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Role of Mitochondria in Regulating Lutein and Chlorophyll Biosynthesis in Chlorella pyrenoidosa under Heterotrophic Conditions

机译:异养条件下线粒体在调控小球藻中叶黄素和叶绿素生物合成中的作用

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摘要

The green alga Chlorella pyrenoidosa can accumulate lutein and chlorophyll under heterotrophic conditions. We propose that the mitochondrial respiratory electron transport chain (mRET) may be involved in this process. To verify this hypothesis, algal cells were treated with different mRET inhibitors. The biosynthesis of lutein and chlorophyll was found to be significantly stimulated by salicylhydroxamic acid (SHAM), whereas their contents substantially decreased after treatment with antimycin A and sodium azide (NaN3). Proteomic studies revealed profound protein alterations related to the redox and energy states, and a network was proposed: The up-regulation of peroxiredoxin reduces oxidized glutathione (GSSG) to reduced glutathione (GSH); phosphoenolpyruvate carboxykinase (PEPCK) catalyzes the conversion of oxaloacetic acid to phosphoenolpyruvate, and after entering the methylerythritol phosphate (MEP) pathway, 4-hydroxy-3-methylbut-2-en-1yl diphosphate synthase reduces 2-C-methyl-d-erythritol-2,4-cyclodiphosphate (ME-Cpp) to 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate (HMBPP), which is closely related to the synthesis of lutein; and coproporphyrinogen III oxidase and ChlI play important roles in the chlorophyll biosynthetic pathway. These results supported that for the heterotrophic C. pyrenoidosa, the signaling, oriented from mRET, may regulate the nuclear genes encoding the enzymes involved in photosynthetic pigment biosynthesis.
机译:绿藻类小球藻可以在异养条件下积累叶黄素和叶绿素。我们建议线粒体呼吸电子运输链(mRET)可能参与此过程。为了验证该假设,用不同的mRET抑制剂处理藻类细胞。水杨基异羟肟酸(SHAM)可显着刺激叶黄素和叶绿素的生物合成,而抗霉素A和叠氮化钠(NaN3)处理后其含量则明显降低。蛋白质组学研究揭示了与氧化还原和能量状态相关的深远蛋白质改变,并提出了一个网络:过氧化物酶毒素的上调将氧化型谷胱甘肽(GSSG)还原为还原型谷胱甘肽(GSH);磷酸烯醇丙酮酸羧激酶(PEPCK)催化草酰乙酸向磷酸烯醇丙酮酸的转化,进入甲基赤藓醇磷酸酯(MEP)途径后,4-羟基-3-甲基丁-2-烯丙基二磷酸合酶还原2-C-甲基-d-赤藓醇-2,4-环二磷酸酯(ME-Cpp)变成1-叶酸-2-甲基-2-(E)-丁烯基4-二磷酸酯(HMBPP),与叶黄素的合成密切相关;卟啉原原Ⅲ氧化酶和Chl在叶绿素的生物合成途径中起重要作用。这些结果支持对于异养梭状芽孢杆菌,从mRET定向的信号转导可能调节编码光合作用色素生物合成中涉及的酶的核基因。

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