Organophosphate Hydrolase Is a Lipoprotein and Interacts with Pi-specific Transport System to Facilitate Growth of Brevundimonas diminuta Using OP Insecticide as Source of Phosphate*

Organophosphate hydrolase (OPH), encoded by the organophosphate degradation (opd) island, hydrolyzes the triester bond found in a variety of organophosphate insecticides and nerve agents. OPH is targeted to the inner membrane of Brevundimonas diminuta in a pre-folded conformation by the twin arginine transport (Tat) pathway. The OPH signal peptide contains an invariant cysteine residue at the junction of the signal peptidase (Spase) cleavage site along with a well conserved lipobox motif. Treatment of cells producing native OPH with the signal peptidase II inhibitor globomycin resulted in accumulation of most of the pre-OPH in the cytoplasm with negligible processed OPH detected in the membrane. Substitution of the conserved lipobox cysteine to serine resulted in release of OPH into the periplasm, confirming that OPH is a lipoprotein. Analysis of purified OPH revealed that it was modified with the fatty acids palmitate and stearate. Membrane-bound OPH was shown to interact with the outer membrane efflux protein TolC and with PstS, the periplasmic component of the ABC transporter complex (PstSACB) involved in phosphate transport. Interaction of OPH with PstS appears to facilitate transport of Pi generated from organophosphates due to the combined action of OPH and periplasmically located phosphatases. Consistent with this model, opd null mutants of B. diminuta failed to grow using the organophosphate insecticide methyl parathion as sole source of phosphate.

Membrane-associated organophosphate hydrolase (OPH) 3 hydrolyzes the triester bond found in a variety of organophos-phate insecticides and nerve agents (1,2). The 39-kDa monomer requires Zn ϩ ions as cofactor (3). OPH is encoded by the opd (organophosphate degrading) gene found on dissimilar plasmids and the opd gene has recently been shown to be a part of an integrative mobilizable element (IME) (4). Due to the mobile nature of the opd island, identical opd genes are found among bacterial strains isolated from different geographical regions (4,5). Although its physiological substrate is unknown, OPH hydrolyzes paraoxon at a rate approaching the diffusion limit (k cat /K m 10 8 M Ϫ1 s Ϫ1 ) (6). Considering its catalytic efficiency and broad substrate range, it has been assumed that OPH has evolved to degrade organophosphate (OP) insecticides accumulated in agricultural soils (7). Structural analysis shows that OPH contains a TIM barrel-fold as seen in most of the members of amidohydrolase superfamily proteins (8).
OPH associates with cell membranes and membrane-associated OPH has been purified from a number of sources (3, 9 -13). Analysis of the amino acid sequences of OPH proteins indicates that all of them contain a predicted signal peptide harboring a well defined twin-arginine (Tat) motif. Twin-arginine signal peptides serve to target proteins to the twin-arginine protein transport (Tat) pathway, which translocates folded proteins across the bacterial cytoplasmic membrane (14). Proteinase K treatment confirmed that OPH is exported to the periplasmic side of the inner membrane in Brevundimonas diminuta and dependence on the Tat pathway was demonstrated because substitution of the invariant arginine residues of the Tat signal peptide affected both processing and localization of OPH (15). However, the mechanism by which OPH is anchored to the inner membrane and the physiological role of OPH are currently unclear. In this report we demonstrate that OPH is a lipoprotein and that it plays an essential role in the acquisition of phosphate from OP insecticides.

Experimental Procedures
Media, Strains, and Plasmids-Strains and plasmids used in the present work are shown in Table 1. Primers used for PCR amplification and site-directed mutagenesis are listed in Table  2. B. diminuta cultures were grown either in LB medium or in HEPES minimal medium. HEPES minimal medium was pre-pared by dissolving 0.2 g of KCl, 0.2 g of MgSO 4 ⅐7H 2 0, 40 mg of CaNO 3 ⅐4H 2 O, 80 mg of (NH 4 ) 2 HPO 4 , and 1 mg of Fe 2 SO 4 in 1 liter of 50 mM HEPES, pH 7.4. The medium also contained an essential amino acid mixture (0.07 mM), pantothenate (0.5 mg), vitamin B-12 (0.001 mg), and biotin (0.001 mg) along with sodium acetate (2%) as carbon source. The (NH 4 ) 2 HPO 4 was omitted when methyl parathion (0.6 mM) was used as sole phosphate source. When required, polymyxin (10 g/ml), chloroamphenicol (30 g/ml), or tetracycline (20 g/ml) were supple-mented to the growth medium. All chemicals used in this study were procured from Sigma, unless otherwise specified all restriction and other enzymes used in DNA manipulations were from ThermoScientific. Routine DNA manipulations were performed following standard procedures (16).
Carbonate and Urea Extraction-Total membrane preparations were made from B. diminuta following standard procedures (17). The cytoplasmic membrane was isolated by following the discontinuous sucrose gradient method described   (18) and equal amounts of membrane was resuspended in buffer containing different concentrations of sodium carbonate, pH 11.5, or urea (2-8 M as indicated). After a 1-h incubation at room temperature the samples were centrifuged at 227,226 ϫ g using a TLA 120.2 rotor (Beckman coulter) for 45 min to pellet the washed membranes. Detection of OPH in the wash supernatant and membrane fractions was achieved by Western blots using anti-OPH antibodies (15). The quantity of OPH in membrane and supernatant fractions were densitometrically determined by comparing with the OPH signal obtained with untreated membrane. Globomycin Treatment-The opd null mutant, B. dimimuta DS010 containing the plasmid pSM5 was grown in LB medium to mid-log phase (0.6 OD at 600 nm) and 50 g/ml of globomycin (Sigma) was added to the culture medium 1 h before the expression of OPH was induced by addition of 3 mM isopropyl ␤-D-galactopyranoside (IPTG) (19,20). After 6 h of induction, the culture was harvested, washed in SET buffer (500 mM sucrose, 5 mM EDTA, and 20 mM Tris-HCl, pH 8.0), and used to prepare periplasmic, cytosolic, and total membrane fractions as described previously (21,22). OPH-specific signals in the subcellular fractions were detected by performing Western blot analysis.
Generation of OPH C24S -The invariant cysteine residue in the lipobox motif of the OPH signal peptide was modified to serine by performing QuikChange TM site-directed mutagenesis (Stratagene). Plasmid pSM5 was used as template and the cysteine to serine codon substitution was confirmed by sequencing. The resulting plasmid coding for OPH C24S was designated pCSOPH. The B. diminuta DS010 (pCSOPH) cultures were grown to mid-log phase and the expression of OPH C24S was induced overnight by supplementation with 3 mM IPTG. The cells expressing OPH C24S were subsequently harvested, washed, and fractionated into periplasm, cytoplasm, and total membrane for the detection of OPH. A similar fractionation procedure was undertaken with B. diminuta DS010 (pSM5) to assess membrane anchorage of OPH in wild type cells.
Solubilization of OPH from the Inner Membrane-Inner membrane preparations were isolated from a 10-liter overnight culture of B. diminuta following procedures described elsewhere (18). The isolated inner membrane was resuspended in minimal amounts of buffer (20 mM Tris-HCl, pH 8.0, 150 mM NaCl, 2% glycerol) and after estimating the protein concentration the buffer volume was adjusted to give a final protein concentration of 5 mg/ml. Triton X-100 (2 g/g of protein), Triton X-114 (2 g/g of protein), n-dodecyl ␤-D-maltoside (DDM) (1 g/g of protein), and digitonin (8 g/g of protein) were separately added to aliquots of the membrane suspension and samples were incubated with gentle rotation (10 rpm) for 1 h at 4°C. Subsequently, the samples were subjected to ultracentrifugation (117,000 ϫ g) and the clarified supernatants, containing solubilized protein, were removed into prechilled tubes. The detergent-insoluble fraction was resuspended in an equal volume of buffer and the OPH activity was estimated in both detergent-soluble and detergent-insoluble fractions (3). The percent of OPH released from the membrane was calculated by comparing the total OPH activity associated with the untreated membrane. Subsequently, for identification of fatty acids attached to OPH, the protein was solubilized using 1.5% Triton X-100 as it disrupts interactions of OPH with other proteins and facilitates purification of OPH without interacting partners.
Affinity Purification of OPH and Identification of Fatty Acids-For purification of OPH-specific antibodies, 10 mg of pure OPH, purified as described elsewhere (23), was coupled to 400 l of CNBr-activated Sepharose TM 4B (GE Healthcare) following the manufacturer's protocol. Aliquots of OPH antisera (15) were passed through the OPH-coupled Sepharose column at a flow rate of 0.5 ml per min. The flow-through was collected carefully and reloaded onto the column to ensure complete binding of OPH-specific antibodies to the column. The unbound antibodies and serum proteins were removed by washing the column with 3 column volumes of wash buffer (20 mM Tris-HCl, pH 7.6). The bound anti-OPH antibodies were eluted (0.1 M glycine-HCl, pH 2.5) as 1-ml fractions into prechilled tubes containing 100 l of 1 M Tris-HCl, pH 9.0, to ensure quick neutralization of the eluate. The antibody fractions were then pooled and dialyzed against coupling buffer (10 mM sodium phosphate, pH 7.2, 150 mM NaCl).
For coupling to protein A/G beads, approximately 1 mg of purified anti-OPH antibodies were mixed with 500 l of protein A/G-agarose plus beads (ThermoScientific) equilibrated with coupling buffer and kept for 1 h at 4°C with gentle shaking. The contents were loaded onto a column and the excess unbound antibodies were removed by washing the column with 3 column volumes of coupling buffer. The anti-OPH antibodies bound to protein A/G-agarose beads were covalently linked by adding one column void volume of cross-linking buffer (10 mM sodium phosphate, pH 7.2, 150 mM NaCl), 2.5 mM disuccinimidyl suberate to the column. The column was left for 1 h at room temperature to complete cross-reaction and excess disuccinimidyl suberate was quenched by washing the column with 25 mM Tris-HCl, pH 7.6. The OPH-antibody cross-linked protein A/G-agarose beads were then taken into a clean tube and suspended in 1 ml of prechilled binding buffer (20 mM Tris-HCl, pH 7.6, 150 mM NaCl, 2% glycerol). Immediately, Triton X-100solubilized membrane proteins of B. diminuta were added to the beads and left overnight at 4°C with head to head rotation. After incubation the contents were loaded onto a column, washed thoroughly with wash buffer, and the bound proteins were then eluted with glycine-HCl, pH 2.5, prior to neutralization with 100 mM Tris-HCl, pH 9.0. About 100 g of immunopurified OPH was esterified using methanolic-HCl (24). The fatty acid methyl esters generated from OPH were then analyzed using Agilent GC/MS equipped with a quadrupole mass selective detector. Control samples were prepared from the periplasmic fraction of B. diminuta DS010 (pCSOPH) and treated identically to identify the fatty acid methyl esters.
Identification of the OPH Interactome-To identify interacting proteins, OPH was affinity purified using two different approaches. Before proceeding with the purification of OPH, the cell pellet collected from wild type B. diminuta was resuspended in PBS buffer (1 g/10 ml) before treatment with 25 mM formaldehyde (25, 26). The formaldehyde cross-linked cell pellet was sonicated (10 cycles of 20-s ON and 40-s OFF) and the membrane fraction was isolated following established procedures (27). The membrane pellet was extracted three times with 5 ml of chloroform:methanol (1:3) and the precipitated proteins were resolubilized in phosphate buffer (0.1 M phosphate buffer, pH 7.6, 350 mM NaCl, 5% glycerol, 1% DDM, and 50 mM imidazole). The first approach involved immunopurification using anti-OPH antibody cross-linked protein A/G-agarose beads. The resolubilized cross-linked OPH complex was passed through the column containing the antibody-linked beads at a flow rate of 0.5 ml/min. The flow-through was repeatedly passed through the column until negligible amounts of OPH was detected in the flow-through sample. After washing the column with 3 column volumes of wash buffer (20 mM Tris-HCl, pH 7.6, 150 mM NaCl, 2% glycerol, 0.1% DDM), the bound cross-linked OPH complex was eluted as described above, and subsequently analyzed both under native and denaturing conditions. Blue native-PAGE (28) and gel filtration (Superose 6, 10/300 GL, GE Healthcare) were performed to assess the molecular mass of the OPH complex. Tricine-PAGE (29) was performed to visualize polypeptides coeluting with OPH.
In an alternative approach, a deca-histidine-tagged OPH variant (OPH 10xHis ) was generated. To achieve this, a DNA fragment encoding 10 histidine residues was introduced into the opd gene, between nucleotide positions 420 and 426 that encodes amino acids in a loop region of OPH. First, a BamHI restriction site was introduced into opd by performing QuikChange mutagenesis between nucleotide positions 420 and 426 using plasmid pSM5 as template. Next, the synthetic DNA fragment encoding the 10 histidine residues was prepared as a BglII fragment and inserted in-frame into the opd gene at the generated BamHI site. The resultant plasmid was designated pOPH141HIS. Plasmid pOPH141HIS was mobilized into B. diminuta DS010, and B. diminuta DS010 (pOPH141HIS) cells were then induced to express OPH 10xHis by addition of IPTG at a final concentration of 3 mM. After incubation with IPTG for 5 h the cells were harvested and the cell pellet was resuspended in PBS buffer (1 g/10 ml) and treated with 25 mM formaldehyde to cross-link OPH. The formaldehyde crosslinked cell pellet was processed as described earlier to obtain total membrane pellet. The pellet was then extracted three times with 5 ml of chloroform:methanol (1:3) and the precipitated proteins were resolubilized before loading the soluble proteins onto a nickel-charged immobilized metal affinity chromatography (IMAC). Following washing with phosphate buffer, bound protein was eluted with 500 mM imidazole in phosphate buffer and analyzed both on blue native and Tricine-PAGE. The affinity purified OPH complexes were subjected to tryptic digestion and mass spectrometry (LTQ-Orbitrap XL ETD mass spectrometer) as described elsewhere (30) to establish the identity of OPH interacting proteins.
Bacterial Two-hybrid System-Protein-protein interactions were studied by the bacterial two-hybrid system (BACTH, Euromedex) following protocols described elsewhere (31). The T25 and T18 domains were separately fused to the N or C termini of the target proteins (OPH and PstS). The fusions were produced independently by cloning the opd and pstS genes in either pKNT25 or pUT18C. Cells of Escherichia coli strain BTH101 (Euromedex) were transformed with different combi-nations of fusion plasmids i.e. pUT18CPstS-pKNT25OPH and pUT18COPH-pKNT25PstS. The combinations pUT18CPstS-pKNT25 and pUT18COPH-pKNT25 served as controls. ␤-Galactosidase assay was performed as described elsewhere (32).
Pulldown Assay of Coexpressed Proteins-Interaction of OPH with a phosphate-binding protein, PstS, and a efflux pump component, TolC, was determined by performing coexpression pulldown assays (33). Initially, an opd gene variant engineered to code for OPH with C-terminal AviTag was generated. Two complementary oligos specifying the AviTag sequence (Avi-Tag-F and AviTag-R; Table 2) were annealed, digested with XhoI and HindIII, and cloned into similarly digested plasmid pSM5 to give plasmid pOPHV400, this procedure results in insertion of the AviTag coding sequence in-frame with opd. Next, the opd gene from plasmid pOPHV400 was excised as an EcoRI and HindIII fragment and cloned into one of the multiple cloning sites of pETduet1 vector that had been similarly digested. Subsequently, the birA gene was cloned as an NdeI and XhoI fragment into the second multiple cloning site of this construct. The cloning strategy places birA under control of the T7 promoter, allowing for regulatable expression of biotin ligase, the enzyme required to ligate biotin at the conserved lysine residue of the AviTag. The resulting pETduet1 derivative, designated pAVB400, codes for both OPH CAviTag and the biotin ligase. The pstS gene was amplified from B. diminuta and cloned initially in pET23b as an NdeI-XhoI fragment. The generated recombinant plasmid, pPST300, codes PstS C6His . After confirming expression of PstS C6His , pstS was amplified from pPST300 using primers PstSPMB-F and PstSPMB-R, respectively, and cloned into similarly digested pMMB206 to give plasmid pLPST300, which encodes PstS C6His controlled by the tac promoter of the vector. E. coli ArcticExpress cells harboring pAVB400 were transformed with pLPST300 and the expression of OPH CAviTag and PstS C6His was induced following standard procedures. The total cell lysate was prepared and the clear lysate was used to isolate OPH CAviTag and any interacting partners using streptavidin magnetic beads (Dynabeads M-280 Streptavidin, Invitrogen) following the manufacturer's protocols. The proteins bound to magnetic beads were analyzed by 12.5% SDS-PAGE and probed either with anti-OPH or anti-His antibodies to detect OPH CaviTag and PstS C6His . Cell lysates prepared either from ArcticExpress (pAVB400) or ArcticExpress (pLPST300) cells treated in a similar manner served as controls.
OPH-TolC Interactions-The tolC gene was amplified from B. diminuta and cloned as a BglII-EcoRI fragment into similarly digested pRSETA. As the cloning strategy facilitates in-frame fusion of the vector-specified His tag to tolC, the resulting recombinant plasmid, pTOLC400, codes for TolC N6His . Similarly, the opd gene was amplified from B. diminuta as an EcoRI-HindIII fragment and cloned into similarly digested pMMB206. The resulting recombinant plasmid, pTLOPH, codes for OPH without any affinity tag, expressed under control of the tac promoter. The TolC N6His and OPH were coexpressed by adding 1 mM IPTG to the mid-log phase cultures of ArcticExpress (pTLOPH400 ϩ pTOLC400). Similarly, the expression of TolC N6His and OPH were induced from ArcticExpress (pTLOPH400) and ArcticExpress (pTLOPH400) cells before preparing clear lysate (4 ml) from 50 ml of culture. The lysate was then incubated overnight with 20 l of MagneHis beads (Promega) at 4°C with constant mixing. After incubation, the beads were collected and washed following the manufacturer's protocol and the presence of TolC N6His and OPH were detected by performing immunoblots probed either with anti-OPH or anti-His antibodies.

OPH Is Tightly Bound to the B. diminuta Inner Membrane-
It has previously been demonstrated that OPH is associated with the inner membrane of B. diminuta (15). To probe the nature of the interaction of OPH with the membrane, we first determined whether the protein could be released from membrane fractions following washing under alkaline conditions using sodium carbonate (Fig. 1A), or under strong denaturing conditions in the presence of urea (Fig. 1B). At concentrations of sodium carbonate normally used to extract peripheral membrane proteins (0.1-0.5 M) (34), very little OPH was released from the membrane, suggesting a relatively tight association with the bilayer. However, at higher concentrations of carbonate, significant levels of OPH were released (Fig. 1A). Likewise the protein was also relatively refractory to extraction by urea, with most of the protein remaining associated with the membrane fraction even in the presence of 8 M urea (Fig. 1B). This behavior is consistent with OPH being an integral protein of the inner membrane rather than associating with the membrane by electrostatic interaction or through binding to other inner membrane proteins.
OPH Is a Lipoprotein-The Tat system is known to assemble some membrane-anchored proteins (20,35,36). In bacteria these usually have either a single transmembrane domain at the C terminus (35) or an N-terminal non-cleaved twin-arginine signal anchor sequence (37). However, bioinformatic analysis supported by structural studies show that OPH has no C-terminal hydrophobic helical domain (38) and the N-terminal signal peptide of OPH is cleaved off during biosynthesis and therefore cannot serve as a signal anchor (15).
A third class of bacterial membrane proteins that are known to be assembled by the Tat pathway is lipoproteins (20,39,40).  In silico analysis of the OPH signal peptide, shown in Fig. 2A, predicts the existence of both signal peptidase II (SpaseII) and multiple signal peptidase I (SpaseI) cleavage sites in pre-OPH, with the SpaseII cleavage site predicted with the highest level of confidence. In addition to the predicted SpaseII cleavage site, a well conserved lipobox containing a cysteine residue was found in the c-region of the signal peptide ( Fig. 2A). To determine whether OPH was a substrate of SpaseII, we treated cells of B. diminuta DS010 (pSM5) with globomycin, which inhibits processing of the prolipoprotein by binding irreversibly to the peptidase (20,41). In support of the in silico prediction, in the globomycin-treated cultures most of the OPH accumulated in the cytoplasmic fraction in an unprocessed form (Fig. 2B, lane 1). This is in contrast with the untreated cells where very little precursor was detectable (Fig. 2B, lane 2). Moreover, there was substantially less mature OPH detectable in the membrane fraction following globomycin treatment (Fig. 2B, lane 3).
To provide additional evidence that OPH is a lipoprotein, we generated a serine substitution of the essential cysteine in the OPH signal sequence lipobox (OPH C24S ) and compared the subcellular location of this variant to that of the wild type protein (Fig. 2, C and D). Unlike the wild type protein where the mature form is found in the membrane fraction (Fig. 2C), most of the processed form of OPH C24S was found in periplasm, with very little seen in the membrane (Fig. 2D). Because SpaseII acts only on acylated prolipoproteins to generate S-lipidated cysteine at the N terminus of the mature protein (42), it is assumed that the mature-sized form of OPH C24S found in the periplasmic fraction results from processing by SpaseI ( Fig. 2A), which is predicted bioinformatically to recognize this signal peptide ( Fig. 2A). Taken together these results demonstrate that OPH is a membraneanchored lipoprotein.

Mature OPH Is Linked to Myristic and Oleic Fatty Acids-
Previous findings have shown that generally diacyl glycerol serves as a lipid anchor for membrane-associated lipoproteins (43). To confirm the nature of the lipid anchor on membranebound OPH and to identify the fatty acid modifications, we extracted fatty acids from affinity purified OPH and OPH C24S (as a negative control) using methanolic HCl extraction (24). The fatty acid methyl esters generated due to transesterification were extracted and analyzed using GC-MS. As shown in Fig. 3, A and B, two novel peaks were identified arising from the mOPH purified from B. diminuta membranes, which were not observed in the control sample derived from OPH C24S . These two peaks corresponded to methyl myristate (C14:0) and methyl oleic acid (C18:1) with 97 and 99% identities (Fig. 3,  C-F). These results demonstrate that OPH is anchored to the membrane through diacylglycerol, which is linked with myristic and oleic groups.
OPH Interacts with Phosphate ABC Transporter-To gain further clues about the physiological role of OPH, we next sought to identify whether it interacted with other cellular proteins. First we developed a strategy to purify OPH in its native state by dispersing the membrane fraction with the non-ionic detergents Triton X-114, DDM, and digitonin. Of the three detergents, DDM facilitated the best release of OPH (liberating ϳ70% of total OPH; data not shown).
Next, we developed a strategy to purify DDM-solubilized OPH. In the crystal structure of OPH the C-terminal region is exposed (38), and we therefore constructed a strain of B. diminuta producing OPH with a C-terminal His 6 tag. However, the DDM-solubilized OPH C6His failed to bind the nickelnitrilotriacetic acid column, suggesting that the C terminus of OPH is not able to interact with the affinity matrix, possibly due to masking of this region by a partner protein subunit. To resolve this problem, we again used the crystal structure of OPH as a reference to introduce an internal His 10 tag internally into a loop region of OPH. This variant, designated OPH 10xHis , bound well to the nickel-affinity matrix following solubilization from the membrane. The affinity-purified OPH 10xHis sample was further analyzed both by BN-PAGE and gel filtration. These two independent experiments both suggested that OPH 10xHis was present in a complex of around 294 kDa (Fig. 4,  A and B). Assuming that the detergent used to solubilize OPH from the membrane may interfere with the determination of an accurate molecular mass for the OPH complex, the isolated membranes from the formaldehyde-treated B. diminuta DS010 (pOPH141HIS) cells were extracted with chloroform:methanol (1:3) to delipidate the sample and the resulting membrane protein precipitate was resolubilized before proceeding with affinity purification of the cross-linked OPH complex. BN-PAGE analysis of the OPH complex isolated in this way coincided with the mass of the OPH complex purified from detergent-solubilized membranes (compare Fig. 4, B with C, lane 3).
To validate these findings we employed a second, independent approach to purify untagged OPH. The membranes isolated from the formaldehyde cross-linked B. diminuta wild type cells were extracted with chloroform:methanol (1:3) and the resolubilized membrane proteins were passed through a protein A column that had been cross-linked with OPH-specific antibodies. The size of the OPH complex obtained following this purification process coincided with the BN-PAGE profile of the OPH complex purified following nickel-affinity column (IMAC) (Fig. 4C, lane 3). We therefore conclude that OPH is present in an ϳ293 kDa complex.
The delipidated OPH complexes purified by immunoaffinity and IMAC were analyzed by Tricine-SDS-PAGE. It can be seen (Fig. 4D) that several protein bands with similar sizes are common between the two samples, although bands with apparent masses of 38, 35, and 15 kDa are more intense in the immunopurified OPH complex. The 35-kDa protein coincided with the size of OPH and its identity was also established by performing a Western immunoblot with anti-OPH antibodies (Fig. 4D). After establishing that OPH is a multiprotein complex, we performed mass spectrometry to obtain unique peptide sequences from proteins copurifying with OPH following IMAC. The obtained peptide sequences were identified using either x!tandem or Mascot web servers. Proteins that matched with more than two peptide sequences are listed in Table 3. From the list of proteins, subunits of the F 1 F o -ATP synthase (␣, ␤, ␥), the phosphate ABC transporter substrate-binding protein (PstS) and efflux pump components AcrB and TolC were identified as candidate OPH interacting partners (Table 3). It is interesting to note that the identified peptides matched with proteins involved either in phosphate uptake (44) or in effluxing of xenobiotics (45), as organophosphates are xenobiotics that also contain a potential source of phosphate.
OPH Interacts with Phosphate-specific Transport Component PstS-As PstS is a periplasmic protein that binds specifically to inorganic phosphate, we chose to further probe potential interaction of OPH with PstS. Initially we undertook bacterial twohybrid analysis to assess OPH-PstS interactions. When PstS was fused to the C terminus of the adenylate cyclase T18 fragment and OPH to the N terminus of the T25 fragment, adeny-late cyclase activity was reconstituted, and strong ␤-galactosidase activity could be measured (Fig. 5A). A similar strong interaction was also seen when OPH was fused to the C terminus of the adenylate cyclase T18 fragment and PstS to the N terminus of the T25 fragment. To confirm that OPH and PstS directly interact, we performed coexpression pulldown assays. To this end we generated compatible plasmids coding for OPH CAviTag (pAVB400) and PstS N6His (pPST300). In addition, plasmid pAVB400 also codes for the biotin ligase, BirA, to facilitate ligation of biotin at the conserved lysine residue of AviTag found at the C terminus of OPH CAviTag . After inducing the production of OPH CAviTag , PstS N6His , and biotin ligase in the heterologous host E. coli, streptavidin-linked beads were used to isolate biotinylated OPH CAviTag . As shown in Fig. 5B, PstS N6His copurified with the biotinylated OPH CAviTag (Fig. 5B,  lane 4), but was not purified by the streptavidin-linked beads in the absence of OPH CAviTag (Fig. 5B, lane 6), providing conclusive proof that OPH and PstS are interaction partners.
Efflux Pump Component TolC Interacts with OPH-Analysis of the OPH interactome indicated that efflux pump components AcrA, AcrB, and TolC also copurified with OPH isolated from B. diminuta (Table 3). We next sought to assess whether there was a direct interaction between OPH and any of these three proteins by heterologous expression and pairwise copurification studies. Unfortunately, we were unable to express B. diminuta AcrA and AcrB in E. coli. However, TolC with an N-terminal His tag was successfully produced in the E. coli Arc-ticExpress strain. We therefore coexpressed untagged OPH along with TolC N6His and isolated TolC N6His from total cell lysates using MagneHis beads. Fig. 5C shows that when TolC N6His was affinity purified, the mature form of OPH was also copurified (Fig. 5C, lane 4). Because OPH produced in the absence of TolC N6His was unable to interact with the beads (Fig.  5C, lane 6), it can be concluded that OPH and TolC can directly interact with each other.
OPH Supports B. diminuta Growth with Methyl Parathion as Sole Phosphate Source-The enzymatic action of OPH generates alkyl phosphates from a variety of organophosphate insecticides due to its triesterase activity (3). These diesters, like diethyl phosphate, may serve as substrates for periplasmically located phosphatases/diesterases, ultimately generating inorganic phosphate (P i ), raising the possibility that interaction of OPH with PstS facilitates the transport of generated inorganic phosphate into the cell. To examine this further, we investigated the ability of B. diminuta to grow in minimal medium using the OP insecticide methyl parathion as sole source of phosphate. As shown in Fig. 6, B. diminuta DS010 alone was unable to grow using methyl parathion as phosphate source, but when carrying plasmid pSM5, encoding OPH, good growth was seen. These results show that OPH is required to support growth using organophosphates as a source of phosphate.

Discussion
In this study we have investigated the interaction of the organophosphate hydrolase, OPH, from B. diminuta, with the cytoplasmic membrane and with other cellular proteins. Our work has clearly shown that OPH is a lipoprotein, and adds to a growing list of Tat-dependent lipoproteins in bacteria and archaea (20,44,47,48). Interestingly, OPH contains an alanine residue at the ϩ2 position and according to the sorting rules for E. coli lipoproteins (42) should be translocated to the outer  The other components of the ABC-type phosphate acquisition system (PstA, PstB, and PstC) for which PstS is the periplasmic binding protein are also shown. Entry of the model OP compound to periplasm (1) and its OPH-mediated hydrolysis (2) generate alkyl phosphate and p-nitrophenol. P i is generated through the action of periplasmically located phosphatases/diesterases (3), which binds to PstS (4) and is transported into the cytoplasm by the phosphate-specific transport system (5). OM, outer membrane; P, periplasm; IM, inner membrane. membrane by the Lol machinery (the genes for which are found in the genome of B. diminuta). However, a number of exceptions to these sorting "rules" have been seen in other Gramnegative bacteria, for example, in Pseudomonas aeruginosa where lipoproteins having lysine, glycine, and glutamine at the ϩ2 position remain attached to the inner membrane (49). It appears for B. diminuta an alanine at the ϩ2 position also permits inner membrane retention.
Copurification studies using two independent approaches showed that OPH was present as a large multiprotein complex that includes other inner membrane proteins such as a predicted PhoR-like histidine kinase, periplasmic proteins such as PstS, and outer membrane proteins TolC and AcrA. Further support for an OPH complex was provided by demonstrating a direct interaction between OPH and PstS, and between OPH and TolC. Growth studies showed that the indirect liberation of organic phosphates from methyl parathion mediated by OPH can support growth with this compound as the sole phosphate source. These findings point to a potential model whereby the triesterase activity of OPH generates phosphodiesters from a variety of OP insecticides, which are converted to inorganic phosphates by periplasmically located phosphatases (Fig. 7). The PstS protein, identified here as an interacting partner of OPH, is a known component of an established phosphotransfer system (44), and it binds to inorganic phosphate, facilitating its transport across the inner membrane. During OPH-mediated hydrolysis of OP insecticides, in addition to alkyl phosphates, aromatic compounds like p-nitrophenol are also generated. Products such as p-nitrophenol are more toxic than the parent compounds and if they are not quickly metabolized they need to be effluxed for the survival of the organism. In this context, OPH interactions with efflux pumps may serve to quickly eliminate toxic degradation products from the intracellular environment.
Author Contributions-S. P., H. P., and A. N. performed the experiments. T. P. and D. S. conceived the idea and drafted the manuscript.