Gao Beile, Gupta Radhey S
Department of Biochemistry and Biomedical Science, McMaster University, Hamilton, Canada L8N 3Z5.
Int J Syst Evol Microbiol. 2005 Nov;55(Pt 6):2401-2412. doi: 10.1099/ijs.0.63785-0.
Gram-positive bacteria with a high G+C content are currently recognized as a distinct phylum, Actinobacteria, on the basis of their branching in 16S rRNA trees. Except for an insert in the 23S rRNA, there are no unique biochemical or molecular characteristics known at present that can distinguish this group from all other bacteria. In this work, three conserved indels (i.e. inserts or deletions) are described in three widely distributed proteins that are distinctive characteristics of the Actinobacteria and are not found in any other groups of bacteria. The identified signatures are a 2 aa deletion in cytochrome-c oxidase subunit 1 (Cox1), a 4 aa insert in CTP synthetase and a 5 aa insert in glutamyl-tRNA synthetase (GluRS). Additionally, the actinobacterial specificity of the large insert in the 23S rRNA was also tested. Using primers designed for conserved regions flanking these signatures, fragments of most of these genes were amplified from 23 actinobacterial species, covering many different families and orders, for which no sequence information was previously available. All the 61 sequenced fragments, except two in GluRS, were found to contain the indicated signatures. The presence of these signatures in various species from 20 families within this phylum provides evidence that they are likely distinctive characteristics of the entire phylum, which were introduced in a common ancestor of this group. The absence of all four of these signatures in Symbiobacterium thermophilum suggests that this species, which is distantly related to other actinobacteria in 16S rRNA and CTP synthetase trees, may not be a part of the phylum Actinobacteria. The identified signatures provide novel molecular means for defining and circumscribing the phylum Actinobacteria. Functional studies on them should prove helpful in understanding novel biochemical and physiological characteristics of this group of bacteria.
基于16S rRNA树中的分支情况,目前具有高G+C含量的革兰氏阳性菌被公认为一个独特的门——放线菌门。除了23S rRNA中的一个插入片段外,目前还没有已知的独特生化或分子特征能够将该类群与所有其他细菌区分开来。在这项研究中,在三种广泛分布的蛋白质中描述了三个保守的插入或缺失(即插入或删除),它们是放线菌门的独特特征,在任何其他细菌类群中都未发现。鉴定出的特征是细胞色素c氧化酶亚基1(Cox1)中有2个氨基酸的缺失,CTP合成酶中有4个氨基酸的插入,以及谷氨酰胺-tRNA合成酶(GluRS)中有5个氨基酸的插入。此外,还测试了23S rRNA中大型插入片段的放线菌特异性。使用针对这些特征两侧保守区域设计的引物,从23种放线菌物种中扩增出了这些基因的大部分片段,这些物种涵盖了许多不同的科和目,之前没有它们的序列信息。除了GluRS中的两个片段外,所有61个测序片段都被发现含有所示的特征。在该门内20个科的各种物种中存在这些特征,这证明它们可能是整个门的独特特征,是在该类群的共同祖先中出现的。嗜热共生菌中所有这四个特征均不存在,这表明该物种在16S rRNA和CTP合成酶树中与其他放线菌关系较远,可能不属于放线菌门。鉴定出的特征为定义和界定放线菌门提供了新的分子手段。对它们的功能研究应有助于理解这组细菌的新生化和生理特征。