Genomics Data (Sep 2016)

Transcriptome profiling of TDC cluster deletion mutant of Enterococcus faecalis V583

  • Marta Perez,
  • Victor Ladero,
  • Beatriz del Rio,
  • Begoña Redruello,
  • Anne de Jong,
  • Oscar P. Kuipers,
  • Jan Kok,
  • M. Cruz Martin,
  • Maria Fernandez,
  • Miguel A. Alvarez

DOI
https://doi.org/10.1016/j.gdata.2016.06.012
Journal volume & issue
Vol. 9, no. C
pp. 67 – 69

Abstract

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The species Enterococcus faecalis is able to catabolise the amino acid tyrosine into the biogenic amine tyramine by the tyrosine decarboxilase (TDC) pathway Ladero et al. (2012) [1]. The TDC cluster comprises four genes: tyrS, an aminoacyl-tRNA synthetase-like gene; tdcA, which encodes the tyrosine decarboxylase; tyrP, a tyrosine/tyramine exchanger gene and nhaC-2, which encodes an Na+/H+ antiporter and whose role in the tyramine biosynthesis remains unknown [2]. In E. faecalis V583 the last three genes are co-transcribed as a single polycistronic mRNA forming the catabolic operon, while tyrS is transcribed independently of the catabolic genes as a monocistronic mRNA [2]. The catabolic operon is transcriptionally induced by tyrosine and acidic pH. On the opposite, the tyrS expression is repressed by tyrosine concentrations [2]. In this work we report the transcriptional profiling of the TDC cluster deletion mutant (E. faecalis V583 ΔTDC) [2] compared to the wild-type strain, both grown in M17 medium supplemented with tyrosine. The transcriptional profile data of TDC cluster-regulated genes were deposited in the Gene Expression Omnibus (GEO) database under accession no. GSE77864.

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