• 제목/요약/키워드: 2-furaldehyde

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Klebsiella pneumoniae 균주의 세포외막에서 분리한 2-furaldehyde dehydrogenase의 특성에 관한 연구 (Characterization of the Outer Membrane-Associated 2-Furaldehyde Dehydrogenase from Klebsiella pneumoniae)

  • 이준우;강사욱;하영칠;한홍의
    • 미생물학회지
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    • 제26권3호
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    • pp.197-206
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    • 1988
  • Klebsiella pneumoniae의 세포외막으로부터 2-furaldehyde를 2-furoic acid로 산화시키는 2-furaldehyde dehydrogenase를 분리하여 그 특성을 조사하였다. 이 효소는 $\beta$-$NAD^{+}$를 특이적으로 요구하였다. 분리과정중의 효소활성도는 2-furaldehyde를 기질로 사용하고 $\beta$-$NAD^{+}$를 조효소로 사용하면서 high performance liquid chromatography에 의해 측정 되었다. 세포외막은 Percoll의 밀도흉배에 의한 초원심분리방법과 $Mg^{2+}$, Triton X-100으로 용해시킨 후, 초원심분리시키는 방법으로 수집되었다. 세포외막단백질은 EDTA와 lysozyme을 처리함으로서 얻어졌고, 효소는 QAE-Sephadex Q-504 S Sephadex G-100-을 사용하면서 column chromatography 방법에 의해 분리되었다. 본 효소는 $85^{\circ}C$, PH9.5, 그리고 1.5% (vol/vol) Triton X-100의 존재하에서 최대활성을 보여주었다. 효소의 분자량은 nondenaturing polyacrylamide gel e electrophoresis의 결과, 88, 000.으로 추정되었고, 2-furaldehyde에 대한 효소의 Km값은 4.72 mM 이였다.

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Klebsiella pneumoniae 균주의 세포외막으로부터 2-Furaldehyde Dehydrogenase의 부분정제에 관하여 (Partial Purification of the Outer Membrane-Associated 2-Furaldehyde Dehydrogenase from Klebsiella pneumoniae)

  • 이준우;이병웅;강사욱;하영칠;유병설;한홍의
    • 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.

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5-치환 2-Furaldehyde류의 염기도 상수 (Basicity Constants (pKBH+) of 5-Substituted 2-Furaldehydes)

  • 이종팔;임귀택;이용희;구인선;류준하
    • 대한화학회지
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    • 제46권4호
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    • pp.323-330
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    • 2002
  • 5-치환 2-Furaldehyde류의 양성자화 반응을 25$^{\circ}C$, 황산 수용액 속에서 분광광도법으로 조사하여 각 반응물질의 염기도 상수인 p$K_{BH+}$값을 과산도 (execess acidity)법으로 구하였다. 전자 주게 치환기를 가진 5-methyl-2-Furaldehyde의 염기도 상수는 전자 받게 치환기를 가진 5-nitro-2-Furaldehyde의 염기도 상수보다 크게 나타났으며 pK단위로 3.25정도 차이가 나는 것을 알수 있었다. 각 반응기질의 양성자화 반응으로부터 형성된 짝산의 용매화 정도를 나타내는 m값은 본 반응계와 유사한 반응물질인 acetophenone과 비슷한 크기로 나타남을 알 수 있었다. 2-Furaldehyde의 치환기 변화에 따른 염기고 상수의 변화 값인 -${\Delta}pK_{BH+}$과 m의 상관관계가 좋은 직선성을 보였다

시판품 숙지황중의 5-hydroxymethyl-2-furaldehyde (5-HMF) 함량분석 (Quantitative Analysis of 5-hydroxymethyl-2-furaldehyde (5-HMF) in the commercial Rehmanniae Radix Preparata)

  • 김호경;전원경;김영아;고병섭
    • 한국한의학연구원논문집
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    • 제9권1호
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    • pp.129-135
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    • 2003
  • Rehmanniae Radix Preparata attributes good blood circulation and it has been used for the treatment of dizziness, men's sterility, excessive loss of blood and weakness. On the quality control of commercial Rehmanniae Radix Preparata, quantitative determination of 5-hydroxymethyl (5-HMF) using HPLC method has been conducted. Quantitative analysis of S-hydroxymethyl-2-furaldehyde (5-HMF) in commercial Rehmanniae Radix Preparata showed average of $0.136{\pm}0.057%$ in 14 samples collected throughout the regions of Korea.

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Inhibitory Effect of Melanogenesis by 5-Pentyl-2-Furaldehyde Isolated from Clitocybe sp.

  • Kim, Young-Hee;Choo, Soo-Jin;Ryoo, In-Ja;Kim, Bo-Yeon;Ahn, Jong-Seog;Yoo, Ick-Dong
    • Journal of Microbiology and Biotechnology
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    • 제22권6호
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    • pp.814-817
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    • 2012
  • In the continued search for melanogenesis inhibitors from microbial metabolites, we found that the culture broth of Clitocybe sp. MKACC 53267 inhibited melanogenesis in B16F10 melanoma cells. The active component was purified by solvent extraction, silica gel chromatography, Sephadex LH-20 column chromatography, and finally by preparative HPLC. Its structure was determined as 5-pentyl-2-furaldehyde on the basis of the UV, NMR, and MS spectroscopic analysis. The 5-pentyl-2-furaldehyde potently inhibited melanogenesis in B16F10 cells with an $IC_{50}$ value of 8.4 ${\mu}g/ml$, without cytotoxicity.

수치에 따른 숙지황 중의 5-hydroxymethyl-2-furaldehyde 함량분석 (Quantitative Determination of 5-Hydroxymethyl-2-furaldehyde in the Rehmanniae Radix Preparata Samples at Various Processing Stages)

  • 황석연;황방연;최우희;정한진;허재두;이경순;노재섭
    • 생약학회지
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    • 제32권2호통권125호
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    • pp.116-120
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    • 2001
  • In order to determine the content of 5-hydroxymethyl-2-furaldehyde (5-HMF) in the Rehmanniae Radix Preparata, 5-HMF was isolated from the EtOAc fraction of the Rehmanniae Radix Preparata samples and identified by spectroscopic and physicochemical evidences. Twenty one samples prepared on the basis of increasing number of stewing times with wine were analyzed by HPLC. From this analysis, it was revealed that the samples processed under one to nine times of stewing showed increasing pattern in 5-HMF contents. And the samples processed under 9 to 18 times of stewing showed 0.53-0.74% in 5-HMF contents. However, for those samples processed more than 19 times, 5-HMF content profile showed decreasing pattern.

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만삼의 성분에 관한 연구 (A Phytochemical Study on Components of Codonopsis pilosulae Radix)

  • 이인란
    • 약학회지
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    • 제22권1호
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    • pp.1-7
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    • 1978
  • Two yellowish oily liquid compounds, $C_{6}H_{6}O_{3}$(A) bp $189^{\circ}$, $n^{20}_{D}$ 1.3697 and $C_{7}H_{8}O_{3}$(D) bp $164^{\circ}$, $n^{20}_{D}$1.5075, were isolated from root of Codonopsis pilosula (Franch.) Nannfeldt (Campanulaceae). Their structures were identified as 5-(hydroxymethyl)-2-furaldehyde(A) and 5-(methoxymethyl)-2-furaldehyde(D). The latter is a new compound among the known natural products.

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5-Nitro-2-furfurylidend sulfanilamide류의 합성과 항균작용에 관한 연구 (Studies on the Synthesis and Antibacterial Activity of 5-Nitro-2 -furfurylidene Sulfanilamides)

  • 박정섭
    • 미생물학회지
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    • 제12권2호
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    • pp.77-84
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    • 1974
  • In order to study 5-nitro-2-furaldehyde derivatives having more effective antibacterial activity, four new $N^4$-(5-nitro-2-furfurylidene)-$N^1$-substituted sulfanilamides$N^1$-3,4-dimethyl-5-isoxazoyl-$N^4$-5-nitro-2-furfurylidene sulfanilamide, $N^1$-4,6-dimethyl-2-pyrimidyl-$N^4$-5-isoxazoyl-$N^4$-5-nitro-2-furfurylidene sulfanilamide, $N^1$-6-methoxy-3-pyridazinyl-$N^4$-5-nitro-2-furaldehyde with sulfa drugs such as sulfisoxazole, sulfamethazine, sulfamethoxypyridazine, and sulfadimethoxine. All compounds were tested for antibacterial activity in vitro on the following micro-organisms : Staphylococcus aureus, Bacillus subtilis, Escherichia coli, and Proteus vulgaris. Each compound exhibited a fair bacteriostatic activity against each microorganism. Above all, sulfisoxazole derivatives showed higher activity than the others. Each compound was most active against Staphylococcus aureus, whereas least active against proteus vulgaris.

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궐련지의 섬유종류가 담배 연기성분에 미치는 영향 (The comparative analysis of smoke components delivered from cigarette papers manufactured by flax and wood pulp)

  • 김종열;김정열;신창호;이근회;이동욱;제병권
    • 한국연초학회지
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    • 제21권2호
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    • pp.119-127
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    • 1999
  • This study was conducted to evaluate the effect of cigarette papers, flax and wood, on the delivery of mainstream smoke. The main components of cigarette papers were cellulose, hemicellulose, lignin, and pectin. Lignin contents, known as precursor of smoke's phenolic compounds, of the flax and wood cigarette papers were 5.8% and 10.6%, respectively. The pyrolysis products of cigarette papers were similar by the profile of total ion chromatogram. But, the area % of some components, such as 1,3-cyclopentanedione, 3,5- dimethyl cyclopentane-1,2-dione, 2-hydroxy-3-methyl-2-cyclopentenone, dihydro-2(3H)-furanone, 3-methyl-2(5H)-fruanone, and 5-methyl-2-furaldehyde delivered through pyrolysis of the flax cigarette paper were higher than that of wood cigarette paper. Otherwise, the area % of some components, such as 2-methyl-cyclopentene-l-one), 2,3-butanedione, 2-cyclopentene-l-one, and 5-hydroxy-2-methyl-furaldehyde, 2-furaldehyde delivered through pyrolvsis of the wood cigarette paper were higher than that of flax cigarette paper. To identify the difference between two cigarette papers, we used the cigarette column filled with the cut cigarette paper instead of the cut tobacco leaf. The amounts of semi-volatile fraction delivered from flax cigarette paper was more than that of wood cigarette paper. But, by using the cut tobacco, there was no big difference of delivery amount between flax and wood cigarette papers. Also, aroma of TPM by collecting from brening cut tobacco wrapped in flax and wood papers showed a different pattern by the electonic nose system. Although the difference between two cigarette papers by using the cut tobacco was smaller than that of cut cigarette paper, this result indicated that the fax and wood had the different effects on the delivery of smoke components as shown in the sensory test results.

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Quantitative analysis of 5-hydroxymethyl-2-furaldehyde (5-HMF) in the commercial Rehmanniae Radix Preparata

  • Kim, Ho-Kyoung;Jeon, Won-Kyung;Kim, Young-A;Ko, Byung-Seob
    • 대한약학회:학술대회논문집
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    • 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2-2
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    • pp.204.1-204.1
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    • 2003
  • Rehmanniae Radix Preparata attributes good blood circulation and it has been used for the treatment of dizziness, men's sterility, excessive loss of blood and weakness. On the quality control of the commercial Rehmanniae Radix Preparata, quantitative determination of 5-hydroxymethyl-2-furaldehyde (5-HMF) using HPLC method has been conducted. Quantitative analysis of 5-HMF in Rehmanniae Radix Preparata showered average 0.121${\pm}$0.063% in 14 samples collected throughout the regions of Korea. Contents of loss on drying, residue on ignition and residue on acid insoluble ignition showered average 14.084${\pm}$2.804%, 3.415${\pm}$0.790% and 0.807${\pm}$0.474% respectively.

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