Structural basis for the broad specificity of a new family of amino-acid racemases
aCentro de Biología Molecular `Severo Ochoa', Universidad Autónoma de Madrid–Consejo Superior de Investigaciones Científicas (CSIC), 28049 Madrid, Spain, bDepartment of Crystallography and Structural Biology, Instituto de Química-Física `Rocasolano'–CSIC, 28006 Madrid, Spain, cCentro Nacional de Biotecnología–CSIC, 28049 Madrid, Spain, dDivision of Infectious Diseases, Brigham and Women's Hospital and Department of Microbiology and Immunobiology, Harvard Medical School and HHMI, Boston, MA 02115, USA, and eDepartment of Molecular Biology and Laboratory for Molecular Infection Medicine Sweden, Umeå Centre for Microbial Research, Umeå University, Umeå, Sweden
*Correspondence e-mail: firstname.lastname@example.org, email@example.com
Broad-spectrum amino-acid racemases (Bsrs) enable bacteria to generate noncanonical D-amino acids, the roles of which in microbial physiology, including the modulation of cell-wall structure and the dissolution of biofilms, are just beginning to be appreciated. Here, extensive crystallographic, mutational, biochemical and bioinformatic studies were used to define the molecular features of the racemase BsrV that enable this enzyme to accommodate more diverse substrates than the related PLP-dependent alanine racemases. Conserved residues were identified that distinguish BsrV and a newly defined family of broad-spectrum racemases from alanine racemases, and these residues were found to be key mediators of the multispecificity of BrsV. Finally, the structural analysis of an additional Bsr that was identified in the bioinformatic analysis confirmed that the distinguishing features of BrsV are conserved among Bsr family members.
In nature, the majority of D-amino acids (DAA) are found in bacterial cell walls, where D-Ala and D-Glu are key constituents of the short peptides that cross-link the glycan chains within the peptidoglycan (PG) polymer (Vollmer et al., 2008). These DAA are produced from their corresponding L-enantiomers by highly specific alanine and glutamate amino-acid racemases (Alr and MurI), which have distinct structural and catalytic properties (Cava, Lam et al., 2011). Alr (EC 184.108.40.206), which is the best characterized of these enzymes, is a cytoplasmic protein that requires the ubiquitous coenzyme pyroxidal-5-phosphate (PLP) as a cofactor (Richard et al., 2009). Crystallographic studies of Alr from diverse organisms have enabled the identification of the structural determinants and spatial constrains that account for its mono-specificity (Couñago et al., 2009; LeMagueres et al., 2003, 2005; Noda et al., 2004; Shaw et al., 1997; Strych & Benedik, 2002; Wu et al., 2008).
Recently, we demonstrated that diverse bacteria produce and release to the extracellular medium high amounts of DAA that are not canonical components of the cell wall (e.g. D-Ala and D-Glu; Cava, de Pedro et al., 2011; Lam et al., 2009). In Vibrio cholerae, the production of these noncanonical DAA (NCDAA) is dependent upon BsrV (VC1312), a periplasmic broad-spectrum racemase (Bsr) with high sequence homology (E-value of 1 × 10−25, 28% identity) to the primary alanine racemase of V. cholerae, AlrV (VC0372; Fig. 1a and Supplementary Fig. S1a1 Lam et al., 2009). A subset of Alr-related racemases from other organisms have also been reported to accept multiple amino-acid substrates (Kino et al., 2007; Lam et al., 2009; Matsui & Oikawa, 2010; Wu et al., 2008). In V. cholerae, the presence of NCDAA negatively regulates cell-wall metabolism, at least in part owing to their incoporation into PG (Cava, de Pedro et al., 2011; Cava, Lam et al., 2011; Lam et al., 2009). NCDAA have also been reported to influence biofilm stability (Kolodkin-Gal et al., 2010), virulence (Anfora et al., 2007) and sporulation (O'Connor & Zusman, 1997). Susceptibility to NCDAA seems to be more widespread than production of NCDAA, raising the possibility that some bacteria may produce and release NCDAA in order to influence nonproducing species within the same habitat (Cava, de Pedro et al., 2011; Horcajo et al., 2012). Given the important adaptative properties provided by NCDAA, a detailed investigation of multi-specific racemases will be critical to understand NCDAA-controlled processes and for the development of new drugs to combact pathogenic bacteria (Conti et al., 2011).
Here, we explore the capacity of BsrV to utilize a wide variety of substrates using a combination of structural, biochemical, mutational and bioinformatic approaches. Finally, we also define and experimentally validate a molecular footprint of conserved residues that mediate the multispecificity of BrsV and use this signature sequence to identify a large family of BsrV-like multi-specific racemases in bacteria.
All V. cholerae strains used in this study were derived from the sequenced El Tor clinical isolate N16961 (Heidelberg et al., 2000). Plasmids and primers, growth conditions and standard molecular-biology techniques are described in the Supporting Information.
All racemase assays were performed in two fundamental steps: (i) the racemase reaction and (ii) the DAAO reaction coupled to peroxidase and 2,3-diaminophenazine or Marfey's (FDAA) derivatization (Fig. 1b). The formation of the colorimetric product was measured at 492 nm (see Supporting Information). The steady-state kinetics parameters were determined using Microsoft Office 2007 and Solver Macro (De Levie, 2001; see Supporting Information). For competition assays, FDAA derivatization of L and D forms of amino acids and HPLC analysis was performed (see Supporting Information).
Crystallization of BsrV, an R173N174/AA point mutant (ΔCl-BsrV), Aeromonas hydrophila Alr3 (a putative Bsr, renamed BsrAh) and the putative primary alanine racemase from A. hydrophila (AlrAh) was performed using a high-throughput NanoDrop ExtY robot (Innovadyne Technologies Inc.) and the commercial Qiagen screens The JCSG+ Suite and The PACT Suite and the Hampton Research screens Index, Crystal Screen and Crystal Screen 2 following the sitting-drop vapour-diffusion method (see Supporting Information). X-ray data collection was performed at a synchrotron-radiation facility on beamlines ID29 and ID14-4 at the ESRF, Grenoble, France or on the X06SA beamline at SLS, Villigen, Switzerland (see Supporting Information). Data sets were collected using a PILATUS 6M or a Q315r ADSC X-ray detector, and were processed using XDS (Kabsch, 2010) and scaled using SCALA (Evans, 2006) from the CCP4 suite (Winn et al., 2011). The structure was solved by the molecular-replacement method with MOLREP (Vagin & Teplyakov, 2010) from the CCP4 suite and was refined with PHENIX (Adams et al., 2010) and manually improved using Coot (Emsley & Cowtan, 2004; see Supporting Information). The stereochemistry of the models was verified using MolProbity (Chen et al., 2010).
The identification of new putative broad-spectrum racemases and the residues responsible for substrate specificity was performed by searching with BLAST (Altschul et al., 1997) against a nonredundant protein database and filtering, selecting only those mapped onto the UniProt database. The protein data set was aligned using MUSCLE (Edgar, 2004; v.3.8.31). The resulting multiple sequence alignment was filtered using the Jalview (Waterhouse et al., 2009) tool (v.2.7). The identification of specificity-determining positions (SDPs) was carried out using the JDet package (see Supporting Information).
The atomic coordinates and structure factors for BsrV, ΔCl-BsrV mutant, BsrAh and AlrAh (PDB entries 4beu , 4beq , 4bf5 and 4bhy , respectively) have been deposited in the Protein Data Bank, Research Collaboratory for Structural Bioinformatics, Rutgers University, New Brunswick, New Jersey, USA (http://www.rcsb.org/ ).
Comparisons of the substrate specificities of BsrV and AlrV, the presumed alanine-specific racemase from V. cholerae, revealed that BsrV is able to utilize a much broader range of substrates (Figs. 1b, 1c and 1d). Unlike AlrV, which only catalyzes the interconversion of L-Ala and L-Ser and their corresponding D forms (Fig. 1c and Supplementary Fig. S1b), BsrV reversibly racemizes ten of the 19 natural chiral amino acids known, including both non-β-branching aliphatic amino acids (Ala, Leu, Met, Ser, Cys, Gln and Asn) and positively charged amino acids (His, Lys and Arg) (Fig. 1d and Supplementary Figs. S1c and S1d). Additionally, it catalyzes the racemization of several amino acids that are not typically incorporated into proteins (Supplementary Fig. S1e). However, BsrV did not alter the chirality of negatively charged (i.e. Glu and Asp) or aromatic (i.e. Tyr, Trp and Phe) amino acids and displayed minimal activity towards β-branched aliphatic (i.e. Ile, Val and Thr) potential substrates (Fig. 1d).
Kinetic analyses, using individual and pooled substrates, were also performed in order to better characterize the activities of BsrV and AlrV. Most analyses were performed using the His-tagged mature proteins used in structural studies because control assays performed with untagged mature BsrV showed that the affinity tag did not alter the activity of the enzyme (Supplementary Fig. S1f). The kinetic analyses revealed that the catalytic efficiency of BrsV (as reflected by kcat/Km) varies depending upon the amino-acid substrate and suggest that it acts more readily upon lysine, arginine and methionine than upon other substrates (Table 1). Assays using pooled substrates largely confirmed this idea: BsrV incubated with its ten potential L-amino-acid substrates efficiently formed D-Arg and D-Lys, but produced lower amounts of other DAA than when they were assayed singly (Supplementary Figs. S1g and S1h). Consequently, the high production of D-Met and D-Leu by V. cholerae in vivo (the principal products of BrsV; Lam et al., 2009) is likely to reflect the relatively high availability of the corresponding L-amino acids.
Comparative analyses of BsrV and AlrV reaction kinetics revealed that the average kcat of BsrV is higher than that of AlrV. However, the Km values for BsrV were also around tenfold higher than the Km of AlrV for alanine, its preferred substrate, and consequently kcat/Km for alanine racemization by AlrV is higher than that of BsrV for its substrate amino acids (Table 1). These facts fit well with the proposal that the development of catalytic multi-specificity is often accompanied by a reduction in kinetic performance (Babtie et al., 2010; Khersonsky et al., 2006).
Purified BsrV was crystallized and its structure was solved at atomic resolution (1.15 Å; Table 2). As observed for monospecific Alrs, BsrV folds as a globular homodimeric enzyme in which both monomers participate in the elaboration of the active sites (Fig. 2a). Analyses using the DALI server (Holm & Rosenström, 2010) indicate that the closest structural homologues of BsrV are alanine racemases from Bacillus anthracis (AlrBax; Couñago et al., 2009; r.m.sd. of 2.0 Å for 361 Cα atoms) and E. coli (AlrEc; Wu et al., 2008; r.m.s.d. of 2.5 Å for 347 Cα atoms). Since the crystallization of AlrV was unsuccessful, further comparative analyses of BsrV were performed with AlrEc (E-value of 3 × 10−157 to AlrV; Supplementary Fig. S1a). Superimposition of the BsrV and AlrEc structures readily reveals their extensive similarity; nonetheless, substantial differences are also apparent (Fig. 2b and Supplementary Figs. S2 and S3).
The entry channel to the catalytic site is approximately twofold wider in BsrV than in AlrEc (roughly 10 × 14 Å in BsrV compared with 7 × 9.5 Å in AlrEc; Fig. 2b and Supplementary Figs. S2b and S2c). This difference is a direct consequence of shorter loops in the side walls of the catalytic entry site in BsrV and of the different orientation of helix α10 (Fig. 2b and Supplementary Figs. S2b and S2c). In addition, the catalytic entry site has a negative charge in BsrV but not in AlrEc (Supplementary Fig. S2d), perhaps impeding the entry of acidic substrates into the catalytic site and thereby contributing to the selectivity of BsrV for neutral and basic amino acids. BsrV also contains a wider tunnel connecting the entry to the catalytic centre (the narrowest width of the BsrV tunnel is 9.0 Å compared with 6.3 Å in AlrEc).
The structure of BrsV also differs from that of AlrEc owing to the presence of an additional structural element formed from the sequence at the N-terminus of the protein (residues 24APLHIDT30). These amino acids fold into a stable, hinge-like complementary structure between monomers that shifts their relative positions (Figs. 2b and 2c). In BsrV monomers, the relative positions of the N-terminal domain (residues 24–279) and the C-terminal domain (residues 280–410) are offset by a 9° rotation compared with the equivalent domains in AlrEc (Fig. 2c), and an average displacement of 1.5 Å for the whole protein backbone is observed. Consequently, there are dramatic differences between the disposition and conformation of the active sites of BrsV and those of AlrEc (e.g. an increased distance between active sites from 37.6 Å in Alr to 45 Å in BsrV; Fig. 2c, right). The N-terminal structure of BrsV appears to be important for the activity of the enzyme, since a single mutation in this structure (P25E; Fig. 2b and Supplementary S3a) completely abolishes the activity of BrsV towards Ala and Met and dramatically impairs (70% reduction) its activity towards Arg.
In addition to the differences between the relative positions of protein domains in BsrV and AlrEc, comparative structural analyses revealed significant differences between the catalytic centres of the two enzymes. Notably, the enzymes use different means to position their PLP cofactor (Fig. 3a and Supplementary Fig. S3b). In BsrV, a Tyr residue that is conserved among Alrs and is typically involved in coordination of the phosphate moiety of PLP is replaced by a proline residue (Pro391), thereby enlarging the space within the active site. Phosphate coordination in BsrV instead depends on Ser245 and Tyr208 and a network of interactions mediated by water molecules (Fig. 3a and Supplementary Fig. S3b). No differences are observed in the stabilization of the pyridoxal ring, where Arg260 stabilizes the N atom of the ring through its N∊ atom (2.82 Å).
The active site of BrsV also lacks an N-carboxylated lysine (Kcx) that in AlrEc and most alanine racemases stabilizes an arginine involved in substrate binding within the active site (Watanabe et al., 2002). In BsrV, Kcx is replaced by Ala165 and the substrate-binding Arg (Arg173) is then stabilized in the active site by the presence of an ion (Fig. 3a and Supplementary Figs. S3b and S3c). Its tetracoordination (with one water molecule at 3.28 Å, the Nδ2 atom of Asn174 at 3.58 Å, the N∊ atom of Arg173 at 3.67 Å and the Nη2 atom of Arg173 at 3.61 Å) and low B factor suggested that it was chloride (Cl−; Fig. 3a and Supplementary S3c). A Cl− ion has also been found in the monospecific alanine racemase AlrBax; however, unlike in BsrV, coordination of Cl− in AlrBax is mediated by the same residues that interact with Kcx in AlrEc and other enzymes that contain Kcx (Couñago et al., 2009). Furthermore, the position occupied by Asn174 in BsrV (Fig. 3a) contains hydrophobic residues (Leu and Ile) in AlrEc, AlrBax and other monospecific Alrs. Collectively, these analyses provide strong evidence that the presence of a negative charge near the catalytic residue is critical for amino-acid racemization by these enzymes; however, they also illuminate the differing catalytic environments in the active sites of enzymes with distinct specificities.
The relevance of the Cl− to BsrV activity was further investigated by the structural and biochemical characterization of a BsrV R173N174/AA point mutant (ΔCl-BsrV). As expected, analysis of the crystal structure of ΔCl-BsrV (Table 2 and Fig. 3b) revealed that the Cl− was absent. However, the structure of ΔCl-BsrV was otherwise very similar to that of BsrV; the only minor changes observed were in the side chains of Tyr208 and His204 (Fig. 3b). As anticipated, ΔCl-BsrV had a highly reduced or no ability to racemize most amino acids (Fig. 3c and Supplementary Figs. S3d and S3e), consistent with Cl− and Arg173 serving to replace Kcx in stabilizing a variety of substrates in the active site of BsrV.
We hypothesized that the basis for the broad substrate tolerance of BsrV might be recognizable through sequence analysis and therefore searched for a molecular footprint of residues that are conserved among BsrV-like enzymes and differ from those found in monospecific alanine racemases. To initiate this analysis, a representative, nonredundant, set of PLP-dependent amino-acid racemase sequences (Alr and Bsr) from different bacteria were collected and aligned. Multiple sequence alignment (MSA; see §2) revealed differential conservation patterns that allowed clustering of proteins into three subfamilies (Fig. 4a). Subfamily 1 (in red) is composed of 84 proteins and includes AlrV, AlrEc and Alr2 (DadB) from E. coli, which have been experimentally confirmed as alanine-specific racemases (Fig. 1c; Faraci & Walsh, 1988; Lam et al., 2009). Subfamily 2 (in blue) is comprised of 13 proteins, including BsrV (Alr2 from V. cholerae). Of the remaining 39 proteins in the data set, 24 proteins were grouped as subfamily 3 (in green). The 15 outlier proteins (in black) could not be assigned to any of the subfamilies (Fig. 4a). Based on the grouping of the characterized racemases, we assumed that the proteins in subfamily 1 are monospecific alanine racemases, while the proteins in subfamily 2 have a broader substrate spectrum. As no member of subfamily 3 or any of the 15 outlier proteins has been biochemically characterized, these proteins were not considered for further sequence analysis.
Further comparative analyses of subfamilies 1 and 2 (see Supporting Information) enabled the prediction of an initial set of 31 specificity-determining positions (SDPs) that appeared to typify the specific and broad-spectrum racemase subfamilies. After additional refinement with manual inspection of each potential SDP, this approach allowed the selection of 16 sites within these enzymes that appear to constitute a molecular footprint that can be used to distinguish alanine and broad-spectrum racemases (Fig. 4b; discussed further below). Mapping of the broad-spectrum-linked amino-acid loci to the BsrV structure revealed that these amino acids affect or reside within features that distinguish BsrV from AlrV, including placement of the entry sites (Arg119 and Arg121), the size of the catalytic entry site (Pro206, Tyr208, Lys216 and Tyr246) and the catalytic machinery (Cys70, Ala165, Asn167, Gly169, Asn174, Gly263, Asn348, Thr349 and Pro391; see Fig. 5h). Notably, specificity determinants were not found within the N-terminal extension of BsrV, although all of the putative broad-spectrum enzymes appear to possess this signature in the mature protein (relative to Alrs) as well as a putative signal sequence (Supplementary Table S3).
An expanded data set containing 2540 putative PLP racemases was similarly grouped into subfamilies and the identities of these families were determined based on the enrichment of proteins described as `broad-spectrum' or `specific' racemases in the previous analysis (see Supplementary Material). This strategy resulted in the identification of 74 BsrV-like racemases that had probably been mis-annotated previously as being specific racemases. Intriguingly, most Bsr candidates are found in Gram-negative marine bacteria, primarily (54.5%) in members of the Vibrionaceae family (Supplementary Table S4).
To validate our in silico identification of putative broad-spectrum racemases, we performed biochemical and structural characterization of A. hydrophila Alr3 (a putative Bsr, renamed BsrAh) and the putative primary alanine racemase of A. hydrophila (AlrAh), which were identified from the `broad-spectrum' and `specific' subfamilies, respectively (Figs. 4a and 4c, Table 2 and Supplementary Fig. S4 and Table S4). As predicted, structural comparison revealed that AlrAh and BsrAh differ in a manner analogous to that seen for BsrV and AlrEc (Supplementary Fig. S4), and BsrAh exhibits all of the distinguishing structural features of BsrV [i.e. Cl− instead of Kcx, a wider entry channel (shorter flanking loops) for the catalytic site, an N-terminal hinge-like extension and conserved signature residues; Fig. 4c and Supplementary Figs. S4d–S4h]. BsrAh also resembles BsrV in its ability to discriminate between amino-acid substrates and displayed catalytic activity against an identical subset of natural amino acids (Supplementary Figs. S4i and S4j). Therefore, the distinct subfamilies of racemases evident in bioinformatic analyses appear to comprise a functionally distinct subset of amino-acid racemases with broad substrate specificity.
3.7. Molecular modelling of the docking of diverse amino-acid substrates within the BsrV and AlrBs active sites
To unveil the structural determinants that influence substrate stabilization in specific and broad-range racemases, we took advantage of the crystal structure of B. stearothermophilus alanine racemase (AlrBs) in complex with N-(5′-phosphopyridoxyl)-D-alanine (PLP-D-Ala; Watanabe et al., 2002; PDB entry 1l6g ) as the reference since this structure mimics the enzyme–substrate catalytic intermediate. We superimposed AlrBs in complex with PLP-D-Ala on BsrV and substituted the alanine analogue by all of the different kinds of amino-acid substrates, selecting the most stable conformation in each case (Figs. 5a–5f). Whilst AlrBs could only accommodate alanine and serine (not shown) in its catalytic site (Figs. 5b, 5d and 5f and Supplementary Table S5b), the BsrV catalytic pocket appears to accommodate all ten amino acids found to be racemized by this enzyme (Figs. 5a, 5c and 5e). Furthermore, in full agreement with the substrate specificity of BsrV, the remaining nine amino acids present multiple steric clashes when forced to fit into the active site of the enzyme (Supplementary Fig. S5a).
The docking analysis supported two overlapping mechanisms for amino-acid stabilization by BsrV: one for aliphatic residues and another for basic amino acids. Aliphatic amino acids (Ala, Ser, Cys, Leu, Gln and Met) are likely to be stabilized in the active site of BrsV through polar interactions between their carboxylate moiety and Arg173, Tyr299′ and Tyr318′, in a similar way to that defined for Ala in AlrBs (Figs. 5a and 5b). In addition, the amino-acid side chains are stabilized through hydrophobic interactions with Met347′ in BsrV (Figs. 5a, 5c and 5e). Basic amino acids (Arg, Lys and Orn) are stabilized by the same interactions at their carboxylate moieties and, in addition, by hydrogen bonding to Tyr394 and by electrostatic interactions with Asp268 and the PLP phosphate group (Fig. 5e).
Furthermore, docking results neatly explain why BsrV, but not Alrs, racemizes long aliphatic and basic residues. In Alrs, a Tyr residue (Tyr354 in AlrBs) closes the active-site cavity, which accommodates the short chain of the Ala residue (Fig. 5b) but produces steric clashes when longer aliphatic, or basic, residues are docked (Figs. 5d and 5f). The presence of a Pro residue (Pro391) at the equivalent position in BsrV makes sufficient additional space for the proper fitting of both long aliphatic and basic residues (Fig. 5c and 5e).
The differential efficiency of BsrV for its substrates was also in agreement with the docking results. Indeed, the lower activity values found for His and Asn (Supplementary Fig. S1g) can be explained by the limited interactions with Asp268 owing to their shorter side chains (Supplementary Figs. S5c and S5d). Nonetheless, additional elements seem to participate in the stabilization of basic substrates.
To further understand the different specifities of BsrV and AlrV and to assess the significance of each `signature' residue, we examined the activity of purified BsrV containing individual point mutations at these loci (Figs. 5g and 5h and Supplementary Figs. S5f and S5g). Notably, the mutation of any of the signature sites reduced the activity of BsrV, although the extent of the reduction varied among the mutations and among the classes of substrates (i.e. short and long non-β-branching aliphatic chains versus positively charged side chains; Fig. 5g and Supplementary S5g). Structural analysis provides likely explanations for the effects of these mutations on BsrV activity (Fig. 5h and Table 3). The analysis of the activity of each BsrV mutant isoform revealed that five substitutions (R119A, R121A, A165K, N167A and Y208A) reduced the activity below 20% compared with wild-type BsrV for most of the substrates (Fig. 5g). The footprint residues Arg119 and Arg121 are involved in salt-bridge interactions on the back side of the dimer and allow the formation of the N-terminal extension of BsrV. The dramatic effect of their absence confirms our previous conclusion (based on the P25E mutant) that the N-terminal extension is critical for the activity of BsrV towards a variety of substrates. In contrast, the A165K and N167A substitutions are expected to impair Cl− coordination and consequently the stabilization of the catalytic Arg173. Finally, the Y208A mutant should affect the conformation of the entry loop L1 (Table 3) and, as expected, has an especially large effect on the racemization of amino acids with long side chains.
The remaining substitutions have narrower effects, and most frequently limit the activity of BsrV towards long non-β-branching amino acids, possibly because these substrates encounter more steric obstacles in entering and/or being positioned within the active site. Interestingly, a subset of mutations (G169A, N174A and P391N) that prevent the racemization of non-β-branching aliphatic amino acids do not markedly impair the activity of BsrV towards basic substrates. Based on the docking models, it seems likely that the side chains of basic substrates are stabilized by different components within the catalytic site (e.g. PLP, Asp268 and Tyr394; Fig. 5e). Analysis of a D268N mutant further confirmed that Asp268 contributes to the racemization of basic amino acids by BsrV (Supplementary Fig. S5e).
Broad-spectrum amino-acid racemases such as BsrV enable bacteria to generate NCDAA, the varied roles of which in microbial physiology are just beginning to be appreciated (Cava, de Pedro et al., 2011; Kolodkin-Gal et al., 2010, 2012; Lam et al., 2009). Here, we present extensive crystallographic, biochemical and bioinformatic analyses of two broad-spectrum racemases (BsrV and BsrAh) and identify the structural features that enable such enzymes to accommodate a wider range of substrates than related PLP-dependent alanine racemases. We also identify the molecular signature for BsrV-like racemases from diverse microbes that enables them to be distinguished from monospecific alanine racemases.
Although BsrV from V. cholerae has previously been reported to produce primarily D-Met and D-Leu (Lam et al., 2009), we found that this enzyme can also racemize eight additional amino acids typically found in proteins, as well as several nonproteinogenic amino acids. The substrates of BrsV fall into two main classes: non-β-branched aliphatic amino acids (i.e. Ala, Ser, Leu, Cys, Gln, Asn and Met) and basic amino acids (i.e. Arg, Lys and His). Although D forms of the latter class were not detected in vivo, kinetic analyses indicate that they can be readily generated by BsrV, perhaps facilitated by additional stabilizing interactions between these substrates and the active site of BsrV (Figs. 5a, 5c and 5e). Lys and Arg have also been found to be the preferred substrates of a broad-spectrum periplasmic racemase from Pseudomonas taetrolens (Matsui et al., 2009). The enhanced active-site stabilization predicted for basic substrates may account for the resilience of the catalytic activity of mutant BsrV with such substrates relative to large uncharged aliphatic substrates (Fig. 5g). The substrate range of BsrV, which includes activity towards non-natural substrates (e.g. ornithine, norleucine, homoserine, N-acetyl lysine methyl ester, diaminobutyrate and aminobutyrate; Supplementary Fig. S1e), is broader than any other known amino-acid racemase and suggests that it has great potential for biotechnological and industrial applications. Currently, production of DAA is an expensive process that is typically reliant upon inefficient chemical catalysts (Gong et al., 2010; Green et al., 2009; Toth & Richard, 2007).
Interestingly, all of the Bsr-family racemases are encoded by Gram-negative bacteria. Since some Gram-positive organisms (e.g. B. subtilis) have also been reported to produce NCDAA, this result suggests that additional families of broad-spectrum enzymes may remain to be identified. Consistent with this idea, the spectrum of NCDAA produced by B. subtilis includes several amino acids that cannot be generated by BsrV (e.g. D-Tyr and D-Trp; Kolodkin-Gal et al., 2010). Additional broad-spectrum enzymes may not be related to the PLP-dependent racemases such as Alrs and Bsrs, but might instead bear a resemblance to other known racemases, such as MurI.
Comparative structural analyses of BsrV-family broad-spectrum racemases (BsrV and BsrAh) and more restricted enzymes (AlrAh, AlrEc and AlrBs) suggest that the catalytic plasticity of these racemases has three essential determinants: the arrangement and features of the entry site, the width of the channel leading to the active site and its catalytic environment, which is able to accommodate and stabilize substrates of diverse chemical natures. There is no indication that the underlying mechanism of racemization differs between the two enzyme subfamilies since the dominant catalytic moeties (catalytic Lys and Tyr) are found in both. The wider entry site and channel of BsrV are likely to facilitate interaction with amino-acid substrates larger than alanine; indeed, structural, biochemical and modelling analyses suggest that the entry channel of BrsV can also accommodate peptide chains which are markedly larger. The catalytic site of BsrV-like racemases is also less constrained than those of related alanine racemases, apparently owing both to differences in the components of the chambers (e.g. Cl− and Pro391) and to different arrangements of the enzymatic domains that interact to form them. Previous analyses have revealed variability in the relative positioning of racemase N- and C-terminal domains owing to changes in the amino acids at the dimer interface (Couñago et al., 2009). In broad-spectrum racemases, this interface is markedly altered by the presence of a new structure formed from an extended N-terminal sequence. Mutational analyses indicate that the N-terminal extension, as well as the 16 `signature' amino acids that can be used to identify broad-spectrum enzymes, are critical for racemase activity on the full set of substrates. Interestingly, mutations in most signature loci did not revert BsrV to an alanine-specific racemase; instead, its activity towards large aliphatic side chains was often lost, while its activity towards basic amino acids was preserved.
Collectively, given the impact of NCDAA on a variety of cellular processes [e.g. biofilm stability, sporulation and cell communication (Anfora et al., 2007; Kolodkin-Gal et al., 2010; O'Connor & Zusman, 1997)], structural and regulatory characterization of broad-spectrum racemases might open the door to the design of new drugs (Conti et al., 2011) that would challenge the adaptability of pathogenic bacteria to adverse conditions (i.e. during infection).
We thank Stavroula Hatzios for insightful comments on the manuscript and Lourdes Infantes for help in data-mining analysis. Special thanks to F. Lopez-Gallego for providing DAAO. Research in the Cava laboratory is supported by the MINECO, Spain (RYC-2010-06241), Universidad Autonoma de Madrid (UAM-38) and by the Knut and Alice Wallenberg Foundation (KAW). Additionally, this work was supported by the BFU2011-25326 MEC grant (JAH), by the S2010/BMD-2457 grant from CAM (JAH) and by HHMI (MKW).
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