Arnon D I
Proc Natl Acad Sci U S A. 1971 Nov;68(11):2883-92. doi: 10.1073/pnas.68.11.2883.
Historically, the role of light in photosynthesis has been ascribed either to a photolysis of carbon dioxide or to a photolysis of water and a resultant rearrangement of constituent atoms into molecules of oxygen and glucose (or formaldehyde). The discovery of photophosphorylation demonstrated that photosynthesis includes a light-induced phosphorus metabolism that precedes, and is independent from, a photolysis of water or CO(2). ATP formation could best be accounted for not by a photolytic disruption of the covalent bonds in CO(2) or water but by the operation of a light-induced electron flow that results in a release of free energy which is trapped in the pyrophosphate bonds of ATP. Photophosphorylation is now divided into (a) a non-cyclic type, in which the formation of ATP is coupled with a light-induced electron transport from water to ferredoxin and a concomitant evolution of oxygen and (b) a cyclic type which yields only ATP and produces no net change in the oxidation-reduction state of any electron donor or acceptor. Reduced ferredoxin formed in (a) serves as an electron donor for the reduction of NADP by an enzymic reaction that is independent of light. ATP, from both cyclic and noncyclic photophosphorylation, and reduced NADP jointly constitute the assimilatory power for the conversion of CO(2) to carbohydrates (3 moles of ATP and 2 moles of reduced NADP are required per mole of CO(2)).Investigations, mainly with whole cells, have shown that photosynthesis in green plants involves two photosystems, one (System II) that best uses light of "short" wavelength (lambda < 685 nm) and another (System I) that best uses light of "long" wavelength (lambda > 685 nm). Cyclic photophosphorylation in chloroplasts involves a System I photoreaction. Noncyclic photophosphorylation is widely held to involve a collaboration of two photoreactions: a short-wavelength photoreaction belonging to System II and a long-wavelength photoreaction belonging to System I. Recent findings, however, indicate that noncyclic photophosphorylation may include two short-wavelength, System II, photoreactions that operate in series and are joined by a "dark" electron-transport chain to which is coupled a phosphorylation site.
从历史上看,光在光合作用中的作用要么归因于二氧化碳的光解,要么归因于水的光解以及随后组成原子重新排列形成氧气和葡萄糖(或甲醛)分子。光合磷酸化的发现表明,光合作用包括一种光诱导的磷代谢,它先于水或二氧化碳的光解,并且与之独立。ATP的形成最好不是由二氧化碳或水中共价键的光解破坏来解释,而是由光诱导的电子流的运作来解释,这种电子流导致自由能的释放,该自由能被困在ATP的焦磷酸键中。光合磷酸化现在分为:(a)非循环型,其中ATP的形成与光诱导的从水到铁氧还蛋白的电子传递以及伴随的氧气释放相偶联;(b)循环型,其仅产生ATP,并且在任何电子供体或受体的氧化还原状态上不产生净变化。在(a)中形成的还原型铁氧还蛋白作为通过与光无关的酶促反应还原NADP 的电子供体。来自循环和非循环光合磷酸化的ATP以及还原型NADP共同构成了将二氧化碳转化为碳水化合物的同化力(每摩尔二氧化碳需要3摩尔ATP和2摩尔还原型NADP)。主要使用全细胞进行的研究表明,绿色植物中的光合作用涉及两个光系统,一个(光系统II)最有效地利用“短”波长(λ<685nm)的光,另一个(光系统I)最有效地利用“长”波长(λ>685nm)的光。叶绿体中的循环光合磷酸化涉及光系统I光反应。非循环光合磷酸化被广泛认为涉及两个光反应的协作:一个属于光系统II的短波长光反应和一个属于光系统I的长波长光反应。然而,最近的发现表明,非循环光合磷酸化可能包括两个串联运行的短波长光系统II光反应,并由一个“暗”电子传递链连接,该电子传递链与一个磷酸化位点相偶联。