Copper(II) tetrapyrazole-based complex as a new peroxidase-mimetic compound

IF 3.2 2区 化学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Inorganic Biochemistry Pub Date : 2025-04-05 DOI:10.1016/j.jinorgbio.2025.112911
Marek Šebela , Giorgio Zoppellaro , Zdeněk Trávníček
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Abstract

A copper(II) tetrapyrazole-based complex of the composition of [Cu(tpyr)(H2O)(ONO2)]NO3 (1), where tpyr represents a tetradentate N-donor ligand formed by the condensation of 1H-pyrazole-5-carbaldehyde in NaOH/MeOH medium, has been prepared and characterized by elemental analysis, infrared spectroscopy, ultraviolet-visible spectroscopy, mass spectrometry, electron paramagnetic resonance and single-crystal X-ray diffraction. Spectrophotometric measurements demonstrated a remarkable peroxidase activity of the complex, which utilized hydrogen peroxide for the oxidation of phenolic compounds such as guaiacol or 3,5-dichloro-2-hydroxybenzene sulfonic acid. The optimum conditions for this reaction were found at pH 8 in ammonium bicarbonate buffer, although the activity was low but still detectable at pH 5–6 in ammonium acetate. As a peroxidase mimic, the complex exhibited enzyme-like Michaelis-Menten kinetics, showing a hyperbolic dependence of the reaction rate on hydrogen peroxide concentration. The determined Km and kcat values were 651 μmol·l−1 and 6.7 × 10−4 s−1, respectively, compared to 41 μmol·l−1 and 73 s−1 for horseradish peroxidase. EPR spectroscopy of the reaction mixture revealed no change in the copper (II) oxidation state during catalysis, suggesting that the oxidation of guaiacol may occur simultaneously with the reduction of hydrogen peroxide to water at the copper centre.

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铜(II)四吡唑基配合物是一种新的模拟过氧化物酶的化合物
制备了一种由[Cu(tpyr)(H2O)(ONO2)]NO3(1)组成的铜(II)四吡唑基配合物,其中tpyr代表由1h -吡唑-5-乙醛在NaOH/MeOH介质中缩合形成的四齿n给体配体,并通过元素分析、红外光谱、紫外-可见光谱、质谱、电子顺磁共振和单晶x射线衍射对其进行了表征。分光光度测量表明,该复合物具有显著的过氧化物酶活性,该复合物利用过氧化氢氧化酚类化合物,如愈创木酚或3,5-二氯-2-羟基苯磺酸。该反应的最佳条件为碳酸氢铵缓冲液pH为8,虽然活性较低,但在pH为5-6的乙酸铵中仍可检测到。作为过氧化物酶模拟物,该复合物表现出酶样Michaelis-Menten动力学,反应速率与过氧化氢浓度呈双曲线依赖性。测定的Km和kcat分别为651 μmol·l−1和6.7 × 10−4 s−1,而辣根过氧化物酶的Km和kcat分别为41 μmol·l−1和73 s−1。反应混合物的EPR光谱显示,在催化过程中铜(II)的氧化态没有变化,这表明愈创木酚的氧化可能与过氧化氢在铜中心还原成水同时发生。
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来源期刊
Journal of Inorganic Biochemistry
Journal of Inorganic Biochemistry 生物-生化与分子生物学
CiteScore
7.00
自引率
10.30%
发文量
336
审稿时长
41 days
期刊介绍: The Journal of Inorganic Biochemistry is an established international forum for research in all aspects of Biological Inorganic Chemistry. Original papers of a high scientific level are published in the form of Articles (full length papers), Short Communications, Focused Reviews and Bioinorganic Methods. Topics include: the chemistry, structure and function of metalloenzymes; the interaction of inorganic ions and molecules with proteins and nucleic acids; the synthesis and properties of coordination complexes of biological interest including both structural and functional model systems; the function of metal- containing systems in the regulation of gene expression; the role of metals in medicine; the application of spectroscopic methods to determine the structure of metallobiomolecules; the preparation and characterization of metal-based biomaterials; and related systems. The emphasis of the Journal is on the structure and mechanism of action of metallobiomolecules.
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