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August 1, 2000Molecular Microbiology38 citationsOpen Access

The tylosin resistance gene tlrB of Streptomyces fradiae encodes a methyltransferase that targets G748 in 23S rRNA

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MLMingfu LiuFKFinn KirpekarGWGilles P. van Wezel

Key Points

  • The research aims to characterize the function of the tlrB gene in conferring tylosin resistance in Streptomyces bacteria.
  • Introduced tlrB into Streptomyces lividans to assess tylosin resistance.
  • Conducted biochemical analysis on rRNA from Streptomyces species.
  • Utilized mass spectrometry to analyze modified RNA substrates.
  • TlrB modifies nucleotide G748 in 23S rRNA, confirming its role as a methyltransferase.
  • TlrB adds a methyl group to G748 using S-adenosyl methionine as a donor.
  • Identification of homologues suggests TlrB is part of a new subclass of rRNA methyltransferases related to macrolide resistance.

Abstract

tlrB is one of four resistance genes encoded in the operon for biosynthesis of the macrolide tylosin in antibiotic-producing strains of Streptomyces fradiae. Introduction of tlrB into Streptomyces lividans similarly confers tylosin resistance. Biochemical analysis of the rRNA from the two Streptomyces species indicates that in vivo TlrB modifies nucleotide G748 within helix 35 of 23S rRNA. Purified recombinant TlrB retains its activity and specificity in vitro and modifies G748 in 23S rRNA as well as in a 74 nucleotide RNA containing helix 35 and surrounding structures. Modification is dependent on the presence of the methyl group donor, S-adenosyl methionine. Analysis of the 74-mer RNA substrate by biochemical and mass spectrometric methods shows that TlrB adds a single methyl group to the base of G748. Homologues of TlrB in other bacteria have been revealed through database searches, indicating that TlrB is the first member to be described in a new subclass of rRNA methyltransferases that are implicated in macrolide drug resistance.

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Cite This Study

Liu et al. (2000) studied this question.

synapsesocial.com/papers/6a11ccb611d1a9d8e2563459https://doi.org/10.1046/j.1365-2958.2000.02046.x
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