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Voltammetric detection of phytochelatin transported across unmodified and protoplast modified model phospholipid membranes

机译:伏安法检测跨未修饰和原生质体修饰的模型磷脂膜转运的植物螯合素

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Possibility of phytochelatin PC2 transport was examined using developed electrochemical cell with two compartments separated by a phospholipid membrane created in pores of polycarbonate support. At first cell penetrating peptides (transportan 10 and mastoparan X) were used to allow the transfer of phytochelatin PC2. The results demonstrated that transportan 10 is several times more efficient than mastoparan X for transferring of phytochelatin across model membrane. Voltammetry with hanging mercury drop electrode or with solid amalgam electrodes was applied for detection of transported species. For determination of PC2, hanging mercury drop electrode and mercury meniscus-modified silver solid amalgam electrode were suitable. Modified model phospholipid membrane was prepared with parts of protoplasts from barley roots or leaves, and transport of phytochelatin PC2 has been confirmed. Electrochemical impedance spectroscopy was utilized to monitor formation, stability, and qualitatively the transporting process across the supported phospholipid membranes.
机译:使用发达的电化学电池检查了植物螯合素PC2转运的可能性,该电化学电池有两个隔室,该隔室被在聚碳酸酯载体孔中形成的磷脂膜隔开。首先,使用细胞穿透性肽(转运蛋白10和乳清蛋白X)来转运植物螯合PC2。结果表明,转运蛋白10在跨模型膜上转移植物螯合素的效率比马索潘兰X高出几倍。使用悬挂式汞滴电极或固态汞齐电极的伏安法检测运输的物种。对于测定PC2,悬挂式汞滴电极和汞弯月形修饰的银固体汞齐电极是合适的。用大麦根或叶的部分原生质体制备了修饰的模型磷脂膜,并已证实了植物螯合剂PC2的转运。电化学阻抗光谱法用于监测形成,稳定性以及定性地跨支持的磷脂膜的转运过程。

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