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首页> 外文期刊>Folia Microbiologica >On the origin of chloroplasts, import mechanisms of chloroplast-targeted proteins, and loss of photosynthetic ability — review
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On the origin of chloroplasts, import mechanisms of chloroplast-targeted proteins, and loss of photosynthetic ability — review

机译:关于叶绿体的起源,叶绿体靶向蛋白的导入机制和光合能力的丧失—综述

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Primary plastids of green algae (including land plants), red algae and glaucophytes are bounded by two membranes and are thought to be derived from a single primary endosymbiosis of a cyanobacterium in a eukaryotic host. Complex plastids of euglenids and chlorarachneans bounded by three and four membranes, respectively, most likely arose via two separate secondary endosymbioses of a green alga in a eukaryotic host. Secondary plastids of cryptophyta, haptophyta, heterokontophyta and apicomplexan parasites bounded by four membranes, and plastids of dinoflagellates bounded by three membranes could have arisen via a single secondary endosymbiosis of a red alga in a eukaryotic host (chromalveolate hypothesis). However, the scenario of separate tertiary origins (symbioses of an alga possessing secondary plastids in a eukaryotic host) of some (or even most) chromalveolate plastids can be also consistent with the current data. The protein import into complex plastids differs from the import into primary plastids, as complex plastids contain one or two extra membrane(s). In organisms with primary plastids, plastid-targeted proteins contain N-terminal transit peptide which ferries proteins through the protein import machineries (multiprotein complexes) of the two (originally cyanobacterial) membranes. In organisms with complex plastids, the secretory signal sequence directing proteins to endomembrane system and afterwards through extra outermost membrane(s) is generally present upstream of the classical transit peptide. Several free-living as well as parasitic eukaryotes possess non-photosynthetic plastids. These plastids have generally retained the plastid genome, functional plastid transcriptional and translational apparatus, and various metabolic pathways, suggesting that though these plastids lost their photosynthetic ability, they are essential for the mentioned organisms. Nevertheless, some eukaryotes could have lost chloroplast compartment completely.
机译:绿藻(包括陆地植物),红藻和青生植物的原生质体被两个膜所包围,并被认为源自真核宿主中蓝细菌的单一原生质共生。真核宿主中,分别由三层和四层膜束缚的桉树和氯囊虫的复杂质体很可能是通过绿藻的两个单独的次生内共生酶产生的。通过真核宿主中红藻的单个次生内共生作用,可以产生由四个膜所包围的隐藻类,触生植物,异种植物和apicomplexan寄生虫的次生质体,以及被三个膜所束缚的鞭毛藻的质体(在真核宿主中,一次红藻的次生共生)(色藻假说)。但是,某些(或什至大多数)苯丙酸类固醇的第三系起源(藻类在真核宿主中具有次级质体的共生酶)的情况也可以与当前数据相一致。蛋白质导入复杂质体的过程不同于蛋白质导入初级质体的过程,因为复杂质体包含一个或两个额外的膜。在具有初级质体的生物中,以质体为靶标的蛋白质包含N末端转运肽,该肽通过两个(最初为蓝细菌)膜的蛋白质输入装置(多蛋白质复合物)运送蛋白质。在具有复杂质体的生物体中,将蛋白质引导至内膜系统并随后通过额外的最外膜的分泌信号序列通常存在于经典转运肽的上游。几种自由生活的和寄生的真核生物都具有非光合作用的质体。这些质体通常保留了质体基因组,功能性质体转录和翻译设备以及各种代谢途径,这表明尽管这些质体失去了光合能力,但它们对于上述生物是必不可少的。但是,某些真核生物可能会完全失去叶绿体区室。

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