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Comparative Genomic Analysis of N2-Fixing and Non-N2-Fixing Paenibacillus spp.: Organization Evolution and Expression of the Nitrogen Fixation Genes

机译:N2-固定和非N2-固定芽孢杆菌的比较基因组分析:固氮基因的组织进化和表达

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摘要

We provide here a comparative genome analysis of 31 strains within the genus Paenibacillus including 11 new genomic sequences of N2-fixing strains. The heterogeneity of the 31 genomes (15 N2-fixing and 16 non-N2-fixing Paenibacillus strains) was reflected in the large size of the shell genome, which makes up approximately 65.2% of the genes in pan genome. Large numbers of transposable elements might be related to the heterogeneity. We discovered that a minimal and compact nif cluster comprising nine genes nifB, nifH, nifD, nifK, nifE, nifN, nifX, hesA and nifV encoding Mo-nitrogenase is conserved in the 15 N2-fixing strains. The nif cluster is under control of a σ70-depedent promoter and possesses a GlnR/TnrA-binding site in the promoter. Suf system encoding [Fe–S] cluster is highly conserved in N2-fixing and non-N2-fixing strains. Furthermore, we demonstrate that the nif cluster enabled Escherichia coli JM109 to fix nitrogen. Phylogeny of the concatenated NifHDK sequences indicates that Paenibacillus and Frankia are sister groups. Phylogeny of the concatenated 275 single-copy core genes suggests that the ancestral Paenibacillus did not fix nitrogen. The N2-fixing Paenibacillus strains were generated by acquiring the nif cluster via horizontal gene transfer (HGT) from a source related to Frankia. During the history of evolution, the nif cluster was lost, producing some non-N2-fixing strains, and vnf encoding V-nitrogenase or anf encoding Fe-nitrogenase was acquired, causing further diversification of some strains. In addition, some N2-fixing strains have additional nif and nif-like genes which may result from gene duplications. The evolution of nitrogen fixation in Paenibacillus involves a mix of gain, loss, HGT and duplication of nif/anf/vnf genes. This study not only reveals the organization and distribution of nitrogen fixation genes in Paenibacillus, but also provides insight into the complex evolutionary history of nitrogen fixation.
机译:我们在这里提供了Paenibacillus属中31个菌株的比较基因组分析,包括N2固定菌株的11个新基因组序列。壳基因组的大尺寸反映了31个基因组(15个固定N2和固定非N2的Paenibacillus菌株)的异质性,该基因组占泛基因组中大约65.2%的基因。大量的转座因子可能与异质性有关。我们发现在15个N2固定菌株中,包含9个基因nifB,nifH,nifD,nifK,nifE,nifN,nifX,hesA和nifV的最小而紧凑的nif簇是保守的。 nif簇受σ 70 依赖的启动子控制,在启动子中具有GlnR / TnrA结合位点。 Suf系统编码[Fe–S]簇在固氮和固氮菌株中高度保守。此外,我们证明了nif簇使大肠杆菌JM109能够固定氮。系统级联的NifHDK序列表明Paenibacillus和 Frankia 是姐妹组。串联的275个单拷贝核心基因的系统发生表明,祖先的Paenibacillus 不能固定氮。通过与来自 Frankia 相关的来源通过水平基因转移(HGT)获得 nif 簇来产生固定N2的 Paenibacillus 菌株。在进化过程中, nif 簇丢失,产生了一些非N2固定菌株,并且 vnf 编码了V-硝化酶或 anf 获得了编码Fe-氮酶的编码,导致某些菌株进一步多样化。此外,一些固氮菌株也可能具有额外的 nif nif 样基因,这些基因可能是基因重复产生的。芽孢杆菌中固氮的演变涉及增益,损失,HGT和 nif / anf / vnf 基因重复的混合。这项研究不仅揭示了 Paenibacillus 中固氮基因的组织和分布,而且为深入了解固氮的复杂进化史提供了见识。

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