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Interactions of Vitamin K3 with Herring-Sperm DNA Using Spectroscopy and Electrochemistry

机译:光谱法和电化学法研究维生素K3与鲱鱼精DNA的相互作用

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By means of ultraviolet–visible (UV-Vis) and fluorescence spectra, thenbinding ratio between vitamin K3 and herring-sperm DNA in anphysiological pH environment (pH ¼ 7.40) was determined as nK3 : nDNAn¼ 2 : 1, and the binding constants of vitamin K3 binding to DNA atndifferent temperatures were determined as Khn298K ¼ 1.28 6 105nLu0002molnu00031nand Khn310K ¼7.19 6 104nLu0002molnu00031n, which were confirmed using the doublenreciprocal method are DrHmhn¼ u00033.57 6 104nJu0002molnu00031n, DrGmhn¼ u00032.92 6n104nJu0002molnu00031n, and DrSmhn¼ 217.67 Ju0002molnu00031nKu00031n. The driving power of thisnprocess was enthalpy. An intercalation binding of the vitamin K3 withnDNA was supported by a competitive experiment using acridine orangen(AO) as a spectral probe. By combination analysis of the Scatchardnmethod and cyclic voltammetry, we suggested that the interaction modenbetween vitamin K3 and herring-sperm DNAwould be a mixed mode. Thenquinonoid, duality fused-ring of vitamin K3 can intercalate into the basenpairs of DNA, and there is an electrostatic binding along withnintercalation binding.
机译:通过紫外-可见光谱和荧光光谱,确定在生理pH值(pH¼7.40)下维生素K3与鲱鱼精DNA的结合比为nK3:nDNAn¼2:1,并确定了维生素的结合常数确定K3在不同温度下与DNA的结合力为Khn298K¼1.28 6 105nLu0002molnu00031n和Khn310K¼7.196 104nLu0002molnu00031n,使用双正反法确认的是DrHmhn¼u00033.57 6 104nJu0002molnu00031000,Dr.mKn¼¼00000000031n,31该过程的驱动力是焓。使用competitive啶橙(AO)作为光谱探针的竞争实验支持了维生素K3与nDNA的插入结合。通过Scatchardn方法和循环伏安法的组合分析,我们认为维生素K3和鲱鱼精DNA之间的相互作用模式应为混合模式。维生素K3的双醌类双稠环然后可以插入DNA的碱基对中,并且与非嵌入结合存在静电结合。

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