A new member of the Phosphotriesterase-Like Lactonases (PLL) family from the hyperthermophilic archeon Sulfolobus islandicus (SisLac) has been characterized. SisLac is a native lactonase that exhibits a high promiscuous phosphotriesterase activity. SisLac thus represents a promising target for engineering studies, exhibiting both detoxification and bacterial quorum quenching abilities, including human pathogens such as Pseudomonas aeruginosa.
Here, we describe the substrate specificity of SisLac, providing extensive kinetic studies performed with various phosphotriesters, esters, N-acyl-homoserine lactones (AHLs) and other lactones as substrates. Moreover, we solved the X-ray structure of SisLac and structural comparisons with the closely related SsoPox structure highlighted differences in the surface salt bridge network and the dimerization interface. SisLac and SsoPox being close homologues (91% sequence identity), we undertook a mutational study to decipher these structural differences and their putative consequences on the stability and the catalytic properties of these proteins.
We show that SisLac is a very proficient lactonase against aroma lactones and AHLs as substrates. Hence, data herein emphasize the potential role of SisLac as quorum quenching agent in Sulfolobus. Moreover, despite the very high sequence homology with SsoPox, we highlight key epistatic substitutions that influence the enzyme stability and activity.
Citation: Hiblot J, Gotthard G, Chabriere E, Elias M (2012) Structural and Enzymatic characterization of the lactonase SisLac from Sulfolobus islandicus. PLoS ONE 7(10): e47028. https://doi.org/10.1371/journal.pone.0047028
Editor: Fernando Rodrigues-Lima, University Paris Diderot-Paris 7, France
Received: May 28, 2012; Accepted: September 7, 2012; Published: October 10, 2012
Copyright: © Hiblot et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was granted by Direction Generale de l’armement (D.G.A.), France (REI. 2009 34 0045) and Vaincre La Mucoviscidose, France. J.H. and G.G. are PhD students granted by D.G.A. M.E. is a fellow supported by the IEF Marie Curie program (grant No. 252836). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
SisLac (also known as SisPox ) is an enzyme isolated from the archaeon organism Sulfolobus islandicus, which is found in extreme environments like the Yellowstone natural park (U.S.A.) or the Mutnovksy volcano in Kamchatka (Russia) . SisLac belongs to an enzyme family called Phosphotriesterase-Like Lactonase (PLL) that encompasses members from mesophilic organisms (PPH, AhlA, MCP, DrOPH) , ,  as well as thermophilic (SsoPox, SacPox, GsP, GkL) , , ,  representatives. The PLL family is structurally and biochemically related to bacterial Phosphotriesterases (PTEs) . Indeed, some representatives of PLLs were primarily isolated by virtue of their phosphotriesterase activity towards the insecticide paraoxon, and were named paraoxonases (Pox) as was the case with SisLac’s closest homologue, SsoPox, an enzyme isolated from Sulfolobus solfataricus . However, further phylogenetic and biochemical studies has revealed that these enzymes are native lactonases endowed with promiscuous paraoxonase activity and more generally with organophosphate hydrolase activity . Hyperthermophylic PLLs (hPLLs) are appealing enzymes in biotechnology because they possess an intrinsically high stability that often confer high resistance towards harsh conditions and proteases activity , which constitute useful properties for storage and large scale purification.
Interestingly, PTEs exhibit diffusion limit-like second order rates with paraoxon as a substrate , and are also endowed with promiscuous lactonase activity , . The particular link between these two families raises the hypothesis that PTEs have diverged from native lactonases like PLLs , , , . Indeed, both PTEs and PLLs belong to the amidohydrolase superfamily . Despite the relatively low sequence identity between these two families (∼30%), PTEs and PLLs exhibit the same (β/α)8 barrel fold or so-called TIM barrel . At the C-terminus of the barrel, two divalent metal cations constitute the active site , , . The phosphotriesterase activity of PTEs and PLLs is modulated in the presence of various divalent cations, the highest activity being achieved in a cobalt-containing buffer for Pseudomonas diminuta PTE , OpdA  and SsoPox .The active site metal cations’ chemical nature has been investigated using anomalous X-ray scattering and has revealed that both the PTE from Agrobacterium radiobacter (OpdA) and the PLL SsoPox possess an iron/cobalt heterobinuclear center when the expression media is supplemented with cobalt ions , .
The catalytic mechanisms for both the lactonase and phosphotriesterase involve a nucleophilic attack by a water molecule activated by the bi-metallic center. The major difference between the two activities consists of the respective transition state geometries: bi-pyramidal for the phosphotriesters and tetrahedral for the lactones. The fact that these two activities can be catalyzed with significant rates within the same active site suggests an overlap between the stabilization of the corresponding transitions state species, from which the enzymatic promiscuity would stem from , . The active site of PLLs possesses three sub-sites that are remarkably adapted for the lactone binding: a small sub-site, a large sub-site and a hydrophobic channel . The aliphatic chain of the lactones binds within the hydrophobic channel, the large sub-site accommodates the amide group of the N-acyl chain, and the small sub-site positions the lactone ring. AHLs are molecules that mediate bacterial communication (quorum sensing) for many species. These molecules accumulate in the media to reach a certain threshold for which the transcriptional profile of the bacteria is altered . Some studies report that virulence and biofilm life-style are regulated by quorum sensing , , , , and suggest that quenching the quorum sensing (quorum quenching) could be an interesting strategy against multi-resistant pathogen bacteria using AHL based quorum sensing like P. aeruginosa , , , , . By hydrolyzing AHLs, lactonases like PLLs can quench the AHL-mediated communication between bacteria, as seen for AiiA  or for human paraoxonases .
Because of their dual catalytic activities, lactonases and phosphotriesterases, PLLs constitute highly attractive candidate for biotechnological utilization as quorum quenching agent  or OPs biodecontaminant . However, their precise biological function(s) remain(s) unknown. In many cases, PLLs are found in bacteria that do not produce or sense AHLs, which may suggest a role in interfering with the quorum sensing of other organisms or in the metabolism of the AHL molecules. Furthermore, some members of the PLL family efficiently hydrolyze gamma and/or delta oxo-lactones, but not AHLs , . However, the structural features that determine the lactonase specificity of these two classes remain unknown.
In this work we present a structural and biochemical analysis of SisLac. We have performed a detailed kinetic characterization and show that this enzyme hydrolyzes AHLs, but also γ and δ-lactones with high proficiency. Moreover, we provide a characterization of its thermal stability, thermophilicity and structural determinants responsible of its stability. The structural comparison with SsoPox reveals an important dimer interface change. Key amino acids variations between the two close homologues were analyzed by mutagenesis study and revealed their critical involvement in the protein stability and lactonase activity.
Materials and Methods
Strain, Plasmids and Site Directed Mutagenesis
The plasmids preparations were performed in Escherichia coli strain DH5α (Invitrogen). Protein production was performed in E. coli BL21(DE3)-pGro7/GroEL strain (TaKaRa) using plasmids pET22b-StrepTevSisLac and pET22b-SsoPox (provided by GeneArt; Germany). Site directed mutagenesis was performed in 50 µL using Pfu polymerase (Invitrogen) on 100 ng of plasmid encoding corresponding genes and primers referenced in Table S1. The PCR cycle was performed using hybridization temperature of 55°C, elongation time of 12 min during 30 cycles and final elongation of 20 min. The template plasmid was eliminated by Fast Digest DpnI (Fermentas) digestion of 30 min at 37°C followed by inactivation step of 20 min at 80°C. Plasmids were concentrated by classical alcoholic precipitation and then electroporated (Gene-Pulser, Bio-Rad) into E. cloni 5alpha cells (Lucingen), a particularly competent strain of E. coli. Site directed mutagenesis was finally verified by sequencing.
Production-purification of SisLac, SsoPox and SisLac’s Variants
SisLac and its variants were heterologously produced and purified from the Escherichia coli strain BL21(DE3)-pGro7/GroEL (TaKaRa) as previously described  with the only difference being that 0.2% (w/v) arabinose was added at the start of the over-expression in order to induce chaperones expression. A very similar production protocol was used for wt SsoPox. Briefly, protein production was performed in 2 liters of ZYP medium  (100 µg/ml ampicillin, 34 µg/ml chloramphenicol) inoculated by over-night pre-culture at a 1/20 ratio. Cultures grew at 37°C to reach OD600nm = 1.5. The induction of protein production was made by starting the consumption of the lactose in ZYP medium. Subsequently, 0.2 mM CoCl2 was added and the temperature was reduced to 25°C for additional 20 hours. Cells were harvested by centrifugation (3 000 g, 4°C, 10 min), re-suspended in lysis buffer (50 mM HEPES pH 8, 150 mM NaCl, CoCl2 0.2 mM, Lysozyme 0.25 mg/ml, PMSF 0.1 mM DNAseI 10 µg/ml) and stored at −80°C. The frozen cells were thawed and disrupted by three steps of 30 seconds of sonication (Branson Sonifier 450; 80% intensity and microtype limit of 8). Cell debris were removed by centrifugation (12 000 g, 4°C, 30 min). The purified protein being hyperthermostable, host proteins were precipitated by incubation of 30 min at 70°C and harvested by centrifugation (12 000 g, 4°C, 30 min). Other thermostable proteins from the host E. coli were eliminated by ammonium sulfate precipitation (326 g/L), and the overexpressed protein was concentrated by ammonium sulfate precipitation (476 g/L) and suspended in activity buffer (HEPES 50 mM pH 8, NaCl 150 mM, CoCl2 0,2 mM). The remaining ammonium sulfate was removed by dialysis against the activity buffer and the protein sample was subsequently concentrated prior to the size exclusion chromatography step (S75-16-60, GE Healthcare). The yield of protein production varied between 20 and 100 mg of protein per liter of culture after purification. The purity and the protein quality were verified by SDS-PAGE and mass spectrometry.
Oligomerization State Determination
Dynamic light scattering (DLS): experiments were performed at room temperature using zetasizer nano series apparatus (Malvern, UK) and the Zetasizer software. 30 µL of purified wt SsoPox and SisLac (2.5 mg/mL) was used in the activity buffer to measure the hydrodynamic radius of particles in the protein solutions at 633 nm.
Multi-angle Light Scattering Studies: experiments were performed at room temperature using a size exclusion chromatography (KW803 column (Shodex)) carried out on an Alliance 2695 HPLC system (Waters) at a flow rate of 0.5 ml/min. The buffer used was similar to activity buffer despite pH was adjusted to 7.3 using NaOH. The signal was monitored by a three-angle light-scattering detector (MiniDAWNTMTREOS; Wyatt Technology), a quasi-elastic light-scattering instrument (DynaproTM, Wyatt Technology), and a differential refractometer (Optilab rEX, Wyatt Technology). Molecular weight, gyration, and hydrodynamic radii determination were performed by the ASTRA V software (Wyatt Technology) using a dn/dC (specific refractive index increment of the solution) value of 0.185 ml/g.
The time course of ethyl-paraoxon hydrolysis by SisLac at 70°C was monitored following the p-nitrophenolate production at 405 nm (ε405nm = 17 000 M−1cm−1) in 1-cm path length cell with a Cary WinUV spectrophotometer (Varian, Australia) and using the Cary WinUV software. Standard assays (500 µL) were performed in paraoxonase buffer CHES 50 mM pH 9, NaCl 150 mM, CoCl2 0.2 mM, EtOH 6% (v/v), with pH adjusted with NaOH at 70°C.
At 25°C, the phosphotriesterase, esterase and lactonase activities were analyzed monitoring absorbance variations in 200 µL reaction volumes using 96-well plates (6.2-mm path length cell) and a microplate reader (Synergy HT) using the Gen5.1 software at 25°C. For each substrate, assays were performed using organic solvent concentrations below 1%. The monitoring wavelength, the solvent used, the molar extinction coefficient and the concentration range for each substrate (Fig. 1, S1 & S2) are summarized in Table S2. Phosphotriesterase and esterase activities were performed in activity buffer. When required, DTNB at 2 mM was added to the buffer to follow hydrolysis of substrate releasing thiolate group (malathion (Fig. S1V)). Catalytic parameters for some phosphotriesters were also recorded using SDS at concentrations 0.01 and 0.1% (w/v). Lactone hydrolysis assays were performed in lactonase buffer (Bicine 2.5 mM pH 8.3, NaCl 150 mM, CoCl2 0.2 mM, Cresol purple 0.25 mM and 0.5% DMSO) using cresol purple (pKa 8.3 at 25°C) as pH indicator to follow the acidification related to the lactone ring hydrolysis. Molar coefficient extinction was measured by recording absorbance of the buffer over a range of acetic acid concentrations (0–0.35 mM). The absorbance values versus acetic acid concentration were fitted to a linear regression (GraphPad Prism 5 software) with a slope corresponding to molar extinction coefficient (see Table S2). For all experiments, each point was made in triplicate and the Gen5.1 software was used to evaluate the initial velocity at each substrate concentration. Mean values were fitted to the Michaelis-Menten equation using Graph-Pad Prism 5 software to obtain the catalytic parameters. In the case of C4 AHL hydrolysis for which the substrate concentration that enable to determine the enzyme Vmax could not be reached, the catalytic efficiency has been determined by fitting the linear part of the Michaelis-Menten plot to a linear regression.
Chemical structures of (A.) phosphotriesters, (B.) esters, (C.) Acyl-Homoserine Lactones, (D.) 3-oxo-Acyl-Homoserine Lactones (E.) γ-lactones and (F.) δ-lactones are presented. For phosphotriesters, R corresponds to different nature of substituents, LG corresponds to the leaving group which can be F, S-R, O-R or CN. The terminal substituent could be S atom if the molecule is a thionophosphotriester or an O atom if the molecule is an oxonphosphotriester. For esters, R corresponds to different nature of substituent. For AHLs and γ/δ-lactones, R corresponds to different size of acyl chain.
Temperature dependence analysis.
The temperature dependence of the SisLac paraoxonase activity was studied over the temperature range 25–85°C with 10°C increment. The ethyl-paraoxon (2 mM) hydrolysis was monitored in 500 µL at 405 nm (ε405nm = 17 000 M−1cm−1) in 1-cm path length cell with a Cary WinUV spectrophotometer (Varian, Australia) using the Cary WinUV software. Triplicate experiments were performed in paraoxonase buffer with pH adjusted with NaOH to 9 at each temperature.
Activity-based thermal stability.
The residual paraoxonase activity of SisLac after incubation at different temperatures was performed. Incubation time and temperatures tested in this experiment were 390 min at 85°C, 90°C and 95°C in activity buffer. The ethyl-paraoxonase (1 mM) activity was followed at 25°C every 15 min during the first hour of incubation and every 30 min till the end of the experiment (after cooling). Paraoxon hydrolysis was monitored at 405 nm (ε405nm = 17 000 M−1cm−1) with a microplate reader (Synergy HT) and Gen5.1 software in a 6.2 mm path length cell for 200 µL reaction in 96-well plate. Initial velocity at 25°C was used as reference to normalize velocities obtained after incubation at high temperature. Values are represented as fraction of the reference (value 1.0). The half-life of the protein at each temperature was determined by fitting the data to an exponential decay equation using GraphPadPrism 5 software.
Melting temperature determination.
Circular Dichroism (CD) spectra were recorded using Jasco J-810 spectropolarimeter equipped with Pelletier type temperature control system (Jasco PTC-4235) in 1 mm thick quartz cell and using the Spectra Manager software. Measurements were carried out in 10 mM sodium phosphate buffer at pH 8 with a protein concentration of 0.1 mg/mL. For wt SisLac, denaturation was first recorded between 190 to 260 nm with a scattering speed of 20 nm/min every 10°C at temperatures ranging between 20 to 90°C. To determine the melting temperature of proteins (wt SisLac and variants), the denaturation was recorded at 222 nm by increasing the temperature from 20 to 90°C (at 5°C/min) in 10 mM sodium phosphate buffer at pH 8 containing increasing concentrations (0.5–3.5 M) of guanidinium chloride. The theoretical Tm without guanidinium chloride was extrapolated at the y-intercept by a linear fit using the GraphPadPrism 5 software.
pH Dependence Profile Determination
The pH-dependence ethyl-paraoxonase activity (2 mM) profile of SisLac was monitored at 348 nm (the pH-independent isobestic point of p-nitrophenol and p-nitrophenoxide ion; ε348nm = 5 300 M−1cm−1) . To explore the pH range 5–11, different buffers were prepared containing 50 mM monobasic phosphate over the pH range 5–7, 50 mM HEPES for pH 8, 50 mM CHES over the pH range 9–10 and 50 mM dibasic phosphate at pH 11. The buffers also contained 150 mM NaCl and 0.2 mM of CoCl2, and were adjusted with NaOH or HCl. The kinetic measurements were performed at 25°C with a microplate reader (Tecan) and Magellan software in a 6.2 mm path length cell for 200 µL reaction in 96-well plate. Each experiment was made in triplicate and initial velocities were evaluated using Excel software (Microsoft).
Crystallization and Structure Determination
The crystallization procedure of SisLac has been previously described . Diffraction data were collected at the ESRF (Grenoble, France) BM-30A (FIP) beamline using a wavelength of 0.98 Å on an ADSC Quantum Q315 Detector. X-Ray diffraction data were integrated and scaled with the XDS program . The presence of a twin was clearly established using phenix.xtriage  from the PHENIX refinement-program suite . The Molecular replacement using the SsoPox structure as model (PDB code 2vc5) was performed with Phaser . The twin operator (-h, -k, l) and a twofold axis (z) arising from the twinning were determined using phenix.xtriage. The solution was then used for refinement performed using REFMAC5  using the twin option and Coot  for model improvement. The model and structure factor were deposited under the Protein Data Bank (PDB) code 4G2D. Despite the twinning, the electronic density maps were of good quality (Fig. S3; R and Rfree values (0.2649 and 0.2925, respectively; Table 1)).
Structural analysis and comparison, cartoon and ribbon representation were made using PyMOL (www.pymol.org). Surface contacts and interaction analysis was performed using the PROTORP server . Root mean square deviations (r.m.s.d) were computed using Swiss-pdb-viewer software .
This study provides the characterization of SisLac isolated from Sulfolobus islandicus strain M.16.4. Several genomes of S. islandicus are available and encode highly similar (99% sequence identity) orthologs of SisLac (Fig. S4). Sequence comparison with close homologs SsoPox (91% identical) from Sulfolobus solfataricus MT4 & P2  and SacPox (76% identical) from Sulfolobus acidocaldarius DSM 639  (Fig. 2 & S4) reveals that the sequence divergence is mainly localized at the N-terminus and C-terminus of the protein. SisLac displays lower sequence identity with other members of the PLL family of proteins (35% GsP/GkL from Geobacillus sp. , , 28% DrOPH form Deinococcus radiodurans , , 37–38% AhlA/PPH/MCP from mesophilic organisms , ) and ∼ 30% with PTEs (Fig. 2). Despite a very high sequence homology between SsoPox and SisLac, both enzymes exhibit structural and enzymatic differences.
Sequence alignment of SisLac from Sulfolobus islandicus strain M.16.4 (ACR40964.1), SacPox from Sulfolobus acidocaldarius strain DSM 639 (AAY81433.1), SsoPox from Sulfolobus solfataricus strain MT4 (AAW47234.1), GsP from Geobacillus stearothermophilus strain 10, GkL from Geobacillus kaustophilus strain HTA426 (YP_147359.1), DrOPH from Deinococcus radiodurans (AAF10507.1), AhlA from Rhodococcus erythropolis (ACF57853.1), PPH from Mycobacterium tuberculosis (ACF57854.1), MCP from Mycobacterium avium subsp. paratuberculosis K-10 (NP_962602.1), Pseudomonas diminuta PTE and Agrobacterium radiobacter OpdA. Metal coordinating residues and important active site residues are indicated by a black vertical arrow. The β-sheets are indicated by a horizontal black arrow. An alignment of Sulfolobal PLL is provided in Supplementary information.
Biochemical and Biophysical Characterization of SisLac
Oligomeric state analysis.
Size exclusion chromatography, dynamic light scattering and multi angle light scattering experiments were carried out to determine the oligomeric states of SisLac and SsoPox. Using a combination of static plus dynamic light scattering, UV spectrophotometry, and refractometry, SisLac and SsoPox appear to be dimeric at room temperature (25°C) (Fig. 3A–B) (72.57±0.79 kDa and 70.46±0.97 kDa, respectively, versus MWs of SsoPox and SisLac dimers = 71.2 kDa). Moreover, the dynamic light scattering experiments show apparent sizes for SisLac and SsoPox of 80±3 kDa and 82±3 kDa, respectively (Fig. 3C–D). These results confirm that both proteins are dimeric at 25°C. The existence of homodimers is consistent with the crystal structures of SisLac, SsoPox  and other PLLs (DrOPH (PDB ID: 3FDK), GsP (PDB ID: 3F4D) and GkL (PDB ID: 3OJG)).
A–B- Multi-angle light scattering analysis of SsoPox (A.) and SisLac (B.) at 25°C. The molecular weight of particules (dashed line) are represented in function of the elution profile (continuous line) during size exclusion chromatography. C–D- Dynamic light scattering experiments. Intensity (%) of the signal versus molecular weight of particles for SsoPox sample (C.) and SisLac sample (D.).
pH and temperature dependence.
We determined the pH and temperature dependency of SisLac’s catalytic activities. However, because the lactonase assay utilizes a pH indicator, these characteristics could only be determined for the paraoxonase activity. The optimal pH for SisLac’s paraoxonase activity was established by measuring the velocity at pH ranging from 5 to 11 (Fig. 4A). The pH-rate dependence plot displays a bell-shape curve with a wide plateau between pH 7 and 10 (with maximal activity at pH 9). The same dependency what was described for SacPox at 70°C , and only a slightly different pattern was observed for SsoPox (optimum at pH 8 ). The PTE from P. diminuta also exhibits an activity maximum at a pH range of 8–10 . This observation is consistent with the hypothesis of common mechanism shared by these enzyme families.
A- pH dependence of SisLac paraoxonase activity. Velocity obtained against 2 mM ethyl-paraoxon at different pH ranging between pH 5 and pH 11 (see methods for more details). B- Thermophilicity of SisLac. Initial rates for the paraoxonase activity of SisLac were measured at temperatures ranging from 25 up to 85°C. C- Thermal stability of SisLac. Relative residual activity of SisLac after different incubation at 85°C (Black square), 90°C (grey triangle) and 95°C (Grey inverted triangle) for different times yielded half-lives of 84 (±20) min for 85°C, 8.5 (±1.5) min for 90°C and 3.6 (±0.4) min for 95°C.
The temperature dependency was investigated by measuring the paraoxonase activity at temperatures ranging from 25 to 85°C (Fig. 4B). The highest temperature tested (85°C) presented the highest velocity. However, within the tested temperature (imposed by technical limitations), we did not find a maximum. Similarly, no maxima were found in the cases of SsoPox , DrOPH  and GsP . In contrast, SacPox presents a maximum activity around 70°C and the activity decrease above this temperature .
The thermostability of SisLac was evaluated based on its catalytic activity. The residual paraoxonase activity of the enzyme after different incubation times at 80, 90 and 95°C was measured (Fig. 4C). The enzyme exhibited respective half-lives of 84±20 min, 8.5±1.5 min and 3.6±0.4 min at 85, 90 and 95°C. In comparison, SsoPox exhibits a half-life of 4 hours at 95°C, and 90 min at 100°C , and SacPox exhibits a half-life of 5 min at 90°C  (from S. acidocaldarius, living temperatures from 55 to 85°C ).
The thermal stability of SisLac was also determined by circular dichroism at temperatures ranging between 20°C and 90°C (Fig. S5). However, as previously observed for SsoPox , the extreme thermostability of this enzyme does not allow to precisely determine a melting temperature (Tm) by this method. Different concentrations of guanidium chloride were required to further destabilize the protein and the Tm values were extrapolated to zero guanidinium chloride: Tm at 102±2°C for SisLac (Fig. S5) (while SsoPox’s Tm = 106°C ). These values are in the range of the other characterized thermostable PLLs, including DrOPH and GsP whose Tm values are 88.1°C  and 106.6°C , respectively. Notably, the extremophile Deinoccocus radiodurans is a mesophilic bacteria , and DrOPH exhibits an extreme Tm, typical for enzymes from hyperthermophiles or thermophiles (Sulfolobus solfataricus living temperatures from 50 to 87°C , Sulfolobus islandicus from 59 to 91°C , Geobacillus stearothermophilus from 37–70°C , ).
Enzymatic Characterization of SisLac
Kinetic parameters were determined for paraoxon (Fig. S1I) at 70°C and 25°C (Table 2). The catalytic efficiency obtained at 70°C for SisLac (kcat/KM = 6.98(±1.56)×102 M−1s−1) is similar to that reported for SacPox  and SsoPox  (Table S3). The catalytic efficiency at 25°C was about 2.5 folds lower than the efficiency at 70°C (2.60(±0.58)×102 M−1s−1), and is higher than that of GsP (5,47(±0.47)×101 M−1s−1) , GkL (4.5 M−1s−1; at 37°C) , MCP (4.1 M−1s−1)  and DrOPH (1.39±0.11 M−1s−1) . These promiscuous phosphotriesterase catalytic parameters of lactonases ,  contrast with the diffusion limit-like second order rates of P. diminuta PTE with paraoxon as substrate (kcat/KM ∼ 108 M−1s−1) .
The modulation of SisLac phosphotriester hydrolysis by Sodium Dodecyl Sulfate (SDS), which has been previously shown to act as an activator in the case of SsoPox , was also tested (Table 2). Interestingly, the addition of 0.01% SDS yields to a 2.5 folds increase in the paraoxonase catalytic efficiency (6.36(±2.18)×102 M−1s−1), whereas the addition of 0.1% SDS enhanced the efficiency by 25 folds (kcat/KM = 7.14(±4.16)×103 M−1s−1).
Others phosphotriesters (Fig. 1A) were also tested as substrates at 25°C; including methyl-paraoxon (Fig. S1II), parathion (Fig. S1III), methyl-parathion (Fig. S1IV), malathion (Fig. S1V) and CMP-coumarin (Fig. S1VI) (methylphosphonic acid 3-cyano-4-methyl-2-oxo-2H-coumarin-7-yl ester cyclohexyl ester (a cyclosarin derivative in which the fluoro substituent of cyclosarin has been replaced by a cyanocoumarin group )) (Table 3 & S4). These assays showed that SisLac is over 10 times more efficient towards methyl-paraoxon than for (ethyl-)paraoxon (4.26(±1.74)×103 M−1s−1 and 2.60(±0.58)×102 M−1s−1, respectively). In a similar fashion, SisLac shows a clear preference for the methyl-parathion (3.57(±0.3)×101 M−1s−1), as compared with ethyl-parathion for which no catalysis could be detected. This suggests that the bulkiness of the substituent groups of some phosphotriesters affects a catalytically efficient binding. This preference has also been observed for SsoPox and SacPox at 70°C . Moreover, SisLac exhibits a pronounced thiono-effect; methyl-paraoxon and methyl-parathion differ by only one atom (the oxon function on the phosphorus moiety in paraoxon is a thiono in parathion), SisLac hydrolyzes methyl-paraoxon about 100 times more efficiently (4.26(±1.74)×103 M−1s−1 and 3.57(±0.3)×101 M−1s−1, respectively). PTEs does not exhibit such a drastic difference and paraoxon is only a slightly better substrate than parathion , . Kinetics parameters were also recorded for the hydrolysis of another sulfur-containing organophosphate, the insecticide called malathion (1.88±0.43 M−1s−1). SisLac exhibits a similar KM for this substrate than for methyl-parathion, but malathion is a considerably slower substrate than parathion. Finally, SisLac hydrolyzes the nerve agent analog CMP-coumarin with moderate efficiency (4.26(±1.86)×103 M−1s−1) illustrating its potential for organophosphorus detoxification.
Although lactones constitute a specific class of esters (Fig. 1B), no esterase activity was detected within PLL family members with the exception of SsoPox and SacPox (with 2-naphthyl acetate , , p-nitrophenyl butanoate and 2-naphthyl acetate ). It is therefore not surprising that SisLac hydrolyzes p-nitrophenyl-acetate (Fig. S1VIII) with kcat/KM = 1.6(±0.5)×103 M−1s−1, a 50 times higher catalytic efficiency than SsoPox (kcat/KM of 3.12(±0.33)×101 M−1s−1) (Table 4). However, both proteins do not exhibit any detectable activity against phenyl-acetate (Fig. S1VII), p-nitrophenyl-decanoate (Fig. S1IX), nitrophenyl-acetate (Fig. S1X) and 4-acetoxyacetophenone (Fig. S1XI) (Table 4).
PLLs are lactonases that might be involved in quorum quenching mechanisms , . We thus assayed the activity of SisLac on several AHLs (Fig. 1C–D) of different chain lengths with the aim of evaluating SisLac’s specificity (Table 5). These experiments revealed that SisLac exhibits clear preference for AHLs with medium-length aliphatic chains (C8 and C10-AHL). Long chains are strongly disfavored, the efficiency of 3-oxo-C12-AHL hydrolysis (Fig. S2VI) (8.97(±3.45)×102 M−1s−1) is 100 fold lower than that of 3-oxo-C10-AHL (Fig. S2V) (9.63(±1.89)×104 M−1s−1). In addition, 3-oxo-AHLs (Fig. 1D) are overall better substrates for SisLac than unsubstituted (Fig. 1C).
Others lactones were also assayed as substrates (Table 6), such as the γ-lactones (5 atoms lactone ring) (Fig. 1E), δ-lactones (6-atoms lactone ring) (Fig. 1F) and ε-lactone (7 atoms lactone ring) (Fig. S2XI), with alkyl substituent on carbons 4 and 5 of the lactone ring (contrary to the substitution of carbon 2 in AHLs (Fig. 1C) (Table 6). Finally, dihydrocoumarin (Fig. S2XII), an aromatic lactone, was also tested (Table 6). We found that γ-lactones (Fig. 1E) and δ-lactones (Fig. 1F) comprise good substrates for SisLac, δ-lactones being the preferred substrates. Indeed, the best δ-lactone (undecanoic-δ-lactone (Fig. S2XIV), 1.77(±0.04)×106 M−1s−1) is hydrolyzed with over 5-times higher catalytic efficiency than the best γ-lactone (nonanoic-γ-lactone (Fig. S2IX), 2.04(±1.12)×105 M−1s−1). The latter is 2 times a better substrate than the best AHL substrate (3-oxo-C8-AHL (Fig. S2IV), 9.70(±1.84)×104 M−1s−1). Comparison of different lactones possessing different alkyl chain lengths confirmed the trend observed for AHLs, whereby acyl chains containing 7 carbons were preferred by the enzyme. For γ-lactones and δ-lactones, the alkyl chain length preferred by the enzyme is between 5 and 6 carbon atoms, and a similar specificity was observed for MCP, GkL and DrOPH enzymes , , . Interestingly, whereas the short chain C4-AHL (Fig. S2I) is a poor substrate for SisLac, the γ-heptanolide lactone (Fig. S2VIII) (3 carbon atoms in the alkyl side-chain) shows a 104 higher catalytic efficiency. In fact, lactones with very short or without side-chains (dihydrocoumarin (Fig. S2XVII), γ-butyrolactone (Fig. S2VII), δ-valerolactone (Fig. S2XII), ε-caprolactone (Fig. S2XVI)) constitute better substrates than C4-AHL (Fig. S2I).
Structural Analysis of SisLac
SisLac is homodimeric in the crystal structure with overall dimensions of the monomers of being approximately 39×48×56 Å. As for its close homolog SsoPox  and related PLLs like DrOPH , GsP  and GkL , SisLac is roughly globular and exhibits a (β/α)8 barrel topology. The active site consists of a binuclear center located at the C-Terminal of the barrel. Four histidines (His22, His24, His170, His199), one aspartic acid (Asp256) and a carboxylated lysine (residue 137) are coordinating the two metals. The two metal cations (possibly iron and cobalt, as seen for SsoPox  and OpdA ) are bridged by a water molecule that is presumed to be the catalytic nucleophile. The active site includes a long hydrophobic channel that was revealed by structural studies on SsoPox as the binding region of aliphatic chains for the AHL substrates . Indeed, SisLac’s structure is overall very similar to the structure of SsoPox (root-mean-square deviation (r.m.s.d.) for α-carbon atoms (over 314 atoms) of 0.35 Å).
Salt bridge network analysis.
SisLac sequence exhibits approximately the same amino acid content as SsoPox, containing 14.3 versus 16% of uncharged polar residues and 28.7 versus 28% of charged residues. This is no surprising since both enzymes possess high sequence identity (91%) (see sequence alignment, Fig. 2). As described for SsoPox, the charged residues are mainly located at the protein surface, forming complex electrostatic networks  that includes 28 salt bridges implicating 46 residues. This charge network mainly differs by the substitution K14E in SisLac that suppress a salt bridge network between E12-K14-D15 of SsoPox, and consequently creates a local concentration of 3 negative charges within 4 consecutive residues (Fig. 5A).
A- Close view on position 14 in SsoPox (left side) and SisLac (right side) structures. Negatively and positively charged residues are represented as red and blue spheres, respectively. Black dashed lines correspond to the putative salt-bridges in SsoPox. B- Structural comparisons of the dimers of SisLac (violet), SsoPox (red) and P. diminuta PTE (yellow). One monomer was used to superpose the three structures (shown on the right side), thus indicating the conformational shift in the position of the second monomer (left side). The differences are highlighted by blue arrows (P. diminuta PTE versus SsoPox) or by black arrows (SsoPox versus SisLac). When compared to P. diminuta PTE, the rotational shift observed in SisLac is more pronounced than that of SsoPox. C- Close view on position 34 in SsoPox (grey) and SisLac (violet). Black dashed lines correspond to the hydrogen bond between Q34 of each monomer of SsoPox with a distance of 3.2 Å. The black arrow shows the rotational shift that seems to be induced by this substitution.
Dimer interface analysis.
The dimer interface of SisLac comprises 46 residues (44 in SsoPox). The contacting area is almost identical and comprise a typical value for homodimers  (1770 Å2 for SisLac structure, 1750 Å2 for SsoPox structure, lower for other thermostable PLLs: 1728 Å2 for GkL structure, 1632 Å2 for GsP structure and 1473 Å2 for DrOPH structure). The nature of this interface is mainly hydrophobic in both enzymes, but SisLac’s interface tends to be more hydrophobic (56% for SisLac, 52.6% for SsoPox), more charged (SisLac 23.91%, SsoPox 20.45%) and less polar (SisLac 32.61%, SsoPox 36.36%). Four interface residues differ from SisLac to SsoPox but these substitutions do not fully explain the observed differences. Interestingly, the superposition of SisLac and SsoPox monomers shows a relative movement of the second SisLac monomer of about 5 Å relative to SsoPox’s, revealing that the interface area is slightly shifted (Fig. 5B). This reorganization of the dimer interface appears to be due to the substitution Q34Y, although it could also originate from the different crystal packing of both proteins. Whereas the two Q34 interact with each other’s in SsoPox structure, the bulkiness of both Y34 in SisLac imposes a reorientation of the dimer (Fig. 5C). This reorientation increases the monomers interpenetration, and makes one closer to the active site of the other. This trend was previously described while comparing the P. diminuta PTE and SsoPox structures , although these enzymes are far more divergent in sequence (about 30% identity). Although the biological importance and catalytic influence of dimerization for these enzymes remain unclear, second shell active site residues are notably involved in dimer formation.
Key Substitutions between SisLac and SsoPox
The structural analysis revealed that the positions 14 and 34 seem to be the major impacting variations between SisLac and SsoPox structures, that may relate to dimerization changes (position 34) or stability (positions 14, 34). Mutational intermediates between SisLac and SsoPox have been constructed to evaluate the consequences of these substitutions (E14K and Y34Q) for the enzyme stability and activity. All the variants exhibit lower Tm as compared to SisLac (102±2°C) and SsoPox (106°C)  while double variants (Y34Q-E14K) present the highest Tm among the variants (Table 7). The analysis of Tm reveals that the substitution Y34Q and E14K are destabilizing on SisLac background but the combination of both variations tends to restore partially the stability (Table 7). Additionally, the mutants have been characterized for catalytic activity against ethyl/methyl-paraoxon and for the best AHL, δ-lactone and γ-lactone substrates of wt SisLac (Table 8). The efficiency of methyl-paraoxon hydrolysis is similar for wt and the mutants, whereas the mutants exhibit higher catalytic efficiency against ethyl-paraoxon than the wt enzyme. However, the mutants exhibit a dramatically reduced AHLase activity (Table 8). A similar trend is observed with δ/γ-lactones. These results clearly highlight the critical importance of these positions for SisLac stability and activity, and validate our structural analysis.
Catalytic Properties of SisLac
The pH dependence of SisLac was investigated and yields a bell-shaped curve with a pH optimum at pH 9, a consistent behavior with previously characterized PLLs ,  and PTEs . This pH dependence profile is also in agreement with the commonly accepted hydrolysis mechanism where a water molecule activated by the bi-metallic active site serves as nucleophile . Additionally, the metal dependence was assayed and the metal nature was found to modulate the catalytic activities, as previously described in PTEs  and PLLs . Amongst the tested metals, SisLac shows preference for cobalt cations for both lactonase and paraoxonase activities (supplementary information & Fig. S6), as previously reported for the paraoxonase activity of SsoPox  and the lactonase activity of DrOPH , MCP  and GkL . The metal dependence of SisLac may be related to the relative pKa of considered metal with H2O, since the pKa of Co2+/H2O is lower than that of Zn2+/H2O and Mn2+/H2O (8.9 versus 9.0, and 10.6, respectively ), thus Co2+ would better contribute to the activation of the nucleophile. In addition, Co2+ is more electronegative than Zn2+ and Mn2+ (1.88 versus 1.65 and 1.55, respectively ), thus being more efficient for stabilizing the developing negative charge on the transition state.
The catalytic efficiency of paraoxon hydrolysis by SisLac at 25°C (kcat/kM = 2.60(±0.58)×102 M−1s−1) shows that SisLac is endowed with one of the highest paraoxonase activity amongst PLLs , , , , , . Moreover, this activity can be considerably increased by addition of 0.1% SDS (25 folds), suggesting that the enzyme has an interesting potential for catalytic improvement. The potential of this enzyme for organophosphorus compounds bio-decontamination is further illustrated by its ability to hydrolyze the nerve agent analog CMP-coumarin with significant efficiency (kcat/KM = 4.26(±1.86)×103 M−1s−1).
Interestingly, we observed that methyl-paraoxon is a better substrate than ethyl-paraoxon, the same trend being monitored between methyl and ethyl-parathion. The fact that smaller substituents on the phosphorus center are preferred by the enzyme is consistent with the promiscuous nature of paraoxonase activity in SisLac. Moreover, the higher compaction of the SisLac monomer makes active sites closer one to each other in the dimer as compared to SsoPox structure and thus could explain the substrate preference in disfavor of bulkier substrates.
In addition, SisLac exhibits very low catalytic efficiency towards P = S containing organophosphates (e.g. ethyl and methyl-parathion, malathion). The KM values are in the range of the native substrates (hundreds of µM), but the kcat values are extremely low (about 3 orders of magnitude lower than P = O containing OPs), which is a typical behavior for promiscuous activities . PTEs, albeit preferring paraoxon to parathion as a substrate, do not exhibit such a pronounced thiono-effect , . PTEs constitutes a protein family that are believed to have diverged from PLLs like SisLac  in the last few decades to specifically hydrolyzes man-made insecticides . They thus may have evolved to suppress this thiono-effect in order to hydrolyze the most used pesticides (e.g. parathion).
Esterase and Lactonase Activity
PLLs have been previously characterized as poor esterases , and so is SisLac. Amongst the five tested esters, only pNP-acetate is a substrate for SisLac. The natural substrates of PLLs, lactones, being a specific class of esters, it is thus surprising that PLLs exhibit low esterase activity. It might results from a rather good binding to the active site (as suggested by observed KM for pNP-acetate), but with a large fraction of non-productive binding (very low kcat).
PLLs are natural lactonases that might be involved in quorum quenching . Their precise substrates and biological function(s) are however still unknown. Lactones encompass two major families of compounds, the lipophilic aroma (oxo-lactones) and the Acyl Homoserine Lactones (AHLs) involved in quorum sensing. The quorum sensing is common in bacteria, but its existence in the archaeal world remains unclear, despite the finding of AHL-based quorum sensing stimulating molecules in Natronoccocus occultus , the presence of biofilms in Sulfolobus sp.  and the recent characterization of complete carboxylated-AHLs quorum sensing system in methanogenic archaeon .
Our kinetic experiments show that SisLac prefers long aliphatic chain lactones, exhibiting optimal activity when the acyl chain contains 7 carbon atoms, as seen for SsoPox . SisLac show also preference for 3-oxo-AHLs and hydrolyzes poorly short chain AHLs. It is interesting to notice that other PLLs, like AhlA and PPH, hydrolyze short and long chain lactones with similar catalytic efficiency . It is thus possible that within the PLL family, different sub-groups of enzymes exhibit different specificities, and thus possibly different physiological functions. In addition, we show that SisLac is a proficient enzyme against oxo-lactones (best substrate: undecanoic-δ-lactone, kcat/kM = 1.77(±0.04)×106 M−1s−1), and hydrolyzes more efficiently long chain lactones, with a preference for 5 to 6 acyl chain carbon atoms. This preference is similar to that observed for AHLs as substrates, and possibly indicates that oxo-lactones and AHLs acyl chains bind into a similar pocket, most likely the hydrophobic channel connected to the active site that was depicted for SsoPox structure , . However, interestingly, whereas the short chain C4-AHL is a poor substrate for SisLac, the heptanolide-δ-lactone (3 carbon atoms in the acyl chain) shows a 104 higher hydrolysis efficiency. In addition, lactones with very short or without acyl chains (dihydrocoumarin, γ-butyrolactone, δ-valerolactone, ε-caprolactone) constitute better substrates than C4-AHL. Altogether, these features might reveal that γ- and δ-lactones utilize an alternate binding mode for the lactone ring than AHLs, and/or that C4-AHL does not bind in a catalytically relevant fashion to SisLac.
Structural Determinants for Thermal Stability
The major structural determinants explaining the high thermal stability of hPLLs have been documented with the example of SsoPox , the comparison with GsP and DrOPH enzymes , and are part of the classical properties described for hyperthermostable proteins . The structures of these enzymes, including SisLac, exhibit a high number of salt bridges organized in complex networks of charges at the protein surface that may rigidify the global protein architecture. Moreover, the homodimer interface is larger and more hydrophobic (see Results) and the overall structure is more compact than mesophilic counterparts . Here we observed that the interface area between SisLac’s monomers is slightly shifted, as compared with SsoPox structure. This reorganization of the dimer interface is consistent with observations made in solution. Indeed, as observed in crystals, both enzymes are dimeric at 25°C. The importance of hydrophobic contacts within the dimer interface of SisLac and SsoPox explain the dimerization of the proteins. Since the hydrophobic effect increases with temperature, it is highly probable that these enzymes could be dimers at physiological temperatures (50–90°C) , .
Interestingly, both Sulfolobus species from which SisLac and SsoPox enzymes originates lives in similarly extreme environments (S. solfataricus from 50 to 87°C , S. islandicus from 59 to 91°C ) and exhibit similar thermostability (Tm = 102±2°C for SisLac and Tm = 106°C for SsoPox ). Taking advantage from their high sequence identity between the two proteins, we studied the substitution K14E in SisLac (as compared to SsoPox) that breaks a salt bridge network at the C-terminus of the protein, a region concentrating the highest divergences among hPLLs as revealed by sequence alignment (i.e. SsoPox, SacPox and SisLac). E14 engenders in SisLac a cluster of 3 negatively charged residues at the surface of the structure allowing to evaluate the contribution of these electrostatic interactions to the enzyme stability and activity. Moreover, another key substitution occurred between the two enzymes in the homodimerization interface. Q34Y is indeed a key substitution in the interface since it consists in a “pivot” residue, i.e. a residue that contacts its equivalent in the second protein molecule while forming the dimer, and seems to be responsible for the observed dimerization shift between SisLac and SsoPox structures. Q34Y is, moreover, the substitution between SisLac and SsoPox that is the closest in space to the active site (second shell). We therefore studied the effects of this variation on SisLac’s activity and stability.
Surprisingly, whereas K14 in SsoPox is involved in a large network of charged interactions and may contribute to the overall protein rigidity , the variation E14K in SisLac is destabilizing (Tm is decreased by 6°C). The variation of the pivot interface residue Y34Q is also destabilizing on SisLac background (decrease of Tm by 8°C). Interestingly, the double variant E14K-Y34Q that carries two destabilizing mutations exhibits a higher Tm than the single variants, revealing the highly epistatic nature of these positions. Moreover, whereas the promiscuous phosphotriesterase activity is not altered by these substitutions, the lactonase activity, especially the AHLase activity is considerably reduced (by ∼100 folds) as compared to wt. The influence of E14K on SisLac’s catalytic activity is not obvious from a structural analysis. However, position 34 comprises a second shell residue, and the overall dimer interface is in the vicinity of the active site. Mutation of position 34 highly influences the protein dimerization and thus the degree of monomers interpenetration. Monomer active sites being close one to each other, their interpenetration could influence substrate specificities and catalytic efficiencies by fine steric or dynamic constraints which can’t be evaluated by structural analysis. These identified key substitutions, however, does not fully explain the observed different catalytic properties of SisLac and SsoPox. The active site residues and configuration of these two enzymes being similar, these discrepancies might be partly mediated by yet unidentified substitutions distant from the active site.
Reconstructed mutational intermediates between SisLac and SsoPox have lower fitness both in term of stability and AHLase activity. Despite the very high sequence identity between both proteins (91%), it may indicate that the evolutionary route that links them already comprise a fraction of highly epistatic mutations. In other words, the mutations that accumulate at a very early stage of divergence might not only be neutral but a fraction of them are highly cooperative.
Chemical structure of phosphotriesters (I-VI) and esters (VII-XI).
Chemical structure of AHLs (I-VI), γ-lactones (VII-XI), δ-lactones (XII-XV) and other lactones (XVI-XVII).
Electronic density map of Sis Lac at 2.7 Å resolution.
Sequence alignment of PLLs from Sulfolobus species.
Thermostability analysis of Sis Lac by circular dichroism.
Supplementary information for Sis Lac metal preferences.
Primers used for site directed mutagenesis.
Ethyl-paraoxonase comparison between Sso Pox, Sac Pox and Sis Lac.
We are grateful to Prof. Dan S. Tawfik for fruitful discussions and to Dr. Moshe Goldsmith for the kind gift of CMP-coumarin. We thank the AFMB laboratory (Marseille, France) for the access to protein production and crystallization platforms.
The coordinate file and the structure factors file of the SisLac structure have been deposited to the Protein Data Bank under the accession number 4G2D.
Conceived and designed the experiments: ME JH EC. Performed the experiments: ME JH GG. Analyzed the data: ME JH EC. Wrote the paper: ME JH.
- 1. Gotthard G, Hiblot J, Elias M, Chabriere E (2011) Crystallization and preliminary X-ray diffraction analysis of the hyperthermophilic Sulfolobus islandicus lactonase. Acta crystallographica Section F, Structural biology and crystallization communications 67: 354–357.
- 2. Reno ML, Held NL, Fields CJ, Burke PV, Whitaker RJ (2009) Biogeography of the Sulfolobus islandicus pan-genome. Proc Natl Acad Sci U S A 106: 8605–8610.
- 3. Afriat L, Roodveldt C, Manco G, Tawfik DS (2006) The latent promiscuity of newly identified microbial lactonases is linked to a recently diverged phosphotriesterase. Biochemistry 45: 13677–13686.
- 4. Chow JY, Wu L, Yew WS (2009) Directed evolution of a quorum-quenching lactonase from Mycobacterium avium subsp. paratuberculosis K-10 in the amidohydrolase superfamily. Biochemistry 48: 4344–4353.
- 5. Hawwa R, Larsen SD, Ratia K, Mesecar AD (2009) Structure-based and random mutagenesis approaches increase the organophosphate-degrading activity of a phosphotriesterase homologue from Deinococcus radiodurans. J Mol Biol 393: 36–57.
- 6. Merone L, Mandrich L, Rossi M, Manco G (2005) A thermostable phosphotriesterase from the archaeon Sulfolobus solfataricus: cloning, overexpression and properties. Extremophiles 9: 297–305.
- 7. Porzio E, Merone L, Mandrich L, Rossi M, Manco G (2007) A new phosphotriesterase from Sulfolobus acidocaldarius and its comparison with the homologue from Sulfolobus solfataricus. Biochimie 89: 625–636.
- 8. Hawwa R, Aikens J, Turner RJ, Santarsiero BD, Mesecar AD (2009) Structural basis for thermostability revealed through the identification and characterization of a highly thermostable phosphotriesterase-like lactonase from Geobacillus stearothermophilus. Arch Biochem Biophys 488: 109–120.
- 9. Chow JY, Xue B, Lee KH, Tung A, Wu L, et al. (2010) Directed evolution of a thermostable quorum-quenching lactonase from the amidohydrolase superfamily. J Biol Chem 285: 40911–40920.
- 10. Demirjian DC, Moris-Varas F, Cassidy CS (2001) Enzymes from extremophiles. Curr Opin Chem Biol 5: 144–151.
- 11. Omburo GA, Kuo JM, Mullins LS, Raushel FM (1992) Characterization of the zinc binding site of bacterial phosphotriesterase. J Biol Chem 267: 13278–13283.
- 12. Draganov DI (2010) Lactonases with organophosphatase activity: structural and evolutionary perspectives. Chem Biol Interact 187: 370–372.
- 13. Elias M, Dupuy J, Merone L, Mandrich L, Porzio E, et al. (2008) Structural basis for natural lactonase and promiscuous phosphotriesterase activities. J Mol Biol 379: 1017–1028.
- 14. Elias M, Tawfik DS (2012) Divergence and Convergence in Enzyme Evolution: Parallel Evolution of Paraoxonases from Quorum-quenching Lactonases. J Biol Chem 287: 11–20.
- 15. Afriat-Jurnou L, Jackson CJ, Tawfik DS (2012) Reconstructing a missing link in the evolution of a recently diverged phosphotriesterase by active-site loop remodeling. Biochemistry.
- 16. Nagano N, Orengo CA, Thornton JM (2002) One fold with many functions: the evolutionary relationships between TIM barrel families based on their sequences, structures and functions. J Mol Biol 321: 741–765.
- 17. Vanhooke JL, Benning MM, Raushel FM, Holden HM (1996) Three-dimensional structure of the zinc-containing phosphotriesterase with the bound substrate analog diethyl 4-methylbenzylphosphonate. Biochemistry 35: 6020–6025.
- 18. Elias M, Dupuy J, Merone L, Lecomte C, Rossi M, et al. (2007) Crystallization and preliminary X-ray diffraction analysis of the hyperthermophilic Sulfolobus solfataricus phosphotriesterase. Acta Crystallogr Sect F Struct Biol Cryst Commun 63: 553–555.
- 19. Rochu D, Viguie N, Renault F, Crouzier D, Froment MT, et al. (2004) Contribution of the active-site metal cation to the catalytic activity and to the conformational stability of phosphotriesterase: temperature- and pH-dependence. Biochem J 380: 627–633.
- 20. Jackson CJ, Carr PD, Kim HK, Liu JW, Herrald P, et al. (2006) Anomalous scattering analysis of Agrobacterium radiobacter phosphotriesterase: the prominent role of iron in the heterobinuclear active site. Biochem J 397: 501–508.
- 21. Ben-David M, Elias M, Filippi JJ, Dunach E, Silman I, et al. (2012) Catalytic versatility and backups in enzyme active sites: the case of serum paraoxonase 1. J Mol Biol 418: 181–196.
- 22. Hentzer M, Wu H, Andersen JB, Riedel K, Rasmussen TB, et al. (2003) Attenuation of Pseudomonas aeruginosa virulence by quorum sensing inhibitors. EMBO J 22: 3803–3815.
- 23. Popat R, Crusz SA, Diggle SP (2008) The social behaviours of bacterial pathogens. Br Med Bull 87: 63–75.
- 24. Costerton JW, Stewart PS, Greenberg EP (1999) Bacterial biofilms: a common cause of persistent infections. Science 284: 1318–1322.
- 25. Dickschat JS (2009) Quorum sensing and bacterial biofilms. Nat Prod Rep 27: 343–369.
- 26. Jones MB, Peterson SN, Benn R, Braisted JC, Jarrahi B, et al. (2010) Role of luxS in Bacillus anthracis growth and virulence factor expression. Virulence 1: 72–83.
- 27. Amara N, Krom BP, Kaufmann GF, Meijler MM (2011) Macromolecular inhibition of quorum sensing: enzymes, antibodies, and beyond. Chem Rev 111: 195–208.
- 28. Dong YH, Wang LH, Xu JL, Zhang HB, Zhang XF, et al. (2001) Quenching quorum-sensing-dependent bacterial infection by an N-acyl homoserine lactonase. Nature 411: 813–817.
- 29. Dong YH, Xu JL, Li XZ, Zhang LH (2000) AiiA, an enzyme that inactivates the acylhomoserine lactone quorum-sensing signal and attenuates the virulence of Erwinia carotovora. Proc Natl Acad Sci U S A 97: 3526–3531.
- 30. Ma F, Wang Y, Zhang Y, Xiong N, Yang B, et al. (2009) Heterologous expression of human paraoxonases in Pseudomonas aeruginosa inhibits biofilm formation and decreases antibiotic resistance. Appl Microbiol Biotechnol 83: 135–141.
- 31. Reimmann C, Ginet N, Michel L, Keel C, Michaux P, et al. (2002) Genetically programmed autoinducer destruction reduces virulence gene expression and swarming motility in Pseudomonas aeruginosa PAO1. Microbiology 148: 923–932.
- 32. Dong YH, Wang LY, Zhang LH (2007) Quorum-quenching microbial infections: mechanisms and implications. Philos Trans R Soc Lond B Biol Sci 362: 1201–1211.
- 33. Singh BK (2009) Organophosphorus-degrading bacteria: ecology and industrial applications. Nat Rev Microbiol 7: 156–164.
- 34. Xiang DF, Kolb P, Fedorov AA, Meier MM, Fedorov LV, et al. (2009) Functional annotation and three-dimensional structure of Dr0930 from Deinococcus radiodurans, a close relative of phosphotriesterase in the amidohydrolase superfamily. Biochemistry 48: 2237–2247.
- 35. Studier FW (2005) Protein production by auto-induction in high density shaking cultures. Protein Expr Purif 41: 207–234.
- 36. Kabsch W (1993) Automatic processing of rotation diffraction data from crystals of initially unknown symmetry land cell constants. J Appl Cryst 26: 795–800.
- 37. Zwart PH G-KR, Adams PD (Winter 2005) Xtriage and Fest: automatic assessment of X-ray data and substructure structure factor estimation. CCP4 newsletter No.43.
- 38. Adams PD, Grosse-Kunstleve RW, Hung LW, Ioerger TR, McCoy AJ, et al. (2002) PHENIX: building new software for automated crystallographic structure determination. Acta Crystallogr D Biol Crystallogr 58: 1948–1954.
- 39. A. J. McCoy RWG-K, P. D Adams, M. D Winn, L. C Storoni, R. J Read (2007) Phaser crystallographic software. J Appl Cryst 40: 658–674.
- 40. Vagin A, Steiner RS, Lebedev AA, Potterton L, McNicholas S, Long F, Murshudov GN (2004) REFMAC5 dictionary: organisation of prior chemical knowledge and guidelines for its use. Acta Cryst D60: 2284–2295.
- 41. Emsley P, Cowtan K (2004) Coot: model-building tools for molecular graphics. Acta Crystallogr D Biol Crystallogr 60: 2126–2132.
- 42. Reynolds DJ Protorp: a protein-protein interaction analysis tool. Bioinformatics: Submitted.
- 43. Guex N, Peitsch MC (1997) SWISS-MODEL and the Swiss-PdbViewer: an environment for comparative protein modeling. Electrophoresis 18: 2714–2723.
- 44. Poirot O, O’Toole E, Notredame C (2003) Tcoffee@igs: A web server for computing, evaluating and combining multiple sequence alignments. Nucleic Acids Res. 31: 3503–3506.
- 45. Notredame C, Higgins DG, Heringa J (2000) T-Coffee: A novel method for fast and accurate multiple sequence alignment. J Mol Biol 302: 205–217.
- 46. Gouy M, Guindon S, Gascuel O (2010) SeaView version 4: A multiplatform graphical user interface for sequence alignment and phylogenetic tree building. Mol Biol Evol 27: 221–224.
- 47. Del Vecchio P, Elias M, Merone L, Graziano G, Dupuy J, et al. (2009) Structural determinants of the high thermal stability of SsoPox from the hyperthermophilic archaeon Sulfolobus solfataricus. Extremophiles 13: 461–470.
- 48. Dumas DP, Raushel FM (1990) Chemical and kinetic evidence for an essential histidine in the phosphotriesterase from Pseudomonas diminuta. J Biol Chem 265: 21498–21503.
- 49. Auernik KS, Cooper CR, Kelly RM (2008) Life in hot acid: pathway analyses in extremely thermoacidophilic archaea. Curr Opin Biotechnol 19: 445–453.
- 50. Nazina TN, Tourova TP, Poltaraus AB, Novikova EV, Grigoryan AA, et al. (2001) Taxonomic study of aerobic thermophilic bacilli: descriptions of Geobacillus subterraneus gen. nov., sp. nov. and Geobacillus uzenensis sp. nov. from petroleum reservoirs and transfer of Bacillus stearothermophilus, Bacillus thermocatenulatus, Bacillus thermoleovorans, Bacillus kaustophilus, Bacillus thermodenitrificans to Geobacillus as the new combinations G. stearothermophilus, G. th. Int J Syst Evol Microbiol 51: 433–446.
- 51. McMullan G, Christie JM, Rahman TJ, Banat IM, Ternan NG, et al. (2004) Habitat, applications and genomics of the aerobic, thermophilic genus Geobacillus. Biochem Soc Trans 32: 214–217.
- 52. Ng FS, Wright DM, Seah SY (2010) Characterization of a phosphotriesterase-like lactonase from Sulfolobus solfataricus and its immobilization for quorum quenching. Appl Environ Microbiol.
- 53. Merone L, Mandrich L, Porzio E, Rossi M, Muller S, et al. (2010) Improving the promiscuous nerve agent hydrolase activity of a thermostable archaeal lactonase. Bioresour Technol 101: 9204–9212.
- 54. Ashani Y, Gupta RD, Goldsmith M, Silman I, Sussman JL, et al. (2010) Stereo-specific synthesis of analogs of nerve agents and their utilization for selection and characterization of paraoxonase (PON1) catalytic scavengers. Chem Biol Interact 187: 362–369.
- 55. Dumas DP, Caldwell SR, Wild JR, Raushel FM (1989) Purification and properties of the phosphotriesterase from Pseudomonas diminuta. J Biol Chem 264: 19659–19665.
- 56. Khersonsky O, Tawfik DS (2010) Enzyme promiscuity: a mechanistic and evolutionary perspective. Annual review of biochemistry 79: 471–505.
- 57. Raushel FM (2002) Bacterial detoxification of organophosphate nerve agents. Curr Opin Microbiol 5: 288–295.
- 58. Paggi RA, Martone CB, Fuqua C, De Castro RE (2003) Detection of quorum sensing signals in the haloalkaliphilic archaeon Natronococcus occultus. FEMS Microbiol Lett 221: 49–52.
- 59. Koerdt A, Godeke J, Berger J, Thormann KM, Albers SV (2010) Crenarchaeal biofilm formation under extreme conditions. PLoS One 5: e14104.
- 60. Zhang G, Zhang F, Ding G, Li J, Guo X, et al.. (2012) Acyl homoserine lactone-based quorum sensing in a methanogenic archaeon. ISME J.
- 61. Vieille C, Zeikus GJ (2001) Hyperthermophilic enzymes: sources, uses, and molecular mechanisms for thermostability. Microbiol Mol Biol Rev 65: 1–43.