Effect of Culture Conditions on Fatty Acid Profiles of Bacteria and Lipopolysaccharides of the Genus Pseudomonas-GC-MS Analysis on Ionic Liquid-Based Column

Molecules. 2022 Oct 15;27(20):6930. doi: 10.3390/molecules27206930.

Abstract

The profiling of bacterial fatty acids is a well-established technique in identifying and classifying bacteria. Cultivation conditions may affect the biosynthesis, thereby, changing the fatty acid profile in bacteria. The effect of the culture conditions on the fatty acid components of Pseudomonas aeruginosa PAO1, Pseudomonas aeruginosa ATCC 27853, Pseudomonas aeruginosa polyresistant and Pseudomonas putida all are aligned to the genus Pseudomonas. The fatty acids in the lipopolysaccharides of Pseudomonas aeruginosa PAO1 were also examined. The effects of the cultivation conditions were followed by using agar and blood agar media at the characteristic temperatures, 25 °C, 37 °C and 42 °C, respectively, and an analysis was made during the 1st, 3rd and 5th day following inoculation. In addition to quantitative differences, we also experienced qualitative differences in the fatty acid profiles which detect newly appearing fatty acids, due to changes in environmental factors. The application of ionic liquid-based column unveils new possibilities for the analyses of fatty acids in GC-MS experiments for bacterial fatty acid profiling. The validation results (response linearity, limit of detection, limit of quantification, system suitability, intraday and interday repeatability and accuracy) show the high separation efficiency of the ionic liquid-based column in the analyses.

Keywords: Pseudomonas genus; bacteria; cultivation conditions; fatty acid profile; gas chromatography-mass spectrometry; ionic liquid column; lipopolysaccharides.

MeSH terms

  • Agar
  • Fatty Acids / analysis
  • Gas Chromatography-Mass Spectrometry / methods
  • Ionic Liquids*
  • Lipopolysaccharides
  • Pseudomonas aeruginosa
  • Pseudomonas putida*

Substances

  • Fatty Acids
  • Ionic Liquids
  • Lipopolysaccharides
  • Agar

Grants and funding

The research was supported by the ÚNKP-21-3-II New National Excellence Program of the Ministry for Innovation and Technology from the Source of the National Research, Development and Innovation Fund. Authors also acknowledges the financial support of the NKFIH K-125275, K-120193 and the PTE-AOK-KA-2017-19 grants. EM acknowledges the financial support of the Gedeon Richter’s Talentum Foundation. LM acknowledges the financial support of the PTE-AOK-KA-2019-08 grant and AB acknowledges the financial support of the PTE-AOK-KA-2015-16.