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Rhamnolipid Stimulates Uptake of Hydrophobic Compounds by Pseudomonas aeruginosa
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ABSTRACT
The biodegradation of hexadecane by five biosurfactant-producing bacterial strains (
Pseudomonas aeruginosa
UG2
, Acinetobacter calcoaceticus
RAG1,
Rhodococcus erythropolis
DSM 43066,
R. erythropolis
ATCC 19558, and strain BCG112) was determined in the presence and absence of exogenously added biosurfactants. The degradation of hexadecane by
P. aeruginosa
was stimulated only by the rhamnolipid biosurfactant produced by the same organism. This rhamnolipid did not stimulate the biodegradation of hexadecane by the four other strains to the same extent, nor was degradation of hexadecane by these strains stimulated by addition of their own biosurfactants. This suggests that
P. aeruginosa
has a mode of hexadecane uptake different from those of the other organisms. Rhamnolipid also enhanced the rate of epoxidation of the aliphatic hydrocarbon α,ω-tetradecadiene by a cell suspension of
P. aeruginosa
. Furthermore, the uptake of the hydrophobic probe 1-naphthylphenylamine by cells of
P. aeruginosa
was enhanced by rhamnolipid, as indicated by stopped-flow fluorescence experiments. Rhamnolipid did not stimulate the uptake rate of this probe in de-energized cells. These results indicate that an energy-dependent system is present in
P. aeruginosa
strain UG2 that mediates fast uptake of hydrophobic compounds in the presence of rhamnolipid.
American Society for Microbiology
Title: Rhamnolipid Stimulates Uptake of Hydrophobic Compounds by
Pseudomonas aeruginosa
Description:
ABSTRACT
The biodegradation of hexadecane by five biosurfactant-producing bacterial strains (
Pseudomonas aeruginosa
UG2
, Acinetobacter calcoaceticus
RAG1,
Rhodococcus erythropolis
DSM 43066,
R.
erythropolis
ATCC 19558, and strain BCG112) was determined in the presence and absence of exogenously added biosurfactants.
The degradation of hexadecane by
P.
aeruginosa
was stimulated only by the rhamnolipid biosurfactant produced by the same organism.
This rhamnolipid did not stimulate the biodegradation of hexadecane by the four other strains to the same extent, nor was degradation of hexadecane by these strains stimulated by addition of their own biosurfactants.
This suggests that
P.
aeruginosa
has a mode of hexadecane uptake different from those of the other organisms.
Rhamnolipid also enhanced the rate of epoxidation of the aliphatic hydrocarbon α,ω-tetradecadiene by a cell suspension of
P.
aeruginosa
.
Furthermore, the uptake of the hydrophobic probe 1-naphthylphenylamine by cells of
P.
aeruginosa
was enhanced by rhamnolipid, as indicated by stopped-flow fluorescence experiments.
Rhamnolipid did not stimulate the uptake rate of this probe in de-energized cells.
These results indicate that an energy-dependent system is present in
P.
aeruginosa
strain UG2 that mediates fast uptake of hydrophobic compounds in the presence of rhamnolipid.
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