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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

Pseudomonas aeruginosa produces the rhamnolipid biosurfactants. Thin-layer chromatography detects and determines the proportion of mono- and di-rhamnolipids produced by each strain. Quantification of total rhamnolipids involves assessing rhamnose equivalents present in these biosurfactants extracted from the culture supernatants using the orcinol method.

Abstract

The environmental bacterium Pseudomonas aeruginosa is an opportunistic pathogen with high antibiotic resistance that represents a health hazard. This bacterium produces high levels of biosurfactants known as rhamnolipids (RL), which are molecules with significant biotechnological value but are also associated with virulence traits. In this respect, the detection and quantification of RL may be useful for both biotechnology applications and biomedical research projects. In this article, we demonstrate step-by-step the technique to detect the production of the two forms of RL produced by P. aeruginosa using thin-layer chromatography (TLC): mono-rhamnolipids (mRL), molecules constituted by a dimer of fatty acids (mainly C10-C10) linked to one rhamnose moiety, and di-rhamnolipids (dRL), molecules constituted by a similar fatty acid dimer linked to two rhamnose moieties. Additionally, we present a method to measure the total amount of RL based on the acid hydrolysis of these biosurfactants extracted from a P. aeruginosa culture supernatant and the subsequent detection of the concentration of rhamnose that reacts with orcinol. The combination of both techniques can be used to estimate the approximate concentration of mRL and dRL produced by a specific strain, as exemplified here with the type strains PAO1 (phylogroup 1), PA14 (phylogroup 2), and PA7 (phylogroup 3).

Introduction

Pseudomonas aeruginosa is an environmental bacterium and an opportunistic pathogen of great concern due to its production of virulence-associated traits and its high antibiotic resistance1,2. A characteristic secondary metabolite produced by this bacterium is the biosurfactant RL, which is produced in a coordinated manner with several virulence-associated traits such as the phenazine pyocyanin, an antibiotic with redox activity, and the protease elastase3. The tensio-active and emulsification properties of RL have been exploited in different industrial app....

Protocol

This procedure is schematized in Supplementary Figure 1. The reagents and equipment used for the study are listed in the Table of Materials.

1. Detection of mRL and dRL in culture supernatants of P. aeruginosa using TLC

  1. Start with the centrifuged broth of the P. aeruginosa strain of interest, cultivated in liquid medium for 24 h (to reach the stationary phase of growth where RL is.......

Representative Results

In this article, three different P. aeruginosa type strains were utilized to represent three phylogroups, each with varying RL production levels and proportions of mRL and dRL. These strains include PAO1 (a wound isolate from Australia, 195522), PA14 (a plant isolate from the USA, 197723), and PA7 (a clinical isolate from Argentina, 201024). As a negative control, the PAO1 rhlA mutant was employed, which is incapable of RL production. All st.......

Discussion

The most accurate method for detecting and quantifying RL is HPLC coupled with mass spectrometry (MS)7,8,27; however, it requires specialized and expensive equipment that may not be accessible to many researchers. The methods described here can be routinely performed with basic laboratory materials and equipment to detect and estimate RL concentrations, but they have some limitations, particularly their inaccuracy in determining.......

Acknowledgements

The laboratory of GSCh is supported in part by grant IN201222 from Programa de Apoyo a Proyectos de Investigación e Innovación Tecnológica (PAPIIT), Dirección General de Asuntos del Personal Académico -UNAM.

....

Materials

NameCompanyCatalog NumberComments
1-NAPHTHOLSIGMA-ALDRICH70442
ACETIC ACIDJ.T. BAKER9508-02
CENTRIFUGEFor centrifuging tubes 1.5 mL and  50 mL
CHLOROFORMJ.T. BAKER9180-02
DRYING OVEN
ETHERJ.T. BAKER9244-02
GLASS PIPETTESIGMA-ALDRICHCLS706510
HYDROCHLORIC ACIDJ.T. BAKER5622-02
LB
L-RHAMNOSE MONOHYDRATESIGMA-ALDRICHR-3875
METHANOLJ.T. BAKER9049-02
ORCINOL MONOHYDRATESIGMA-ALDRICHO1875
PPGAS BrothTris HCL (0.12M), Potassium Chloride ( 0.02M) Ammonium Chloride (0.02M),  Peptone (1%), pH 7.4   Autoclaved. Add  Glucose (5%) and Magnesium Sulfate (0.0016M)
QUARTZ CELL (CUVETTE)SIGMA-ALDRICHZ276669
RECTANGULAR TLC DEVELOPING TANKFISHER SCIENTIFICK4161801020
RHAMNOLIPIDS SIGMA-ALDRICHR-90
SPECTROPHOTOMETERVIS
SPRAYERSIGMA-ALDRICHZ529710-1EA
SULFURIC ACIDJ.T. BAKER9681-02
TES TUBES 5mLCORNING352002
TLC SILICA GEL 60 F254MERCK1.05554.0001
WATER BATH> 80 °C

References

  1. Moradali, M. F., Ghods, S., Rehm, B. H. A. Pseudomonas aeruginosa lifestyle: A paradigm for adaptation, survival, and persistence. Frontiers in Cell Infection and Microbiology. 7, 1-29 (2017).
  2. Gellatly, S. L., Hancock, R. E. W.

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Pseudomonas AeruginosaRhamnolipidsMono rhamnolipidsDi rhamnolipidsThin layer ChromatographyOrcinol AssayBiosurfactantsVirulenceAntibiotic ResistanceBiotechnology

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