Novel insights into biosynthesis and uptake of rhamnolipids and their precursors
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- Wittgens, A., Kovacic, F., Müller, M.M. et al. Appl Microbiol Biotechnol (2017) 101: 2865. doi:10.1007/s00253-016-8041-3
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The human pathogenic bacterium Pseudomonas aeruginosa produces rhamnolipids, glycolipids with functions for bacterial motility, biofilm formation, and uptake of hydrophobic substrates. Rhamnolipids represent a chemically heterogeneous group of secondary metabolites composed of one or two rhamnose molecules linked to one or mostly two 3-hydroxyfatty acids of various chain lengths. The biosynthetic pathway involves rhamnosyltransferase I encoded by the rhlAB operon, which synthesizes 3-(3-hydroxyalkanoyloxy)alkanoic acids (HAAs) followed by their coupling to one rhamnose moiety. The resulting mono-rhamnolipids are converted to di-rhamnolipids in a third reaction catalyzed by the rhamnosyltransferase II RhlC. However, the mechanism behind the biosynthesis of rhamnolipids containing only a single fatty acid is still unknown. To understand the role of proteins involved in rhamnolipid biosynthesis the heterologous expression of rhl-genes in non-pathogenic Pseudomonas putida KT2440 strains was used in this study to circumvent the complex quorum sensing regulation in P. aeruginosa. Our results reveal that RhlA and RhlB are independently involved in rhamnolipid biosynthesis and not in the form of a RhlAB heterodimer complex as it has been previously postulated. Furthermore, we demonstrate that mono-rhamnolipids provided extracellularly as well as HAAs as their precursors are generally taken up into the cell and are subsequently converted to di-rhamnolipids by P. putida and the native host P. aeruginosa. Finally, our results throw light on the biosynthesis of rhamnolipids containing one fatty acid, which occurs by hydrolyzation of typical rhamnolipids containing two fatty acids, valuable for the production of designer rhamnolipids with desired physicochemical properties.
KeywordsPseudomonas aeruginosa Rhamnolipids Biosurfactant Pseudomonas putida Biosynthesis pathway
The biosurfactant rhamnolipid, first described by Jarvis and Johnson (1949), has various physiological roles and industrial applications (Lang and Wullbrandt 1999; Maier and Soberón-Chávez 2000). Rhamnolipids are produced and secreted to the extracellular milieu mainly by bacteria of the genus Pseudomonas (Abdel-Mawgoud et al. 2010). The opportunistic human pathogen Pseudomonas aeruginosa is among the best rhamnolipid producers (Giani et al. 1997; Müller et al. 2011), although bacteria from the genus Burkholderia also produce rhamnolipids (Häußler et al. 1998; Andrä et al. 2006; Funston et al. 2016).
In P. aeruginosa, rhamnolipids are essential for swarming motility, involved in biofilm formation and act as hemolysins (Köhler et al. 2000; Davey et al. 2003; Tremblay et al. 2007) what makes them to important virulence factors (Kownatzki et al. 1987). Rhamnolipids play a role in shielding of P. aeruginosa cells from host defense, e.g., they inhibit the phagocytosis by macrophages (McClure and Schiller 1996; van Gennip et al. 2009; Alhede et al. 2009). Additionally, rhamnolipids enhance the uptake of hydrophobic substrates like long-chain alkanes, e.g., octadecane (Zhang and Miller 1995; Al-Tahhan et al. 2000; Noordman and Jassen 2002).
Rhamnolipids feature a low toxicity and an enhanced biodegradability in comparison to detergents with petrochemical origin (Maslin and Maier 2000; Johann et al. 2016). Based on their surface active properties, they are used for bioremediation (Nguyen et al. 2008), enhanced oil recovery (Wang et al. 2007), and in cosmetic and food industries (Banat et al. 2010).
In P. aeruginosa, the length of the fatty acid chains in rhamnolipids varies from C8 to C14 with a predominant species containing C10-C10 fatty acid chains in mono- as well as in di-rhamnolipids (Déziel et al. 1999; Abdel-Mawgoud et al. 2010). In contrast, rhamnolipids produced by bacteria from the genus Burkholderia contain long-chain fatty acid with a predominant C14-C14 species (Manso Pajarron et al. 1993; Dubeau et al. 2009). Additionally, mono- and di-unsaturated fatty acids can be found in rhamnolipids, further expanding the existing chemical diversity of rhamnolipids (Abalos et al. 2001) and their potential applications in biotechnology and industry.
Rhamnolipid biosynthesis occurs in three consecutive enzymatic reactions. In the first step, RhlA synthesizes 3-(3-hydroxyalkanoyloxy)alkanoic acids (HAAs) by esterification of two 3-hydroxyacyl molecules bound to acyl carrier protein (ACP) descending from the fatty acid de novo synthesis (Rehm et al. 2001). RhlB links an HAA molecule with dTDP-L-rhamnose descending from glucose-6-phosphate (Olvera et al. 1999; Rahim et al. 2000), to create mono-rhamnolipids (Ochsner et al. 1994a). The last reaction in the di-rhamnolipid synthesis pathway is catalyzed by the rhamnosyltransferase II (RhlC), which joins a second dTDP-L-rhamnose molecule to the mono-rhamnolipids (Rahim et al. 2001). The biosynthesis of mono- and di-rhamno-mono-lipids with a single 3-hydroxyfatty acid is still speculative. Possibly, they descend from direct condensation of a dTDP-L-rhamnose with a 3-hydroxyfatty acid chain by RhlB. These molecules could be used as precursors for synthesis of di-rhamno-mono-lipids by RhlC. Optionally, they could be produced by hydrolysis of one unit from the dimer of esterified fatty acids in mono- and di-rhamno-di-lipids by a still unknown enzyme (Soberón-Chávez et al. 2005).
The genes rhlA and rhlB are organized in a bicistronic operon and encode proteins originally described as two subunits forming a functional rhamnosyltransferase I enzyme complex (Ochsner et al. 1994a). However, evidences that a P. aeruginosa ΔrhlB mutant strain produces HAAs (Déziel et al. 2003) and that heterologous expression of rhlA in Escherichia coli leads to production of HAAs (Zhu and Rock 2008) indicate that RhlA exerts its function independently of RhlB. The gene rhlC is also organized in a bicistronic operon with PA1131, a gene of unknown function (Rahim et al. 2001).
In P. aeruginosa, the two rhl-operons are transcriptionally regulated by the quorum sensing (QS) regulatory network (Ochsner et al. 1994b; Ochsner and Reiser 1995; Pearson et al. 1997) and probably by other signaling systems (Wilhelm et al. 2007; Rosenau et al. 2010; Henkel et al. 2013). The QS autoinducer molecules butanoyl-homoserine-lactone (C4-HSL) and 3-oxo-dodecanoyl-homoserine-lactone (3-oxo-C12-HSL) are synthesized by RhlI and LasI, respectively. After the concentration of autoinducer molecules reaches a threshold, they bind to the regulator proteins RhlR and LasR to induce the expression of the rhl-genes (Williams and Cámara 2009; Reis et al. 2011).
The complex regulatory network controlling the rhamnolipid production in P. aeruginosa and its classification as an opportunistic pathogen are bottlenecks for their production (Müller and Hausmann 2011) and disadvantageous for many industrial applications (Toribio et al. 2010). Searching for an alternative rhamnolipid producing host, the non-pathogenic Pseudomonas putida KT2440 strain was identified as a suitable organism (Ochsner et al. 1995; Wittgens et al. 2011; Behrens et al. 2016; Beuker et al. 2016). It provides both pathways essential for the production of 3-hydroxyfatty acids and dTDP-L-rhamnose used as rhamnolipid precursors (Nelson et al. 2002). Although evolutionary closely related with P. aeruginosa, P. putida is lacking the complex regulatory circuits found in P. aeruginosa, what makes P. putida KT2440 a favorable host for the heterologous production of rhamnolipids and an ideal simplified genetic and physiologic background to study molecular aspects of rhamnolipid biosynthesis.
In this study, we have expressed P. aeruginosa genes involved in rhamnolipid biosynthesis in P. putida KT2440 to address the question if their protein-protein interactions play a role for function and/or stabilization of individual enzymes. A set of expression plasmids containing single genes or operons was used for modular expression of different gene combinations. Chemical analysis of produced rhamnolipids and precursors revealed novel insights in molecular interactions of RhlA and RhlB. Furthermore, we could show that exogenous rhamnolipids and HAAs are taken up by the cell and that they flow into the rhamnolipid biosynthesis pathway. These novel insights in the rhamnolipid biosynthesis pathway can be used for modulation of biochemical properties to create designer rhamnolipids.
Material and methods
Bacterial strains and culture conditions
P. aeruginosa PAO1 (DSM-22644; Hancock and Carey 1979), P. putida KT2440 (DSM-6125; Nelson et al. 2002), and E. coli DH5α (DSM-6897; Grant et al. 1990) were routinely cultivated in 10 ml LB medium (10 g/l tryptone, 5 g/l yeast extract, 10 g/l NaCl) in 100 ml Erlenmeyer flasks. All strains were grown at 150 rpm orbital shaking and 37 °C except P. putida, which were cultivated at 30 °C.
Amplification of rhl-genes and plasmid construction
PCR primers, restriction enzymes and resulting recombinant plasmids or P. aeruginosa mutant strains
Sequence (5′- > 3′)
Recombinant plasmid or mutant strain
additional cloning of rhlC in pVLT33_rhlAB
P. aeruginosa ΔrhlA
P. aeruginosa ΔrhlA
P. aeruginosa ΔrhlC
P. aeruginosa ΔrhlC
Structure homology modeling and site-directed mutagenesis of the rhlA gene
The three-dimensional structure of RhlA was modeled using the Phyre server (Kelley and Sternberg 2009) with Streptomyces lividans chloroperoxidase L (PDB code: 1A88) identified as the best template, with a 14% sequence identity, an E-value of 1 × 10−35 and a 100% prediction confidence. Chloroperoxidase L belongs to the family with an α/β-hydrolase fold and the Ser-His-Asp catalytic triad. The structural superimposition of a RhlA model and a chloroperoxidase L structure was performed using the PyMOL software (DeLano 2002). To inactivate, RhlA Ser102, identified as a catalytic residue of RhlA, was replaced by alanine with the QuikChange® Site-Directed Mutagenesis Kit (Stratagene, Waldbronn, Germany) using the plasmid pVLT33_rhlAB as template and the primer pair rhlA*B (Table 1) as recommend by the supplier.
Production of rhamnolipids and HAAs in recombinant P. putida
P. putida KT2440 was transformed by electroporation as described by Choi et al. (2006). Cells carrying pVLT33-based recombinant plasmids were selected using LB-agar medium or LB liquid medium containing 50 μg/ml kanamycin after incubation at 30 °C.
For the production of rhamnolipids and HAAs, main cultures of 100 ml LB medium in 1 l Erlenmeyer flasks were inoculated to an OD580 of 0.05 using overnight cultures and incubated at 30 °C and 150 rpm. The medium was supplemented with 10 g/l glucose, 50 μg/ml kanamycin, and 0.4 mM isopropyl-β-D-thiogalactopyranoside (IPTG) to induce the expression of rhl-genes. The cell-free culture supernatant was prepared by centrifugation of the cells for 30 min at 2200×g and 4 °C followed by filtration of the supernatant through a cellulose-membrane filter with 0.2 μm pore size (VWR International, Darmstadt, Germany).
Production of rhamnolipids in P. aeruginosa mutant strains
For generating P. aeruginosa rhl-mutant strains, the flanking up- and downstream regions of rhlA and rhlC were amplified as described above using the primer pairs rhlA-up, rhlA-down, rhlC-up, and rhlC-down, respectively (Table 1). PCR products were hydrolyzed with the restriction endonucleases PvuI and MluI (for upstream regions) and MluI and NcoI (for downstream regions). The two products for each gene were ligated into PvuI and NcoI restriction sites of pSUP202 (Simon et al. 1983), creating plasmids pSUP_rhlA and pSUP_rhlC. Recombinant E. coli cells containing this vector and its derivatives were selected by adding 10 μg/ml tetracycline to the medium. An Ω-gentamicin-cassette obtained by hydrolysis of pBSL142 (Alexeyev et al. 1995) with MluI was subsequently cloned into the plasmids pSUP_rhlA and pSUP_rhlC hydrolyzed with MluI creating the plasmids pSUP_rhlA-Gm and pSUP_rhlC-Gm, respectively. Recombinant E. coli cells containing these plasmids were selected by adding 10 μg/ml gentamicin to the medium. P. aeruginosa PAO1 was transformed with the gene mutator plasmids by electroporation (Choi et al. 2006) and selected for gentamicin resistance and tetracycline susceptibility indicating homologous recombination events with a double crossing-over. For this purpose, 30 μg/ml gentamicin or 100 μg/ml tetracycline were supplemented to agar-plates and liquid cultures. The P. aeruginosa mutant strains PAO1ΔrhlA and PAO1ΔrhlC were cultivated in phosphate-limited protease peptone-glucose-ammonium salt medium (PPGAS), containing 5 g/l glucose, 10 g/l peptone, 0.02 M NH4Cl, 0.02 M KCl, 0.12 M Tris-HCl, and 0.0016 M MgSO4 adjusted to pH 7.2 (Zhang and Miller, 1992). The main cultures of 10 ml medium in a 100 ml Erlenmeyer flask were inoculated to an OD580 of 0.05 from an overnight culture and incubated at 37 °C and 150 rpm. Cell-free culture supernatants were prepared by centrifugation of the cells for 30 min at 2200×g and 4 °C followed by filtration of the supernatant through a cellulose-membrane filter with 0.2 μm pore size (VWR International, Darmstadt, Germany).
Extraction of surface active compounds
For the extraction of rhamnolipids and their precursors HAAs, 4 ml of the cell-free culture supernatants were transferred to a new reaction tube and acidified with 40 μl of phosphoric acid (80% (v/v)). To these solutions, 6 ml ethyl acetate were added, the samples were mixed on a vortex shaker and centrifuged for 10 min at 2200×g. The upper ethyl acetate phases containing rhamnolipids and their precursors were removed. The lower phases were used for second extraction according to the same procedure. The two extracts were combined for further analysis.
For the detection of rhamnolipids using thin layer chromatography (TLC), 1.25 ml and for quantification of rhamnolipids and HAAs via HPLC-UV/Vis analysis 2 ml of the extract were evaporated in the vacuum centrifuge.
Thin layer chromatography of rhamnolipids
The dried samples for TLC analysis were dissolved in 20 μl ethanol and 10 μl of these solutions were spotted on silica 60 TLC plates (SIL-G, Macherey-Nagel, Düren, Germany). As a positive control, 10 μl of a 0.1% (w/v) rhamnolipid solution (JBR425, Jeneil Biosurfactant Co., LCC, Saukville, USA) containing mono- and di-rhamnolipids were spotted onto each TLC plate. A mixture of chloroform, methanol, and acetic acid at a ratio of 65:15:2 (v/v/v) was used as mobile phase. To visualize the rhamnolipids, a solution consisting of 0.15 g orcinol-monohydrate, 8.2 ml sulfuric acid, and 42 ml distilled water was sprayed on the TLC plates. The dried plates were incubated at 110 °C for 10 min.
Quantification of rhamnolipids and HAAs by HPLC-UV/Vis
Crystalline Rha-Rha-C10-C10 standard was a gift from former Hoechst AG (Frankfurt a. M., Germany). Rha-C10-C10 and C10-C10 (HAA) standards for HPLC analysis were prepared and purified as described before (Trummler et al. 2003; Magario et al. 2009). The β-hydroxydecanoic acid (C10) standard was obtained from Sigma-Aldrich Chemie GmbH (Steinheim, Germany). For derivatization, triethylamine and 4-bromophenacylbromide were used (Sigma-Aldrich Chemie GmbH) like described by Schenk et al. (1995).
Phenacyl esters of rhamnolipids and β-hydroxydecanoic acids for HPLC analysis were obtained as described before (Schenk et al. 1995) with minor changes. The analysis was performed with a standard HPLC device (Agilent 1100 Series, Agilent Technologies, Waldbronn, Germany) equipped with a Supelcosil® LC-18 Octadecylsilyl (Supelco, Deisenhofen, Germany) reverse phase column (3 mm × 150 mm × 5 μm) at 30 °C. Components of the mobile phase were solution A with 5% (v/v) methanol and solution B with 95% (v/v) methanol in ultrapure water, respectively. To achieve separation, a gradient of solution B from 80 to 100% was used according to the following protocol: from t = 0 to t = 17 min increase of solution B from 80 to 100%, holding 100% solution B up to t = 25 min and decrease back to 80% solution B until t = 30 min, holding 80% solution B for 5 more min to equilibrate. The injection volume was 10 μl. The flow rate was 0.4 ml/min and analytes were monitored at 254 nm. Retention times were 21.5 (±0.1) min for Rha-Rha-C10-C10, 22.2 (±0.1) min for Rha-C10-C10, and 23.3 (±0.1) min for C10-C10.
Chemical analysis of rhamnolipids by HPLC-ESI-MS
For the identification of rhamnolipids via HPLC-ESI-MS, the P. putida strain carrying pVLT33_rhlAB was cultivated in 1 l cultures in 5 l Erlenmeyer flasks and conditions as described before. The rhamnolipids were purified after Déziel et al. (1999) with some modifications. Cells were removed by centrifugation (6740×g, 10 °C, 30 min). The supernatant was acidified to pH 3 with 37% HCl and kept at 4 °C and 80 rpm overnight. The precipitated rhamnolipids were recovered by centrifugation (8280×g, 10 °C, 45 min) and dissolved in 15 ml acidified water (pH 3, adjusted with 37% HCl). The solution was extracted three times with 15 ml ethyl acetate, the organic phases were collected and evaporated under vacuum. The dried rhamnolipids were dissolved in 15 ml of 0.05 M sodium bicarbonate, acidified to pH 2 with 37% HCl and kept overnight at 4 °C. The rhamnolipids were recovered by centrifugation (4650×g, 4 °C, 60 min).
HPLC-MS experiments were carried out on an Agilent 1100 series binary HPLC system (Agilent Technologies, Waldbronn, Germany), combined with a DAD (190–400 nm) and coupled with the triple quadrupole 4000 QTRAP™ mass spectrometer (AB SCIEX, Darmstadt, Germany) equipped with a TurboIon spray source.
Separation was achieved on a ProntoSIL 120-C8-SH (Bischoff Chromatography, Leonberg, Germany) column (2 mm × 150 mm × 3 μm) kept at 20 °C during analysis. The gradient elution was done with deionized water with 0.1% (v/v) formic acid (solution A) and acetonitrile with 0.1% (v/v) formic acid (solution B) at a constant flow rate of 300 μl/min in the following manner: start with 60% solution B isocratic for 4 min, from 4 to 24 min a linear increase from 60% solution B to 90% solution B, followed by a second isocratic step (90% solution B for 10 min). The return to 60% solution B was performed in 1 min and 10 min; isocratic (60% solution B) was used for the re-equilibration. The injection volume was 20 μl.
The MS was used in the negative EMS mode scanning from 200 to 1000 Da. The parameters used were optimized first performing a flow injection analysis (FIA) with a standard and led to the following parameter settings: IS −4500 V, declustering potential (DP) −100 V, curtain gas (N2) 10 arbitrary units (au), source temperature 500 °C, nebulizer gas (N2) 50 au, and heater gas (N2) 20 au. Collision energy (CE) and Q3-entry barrier were set to −5 V and 8 V, respectively, to minimize fragmentation entering the LIT in the full scan mode.
For structural elucidation, MS/MS experiments were performed in negative enhanced product ion (EPI) scan mode. CE in the range between 30 and 70 V were used.
Biosynthesis of HAAs and mono-rhamnolipids in recombinant P. putida
Typical mono- and di-rhamnolipids contain two 3-hydroxyfatty acid chains; however, rhamnolipid congeners with only one 3-hydroxyfatty acid chain were described, too (Syldatk et al. 1985b; Déziel et al. 1999). Two different routes for the biosynthesis of these mono-rhamno-mono-lipids were suggested. The first is of anabolic character and proposes a RhlB catalyzed transfer of a single ACP-activated 3-hydroxyfatty acid to a dTDP-L-rhamnose molecule. The second catabolic approach involves a hypothetic degradation step of common mono-rhamno-di-lipids by an unknown hydrolytic enzyme.
To investigate the biosynthetic pathway for mono-rhamno-mono-lipids, we used P. putida KT2440 for which we previously reported multiple advantages for heterologous rhamnolipid production in comparison with P. aeruginosa (Wittgens et al. 2011; Tiso et al. 2016). The fact that this strain does not produce rhamnolipids itself simplifies the analysis of different rhamnolipid species after the expression of P. aeruginosa PAO1 genes involved in rhamnolipid biosynthesis.
The chemical analysis of the secreted mono-rhamnolipids produced by recombinant P. putida expressing rhlAB by HPLC-ESI-MS revealed six different mono-rhamnolipid congeners containing two 3-hydroxyfatty acids with chain length between C8-C10 and C12-C12 and a predominant C10-C10 species, which correlates with the composition of rhamnolipids known from P. aeruginosa (Abdel-Mawgoud et al. 2010). Beside the predominant mono-rhamno-di-lipids, also two mono-rhamno-mono-lipid congeners (Rha-C8 and Rha-C10) were detectable.
RhlA and RhlB function independently from each other
Surprisingly, P. putida expressing rhlAB produced also mono-rhamno-mono-lipids while these compounds were not detected in the supernatant of P. putida expressing only the rhlB gene, although the function of RhlB for transfer of a single 3-hydroxyacyl-ACP to a dTDP-L-rhamnose molecule has been suggested (Soberón-Chávez et al. 2005). In the literature RhlA and RhlB are described as two subunits of rhamnosyltransferase I forming a heterodimer to build the active enzyme complex (www.ncbi.nlm.nih.gov; Ochsner et al. 1994a; Winsor et al. 2016). We examined the role of this RhlAB complex for the biosynthesis of rhamnolipids and could show that RhlA can exert its function independently of RhlB (Fig. 2b). In addition, our results reveal that RhlB was active after expression of the rhlAB operon but not as single protein in P. putida (Fig. 2c). The fact that RhlB was active in the presence of RhlA but not when rhlA was not co-expressed opened the question if the function of RhlA is to stabilize RhlB through protein-protein interactions or if RhlA indirectly affect the function of RhlB through the supply of HAAs as substrate for RhlB.
Expression of the rhlA*B operon, encoding the inactive RhlA* variant and wild-type RhlB, in P. putida did not result in the production neither of HAAs nor of any mono-rhamnolipid species (data not shown). This confirmed Ser102 being the active site residue of RhlA as no HAAs were synthesized. Furthermore, this result is in conflict with the hypothesis of a functional RhlAB complex, as in this strain inactive RhlA* can form a complex with RhlB; however, RhlB is unable to produce mono-rhamnolipids. Conclusively, RhlB function is dependent on supply of precursors by RhlA rather than on interaction with RhlA.
Synthesis of mono-rhamnolipids by RhlB after uptake of extracellular HAAs as precursors
Synthesis of di-rhamnolipids by RhlC using extracellular mono-rhamnolipids as precursors
Our results demonstrate for the first time that P. putida can take up exogenous HAAs for the synthesis of mono-rhamnolipids. Therefore, we tested if mono-rhamnolipids can be imported by P. putida cells as well and if they flow into the di-rhamnolipid biosynthesis pathway, which relies on RhlC. In addition, we investigated the function of PA1131, which is organized in a bicistronic operon together with rhlC and has been supposed to play a role in rhamnolipid secretion (Rahim et al. 2001), but experimental evidences were currently missing.
Our results demonstrate that P. putida indeed can take up mono-rhamnolipids from the medium and use them as a precursor for the subsequent synthesis of di-rhamnolipids. Moreover, under the experimental conditions tested here, the protein of unknown function PA1131 has neither quantitative nor qualitative influence on rhamnolipid biosynthesis and does not appear to be involved in excretion of rhamnolipids.
P. aeruginosa can also import extracellular mono-rhamnolipids as precursors for RhlC-dependent di-rhamnolipid synthesis
The discovery of rhamnolipid precursor uptake by P. putida motivated us to examine if similar processes can be observed for the native rhamnolipid producer P. aeruginosa.
The biosynthesis of mono-rhamnolipids requires the two enzymes RhlA and RhlB, which are encoded by genes organized in the bicistronic rhlAB operon. These enzymes according to presently accepted hypotheses fulfill their functions in the form of a heterodimeric rhamnosyltransferase I enzyme complex (Ochsner et al. 1994a). Hence, in the Pseudomonas database (Winsor et al. 2016), RhlA and RhlB are respectively annotated as chain A and chain B of rhamnosyltransferase I. We could show that in P. putida RhlA with its 3-hydroxyacyl-ACP:3-hydroxyacyl-ACP O-3-hydroxyacyltransferase activity is responsible for the production of the rhamnolipid precursor molecule HAA and is not dependent on the expression of rhlB, what is also known from experiments with E. coli as a model host organism (Lépine et al. 2002; Déziel et al. 2003; Zhu and Rock 2008). However, if the hypotheses were true that RhlB could catalyze the acylation of dTDP-L-rhamnose with one ACP activated 3-hydroxyfatty acid (Soberón-Chávez et al. 2005), the production of mono-rhamno-mono-lipids were expected at least, but single expression of the rhlB gene in P. putida did not result in any rhamnolipid production. The same result was achieved when the mutagenized rhlA*B operon containing an inactive RhlA was expressed. RhlA inactivation was done in order to separate the postulated dual functionality of this protein as an enzyme and as a stabilizing function for RhlB in the postulated complex. However, since extracellularly provided HAAs are a substrate for rhamnolipid biosynthesis in P. putida expressing the single rhlB gene or the rhlA*B operon, we conclude that RhlB is active as a single enzyme and is most likely not a subunit of the rhamnosyltransferase I enzyme complex. Thus, RhlB fulfills the role as rhamnosyltransferase I independent of the assistance of RhlA for its stabilization, but strongly requires the RhlA product HAA as substrates for its own activity.
Given that RhlB cannot use single 3-hydroxyfatty acids for the synthesis of mono-rhamno-mono-lipids, these relatively rare rhamnolipid species containing only one fatty acid chain then have to descend from hydrolysis of typical and more abundant rhamnolipid species containing the normal dimer of two 3-hydroxyfatty acids. Since mono-rhamno-mono-lipids also occur in P. putida, it is reasonable to suspect that P. putida as well as P. aeruginosa contain at least one enzymatic activity, which is able to hydrolyze the ester bond between the two 3-hydroxyfatty acids of rhamnolipids. Taking into account the typical chain lengths of fatty acids of 8 to 14 carbon atoms, the most probable enzymes for this activity can be expected to belong to the esterase or lipase family of hydrolases. P. aeruginosa, for which these rhamnolipid species were first described (Syldatk et al. 1985a; Déziel et al. 1999), produces several lipolytic enzymes (Wilhelm et al. 1999; Leščić Ašler et al. 2010; Funken et al. 2011; Kovačić et al. 2013; Kovacic et al. 2016). However, 80 putative are predicted for P. aeruginosa (Jaeger and Kovacic 2014) and about half as many for P. putida (Nelson et al. 2002; Winsor et al. 2016). The identification of the individual enzymes responsible for modification of rhamnolipids by processing of fatty acids will be the aim of a further study and may provide a tool to enlarge the product range for designer rhamnolipids containing hydrophobic moieties composed of uneven numbers of fatty acids. Since rhamnolipid species containing, e.g., only one fatty acid feature an entirely different chemical proportion between the hydrophilic and hydrophobic molecule domain in comparison to typical rhamnolipids, they are considerably different and thus highly interesting for various novel applications, because their characteristics strongly affect the physicochemical properties of surfactants (Winsor 1954; Salager et al. 1979; Acosta et al. 2008).
Furthermore, extracellularly provided mono-rhamnolipids were converted to di-rhamnolipids by RhlC in recombinant P. putida. This reaction could be observed upon expression of rhlC as a single gene and also by expression of the PA1131-rhlC operon. The gene PA1131 was predicted to probably encode a transporter of the major facilitator superfamily (MFS) and the genetically organization in an operon together with rhlC consequently led to the hypothesis that the resulting protein might be involved in rhamnolipid production and/or secretion (Rahim et al. 2001). However, the additional expression of this gene had no influence on the rhamnolipid production or secretion in the recombinant P. putida strains. In addition, the genome of P. putida (Nelson et al. 2002) does not contain any gene for a homologous protein that could substitute or complement the suggested role as a membrane transporter, suggesting that PA1131 has probably a role different from rhamnolipid transport and thus may be, if at all, more indirectly linked to rhamnolipid production.
Furthermore, this is the first report that exogenously added HAAs and mono-rhamnolipids can cross both membranes of the original host P. aeruginosa and of the heterologous host P. putida to reach the cytoplasm, where all the proteins responsible for rhamnolipid biosynthesis are located (Rahim et al. 2001; Winsor et al. 2016). This suggests that beside the yet unknown exporter for HAAs and rhamnolipids, there probably may exist an importer system for the resumption of these compounds. However, the mechanism behind this retrograde transport is currently completely unknown as are candidate proteins for this functionality. A simple diffusion of the tensioactive molecules seems rather unlikely because their transport by diffusion would require close and direct interactions of HAA and rhamnolipids with the lipid bilayers of the cell membranes. One function of rhamnolipids is to emulsify hydrophobic substrates like long-chain hydrocarbons and oil in the extracellular milieu (Zhang and Miller 1992; Patel and Desai 1997) or to bind to the cell surface and to modify its overall hydrophobicity, which in turn leads to the enhanced uptake of these substrates into the cell (Zhang and Miller 1994; Noordman and Janssen 2002). In this process, below its critical micelle concentration (CMC), the hydrophilic moiety of rhamnolipids interacts with O-antigen component of lipopolysaccharides (LPS) in the outer membrane of Gram-negative bacteria to increase its hydrophobicity (Zhong et al. 2008). Above the CMC, rhamnolipids remove LPS from the outer membrane, which still leads to an increase in hydrophobicity due to the resulting lack of polar sugar residues on the cell surface (Al-Tahhan et al. 2000; Sotirova et al. 2009). It is still speculative, if rhamnolipids only permit the interaction between cell surface and hydrophobic substrates or if the cells can absorb larger adducts of substrate molecules or particles emulsified by micelles of rhamnolipids or HAAs, which also show tensioactive properties (Lépine et al. 2002). Speculative, but possibly rhamnolipid producing organisms use a cycle of HAA and rhamnolipid secretion, emulsification of hydrophobic compounds, and their reabsorption into the cell to metabolize the encased substrate and to recycle the surfactants.
Surprisingly, the decreasing amounts of HAAs and mono-rhamnolipids presented in the experiments do not quantitatively reflect the increasing amount of mono- and di-rhamnolipids, respectively. This difference indicates that P. putida can actively degrade the surfactants and is probably able to metabolize the breakdown products of these molecules. The hypothetical lipolytic enzyme responsible for the hydrolysis of rhamnolipids and probably also free HAAs into free fatty acids and mono-rhamno-mono-lipids may be also the catalyst in this process. For complete degradation of the latter, a second enzyme similar to the naringinase from Aspergillus niger (Trummler et al. 2003) would be essentially required to hydrolyze the β-glycosidic bond and release the rhamnose moiety. The identification of these enzymes will be one topic of further investigations to step forward to understand the complete biochemistry of rhamnolipid production and metabolism, to create a toolbox of enzymatic activities on HAAs and rhamnolipids and—in perspective—to open novel strategies based on these enzymes for the production of tailor made rhamnolipid molecules with specific properties for biomedical and conventional applications in biotechnology and industry.
The authors are grateful to the Fachagentur Nachwachsende Rohstoffe e. V. (FNR) and the Deutsche Bundesstiftung Umwelt (DBU) for providing financial support.
AW planned and executed the experiments, created figures, and drafted most of the manuscript; FK performed structure homology modeling and drafted parts of the manuscript; MMM and MG carried out quantification of surface active compounds; BSS and DH executed structural analysis of rhamnolipids and critically read the manuscript; TT assisted the plasmid characterization and critically read the manuscript; LMB took part in initiating the research and critically read the manuscript; MH and RH coordinated the HPLC experiments and critically read the manuscript; CS and SW took part in initiating the research and critically read the manuscript; FR initiated the project, supervised the research, coordinated the study, and critically read the manuscript. All authors read and approved the final manuscript.
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Conflict of interest
The authors declare that they have no conflict of interest.
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