Literature DB >> 8948633

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

R Himmelreich1, H Hilbert, H Plagens, E Pirkl, B C Li, R Herrmann.   

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.

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Year:  1996        PMID: 8948633      PMCID: PMC146264          DOI: 10.1093/nar/24.22.4420

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  60 in total

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Review 5.  Repair of oxidative damage to DNA: enzymology and biology.

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Review 7.  The sigma factors of Bacillus subtilis.

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8.  The proline-rich P65 protein of Mycoplasma pneumoniae is a component of the Triton X-100-insoluble fraction and exhibits size polymorphism in the strains M129 and FH.

Authors:  T Proft; H Hilbert; G Layh-Schmitt; R Herrmann
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9.  Identification and characterization of hitherto unknown Mycoplasma pneumoniae proteins.

Authors:  T Proft; R Herrmann
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10.  Codon reading scheme in Mycoplasma pneumoniae revealed by the analysis of the complete set of tRNA genes.

Authors:  P Simoneau; C M Li; S Loechel; R Wenzel; R Herrmann; P C Hu
Journal:  Nucleic Acids Res       Date:  1993-10-25       Impact factor: 16.971

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  318 in total

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Authors:  R H Waldo; P L Popham; C E Romero-Arroyo; E A Mothershed; K K Lee; D C Krause
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5.  Genotyping of Mycoplasma pneumoniae clinical isolates reveals eight P1 subtypes within two genomic groups.

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Journal:  J Clin Microbiol       Date:  2000-03       Impact factor: 5.948

6.  The effect of nucleotide bias upon the composition and prediction of transmembrane helices.

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7.  Decoupling of genome size and sequence divergence in a symbiotic bacterium.

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Journal:  J Bacteriol       Date:  2000-07       Impact factor: 3.490

8.  Whole-genome trees based on the occurrence of folds and orthologs: implications for comparing genomes on different levels.

Authors:  J Lin; M Gerstein
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9.  Thermophilic bacteria strictly obey Szybalski's transcription direction rule and politely purine-load RNAs with both adenine and guanine.

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10.  P48 major surface antigen of Mycoplasma agalactiae is homologous to a malp product of Mycoplasma fermentans and belongs to a selected family of bacterial lipoproteins.

Authors:  S Rosati; S Pozzi; P Robino; B Montinaro; A Conti; M Fadda; M Pittau
Journal:  Infect Immun       Date:  1999-11       Impact factor: 3.441

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