首页> 美国卫生研究院文献>The Journal of Biological Chemistry >Outer Membrane Proteins Derived from Non-cyanobacterial Lineage Cover the Peptidoglycan of Cyanophora paradoxa Cyanelles and Serve as a Cyanelle Diffusion Channel
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Outer Membrane Proteins Derived from Non-cyanobacterial Lineage Cover the Peptidoglycan of Cyanophora paradoxa Cyanelles and Serve as a Cyanelle Diffusion Channel

机译:源自非蓝细菌谱系的外膜蛋白覆盖了Cyanophora paradoxa Cyanelles的肽聚糖并作为Cyanelle扩散通道。

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摘要

The cyanelle is a primitive chloroplast that contains a peptidoglycan layer between its inner and outer membranes. Despite the fact that the envelope structure of the cyanelle is reminiscent of Gram-negative bacteria, the Cyanophora paradoxa genome appears to lack genes encoding homologs of putative peptidoglycan-associated outer membrane proteins and outer membrane channels. These are key components of Gram-negative bacterial membranes, maintaining structural stability and regulating permeability of outer membrane, respectively. Here, we discovered and characterized two dominant peptidoglycan-associated outer membrane proteins of the cyanelle (∼2 × 106 molecules per cyanelle). We named these proteins CppF and CppS (cyanelle peptidoglycan-associated proteins). They are homologous to each other and function as a diffusion channel that allows the permeation of compounds with Mr <1,000 as revealed by permeability measurements using proteoliposomes reconstituted with purified CppS and CppF. Unexpectedly, amino acid sequence analysis revealed no evolutionary linkage to cyanobacteria, showing only a moderate similarity to cell surface proteins of bacteria belonging to Planctomycetes phylum. Our findings suggest that the C. paradoxa cyanelle adopted non-cyanobacterial lineage proteins as its main outer membrane components, providing a physical link with the underlying peptidoglycan layer and functioning as a diffusion route for various small substances across the outer membrane.
机译:氰化物是原始叶绿体,在其内膜和外膜之间包含肽聚糖层。尽管事实是,氰基的包膜结构使人联想到革兰氏阴性细菌,但是,Cyanophora paradoxa基因组似乎缺乏编码假定的肽聚糖相关外膜蛋白和外膜通道同源物的基因。这些是革兰氏阴性细菌膜的关键组成部分,分别维持结构稳定性和调节外膜的渗透性。在这里,我们发现并表征了氰基的两个主要的肽聚糖相关的外膜蛋白(每个氰基约2×10 6 分子)。我们将这些蛋白命名为CppF和CppS(氰基肽聚糖相关蛋白)。它们彼此同源,并起扩散通道的作用,如使用纯化的CppS和CppF重构的蛋白脂质体进行的渗透性测量所揭示,Mr <1,000的化合物可以渗透。出乎意料的是,氨基酸序列分析显示没有与蓝细菌的进化联系,仅显示出与属于门生菌的细菌的细胞表面蛋白中等程度的相似性。我们的发现表明,C。paradoxa cyanelle采用非蓝细菌谱系蛋白作为其主要外膜成分,提供了与下面的肽聚糖层的物理连接,并充当了各种小物质穿过外膜的扩散途径。

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