Zen'kevich E I, Losev A P
Mol Biol (Mosk). 1976 Mar-Apr;10(2):294-304.
The addition of water to dioxane solution of protochlorophyll (PChl) and 4-vinyl-protochlorophyll (4VPChl) results in a number of transformations related with pigment molecule associations into polymer formations and with their conversion. By variation of pigment concentration and composition of binar mixture of solvents a set of aggregated forms with different electronic spectra can be obtained. At the first stage the monomeric pigment converts into polymer with long-wavelenght absorption maximum of 633 nm (P633). During 1-3 hours P633 converts into other aggregated forms: either P639 or P645 depending on the proportion of dioxane and water. The pigment aggregates are characterized by fluorescence (quantum yield less than or equal to 1%) with maxima close to the main maxima of absorption spectra. Alongside with the main aggregated forms of PChl and 4VPChl the presence of a small number of longer-wavelength aggregates in solutions is established by fluorescence spectra. The investigation of dependence of fluorescence spectra on excitation wavelength, as well as of fluorescence excitation spectra of pigments in binary mixture shows that the long-wavelength aggregates can form part of complex associate and be effective trapping centres of electronic excitation of shorter wavelength aggregated forms. The phenomenon of 4VPChl association in concentrated solutions of castor oil (c greater than-10(-2) m/l) is discovered, which is especially marked after a long storage of the solutions at lower temperature (t=-2 degrees C). Under these conditions the two aggregated forms P640 and P650 alongside with monomer are present. The aggregate P650 is characterized by fluorescence with maximum of 655 nm and spectrally similar to the natural form of photoactive protochlorophyll. The experimental data show that the protochlorophyll pigments form a set of aggregated forms and that the medium conditions favour the predominance of some of the forms and their interconversion. The results obtained evidence that the main reason of the long-wavelength shift of electronic spectra for PChl natural forms is the intermolecular interaction related with the association of pigment monomeric molecules.
向原叶绿素(PChl)和4-乙烯基原叶绿素(4VPChl)的二氧六环溶液中加水会导致许多与色素分子缔合成聚合物结构及其转化相关的转变。通过改变色素浓度和二元混合溶剂的组成,可以获得一组具有不同电子光谱的聚集形式。在第一阶段,单体色素转化为聚合物,其长波长吸收最大值为633nm(P633)。在1-3小时内,P633转化为其他聚集形式:根据二氧六环和水的比例,要么是P639,要么是P645。色素聚集体的特征是荧光(量子产率小于或等于1%),其最大值接近吸收光谱的主要最大值。除了PChl和4VPChl的主要聚集形式外,通过荧光光谱确定溶液中存在少量长波长聚集体。对荧光光谱对激发波长的依赖性以及二元混合物中色素的荧光激发光谱的研究表明,长波长聚集体可以形成复杂缔合体的一部分,并成为较短波长聚集形式的电子激发的有效俘获中心。发现了蓖麻油浓溶液(c大于10^(-2) m/l)中4VPChl的缔合现象,在较低温度(t = -2℃)下长时间储存溶液后尤为明显。在这些条件下,除了单体外,还存在两种聚集形式P640和P650。聚集体P650的特征是荧光最大值为655nm,光谱上类似于光活性原叶绿素的天然形式。实验数据表明,原叶绿素色素形成了一组聚集形式,并且介质条件有利于某些形式的优势及其相互转化。所获得的结果证明,PChl天然形式电子光谱长波长位移的主要原因是与色素单体分子缔合相关的分子间相互作用。