Rangan Parimalan, Wankhede Dhammaprakash P, Subramani Rajkumar, Chinnusamy Viswanathan, Malik Surendra K, Baig Mirza Jaynul, Singh Kuldeep, Henry Robert
ICAR-National Bureau of Plant Genetic Resources, PUSA Campus, New Delhi, 110012, India.
Queensland Alliance for Agriculture and Food Innovation, University of Queensland, Brisbane, QLD, 4072, Australia.
Photosynth Res. 2022 Sep;153(3):125-134. doi: 10.1007/s11120-022-00926-7. Epub 2022 Jun 1.
Carbon concentrating mechanisms (CCMs) in plants are abaptive features that have evolved to sustain plant growth in unfavorable environments, especially at low atmospheric carbon levels and high temperatures. Uptake of CO and its storage in the aerenchyma tissues of Lycopsids and diurnal acidity fluctuation in aquatic plants during the Palaeozoic era (ca. 300 Ma.) would represent the earliest evolution of a CCM. The CCM parts of the dark reactions of photosynthesis have evolved many times, while the light reactions are conserved across plant lineages. A C type CCM, leaf C photosynthesis is evolved in the PACMAD clade of the Poaceae family. The evolution of C photosynthesis from C photosynthesis was an abaptation. Photosynthesis in reproductive tissues of sorghum and maize (PACMAD clade) has been shown to be of a weaker C type (high CO compensation point, low carbon isotope discrimination, and lack of Rubisco compartmentalization, when compared to the normal C types) than that in the leaves (normal C type). However, this does not fit well with the character polarity concept from an evolutionary perspective. In a recent model proposed for CCM evolution, the development of a rudimentary CCM prior to the evolution of a more efficient CCM (features contrasting to a weaker C type, leading to greater biomass production rate) has been suggested. An intermediate crassulacean acid metabolism (CAM) type of CCM (rudimentary) was reported in the genera, Brassia, Coryanthes, Eriopsis, Peristeria, of the orchids (well-known group of plants that display the CAM pathway). Similarly, we propose here the evolution of a rudimentary CCM (C-like type pathway) in the non-foliar tissues of the Poaceae, prior to the evolution of the C pathway as identified in the leaves of the C species of the PACMAD clade.
植物中的碳浓缩机制(CCMs)是一种适应性特征,其进化目的是在不利环境中维持植物生长,特别是在低大气碳水平和高温环境下。在古生代(约3亿年前),石松类植物气腔组织中CO的吸收及其储存以及水生植物的昼夜酸度波动,可能代表了CCM的最早进化。光合作用暗反应中的CCM部分已经进化了很多次,而光反应在植物谱系中是保守的。在禾本科的PACMAD分支中进化出了C4型CCM,即叶片C4光合作用。从C3光合作用进化到C4光合作用是一种适应。与叶片(正常C4类型)相比,高粱和玉米(PACMAD分支)生殖组织中的光合作用表现出较弱的C4类型(高CO2补偿点、低碳同位素歧视以及缺乏Rubisco区室化)。然而,从进化的角度来看,这与性状极性概念不太相符。在最近提出的CCM进化模型中,有人提出在更高效的CCM进化之前(其特征与较弱的C4类型相反,导致更高的生物量生产率),先发展出一种初级CCM。在兰花的Brassia、Coryanthes、Eriopsis、Peristeria属(显示CAM途径的著名植物类群)中报道了一种中间型景天酸代谢(CAM)类型的CCM(初级)。同样,我们在此提出,在PACMAD分支C4物种叶片中鉴定出的C4途径进化之前,禾本科非叶组织中先进化出一种初级CCM(类似C4的途径)。