Strain-specific genomic regions of Ruminococcus flavefaciens FD-1 as revealed by combinatorial random-phase genome sequencing and suppressive subtractive hybridization

Environ Microbiol. 2004 Apr;6(4):335-46. doi: 10.1111/j.1462-2920.2004.00576.x.

Abstract

Two closely related strains of the Gram-positive, cellulolytic ruminal bacterium Ruminococcus flavefaciens were compared at the genomic level by suppressive subtractive hybridization. The two strains investigated in this study differ by 1.94% in their respective 16S rDNA genes. Three hundred and eighty-four PCR-amplified products were cloned and then screened for their strain identity by dot blot hybridization. Based on redundancy percentages of the clones sequenced, 9.5% of the genome of the R. flavefaciens FD-1 strain is not present in the JM1 strain. The majority of identities of individual cloned subtracted products (642 bp average length) bore no relation to deposited sequences in GenBank (42% of the subtracted library), whereas of those with putative assigned functions 7% are loosely associated with fibre-degradation, 6% with insertion elements, transposons and phage-like ORFs, 5% with cell membrane associated proteins and 3% with signal transduction. Subtracted sequences were then supplemented with the draft (2 x coverage) genome sequence of R. flavefaciens FD-1 to indicate potential regions of rearrangement within the genome, including a novel insertion sequence.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Base Sequence
  • Cellulase / genetics
  • DNA Transposable Elements
  • Databases, Nucleic Acid
  • Gene Library
  • Genome, Bacterial*
  • Molecular Sequence Data
  • Nucleic Acid Hybridization*
  • RNA, Ribosomal, 16S / analysis
  • Ruminococcus / classification
  • Ruminococcus / genetics*
  • Sequence Analysis, DNA*

Substances

  • DNA Transposable Elements
  • RNA, Ribosomal, 16S
  • Cellulase