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胶束和脂质双层表面锰叶绿素衍生物催化 CI 酸性橙 7 的过氧化物褪色。

Peroxide decoloration of CI Acid Orange 7 catalyzed by manganese chlorophyll derivatives at the surfaces of micelles and lipid bilayers.

机构信息

Department of Life and Materials Engineering, Nagoya Institute of Technology, Gokiso-cho, Showa-ku, Nagoya, Aichi 466-8555, Japan.

出版信息

Langmuir. 2010 Jun 1;26(11):7774-82. doi: 10.1021/la904574m.

Abstract

Manganese-substituted chlorophyll a derivatives (MnChls) were synthesized. We first report peroxidative oxidation of an azo dye, CI Acid Orange 7, catalyzed by MnChls at the surfaces of micelles and lipid bilayers with hydrogen peroxide (H(2)O(2)) under mild conditions (pH 8.0, 25 degrees C). Peroxide decoloration depended upon the structures of MnChls, surfactants, lipids, and the presence of imidazole. Surprisingly, a largest decoloration rate was observed for MnChls dimer, MnPChlide a-K(MnPChlide a)-His 5 in cetyltrimethylammonium bromide (CTAB) micellar solution, especially when imidazole was present: this observation is analogous to the decoloration using horseradish peroxidase (HRP). Interestingly, the dimer complexes showed enhanced decoloration in comparison to the corresponding MnChls monomer in the micellar solution. In contrast, the MnChls monomer showed enhanced decoloration in comparison with the MnChls dimer in liposomal suspensions. Further, the imidazole residue covalently linked to the MnChls plays an important role in increasing the decoloration in both micellar and liposomal suspensions as well as in addition of imidazole into the solutions. It is interesting that the electron paramagnetic resonance (EPR) spectra of MnPChlide a ME 2, MnPChlide a-His 3, and MnMPMME-His 7 have 16 peaks around g = 2 in Egg PC or DMPC liposomal suspension with H(2)O(2), which is typical of a mixed-valence Mn(III)-Mn(IV) complex with coupling between two ions. The higher decoloration performance obtained by the monomer porphyrin compounds at the surface of the lipid bilayers appears to be related to the stability of this mixed-valence Mn(III)-Mn(IV) species formed in the lipid bilayers. This finding should provide useful information to note that MnChls, which are easily found in a number of biological systems, are involved in functions such as hydrogen peroxide decomposition in bacteria and the oxidation of water during photosynthesis as well as the peroxidases function such as the peroxidative decoloration as bleaching agents.

摘要

锰取代叶绿素 a 衍生物(MnChls)被合成。我们首次报道在温和条件下(pH8.0,25°C),在胶束和脂质双层表面,用过氧化氢(H2O2)催化 MnChls 对偶氮染料 CI 酸性橙 7 的过氧化氧化作用。过氧化物褪色取决于 MnChls、表面活性剂、脂质的结构以及咪唑的存在。令人惊讶的是,在十六烷基三甲基溴化铵(CTAB)胶束溶液中,MnPChlide a-K(MnPChlide a)-His5 的 MnChls 二聚体观察到最大的褪色率,特别是当存在咪唑时:这一观察结果类似于辣根过氧化物酶(HRP)的褪色。有趣的是,与胶束溶液中的相应 MnChls 单体相比,二聚体复合物显示出增强的褪色。相比之下,在脂质体悬浮液中,MnChls 单体比 MnChls 二聚体显示出增强的褪色。此外,与 MnChls 共价连接的咪唑残基在胶束和脂质体悬浮液中以及在添加咪唑进入溶液中都对增加褪色起着重要作用。有趣的是,在 Egg PC 或 DMPC 脂质体悬浮液中,MnPChlide aME2、MnPChlide a-His3 和 MnMPMME-His7 的电子顺磁共振(EPR)光谱在 g=2 周围有 16 个峰,这是与两个离子之间的偶联的混合价态 Mn(III)-Mn(IV)络合物的典型特征。在脂质双层表面,单体卟啉化合物表现出更高的褪色性能,这似乎与在脂质双层中形成的这种混合价态 Mn(III)-Mn(IV)物种的稳定性有关。这一发现应该提供有用的信息,即 MnChls 很容易在许多生物系统中找到,它们参与了细菌中过氧化氢的分解以及光合作用中水的氧化等功能,以及过氧化物酶的功能,如作为漂白剂的过氧化褪色。

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