• 제목/요약/키워드: Lineweaver-Burk plot

검색결과 56건 처리시간 0.024초

Anti-Cariogenicity of NCS (Non-Cariogenicity Sugar) Produced by Alkalophilic Bacillus sp. S-1013

  • Ryu, Il-Hwan;Kim, Sun-Sook;Lee, Kap-Sang
    • Journal of Microbiology and Biotechnology
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    • 제14권4호
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    • pp.759-765
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    • 2004
  • The NCS inhibited the activity of glucosyltransferase which was produced by Streptococcus mutans JC-2, and the rate of inhibition at $100\muM<$ and $200\muM$ were 74.0% and 99.8%, respectively. It was stable in alkali condition, but unstable in acid condition. It was also stable up to $80^{\circ}C$. The kinetic study of the inhibition by NCS was carried out by Lineweaver-Burk plot and Dixon plot. It was non-competitive inhibition, determined by the two plots and $K_i$ and $K_i$ values were $15\muM$ and $19.3\muM$ respectively. The NCS did not show cytotoxicity against human gingival cells at $K_i$ ($15\muM$, $150\muM$, $1,500\mu$ M) concentrations. It had less cytotoxicity than chlohexidin, which has usually been used as the agent of anticaries. To evaluate the industrial applicability of the NCS, human pluck tooth was used. The inhibitory rates of tooth calcification and calcium ion elution by the NCS were 41 % and 2.5 times, respectively. These results suggested that NCS from Bacillus sp. S-1013 is an efficient anticaries agent.

Streptomyces polychromogenes IFO 13072가 생산하는 Cholesterol Oxidase의 정제 및 효소학적 특성 (Purification and Characterization of Cholesterol Oxidase Produced by Streptomyces polychromogenes IFO 13072.)

  • 김현수;성림식;이경화;이용직;이인선;유대식
    • 한국미생물·생명공학회지
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    • 제30권2호
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    • pp.142-150
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    • 2002
  • Cholesterol oxidase(EC 1.1.3.6)는 cholesterol을 산화 또는 이성화시키는 효소로, 혈중 cholesterol 측정 등의 임상진단용 시약에 이용되고 있으며, 여러 종류의 미생물에서 분리, 연구되어 왔다. 현재에는 농업 및 식품 등에도 응용이 기대되고 있는 매우 유용한 효소이다. 본 실험은 공시균인 Streptomyces polychromogenes IFO 13072의 효소 생산 조건과 cholesterol oxidase의 정제 및 효소학적 특성을 조사하였다. 효소 생산 조건을 검토한 결과, 탄소원으로 1% dextrin, 유기 질소원으로는 0.5% casamino acid, 무기 질소원으로는 0.5% sodium nitrate가 효소생산에 우수하였으며, 이들 탄소원, 질소원 이외 0.1% $KH_2$$PO_4$, 0.05% $MgSO_4$$7H_2$O가 함유된 배지를 생산 최적 배지로 사용하였다. 본 효소의 정제는 30-80% 포화의 ($NH_4$)$_2$$SO_4$ 침전 및 cholesterol affinity column chromatography를 통하여 23.2%의 수율로 정제되었다. 정제된 효소는 SDS-PAGE에서 단일한 밴드를 보였으며, 분자량은 약 52,000 Da으로 추정되었다. 본 효소의 특성을 검토한 결과, 최적 온도와 최적 pH는 각각 $37^{\circ}C$, pH 7.0이었으며, 효소의 안정성은 온도 $25^{\circ}C$, pH 6.0~7.0의 범위까지 안정한 것으로 나타났다. 또한 본 효소는 금속이온으로 Hg와 Fe 이온의 존재시 크게 저해를 받았고, dithiothreitol과 mercaptoethanol, Isonicotinic acid와 같은 저해제에 의해서 상당히 실활 되었다. 본 cholesterol oxidase의 Michaelis 상수는 cholesterol을 기질로 하여 Lineweaver-Burk plot 분석에서 25 mM로 추산되었다

옥수수(Zea mays) 뿌리의 초기 생장에 미치는 CsCl의 영향 (Effects of CsCl on the Early Root Growth of Maize (Zea mays))

  • 박웅준
    • 생명과학회지
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    • 제20권2호
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    • pp.298-303
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    • 2010
  • 본 연구에서는 발아 후 2일된 옥수수 유식물의 뿌리 생장에 미치는 영향을 조사하였다. 5 mM에서 30 mM에 이르는 CsCl을 처리하였을 때 옥수수 뿌리와 자엽초 마디 위쪽 shoot의 생중량이 감소하였다. 뿌리의 길이 생장도 역시 동일한 농도 범위의 CsCl에 의하여 감소하였는데 CsCl을 처리할 때 60 mM의 KCl을 함께 처리하면 CsCl에 의하여 감소되었던 신장 생장이 일부 회복되었다. CsCl과 KCl의 관계를 Lineweaver-Burk plot으로 분석한 결과 10 mM - 30 mM CsCl은 KCl과 경쟁 관계에 있는 것으로 나타났지만 5 mM CsCl은 경쟁관계에서 벗어나는 것으로 나타나 주변의 CsCl 농도에 따라 KCl의 작용 모드가 다른 또 하나의 메커니즘이 존재하는 것으로 사료되었다. CsCl의 농도에 따라서 KCl과의 상호작용 모드가 달라지는 현상은 CsCl에 의하여 유도되는 옥수수뿌리 정단 하부의 횡축 팽창에서도 관찰되었다. 또한, CsCl은 10 mM 이상에서 농도 증가에 비례하여 $K^+$ transporter인 ZmKUP1의 발현을 유도하였지만 5 mM CsCl의 ZmKUP1 발현 효과는 뚜렷하게 관찰되지 않았다. 한편, CsCl 존재 하에서도 근단 분열 조직의 수축은 관찰되지 않았다. 종합하면, 외부에서 처리된 CsCl은 2일된 옥수수 유식물의 뿌리의 생중량과 신장을 감소시켰으며 정단 하부의 횡축 팽창을 유도하고 ZmKUP1의 발현을 촉진하였다. 그러나 근단 분열조직의 수축은 없었으므로 CsCl의 효과는 주로 세포 팽창과 관련되는 것으로 판단되며 $Cs^+$$K^+$의 경쟁 및 비경쟁적 상호작용을 모두 포함하는 복합적인 메커니즘이 존재하는 것으로 사료된다.

한외여과 알로에 농축액의 Urease 저해 및 무기물 응집 활성 (Urease Inhibition and Flocculating Activity of Concentrated Aloe vera Gel by Using Ultrafiltration Process)

  • 백진홍;김성아;이신영
    • KSBB Journal
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    • 제23권3호
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    • pp.239-244
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    • 2008
  • For physiological function of aloe concentrate by ultrafiltration (UF) process, jack bean urease inhibitory activity and bentonite flocculating activity of UF aloe concentrate was investigated and compared with fresh aloe gel. Urease inhibitory activity of UF aloe concentrate ranged from 87 to 90% in 1 mL sample. Also, urease inhibitory activity of UF aloe concentrate increased about 10% by heat treatment showing the heat stability. From Lineweaver-Burk plot for UF aloe concentrate, urease inhibition pattern indicated general non-competitive inhibition. From flocculation test of UF aloe concentrate about 1% (w/v) bentonite suspension, maximum flocclulating activity of 97% was obtained at 0.5 mL addition of UF aloe concentrate/ 5 ml bentonite suspension. However, flocculating activity of 81% was obtained at 1 mL addition of UF aloe concentrate/ 5 mL bentonite suspension, which was typical flocculating behavior of polymers with re-dispersion at overdose area. FT-IR spectra of UF aloe concentrate showed the characteristic patterns of $\beta$-binding polysaccharide and less deacetylation indicating higher level of bioactive polysaccharide content.

Anticaries Activity of Antimicrobial Material from Bacillus alkalophilshaggy JY-827

  • Chun, Ju-Yean;Ryu, Il-Hwan;Park, Jung-Sun;Lee, Kap-Sang
    • Journal of Microbiology and Biotechnology
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    • 제12권1호
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    • pp.18-24
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    • 2002
  • The present study was performed to investigate the excellent microbial anticaries substance, aminoglycoside antibiotic, which is more effective than chlorhexidine for the treatment of dental caries. The aminoglycoside antibiotic against Streptococcus mutans JC-2 from a novel alkaliphilic Bacillus alkalophilshaggy JY-827 exhibited no significant difference at the treatment concentration of $2.5{\times}10^{-7}M$, however, it inhibited the activity of the Streptococcus mutans glucosyltransferase by 70.2% and 99.8% at the concentrations of $2.5{\times}10^{-7}$M\;and\;2.5{\times}10^{-6}M$, respectively. Lineweaver-Burk plot of the inhibitory aminoglycoside antibiotic showed competitive inhibition, with $K_i$ value of $6.4{\times}10^{-6}$ M. The aminoglycoside antibiotic did not show any cytotoxicity against human gingival cells. To evaluate the industrial applicability of the aminoglycoside antibiotic, a toothpaste containing this substance was prepared and tested on the extracted human teeth. The inhibitory rate of tooth calcification and calcium ion elution by the aminoglycoside antibiotic were 50% and 2.5 times, respectively. These results suggested that the aminoglycoside antibiotic from Bacillus alkalophilshaggy JY-827 is an effective agent against dental caries.

Tyrosinase Inhibiting and DPPH Radical Scavenging Activities of Rosmarinic Acid and Its Methyl ester from Salvia miltiorrhiza

  • Kang, Hye-Sook;Kim, Hyeung-Rak;Chung, Hae-Young;Choi, Jae-Sue
    • 대한약학회:학술대회논문집
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    • 대한약학회 2002년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2
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    • pp.383.3-384
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    • 2002
  • Rosmarinic acid (1) and methyl rosmarinic acid (2), isolated from the ethyl acetate soluble fraction of the methanolic extract of Salvia miltiorrhiza Bunge (Lamiaceae) were found to be the tyrosinase inhibitors and scavengers of 1, 1-diphenyl-2-picrylhydrzyl (DPPH) radical. Compounds 1 and 2 inhibited the oxidation of L-tyrosine catalyzed by mushroom tyrosinase with $IC_{50}$/ of 16.8 $\mu\textrm{M}$ and 21.5 $\mu\textrm{M}$. respectively. It compared well with kojic acid. a well-known tyrosinase inhibitor. with an $IC_{50}$ of 22.4 $\mu\textrm{M}$. The inhibitory kinetics, analyzed by a Lineweaver-Burk plot, found rosmarinic acid and its methyl ester to be competitive inhibitors with $K_{i}$ of $2.35{\times}10^{-5}M$ and $1.52{\times}10^{-5}M$ respectively. In addition, compounds 1 and 2 showed the scavenging activities on DPPH radical, with $IC_{50}$ of 4.27 $\mu\textrm{M}$ and 3.05 $\mu\textrm{M}$. respectively. These scavenging effects were more potent than that of L-ascorbic acid ($IC_{50}$ = 11.75$\mu\textrm{M}$).

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Monascus purpureus P-57 변이주가 생산하는 홍국색소의 항산화효과 (Antioxidant Activity of Monascus Pigment of Monascus purpureus P-57 Mutant)

  • 박치덕;정혁준;이항우;김현수;유대식
    • 미생물학회지
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    • 제41권2호
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    • pp.135-139
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    • 2005
  • Monascus purpureue KCCM 60016으로부터 색소생성 이 우수한 변이주 P-57이 생성한 홍국색소의 항산화 활성을 조사하였다. 홍국색소는 chloroform에 아주 잘 추출되며, 특히 hexane에서는 황색색소가 특이적으로 높게 추출되었다. DPPH radical소거 효과는 hexane분획, chloroform 분획, ethyl acetate분획, butanol 분획, water 분획의 순으로 높게 나타났다. Xanthine oxidase저해효과는 hexane분획, chloroform분획, ethyl acetate 분획의 순으로 높게 나타났으며, hexane 분획물의 경우 5 ppm에서 $41.2\%$, 50 ppm에서 $82.4\%$로 높은 저해율을 보였으며, 저해기작은 비경쟁적 저해였다.

현호색의 Acetylcholinesterase 활성 저해 성분 및 그 작용기전 (An Acetylcholinesterase Inhibitor Isolated from Corydalis Tuber and Its Mode of Action)

  • 황세영;장영표;변순정;전미희;김영중
    • 생약학회지
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    • 제27권2호
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    • pp.91-95
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    • 1996
  • In the course of searching for acetylcholinesterase inhibitors from crude drugs, it was found that total MeOH extract of Corydalis Tuber showed significant inhibitory effect on acetylcholinesterase. To isolate acetylcholinesterase inhibitors from Corydalis Tuber, total MeOH extract of the the crude drug was subjected to activity guided fractionation. The MeOH extract was suspended in water and fractionated with methylene chloride and subjected to acid-base fractionation. Silica gel column chromatography of the basic fraction which showed significant inhibitory effect on acetylcholinesterase was carried out and 5 subfractions (1-5) were obtained. From subtraction 4, compound I was isolated. The structure of isolated compound I was identified by spectroscopic parameters of $^1H-NMR$, $^{13}C-NMR$, EI-MS and FAB-MS. The compound I was identified as berberine. It was found from the Lineweaver-Burk plot that berberine was a reversible and specific inhibitor of acetylcholinesterase having 90% inhibitory effect at the concentration of $2.5{\mu}M$.

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미생물 세포 기반의 에폭사이드 가수분해효소 활성 측정을 위한 분광학적 분석법 최적화 (Optimization of Microbial Cell-Based Spectrometric Assay for the Analysis of Epoxide Hydrolase Activity)

  • 김희숙;이은열
    • 생명과학회지
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    • 제15권1호
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    • pp.136-140
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    • 2005
  • 다양한 라세믹 에폭사이드 기질에 대한 입체선택적 가수분해 반응을 촉매하는 epoxide hydrolase 활성을 측정할 수 있는 미생물 세포 기반의 자외선 활성 분석법을 최적화하였다. 2.5 mg/ml의 세포 농도에서도 비교적 쉽게 흡광도 변화량을 인식할 수 있는 흡광도 범위인 0.5 이상을 얻을 수 있고, 반응 동력학 분석에도 응용할 수 있었다. 기존의 GC, HPLC 분석 법 보다 분석 시간을 줄일 수 있으며, 효소를 별도로 분리$\cdot$정제하지 않고 미생물 세포 자체의 epoxide hydrolase활성 분석이 가능하므로 상업적 특성이 우수한 epoxide hydrolase을 가진 미생물을 효율적으로 선별하는데 응용될 수 있을 것으로 기대된다.

Characterization of Calcium-Activated Bifunctional Peptidase of the Psychrotrophic Bacillus cereus

  • Kim Jong-Il;Lee Sun-Min;Jung Hyun-Joo
    • Journal of Microbiology
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    • 제43권3호
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    • pp.237-243
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    • 2005
  • The protease purified from Bacillus cereus JH108 has the function of leucine specific endopeptidase. When measured by hydrolysis of synthetic substrate (N-succinyl-Ala-Ala-Pro-Leu-p-nitroanilide), the enzyme activity exhibited optimal activity at pH 9.0, $60^{\circ}C$. The endopeptidase activity was stimulated by $Ca^{++},\;Co^{++},\;Mn^{++},\;Mg^{++},\;and\;Ni^{++}$, and was inhibited by metal chelating agents such as EDTA, 1,10-phenanthroline, and EGTA. Addition of serine protease inhibitor, PMSF, resulted in the elimination of the activity. The endopeptidase activity was fully recovered from the inhibition of EDTA by the addition of 1 mM $Ca^{++}$, and was partially restored by $Co^{++}\;and\;Mn^{++}$, indicating that the enzyme was stabilized and activated by divalent cations and has a serine residue at the active site. Addition of $Ca^{++}$ increased the pH and heat stability of endopeptidase activity. These results show that endopeptidase requires calcium ions for activity and/or stability. A Lineweaver-Burk plot analysis indicated that the $K_m$ value of endopeptidase is 0.315 mM and $V_{max}$ is 0.222 ) is $0.222\;{\mu}mol$ of N-succinyl-Ala-Ala-Pro-Leu-p-nitroanilide per min. Bestatin was shown to act as a competitive inhibitor to the endopeptidase activity.