Krasnovsky A A
Orig Life. 1976 Apr;7(2):133-43. doi: 10.1007/BF00935657.
The principles of biological evolution of photosynthesis are established, but the ways of chemical evolution are unclear yet. The model systems will help to elucidate the problem. Every type of photosynthesis requires photoreceptor absorbing solar radiation. We studied as photoreceptors inorganic components of Earth crust, some coenzymes and porphyrins of abiogenic and biogenic origin. By the aid of inorganic photosensitizers (TiO2, ZnO) the models of photosystems I and II were constructed. Photochemical activation of some coenzymes may serve as an intermediate step from heterotrophic 'dark' to 'light' metabolism. The further evolution led to the separation of catalytic and photosensitizing functions. Porphin, chlorin and bacteriochlorin were formed by abiogenic synthesis. Magnesium complexes of porphyrins are active being excited by light. They are capable to reversible acceptance or donation of an electron to partner molecule. Excited Mg-complexes of porphyrins (P) are capable to transfer an electron from electron-donor (D) to electron-acceptor (A) accompanied by conversion of light quanta energy into potential chemical energy. The primary electron transfer unit (D-P-A) was incorporated into primary membrane. The transition from random to anisotropic arrangement of (D-P-A) in the membrane was plausable as a step of evolution; charge translocation appeared. (D-P-A) units created in the period of chemical evolution were probably used in the course of biological evolution. The (D-P-A) units were coupled with noncyclic and cyclic electron transfer resulting in ATP formation; coupling of two (D-P-A) units led to H2O oxidation and NADP reduction in photosynthetic organisms. The improvement of pigments biosynthesis created the phenomenon of excitation energy migration from the bulk of the pigment to (D-P-A) unit, being reactive center. The models described points the plausible steps of chemical evolution; the real sequence of events will be probably disclosed in the studies of precambrian rocks and space exploration.
光合作用的生物进化原理已确立,但化学进化的方式尚不清楚。模型系统将有助于阐明这一问题。每种光合作用类型都需要光感受器来吸收太阳辐射。我们研究了地壳中的无机成分、一些非生物起源和生物起源的辅酶及卟啉作为光感受器。借助无机光敏剂(TiO₂、ZnO)构建了光系统I和光系统II的模型。一些辅酶的光化学活化可能是从异养“暗”代谢到“光”代谢的中间步骤。进一步的进化导致了催化功能和光敏功能的分离。卟吩、二氢卟吩和细菌二氢卟吩通过非生物合成形成。卟啉的镁配合物在光激发下具有活性。它们能够可逆地接受或向伙伴分子提供电子。激发态的卟啉镁配合物(P)能够将电子从电子供体(D)转移到电子受体(A),同时将光量子能量转化为潜在的化学能。初级电子转移单元(D-P-A)被整合到初级膜中。(D-P-A)在膜中从随机排列到各向异性排列的转变被认为是进化的一个步骤;电荷转移出现了。在化学进化时期产生的(D-P-A)单元可能在生物进化过程中被利用。(D-P-A)单元与非循环和循环电子转移相偶联,导致ATP形成;两个(D-P-A)单元的偶联导致光合生物中H₂O氧化和NADP还原。色素生物合成的改进产生了激发能从大量色素向作为反应中心的(D-P-A)单元迁移的现象。所描述的模型指出了化学进化的合理步骤;实际的事件顺序可能会在前寒武纪岩石研究和太空探索中被揭示。