Osmotic Adaptation of <i>Thermus thermophilus</i> RQ-1: Lesson from a Mutant Deficient in Synthesis of Trehalose

  • Zélia Silva
    Departamento de Bioquímica and Centro de Neurociências de Coimbra, Universidade de Coimbra, 3004-517 Coimbra
  • Susana Alarico
    Departamento de Bioquímica and Centro de Neurociências de Coimbra, Universidade de Coimbra, 3004-517 Coimbra
  • Ana Nobre
    Departamento de Bioquímica and Centro de Neurociências de Coimbra, Universidade de Coimbra, 3004-517 Coimbra
  • Reinhold Horlacher
    Department of Biology, University of Constance, 78457 Constance, Germany
  • Joey Marugg
    Departamento de Bioquímica and Centro de Neurociências de Coimbra, Universidade de Coimbra, 3004-517 Coimbra
  • Winfried Boos
    Department of Biology, University of Constance, 78457 Constance, Germany
  • Ana I. Mingote
    Instituto de Tecnologia Química e Biológica, Universidade Nova de Lisboa, 2780-156 Oeiras, Portugal
  • Milton S. da Costa
    Departamento de Bioquímica and Centro de Neurociências de Coimbra, Universidade de Coimbra, 3004-517 Coimbra

Abstract

<jats:title>ABSTRACT</jats:title> <jats:p> Strains of <jats:italic>Thermus thermophilus</jats:italic> accumulate primarily trehalose and smaller amounts of mannosylglycerate in response to salt stress in yeast extract-containing media (O. C. Nunes, C. M. Manaia, M. S. da Costa, and H. Santos, Appl. Environ. Microbiol. 61:2351-2357, 1995). A 2.4-kbp DNA fragment from <jats:italic>T. thermophilus</jats:italic> strain RQ-1 carrying <jats:italic>otsA</jats:italic> (encoding trehalose-phosphate synthase [TPS]), <jats:italic>otsB</jats:italic> (encoding trehalose-phosphate phosphatase [TPP]), and a short sequence of the 5′ end of <jats:italic>treS</jats:italic> (trehalose synthase [TreS]) was cloned from a gene library. The sequences of the three genes (including <jats:italic>treS</jats:italic> ) were amplified by PCR and sequenced, revealing that the genes were structurally linked. To understand the role of trehalose during salt stress in <jats:italic>T. thermophilus</jats:italic> RQ-1, we constructed a mutant, designated RQ-1M6, in which TPS ( <jats:italic>otsA</jats:italic> ) and TPP ( <jats:italic>otsB</jats:italic> ) genes were disrupted by gene replacement. Mutant RQ-1M6 accumulated trehalose and mannosylglycerate in a medium containing yeast extract and NaCl. However, growth in a defined medium (without yeast extract, known to contain trehalose) containing NaCl led to the accumulation of mannosylglycerate but not trehalose. The deletion of <jats:italic>otsA</jats:italic> and <jats:italic>otsB</jats:italic> reduced the ability to grow in defined salt-containing medium, with the maximum salinity being 5% NaCl for RQ-1 and 3% NaCl for RQ-1M6. The lower salt tolerance observed in the mutant was relieved by the addition of trehalose to the growth media. In contrast to trehalose, the addition of glycine betaine, mannosylglycerate, maltose, and glucose to the growth medium did not allow the mutant to grow at higher salinities. The results presented here provide crucial evidence for the importance of the TPS/TPP pathway for the synthesis and accumulation of trehalose and the decisive contribution of this disaccharide to osmotic adaptation in <jats:italic>T. thermophilus</jats:italic> RQ-1. </jats:p>

Journal

  • Journal of Bacteriology

    Journal of Bacteriology 185 (20), 5943-5952, 2003-10-15

    American Society for Microbiology

Citations (1)*help

See more

Details 詳細情報について

Report a problem

Back to top