Beyond Chloride Brines: Variable Metabolomic Responses in the Anaerobic Organism Yersinia intermedia MASE-LG-1 to NaCl and MgSO4 at Identical Water Activity

نویسندگان

  • Petra Schwendner
  • Maria Bohmeier
  • Petra Rettberg
  • Kristina Beblo-Vranesevic
  • Frédéric Gaboyer
  • Christine Moissl-Eichinger
  • Alexandra K. Perras
  • Pauline Vannier
  • Viggó T. Marteinsson
  • Laura Garcia-Descalzo
  • Felipe Gómez
  • Moustafa Malki
  • Ricardo Amils
  • Frances Westall
  • Andreas Riedo
  • Euan P. Monaghan
  • Pascale Ehrenfreund
  • Patricia Cabezas
  • Nicolas Walter
  • Charles Cockell
چکیده

Growth in sodium chloride (NaCl) is known to induce stress in non-halophilic microorganisms leading to effects on the microbial metabolism and cell structure. Microorganisms have evolved a number of adaptations, both structural and metabolic, to counteract osmotic stress. These strategies are well-understood for organisms in NaCl-rich brines such as the accumulation of certain organic solutes (known as either compatible solutes or osmolytes). Less well studied are responses to ionic environments such as sulfate-rich brines which are prevalent on Earth but can also be found on Mars. In this paper, we investigated the global metabolic response of the anaerobic bacterium Yersinia intermedia MASE-LG-1 to osmotic salt stress induced by either magnesium sulfate (MgSO4) or NaCl at the same water activity (0.975). Using a non-targeted mass spectrometry approach, the intensity of hundreds of metabolites was measured. The compatible solutes L-asparagine and sucrose were found to be increased in both MgSO4 and NaCl compared to the control sample, suggesting a similar osmotic response to different ionic environments. We were able to demonstrate that Yersinia intermedia MASE-LG-1 accumulated a range of other compatible solutes. However, we also found the global metabolic responses, especially with regard to amino acid metabolism and carbohydrate metabolism, to be salt-specific, thus, suggesting ion-specific regulation of specific metabolic pathways.

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عنوان ژورنال:

دوره 9  شماره 

صفحات  -

تاریخ انتشار 2018