• 제목/요약/키워드: Redox mechanism

검색결과 139건 처리시간 0.026초

Assembly Mechanism of [$Fe_2S_2$] Cluster in Ferredoxin from Acidithiobacillus ferrooxidans

  • Chen, Qian;Mo, Hongyu;Tang, Lin;Du, Juan;Qin, Fang;Zeng, Jia
    • Journal of Microbiology and Biotechnology
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    • 제21권2호
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    • pp.124-128
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    • 2011
  • Ferredoxin is a typical iron-sulfur protein that is ubiquitous in biological redox systems. This study investigates the in vitro assembly of a [$Fe_2S_2$] cluster in the ferredoxin from Acidithiobacillus ferrooxidans in the presence of three scaffold proteins: IscA, IscS, and IscU. The spectra and MALDI-TOF MS results for the reconstituted ferredoxin confirm that the iron-sulfur cluster was correctly assembled in the protein. The inactivation of cysteine desulfurase by L-allylglycine completely blocked any [$Fe_2S_2$] cluster assembly in the ferredoxin in E. coli, confirming that cysteine desulfurase is an essential component for iron-sulfur cluster assembly. The present results also provide strong evidence that [$Fe_2S_2$] cluster assembly in ferredoxin follows the AUS pathway.

전자에너지 손실분광 분석법을 이용한 광물에서의 정량적 철 산화수 측정과 분석 (Electron Energy Loss Spectroscopy (EELS) Application to Mineral Formation)

  • 양기호;김진욱
    • 한국광물학회지
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    • 제29권2호
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    • pp.73-78
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    • 2016
  • 점토 광물의 구조 내에 들어 있는 철의 산화수는 퇴적환경의 산화/환원 조건에 대한 정보를 제공하여 준다. 이러한 광물형성의 메커니즘을 밝히기 위해서는 고해상도를 가진 전자현미경을 이용한 나노 스케일 분석이 불가피하다. 투과전자현미경에 장착되어있는 전자에너지 손실분광 분석법(EELS)을 이용하여 정량적 철 산화수 분석을 논트로나이트 점토광물 구조 내 철의 환원으로 인한 K-논트로나이트의 형성의 예를 들어 설명하고자 한다. 철 산화/환원의 정량적 분석을 통하여 퇴적물의 위치에 따른 철 산화도 측정은 광물변화에 대한 연구를 용이하게 해준다. 따라서 본 논문은 전자에너지 손실분광의 분석방법 및 장점을 소개함을 목적으로 한다.

Chromatic Characteristics of Copper Glaze as a Function of Copper Oxide Addition and Sintering Atmosphere

  • No, Hyunggoo;Kim, Soomin;Kim, Ungsoo;Cho, Wooseok
    • 한국세라믹학회지
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    • 제54권1호
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    • pp.61-65
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    • 2017
  • Examined in this study were the effects of copper oxide (II) addition and sintering conditions on the chromatic characteristics of copper glaze. Oxidatively sintered samples exhibited the negative increase of $CIEa^*$ and the positive increase of $CIEb^*$ with the increase of CuO concentration, leading to Green and Green-Yellow coloration. On the other hand, $CIEa^*$ and $CIEb^*$ of reductively sintered samples were positively increased in direct proportion. The green color of oxidatively sintered samples was originated from the $Cu^{2+}$ ions formed by the dissolution of CuO. The reductively sintered samples resulted in dull tone red color with low chroma. Such behavior seems to be influenced by the interplay of metal Cu aggregation, metal Cu globule, and $Cu_2O$ formed in the glaze layer through the redox interaction of CuO during the sintering process.

항산화효소의 암 예방 효과 및 발암 억제 기전 (The Chemopreventive Effects of Antioxidant Enzyme)

  • 정화진;조윤주;원장원;서영록
    • 한국환경성돌연변이발암원학회지
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    • 제26권2호
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    • pp.45-47
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    • 2006
  • The reactive oxygen species (ROS) caused the damage of macro molecules, many degenerative disease and cancer, which was produced in process of the aerotropic metabolic pathway as well as in response to the various genotoxic stresses. Recently, redox systems including the number of antioxidant proteins such as catalase, glutathione peroxidase, heam-containing peroxidase, peroxiredoxin and superoxide dismutase (SOD) has been reported to have chemopreventive effects. Antioxidant proteins has been known to have the activity directly removing ROS and affecting the protein-protein interaction and cell signaling to induce the cellular responses. We need to understand the mechanism of antioxidants prevent DNA damage from oxidative stresses for researching the cancer prevention and providing the development of cancer therapeutic drug.

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Phthalate 완충용액에서 전해 석출한 철족 원소의 산화 용해 반응 (Anodic Dissolution of Electrodeposited Iron Group Elements in Phthalate Buffer Solution)

  • 천정균;김연규
    • 대한화학회지
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    • 제51권1호
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    • pp.14-20
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    • 2007
  • 금(Au) 전극 위에 전해 석출한 철족 원소(Fe, Co, Ni)를 전극으로 phthalate 완충 용액에서 철족 원소의 부식과정을 조사하였다. Phthalate 완충용액의 pH의 변화에 대한 부식전위와 부식전류를 측정하여 각 원소(Fe, Co, Ni)전극의 산화반응과 환원반응에 대한 Tafel 기울기를 구하였으며 Tafel 기울기를 포함한 정량적인 전기화학 인자를 측정하여 전극의 산화반응과 환원반응에 대한 반응 메커니즘을 제안하였다. Phthalate 완충 용액에 존재하는 화학 종의 흡착은 철족 원소 전극의 산화반응에 영향을 미치는 것으로 보인다.

음이온성 아크릴아미드와 아크릴산의 역유화 중합에 관한 연구 (A Study on the Inverse Emulsion Polymerization of Anionic Arcrylamide and Acrylic Acid)

  • 이기창;최희천;최봉종;이광일
    • 한국응용과학기술학회지
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    • 제6권1호
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    • pp.1-7
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    • 1989
  • To developed new process for obtaining maximum molecular weight of anionic acrylamide and acrylic acid copolymer by inverse emulsion polymerization. Concentration of initiator, reducing agent, surfactant and mole ratio of acrylamide-acrylic acid were studied for the process. Semi-batch processes with method of redox, control of reaction temperature, feeding method of monomer and reaction time, was suitable for maximum molecular weight of P(AMAC) from this process obtained $3.09\;{\time}\;10^6({\bar{M}}n.)$ and $4.41\;{\time}\;10^6({\bar{M}}w.)$ in molecular weight measured by the intrinsic viscosity method. inverse emulsion polymerization mechanism of P(AMAC) does not followed the Smith-Ewart and Medvedev theory, but selected for concentration of initiator, reducing agent, surfactant, water solubility of monomer.

Kinetics and Mechanistic Chemistry of Oxidation of Butacaine Sulfate by Chloramine-B in Acid Medium

  • Shubha, Jayachamarajapura Pranesh;Kotabagi, Vinutha;Puttaswamy, Puttaswamy
    • Bulletin of the Korean Chemical Society
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    • 제33권11호
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    • pp.3539-3543
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    • 2012
  • Butacaine sulfate is an ester of p-aminobenzoic acid which has been widely used as a local anaesthetic and it is a long standing agent particularly for spinal anaesthesia. For this reason, a kinetic study of oxidation of butacaine sulfate by sodium N-chlorobenzenesulfonamide (chloramine-B or CAB) has been carried out in $HClO_4$ medium at 303 K in order to explore this redox system mechanistic chemistry. The rate shows a first-order dependence on both $[CAB]_o$, and $[substrate]_o$, and a fractional-order dependence on acid concentration. Decrease of dielectric constant of the medium, by adding methanol, increases the rate of the reaction. Variation of ionic strength and addition of benzenesulfonamide or NaCl have no significant effect on the rate. The reaction was studied at different temperatures and the activation parameters have been evaluated. The stoichiometry of the reaction has been found to be 1:2 and the oxidation products have been identified by spectral analysis. The observed results have been explained by plausible mechanism and the related rate law has been deduced.

Inhibition of Invasion and Induction of Apoptosis by Curcumin in H-ras-Transformed MCF10A Human Breast Epithelial Cells

  • Kim, Mi-Sung;Kang, Hye-Jung;Moon, Aree
    • Archives of Pharmacal Research
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    • 제24권4호
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    • pp.349-354
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    • 2001
  • Curcumin, a dietary pigment in turmeric, posseses anti-carcinogenic and anti-metastatic properties. The present study was conducted to study in vitro chemopreventive effects of curcumin in transformed breast cells. Here, we show that curcumin inhibits H-ras-induced invasive phenotype in MCF10A human breast epithelial cells (H-ras MCF10A) and downregulates matrix metalloproteinase (MMP)-2 dose-dependently. Curcumin exerted cytotoxic effect on H-ras MCF10A cells in a concentration-dependent manner. Curcumin-induced cell death was mainly due to apoptosis in which a prominent downregulation of Bcl-2 and upregulation of Bax were involved. We also suggest a possible involvement of caspase-3 in curcumin-induced apoptosis. Curcumin treatment resulted in the production of reactive oxygen species (ROS) in H-ras MCF10A cells. Apoptotic event by curcumin was significantly inhibited by pretreatment of an antioxidant N-acetyl-$_L$-cysteine (NAC), suggesting redox signaling as a mechanism responsible for curcumin-induced apoptosis in H-ras MCF10A cells. Taken together, our results demonstrate that curcumin inhibits invasion and induces apoptosis, proving the chemopreventive potential of curcumin .

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Nitric Oxide-induced Protein S-nitrosylation Causes Mitochondrial Dysfunction and Accelerates Post-ovulatory Aging of Oocytes in Cattle

  • Niu, Ying-Jie;Zhou, Dongjie;Zhou, Wenjun;Nie, Zheng-Wen;Kim, Ju-Yeon;Oh, YoungJin;Lee, So-Rim;Cui, Xiang-Shun
    • 한국동물생명공학회지
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    • 제35권1호
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    • pp.102-111
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    • 2020
  • Nitric oxide (NO)-induced protein S-nitrosylation triggers mitochondrial dysfunction and was related to cell senescence. However, the exact mechanism of these damages is not clear. In the present study, to investigate the relationship between in vitro aging and NO-induced protein S-nitrosylation, oocytes were treated with sodium nitroprusside dihydrate (SNP), and the resultant S-nitrosylated proteins were detected through biotin-switch assay. The results showed that levels of protein S-nitroso thiols (SNO)s and expression of S-nitrosoglutathione reductase (GSNOR) increased, while activity and function of mitochondria were impaired during oocyte aging. Addition of SNP, a NO donor, to the oocyte culture led to accelerated oocyte aging, increased mitochondrial dysfunction and damage, apoptosis, ATP deficiency, and enhanced ROS production. These results suggested that the increased NO signal during oocyte aging in vitro, accelerated oocyte degradation due to increased protein S-nitrosylation, and ROS-related redox signaling.

Interaction Metal Ions with NADH Model Compounds. Cupric Ion Oxidation of Dihydronicotinamides

  • Park, Joon-Woo;Yun, Sung-Hoe;Koh Park, Kwang-Hee
    • Bulletin of the Korean Chemical Society
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    • 제9권5호
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    • pp.298-303
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    • 1988
  • Kinetic studies on cupric ion ($Cu^{2+}$) oxidation of 1-benzyl- and 1-aryl-1,4-dihydronicotinamides (XNAH) in aqueous solution were performed. In the presence of dioxygen ($O_2$), the reaction followed first order kinetics with respect to both XNAH and $Cu^{2+}$. The oxidation reaction was found to be independent and parallel to the acid-catalyzed hydration reaction of XNAH. The catalytic role of $Cu^{2+}$ for the oxidation of XNAH in the presence of $O_2$ was attributed to $Cu^{2+}/Cu^+$ redox cycle by the reactions with XNAH and $O_2$. The second order rate constants of the Cu2+ oxidation reaction kCu, and acid-catalyzed hydration reaction $k_H$ were strongly dependent on the nature of the substituents in 1-aryl moiety. The slopes of log $k_{Cu}$ vs log $K_H$ and log $k_{Cu}$ vs ${\sigma}_p$ of the substituents plots were 1.64 and -2.2, respectively. This revealed the greater sensitivity of the oxidation reaction rate to the electron density on the ring nitrogen than the hydration reaction rate. A concerted two-electron transfer route involving XNAH-$Cu^{2+}$ complex was proposed for mechanism of the oxidation reaction.