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1.
Appl Environ Microbiol ; 78(24): 8611-22, 2012 Dec.
Article in English | MEDLINE | ID: mdl-23042167

ABSTRACT

Rhamnolipids have multiple potential applications as "green" surfactants for industry, remediation, and medicine. As a result, they have been intensively investigated to add to our understanding of their biosynthesis and improve yields. Several studies have noted that the addition of a fatty acid cosubstrate increases rhamnolipid yields, but a metabolic explanation has not been offered, partly because biosynthesis studies to date have used sugar or sugar derivatives as the carbon source. The objective of this study was to investigate the role of fatty acid cosubstrates in improving rhamnolipid biosynthesis. A combination of stable isotope tracing and gene expression assays was used to identify lipid precursors and potential lipid metabolic pathways used in rhamnolipid synthesis when fatty acid cosubstrates are present. To this end, we compared the rhamnolipids produced and their yields using either glucose alone or glucose and octadecanoic acid-d(35) as cosubstrates. Using a combination of sugar and fatty acids, the rhamnolipid yield was significantly higher (i.e., doubled) than when glucose was used alone. Two patterns of deuterium incorporation (either 1 or 15 deuterium atoms) in a single Rha-C(10) lipid chain were observed for octadecanoic acid-d(35) treatment, indicating that in the presence of a fatty acid cosubstrate, both de novo fatty acid synthesis and ß-oxidation are used to provide lipid precursors for rhamnolipids. Gene expression assays showed a 200- to 600-fold increase in the expression of rhlA and rhlB rhamnolipid biosynthesis genes and a more modest increase of 3- to 4-fold of the fadA ß-oxidation pathway gene when octadecanoic acid was present. Taken together, these results suggest that the simultaneous use of de novo fatty acid synthesis and ß-oxidation pathways allows for higher production of lipid precursors, resulting in increased rhamnolipid yields.


Subject(s)
Fatty Acids/metabolism , Glycolipids/metabolism , Pseudomonas aeruginosa/metabolism , Carbohydrate Metabolism , Gene Expression Profiling , Isotope Labeling , Isotopes/metabolism , Metabolic Networks and Pathways/genetics , Oxidation-Reduction , Pseudomonas aeruginosa/genetics
2.
Appl Microbiol Biotechnol ; 88(4): 953-63, 2010 Oct.
Article in English | MEDLINE | ID: mdl-20706835

ABSTRACT

While variable production of the biosurfactant, rhamnolipid, by Pseudomonas aeruginosa has been shown to be dependent on growth conditions, no research has evaluated potential relationships between rhamnolipid production and the presence of heavy metals. The current investigation evaluates the influence of Cd(2+) on rhamnolipid synthesis. Cultures grown in the presence of 0.45 and 0.89 mM Cd(2+) were monitored for rhlB/rhlC expression, rhamnolipid yield, and the ratio of monorhamnolipid (RL1) and dirhamnolipid (RL2) produced. Results show a Cd-induced enhancement of rhlB expression in mid-stationary phase (53 h). In addition, sustained production of rhamnolipid through late stationary growth phase (96 h) was observed for Cd-amended cultures, unlike Cd-free control cultures that ceased rhamnolipid production by mid-stationary growth phase. Most significant was an observed increase in the ratio of RL2 to RL1 congeners produced by cultures grown in the presence of Cd(2+). Previous results have shown that the complexation constant for RL2-Cd is several orders of magnitude larger than that of RL1-Cd thus the preferential production of RL2 in the presence of Cd(2+) impacts its bioavailability and toxicity both for the cell and in the surrounding environment.


Subject(s)
Cadmium/metabolism , Glycolipids/biosynthesis , Pseudomonas aeruginosa/genetics , Transcription, Genetic , Gene Expression Regulation, Bacterial , Genes, Bacterial , Pseudomonas aeruginosa/growth & development , Pseudomonas aeruginosa/metabolism , Surface-Active Agents/metabolism
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