technology
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    • 제20권1호
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    • pp.60-71
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    • 1992
  • To investigate the delignification behaviour in solvolysis pulping process, Populus alba ${\times}$ glandulosa H. and Pinus Kuraiensis S. et Z. were cooked with p-cresol and vater solvent(2:8, 5:5, 8:2 v/v) at $175^{\circ}C$ for 9 cooking time levels(20, 40, 60, 80, 100, 120, 140, 160, 180, min). Pulp yield, residual lignin content, de lignification rate, decarborhydration rate were determined. Delignification behaviours were analyzed by TEM. 1. The p-cresol-water solvent cooking of P. alba ${\times}$ glandulosa showed good delignification at the solvent system which the mixture ratio of p-cresol and water were 2:8(v/v), while the cooking of P. koraiensis with the p-cresol and water mixture ratio of 5:5 was no good. 2. P. alba ${\times}$ glandulosa showed three step-delignification phenomena at the solvent system which the mixture ratio of p-cresol and water were 2:8(v/v) anti 5:5(v/v). But P. koraiensis showed a first order delignification reaction at the same mixture ratio of p-cresol and water solvent system. 3. In TEM micrograph obtained for the solvent system which the mixture ratio of p-cresol and water was 5:5(v/v), the partial delignification of the cell corner of P. alba ${\times}$ glandulosa and P. koraiensis were observed at 60min. of cooking time. Complete delignification at the cell corner of P. alba ${\times}$ glandulosa was observed at 160min. and that of P. koraiensis was observed of 180min. of cooking time. 4. In optical microscopic observation, fiber separation of P. alba ${\times}$ glandulosa occured at 120min. and that of P. koraiensis began at 140min. of cooking time. 5. At the solvent system which the mixture ratio of p-cresol and water was 5:5(v/v), middle layer on secondary wall($S_2$) and cell corner of P. alba ${\times}$ glandulosa were more selectively delignified than primary wall(P) and outer layer on secondary wall($S_1$). However P. koraiensis did not showed any difference in delignification between cell wall layers and cell corner.

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용매 고분자막 상에 고정된 나트륨 이온선택성 물질의 착물형성상수 결정 (Determination of Complex Formation Constant of Sodium-Selective Ionophores in Solvent Polymeric Membranes)

  • 강태영;김성배;오현준;한상현;차근식;남학현
    • 분석과학
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    • 제13권4호
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    • pp.466-473
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    • 2000
  • 용매고분자막 상에 칼륨과 다양한 나트륨이온 선택성 중성 운반체의 착물형성상수(${\beta}_{MLn}$)를 고분자막형 광센서(optode)와 이온선택성 전극(ISE)을 이용하여 결정하였다. 수소이온선택성 발색물질(chromoionophore : ETH 5294)에 가장 널리 쓰이는 나트륨 이온선택성 물질들(4-tert-butylcalix[4]arenetetraacetic acid tetraethyl ester, ETH 2120, bis[(12-crown-4)methyl] dodecyl-methylmalonate 및 monensin methyl ester)을 첨가한 막과 첨가하지 않은 막으로 두 가지 다른 조성의 PVC 막을 제작하여, 일정 pH(0.05 M Tris-HCl, pH7.2)에서 알칼리금속 양이온(나트륨과 칼륨)의 농도 변화에 따른 광학적 감응을 측정하고, 또 일정한 알칼리금속 양이온 농도(0.1M)에서 pH변화에 따른 광학적 감응을 측정하였다. 또한 유사한 조성의 막을 각각 재래식 전극체에 장착하고 일정한 알칼리금속 양이온의 농도(0.1M)에서 pH 변화에 따른 전위치를 측정하였다. 양이온/수소이온의 활동도 비($a_{M^+}/a_{H^+}$)와 상대흡광도로 도시한 광센서 감응곡선과 수소이온농도에 따른 전위차 감응곡선으로부터 나트륨 이온선택성 리간드들의 착물형성상수를 결정하였다. 목적이온과 방해이온에 대한 착물형성상수들의 비로부터 얻어진 값은 실험적으로 얻어진 이온선택성 전극의 선택계수와 근접함을 확인하였다.

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The Influence of Mixed Solvents Volatility on Charge State Distribution of Peptides During Positive Electrospray Ionization Mass Spectrometry

  • Nielsen, Birthe V.;Abaye, Daniel A.;Nguyen, Minh T.L.
    • Mass Spectrometry Letters
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    • 제8권2호
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    • pp.29-33
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    • 2017
  • Understanding the mechanisms that control and concentrate the observed electrospray ionisation (ESI) response from peptides is important. Controlling these mechanisms can improve signal-to-noise ratio in the mass spectrum, and enhances the generation of intact ions, and thus, improves the detection of peptides when analysing mixtures. The effects of different mixtures of aqueous: organic solvents (25, 50, 75%; v/v): formic acid solution (at pH 3.26) compositions on the ESI response and charge-state distribution (CSD) during mass spectrometry (MS) were determined in a group of biologically active peptides (molecular wt range 1.3 - 3.3 kDa). The ESI response is dependent on type of organic solvent in the mobile phase mixture and therefore, solvent choice affects optimal ion intensities. As expected, intact peptide ions gave a more intense ESI signal in polar protic solvent mixtures than in the low polarity solvent. However, for four out of the five analysed peptides, neither the ESI response nor the CSD were affected by the volatility of the solvent mixture. Therefore, in solvent mixtures, as the composition changes during the evaporation processes, the $pK_b$ of the amino acid composition is a better predictor of multiple charging of the peptides.