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细菌多聚磷酸激酶向真核生物的水平转移:对冰河时代和陆地殖民化的影响。

Horizontal transfer of bacterial polyphosphate kinases to eukaryotes: implications for the ice age and land colonisation.

作者信息

Whitehead Michael P, Hooley Paul, W Brown Michael R

机构信息

School of Applied Sciences, University of Wolverhampton, Wolverhampton, UK.

出版信息

BMC Res Notes. 2013 Jun 5;6:221. doi: 10.1186/1756-0500-6-221.

Abstract

BACKGROUND

Studies of online database(s) showed that convincing examples of eukaryote PPKs derived from bacteria type PPK1 and PPK2 enzymes are rare and currently confined to a few simple eukaryotes. These enzymes probably represent several separate horizontal transfer events. Retention of such sequences may be an advantage for tolerance to stresses such as desiccation or nutrient depletion for simple eukaryotes that lack more sophisticated adaptations available to multicellular organisms. We propose that the acquisition of encoding sequences for these enzymes by horizontal transfer enhanced the ability of early plants to colonise the land. The improved ability to sequester and release inorganic phosphate for carbon fixation by photosynthetic algae in the ocean may have accelerated or even triggered global glaciation events. There is some evidence for DNA sequences encoding PPKs in a wider range of eukaryotes, notably some invertebrates, though it is unclear that these represent functional genes.Polyphosphate (poly P) is found in all cells, carrying out a wide range of essential roles. Studied mainly in prokaryotes, the enzymes responsible for synthesis of poly P in eukaryotes (polyphosphate kinases PPKs) are not well understood. The best characterised enzyme from bacteria known to catalyse the formation of high molecular weight polyphosphate from ATP is PPK1 which shows some structural similarity to phospholipase D. A second bacterial PPK (PPK2) resembles thymidylate kinase. Recent reports have suggested a widespread distribution of these bacteria type enzymes in eukaryotes.

RESULTS

On - line databases show evidence for the presence of genes encoding PPK1 in only a limited number of eukaryotes. These include the photosynthetic eukaryotes Ostreococcus tauri, O. lucimarinus, Porphyra yezoensis, Cyanidioschyzon merolae and the moss Physcomitrella patens, as well as the amoeboid symbiont Capsaspora owczarzaki and the non-photosynthetic eukaryotes Dictyostelium (3 species), Polysphondylium pallidum and Thecamonas trahens. A second bacterial PPK (PPK2) is found in just two eukaryotes (O. tauri and the sea anemone Nematostella vectensis). There is some evidence for PPK1 and PPK2 encoding sequences in other eukaryotes but some of these may be artefacts of bacterial contamination of gene libraries.

CONCLUSIONS

Evidence for the possible origins of these eukaryote PPK1s and PPK2s and potential prokaryote donors via horizontal gene transfer is presented. The selective advantage of acquiring and maintaining a prokaryote PPK in a eukaryote is proposed to enhance stress tolerance in a changing environment related to the capture and metabolism of inorganic phosphate compounds. Bacterial PPKs may also have enhanced the abilities of marine phytoplankton to sequester phosphate, hence accelerating global carbon fixation.

摘要

背景

在线数据库研究表明,源自细菌型PPK1和PPK2酶的真核生物多聚磷酸激酶(PPK)的令人信服的例子很少,目前仅限于少数简单的真核生物。这些酶可能代表了几个独立的水平转移事件。对于缺乏多细胞生物所具备的更复杂适应能力的简单真核生物而言,保留此类序列可能有利于耐受诸如干燥或营养耗竭等压力。我们提出,通过水平转移获得这些酶的编码序列增强了早期植物在陆地上定殖的能力。海洋中光合藻类通过隔离和释放无机磷酸盐以进行碳固定的能力的提高可能加速甚至引发了全球冰川事件。有证据表明,在更广泛的真核生物中存在编码PPK的DNA序列,尤其是一些无脊椎动物,不过尚不清楚这些是否代表功能基因。多聚磷酸盐(poly P)存在于所有细胞中,发挥着广泛的重要作用。主要在原核生物中进行研究,对真核生物中负责多聚磷酸盐合成的酶(多聚磷酸激酶PPK)了解甚少。已知能催化由ATP形成高分子量多聚磷酸盐的细菌中,特征最明确的酶是PPK1,它与磷脂酶D在结构上有一些相似之处。第二种细菌PPK(PPK2)类似于胸苷酸激酶。最近的报告表明,这些细菌型酶在真核生物中广泛分布。

结果

在线数据库显示,仅在有限数量的真核生物中存在编码PPK1的基因证据。这些包括光合真核生物莱茵衣藻、纤细角毛藻、条斑紫菜、聚球藻,以及苔藓小立碗藓,还有变形虫共生体奥氏嗜囊菌和非光合真核生物盘基网柄菌(3个物种)、苍白聚孢黏菌和特拉氏嗜囊菌。第二种细菌PPK(PPK2)仅在两种真核生物(莱茵衣藻和海葵星状海葵)中发现。在其他真核生物中存在PPK1和PPK2编码序列的一些证据,但其中一些可能是基因文库细菌污染的假象。

结论

本文提供了这些真核生物PPK1和PPK2可能的起源以及通过水平基因转移潜在的原核生物供体的证据。提出在真核生物中获得并维持原核生物PPK的选择优势在于增强在与无机磷酸盐化合物捕获和代谢相关的变化环境中的胁迫耐受性。细菌PPK也可能增强了海洋浮游植物隔离磷酸盐的能力,从而加速全球碳固定。

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