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首页> 外文期刊>RSC Advances >Development of a multifunctional biomimicking L- cysteine based oxovanadium(IV) complex: synthesis, DFT calculations, bromo-peroxidation and nuclease activity
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Development of a multifunctional biomimicking L- cysteine based oxovanadium(IV) complex: synthesis, DFT calculations, bromo-peroxidation and nuclease activity

机译:发展多功能生物纤米的L-半胱氨酸基氧化物(IV)复合物:合成,DFT计算,溴过氧化和核酸酶活性

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摘要

An oxovanadiumcomplex [VO(sal-L-cys)(phen)] (sal-L-cys =Schiff base derived fromsalicylaldehyde and L- cysteine; phen =1,10-phenanthroline) has been synthesized and characterized by spectroscopic studies (IR, UV-vis, ESI-MS and EPR studies). The structure of the complex has been optimized by density functional theory (DFT) calculations. Time-dependent DFT (B3LYP) calculations were used to establish and understand the nature of the electronic transitions observed in UV-vis spectra of the ligand and the complex. The multifunctionality of this oxovanadium complex has been exhibited by the application of it as a catalyst in peroxidative bromination of phenol red to demonstrate vanadium dependent bromoperoxidase activity, whereas nuclease activity has been established by DNA cleavage. The interaction of DNA with this structurally characterized oxovanadium complex has been studied by various physicochemical tools like UV-vis, fluorescence, and viscosity measurement studies. The intrinsic binding constant of the complex with DNA has been determined by electronic absorption studies and calculated to be (3.51 ± 0.02) × 10~4 M~(-1) . The spectroscopic studies and the viscosity measurements indicate that the complex binds CT DNA by an intercalative mode. The ability of the complex to induce DNA cleavage was studied by gel electrophoresis techniques. The complex has been found to promote cleavage of pUC19 plasmid DNA from the super coiled (SC) form I to nicked coiled (NC) relaxed form II.
机译:氧化钒瘤复合[VO(SAL-L-CYS)(PhO)(Sal-L-Cys = Schiff碱来自苏丙基甲醛和L-半胱氨酸; Phen = 1,10-菲咯啉)已经合成并通过光谱研究表征(IR, UV-Vis,ESI-MS和EPR研究)。复合物的结构已被密度泛函理论(DFT)计算优化。使用时间依赖性DFT(B3LYP)计算来建立和理解在配体和复合物的UV-Vis光谱中观察到的电子转变的性质。通过在酚红的过氧化溴化溴化溴化溴化溴化溴化溴化钒中的催化剂上展示了该氧化钒络合物的多官能,以证明钒依赖性溴氧化酶活性,而DNA切割已经建立了核酸酶活性。 DNA与该结构表征氧化钒络合物的相互作用已经通过紫外 - Vis,荧光和粘度测量研究等各种物理化学工具研究。通过电子吸收研究确定复合物的固有结合常数,并计算为(3.51±0.02)×10〜4m〜(-1)。光谱研究和粘度测量表明该复合物通过插入模式结合CT DNA。通过凝胶电泳技术研究了复合物诱导DNA切割的能力。已经发现该综合体促进从超级卷绕(SC)I形式I中的PUC19质粒DNA的切割,以划接卷材卷曲(NC)松弛的形式II。

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  • 来源
    《RSC Advances》 |2015年第114期|共12页
  • 作者单位

    Department of Chemistry Jadavpur University Kolkata 700032 India.;

    Department of Chemistry Jadavpur University Kolkata 700032 India.;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

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