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肺炎支原体细菌基因组的全序列分析。

Complete sequence analysis of the genome of the bacterium Mycoplasma pneumoniae.

作者信息

Himmelreich R, Hilbert H, Plagens H, Pirkl E, Li B C, Herrmann R

机构信息

Zentrum für Molekulare Biologie Heidelberg, Mikrobiologie, Universität Heidelberg, Germany.

出版信息

Nucleic Acids Res. 1996 Nov 15;24(22):4420-49. doi: 10.1093/nar/24.22.4420.

Abstract

The entire genome of the bacterium Mycoplasma pneumoniae M129 has been sequenced. It has a size of 816,394 base pairs with an average G+C content of 40.0 mol%. We predict 677 open reading frames (ORFs) and 39 genes coding for various RNA species. Of the predicted ORFs, 75.9% showed significant similarity to genes/proteins of other organisms while only 9.9% did not reveal any significant similarity to gene sequences in databases. This permitted us tentatively to assign a functional classification to a large number of ORFs and to deduce the biochemical and physiological properties of this bacterium. The reduction of the genome size of M. pneumoniae during its reductive evolution from ancestral bacteria can be explained by the loss of complete anabolic (e.g. no amino acid synthesis) and metabolic pathways. Therefore, M. pneumoniae depends in nature on an obligate parasitic lifestyle which requires the provision of exogenous essential metabolites. All the major classes of cellular processes and metabolic pathways are briefly described. For a number of activities/functions present in M. pneumoniae according to experimental evidence, the corresponding genes could not be identified by similarity search. For instance we failed to identify genes/proteins involved in motility, chemotaxis and management of oxidative stress.

摘要

肺炎支原体M129菌株的全基因组已被测序。其大小为816,394个碱基对,平均G+C含量为40.0摩尔%。我们预测有677个开放阅读框(ORF)以及39个编码各种RNA种类的基因。在预测的ORF中,75.9%与其他生物体的基因/蛋白质有显著相似性,而只有9.9%与数据库中的基因序列没有任何显著相似性。这使我们能够初步为大量的ORF进行功能分类,并推断出这种细菌的生化和生理特性。肺炎支原体从祖先细菌进化过程中基因组大小的减少可以通过完整合成代谢(如无氨基酸合成)和代谢途径的丧失来解释。因此,肺炎支原体在自然环境中依赖专性寄生的生活方式,这需要提供外源性必需代谢物。本文简要描述了所有主要的细胞过程和代谢途径类别。根据实验证据,对于肺炎支原体中存在的许多活性/功能,通过相似性搜索无法鉴定出相应的基因。例如,我们未能鉴定出参与运动性、趋化性和氧化应激管理的基因/蛋白质。

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