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Effect of Sodium Dodecyl Sulfate on Structure and Spectroscopic Characteristics of Water-Soluble Chlorophyll Protein Complex Isolated from Stems ofLepidium virginicum

机译:十二烷基硫酸钠对从初蕊茎中分离的水溶性叶绿素蛋白复合物结构及光谱特性的影响

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The relationship between structure and spectroscopic characteristics of the watersoluble chlorophyll protein complex isolated from stems ofLepidium virginicum(CP663S) was studied. Addition of 0.08SDS induced a red shift of the 663 nm absorption maximum. At the same time, under excitation at 435 nm, the maximum of fluorescence emission shifted from 672 nm to 675 nm and the fluorescence yield increased. When CP663S was excited at 480 nm, the 660 nm emission band of chlorophyllbbecame more prominent. Fluorescence lifetime of emission from chlorophyllaincreased on addition of SDS. The energy transfer from chlorophyllbto chlorophyllawas decreased by the SDS addition, as judged by the fluorescence spectra and lifetime measurement. Symmetrical positive and negative peaks of the circular dichroism (CD) spectrum around 669 nm, which indicate the interaction between chlorophyllamolecules at short distances, disappeared after addition of SDS. These SDS-induced changes of spectroscopic characteristics occurred in similar SDS concentration ranges and were reversible. SDS polyacrylamide gel electrophoresis cleaved CP663S into subunits. Chlorophyll molecules moved with protein moieties. Glutaraldehyde treatment suppressed the effects of SDS on absorption, fluorescence and CD characteristics. We conclude that chlorophyll molecules in CP663S are in the hydrophobic region of the protein and the interaction between chlorophyllamolecules occurs at short distances. Changes of spectroscopic characteristics are a result of cleavage of CP663S.
机译:研究了从Lepidium virginicum(CP663S)茎中分离得到的水溶性叶绿素蛋白复合物的结构与光谱特性的关系。添加 0.08%SDS 可引起 663 nm 最大吸收的红移。同时,在435 nm激发下,荧光发射的最大值从672 nm转移到675 nm,荧光产率增加。当CP663S在480 nm处被激发时,叶绿素的660 nm发射带变得更加突出。叶绿素发射的荧光寿命随着SDS的添加而增加。从叶绿素到叶绿素的能量转移因SDS的添加而减少,通过荧光光谱和寿命测量来判断。加入SDS后,669 nm左右的圆二色性(CD)光谱的对称正负峰消失了,表明叶绿素分子之间的短距离相互作用。这些SDS诱导的光谱特性变化发生在相似的SDS浓度范围内,并且是可逆的。SDS聚丙烯酰胺凝胶电泳将CP663S切割成亚基。叶绿素分子随蛋白质部分移动。戊二醛处理抑制了SDS对吸收、荧光和CD特性的影响。我们得出结论,CP663S中的叶绿素分子位于蛋白质的疏水区域,叶绿素分子之间的相互作用发生在短距离内。光谱特性的变化是CP663S裂解的结果。

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