Raven John A, Giordano Mario, Beardall John
Division of Plant Sciences, University of Dundee at SCRI, Scottish Crop Research Institute, Invergowrie, Dundee DD2 5DA, United Kingdom.
Physiol Plant. 2008 May;133(1):4-14. doi: 10.1111/j.1399-3054.2007.01024.x.
Regarding inorganic carbon as 'just another' chemical resource used in the growth of aquatic photolithotrophs, we ask three questions and then attempt to answer them. (1) How common are catalysed chemical changes of the resource outside the cell, and accumulation of the resource inside the cell prior to assimilation, for the diverse chemical resources used? (2) Do acquisition and assimilation meet evolutionary optimality criteria with respect to the use of other resources? (3) Are there clues to the evolutionary origin of inorganic carbon concentrating mechanism (CCMs) in the mechanisms of acquisition of other resources and vice versa? Evidence considered includes molecular genetic similarities between CCM components and components of other resource acquisition mechanisms, and palaeogeochemical evidence on the timing of restrictions on the availability of the resources such that extracellular transformation of materials, and their accumulation within cells prior to assimilation, are needed. Provisional answers to the questions are as follows: (1) Many common chemical resources other than inorganic carbon are subject to extracellular chemical conversion and/or accumulation prior to assimilation, e.g. ammonium, nitrate, urea, amino acids, organic and inorganic phosphate and iron; (2) There is some evidence for optimality of CCMs and of less complex resource acquisition processes, exemplified by NH(4)(+) entry and assimilation, though many more data are needed and (3) There are molecular genetic similarities between CCM components and transporters for other solutes and components of respiratory NADH dehydrogenases that are consistent with their use in CCMs representing a derived evolutionary state. Palaeogeochemical evidence suggests that CCMs evolved later than did at least some of the extracellular chemical transformation and/or accumulation mechanisms for other resources.
将无机碳视为水生光合自养生物生长过程中使用的“另一种”化学资源,我们提出三个问题,然后尝试回答。(1)对于所使用的各种化学资源而言,细胞外资源的催化化学变化以及同化之前资源在细胞内的积累有多普遍?(2)就其他资源的利用而言,获取和同化是否符合进化最优标准?(3)在其他资源的获取机制中是否存在无机碳浓缩机制(CCM)进化起源的线索,反之亦然?所考虑的证据包括CCM组分与其他资源获取机制组分之间的分子遗传相似性,以及关于资源可用性限制时间的古地球化学证据,这些证据表明需要进行物质的细胞外转化及其在同化之前在细胞内的积累。这些问题的初步答案如下:(1)除无机碳外,许多常见化学资源在同化之前会经历细胞外化学转化和/或积累,例如铵、硝酸盐、尿素、氨基酸、有机和无机磷酸盐以及铁;(2)有一些证据表明CCM以及不太复杂的资源获取过程具有最优性,以NH₄⁺的进入和同化为例,不过还需要更多数据;(3)CCM组分与其他溶质转运蛋白以及呼吸NADH脱氢酶组分之间存在分子遗传相似性,这与它们在CCM中的使用代表一种衍生进化状态相一致。古地球化学证据表明,CCM的进化晚于至少一些其他资源的细胞外化学转化和/或积累机制。