Montgomery Beronda L, Lechno-Yossef Sigal, Kerfeld Cheryl A
MSU-DOE Plant Research Laboratory, Michigan State University, East Lansing, MI 48824, USA Department of Biochemistry and Molecular Biology, Michigan State University, East Lansing, MI 48824, USA.
MSU-DOE Plant Research Laboratory, Michigan State University, East Lansing, MI 48824, USA.
J Exp Bot. 2016 May;67(10):2931-40. doi: 10.1093/jxb/erw162. Epub 2016 Apr 25.
Here we consider the cyanobacterial carbon-concentrating mechanism (CCM) and photorespiration in the context of the regulation of light harvesting, using a conceptual framework borrowed from engineering: modularity. Broadly speaking, biological 'modules' are semi-autonomous functional units such as protein domains, operons, metabolic pathways, and (sub)cellular compartments. They are increasingly recognized as units of both evolution and engineering. Modules may be connected by metabolites, such as NADPH, ATP, and 2PG. While the Calvin-Benson-Bassham Cycle and photorespiratory salvage pathways can be considered as metabolic modules, the carboxysome, the core of the cyanobacterial CCM, is both a structural and a metabolic module. In photosynthetic organisms, which use light cues to adapt to the external environment and which tune the photosystems to provide the ATP and reducing power for carbon fixation, light-regulated modules are critical. The primary enzyme of carbon fixation, RuBisCO, uses CO2 as a substrate, which is accumulated via the CCM. However RuBisCO also has a secondary reaction in which it utilizes O2, a by-product of the photochemical modules, which leads to photorespiration. A complete understanding of the interplay among CCM and photorespiration is predicated on uncovering their connections to the light reactions and the regulatory factors and pathways that tune these modules to external cues. We probe this connection by investigating light inputs into the CCM and photorespiratory pathways in the chromatically acclimating cyanobacterium Fremyella diplosiphon.
在此,我们利用从工程学借鉴的概念框架:模块化,在光捕获调节的背景下考虑蓝藻的碳浓缩机制(CCM)和光呼吸作用。广义而言,生物“模块”是半自主功能单元,如蛋白质结构域、操纵子、代谢途径和(亚)细胞区室。它们越来越被视为进化和工程的单元。模块可能通过代谢物连接,如NADPH、ATP和2PG。虽然卡尔文-本森-巴斯姆循环和光呼吸挽救途径可被视为代谢模块,但蓝藻CCM的核心羧酶体既是结构模块也是代谢模块。在利用光信号适应外部环境并调节光系统以提供用于碳固定的ATP和还原力的光合生物中,光调节模块至关重要。碳固定的主要酶核酮糖-1,5-二磷酸羧化酶/加氧酶(RuBisCO)以CO2为底物,CO2通过CCM积累。然而,RuBisCO也有一个副反应,即它利用光化学模块的副产物O2,这会导致光呼吸。对CCM和光呼吸之间相互作用的全面理解取决于揭示它们与光反应以及将这些模块调节至外部信号的调节因子和途径的联系。我们通过研究在能进行色适应的蓝藻双岐颤藻中输入到CCM和光呼吸途径的光来探究这种联系。