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In Haloferax volcanii, AglD adds the final hexose to the N-linked pentasaccharide decorating the S-layer glycoprotein. Not knowing the natural substrate of the glycosyltransferase, together with the challenge of designing assays compatible with hypersalinity, has frustrated efforts at biochemical characterization of AglD activity. To circumvent these obstacles, an in vivo assay designed to identify amino acid residues important for AglD activity is described. In the assay, restoration of AglD function in an Hfx. volcanii aglD deletion strain transformed to express plasmid-encoded versions of AglD, generated through site-directed mutagenesis at positions encoding residues conserved in archaeal homologues of AglD, is reflected in the behavior of a readily detectable reporter of N-glycosylation. As such Asp110 and Asp112 were designated as elements of the DXD motif of AglD, a motif that interacts with metal cations associated with nucleotide-activated sugar donors, while Asp201 was predicted to be the catalytic base of the enzyme.
Although the presence of N-glycosylated proteins in Archaea has been known for over 30 years , the pathways responsible for this posttranslational modification have only recently been addressed. In Methanococcus voltae, Methanococcus maripaludis, and Haloferax volcanii, products of the agl genes have been shown to participate in the assembly of oligosaccharides decorating various glycoproteins in these species [2–4]. At present, however, apart from the oligosaccharyltransferase, AglB [5–7], virtually nothing is known of the catalytic workings of the different Agl proteins. Of the Hfx. volcanii Agl proteins identified to date, at least five (i.e., AglD, AglE, AglG, AglI, and AglJ) are predicted to act as glycosyltransferases (GTs), enzymes that catalyze the formation of glycosidic bonds through the transfer of the sugar moieties from nucleotide-activated saccharides to appropriate targets .
Based on their amino acid similarities, GTs can be classified into 91 family groups (http://www.cazy.org/fam/acc_GT.html; January, 2009), varying in size and number of functions fulfilled by family members [9, 10]. Furthermore, the different GT families can be clustered based on whether the canonical GT-A or GT-B fold is employed and whether sugar stereochemistry is retained or inverted upon addition of a glycosyl donor . Still, the ability to predict the function of a given GT or to define its catalytic mechanism remains a challenge. This is particularly true in the case of the GT2 family, an ancient group of GT-A fold-bearing GTs containing over 10,000 members derived from various sources and serving at least 12 distinct functions [11, 12]. Like all GT-A fold-bearing GTs, GT2 family members contain a DXD signature motif, shown to interact with a divalent cation (usually Mg2+ or Mn2+) that facilitates the leaving of the nucleoside diphosphate group of a nucleotide-activated sugar donor as part of the SN2-like displacement mechanism believed to be employed by these enzymes [11, 13–17]. The DXD motif also serves to divide the GT-A fold into two portions. The N-terminal portion, containing the sequence that assigns the protein to the GT2 family , binds the nucleotide-activated sugar donor [19–22]. By contrast, the C-terminal portion is highly variable and generally serves to recognize the acceptor . Despite such variability, the C-terminal portion of GT2 family members includes a conserved Asp or Glu residue that presumably serves as the catalytic base, thought to assist in the protonation of the nucleophilic hydroxyl group of the acceptor saccharide [11, 21, 23–25].
The GT2 glycosyltransferase family includes Hfx. volcanii AglD, previously shown to participate in adding the final hexose to the pentasaccharide comprising two hexoses, two hexuronic acids, and a methylated ester of hexuronic acid decorating at least two sequons of the S-layer glycoprotein [26, 27]. However, due to the fact that its natural substrates have yet to be defined and the challenge of devising in vitro assays for haloarchaeal enzymes due to their hypersaline requirements, little is known of the catalytic workings of AglD. Towards remedying the situation, an in vivo approach has been developed in which the ability of plasmid-encoded versions of AglD, modified through site-directed mutagenesis, to restore the absent function to an aglD deletion strain, was tested. Results obtained employing this novel assay point to Asp110-Thr111-Asp112 as corresponding to the DXD motif and Asp201 as corresponding to the catalytic base of Hfx. volcanii AglD.
The Hfx. volcanii background strain WR536 (H53) and the same strain deleted for aglD were grown in complete medium containing 3.4MNaCl, 0.15MMgSO4·7H20, 1mMMnCl2, 4mMKCl, 3mMCaCl2, 0.3% (w/v) yeast extract, 0.5% (w/v) tryptone and 50mM Tris-HCl, pH 7.2, at 42°C . A complete description of the aglD deletion strain and the protocol used to delete the gene have been previously published .
To assay AglD activity, Hfx. volcanii cells deleted of aglD  were transformed to express plasmid-encoded versions of AglD that included an N-terminally fused Clostridium thermocellum cellulose-binding domain (CBD) . To introduce nonnative residues into AglD, the plasmid-encoded version of aglD (GenBank accession number CAM91696.1) was modified by site-directed mutagenesis. Restoration of AglD function lost as a result of deletion of the genomic copy of the encoding gene was determined by the ability of the transformed cells to reverse the enhanced SDS-PAGE migration of the S-layer glycoprotein and loss of PAS glycostaining of the same reporter, that is, novel traits of the S-layer glycoprotein that appeared in cells lacking AglD.
Mutated versions of aglD were generated by site-directed mutagenesis using the Quikchange (Stratagene) protocol, performed according to the manufacturer's instructions, with plasmid pWL-CBD-AglD, encoding CBD-AglD , serving as template. Oligonucleotide primers used to introduce the various mutations are listed in Supplementary Table1 (available online at doi:10.1155/2010/315108). The introduction of mutations was confirmed by sequencing, performed both before and following introduction of plasmid-encoded mutated aglD into Hfx. volcanii.
Periodic acid-Schiff (PAS) reagent glycoprotein staining was performed as described previously . Immunoblots were performed using polyclonal antibodies raised against the C. thermocellum CBD (obtained from Ed Bayer, Weizmann Institute of Science; 1:10,000). Antibody binding was detected using goat antirabbit horseradish peroxidase-(HRP-) conjugated antibodies (1:4000, BioRad, Hercules, CA) and an ECL-enhanced chemiluminescence kit (Amersham, Buckingham, UK).
As a first step towards describing AglD function, efforts were directed at creating an assay to allow for characterization of the activity of the enzyme. Accordingly, cells deleted of the encoding gene were transformed with a plasmid encoding a version of the protein designed to include an N-terminally fused Clostridium thermocellum cellulose-binding domain (CBD) . As previously reported , an 85kDa band, corresponding to the predicted molecular mass of the 17kDa CBD moiety and the 68kDa AglD protein, was expressed in the transformed cells and recognized in an immunoblot using antiCBD antibodies (not shown).
Deletion of aglD results in the absence of the final hexose of the pentasaccharide decorating the Hfx. volcanii S-layer glycoprotein . As such, the S-layer glycoprotein in the deletion strain migrates faster in SDS-PAGE than does the native protein in the background strain . Moreover, the S-layer glycoprotein is not recognized by PAS glycostain in the mutant strain. However, as reflected in Figure 1, the S-layer glycoprotein from cells of the aglD-deleted strain transformed to express CBD-tagged AglD migrated to the same position as did the protein from the background strain and was similarly PAS-stained. As such, complementation of Hfx. volcanii cells lacking aglD with an AglD-encoding plasmid restores the absent activity to the deletion strain.
To demonstrate the involvement of a given AglD residue in the activity of the enzyme, the return of AglD activity to the aglD deletion strain, upon introduction of a plasmid-encoded version of AglD modified at the amino acid position in question, was assessed. In these experiments, the SDS-PAGE migration of the S-layer glycoprotein from cells of the background strain, from cells deleted of aglD, and from AglD-lacking cells transformed to express select mutant AglD proteins was addressed. In addition, the S-layer glycoprotein in each of the three populations of Hfx. volcanii cells was subjected to PAS glycostaining. While this in vivo approach cannot distinguish between residues necessary for catalytic activity from those important for proper AglD folding, it, nonetheless, offers a facile route for identifying important AglD residues until such time as AglD activity can be directly assayed in vitro.
To select candidate residues for site-directed mutagenesis, the Hfx. volcanii AglD sequence was aligned with selected homologous archaeal sequences using ClustalW (http://www.ebi.ac.uk/Tools/clustalw2/index.html). It should be noted, however, that it is not yet known whether the various homologues considered indeed catalyze the same reaction as does Hfx. volcanii AglD. Indeed, it remains to be confirmed that N-glycosylation occurs in all of the species listed. Nonetheless, such alignment revealed the presence of a stretch of amino acids in the N-terminal region of AglD showing substantial overlap with similarly situated regions in the various archaeal homologues considered (Figure 2). In the Hfx. volcanii protein, this stretch corresponds to the region between Asp110 and Glu203, a portion of the protein previously localized to the cytoplasm  and which includes seven residues absolutely conserved in the sequences considered, namely, Asp110, Asp112, Asp133, Arg139, Arg152, Asp173, and Gly177. Between Asp133 and Arg139, between Trp198 and Glu203, and in the region surrounding Asp173 and Gly177, several highly conserved residues were also detected. To determine whether any of these residues contribute to AglD function, the corresponding aglD codons were modified by site-directed mutagenesis using the primer pairs listed in Supplementary Table 1, and the ability of plasmid-encoded versions of the mutant proteins to restore AglD function in the aglD deletion strain was considered.
The GT-A fold found in GT2 family members includes a DXD motif that contributes to the catalytic activity of the enzyme [11, 13, 14, 16, 17]. Sequence alignment-based examination of the Hfx. volcanii AglD sequence points to Asp110-Thr111-Asp112 as comprising this motif (Figure 2). To directly test this hypothesis, the site-directed mutagenesis approach described above was enlisted. Figure 3 addresses the effects of replacing either AglD Asp110 or Asp112 with other residues. Transformation of AglD-lacking cells to express AglD D110A resulted in both the failure of plasmid-encoded AglD to restore S-layer glycoprotein migration to the position of this reporter in the background strain as well as the lost ability of PAS glycostain to label the S-layer glycoprotein. The same was true in cells transformed to express AglD D110E, a mutation that retains the negative charge at this position (Figure 3), or upon introduction of an Asn residue at this position (not shown).
When AglD Asp112 of the plasmid-encoded protein was replaced with an Asn, no recovery of AglD function in the transformed aglD deletion strain was realized, reflected in the inability of cells expressing the mutated version of AglD to restore SDS-PAGE migration and PAS glycostaining of the S-layer glycoprotein, as realized in the background strain (Figure 3). By contrast, transformation of the deletion strain to express AglD D112E led to a restoration of SDS-PAGE migration of the S-layer glycoprotein to the position seen in background cells but only a partial recovery (6% ± 0.5% (standard deviation), n = 3) of PAS glycostaining (Figure 3).
The importance of Asp110 and Asp112 for Hfx. volcanii AglD activity points to these two residues as comprising the DXD motif found in GT-A fold-bearing GTs. However, while the Asp residue at position 110 is apparently essential for activity, the presence of Glu at position 112 yields a functional enzyme that apparently acts differently from the native enzyme, as reflected in the limited PAS staining detected with this mutant.
In addition to the DXD motif considered above, the activity of GT2 family members also relies on an Asp or Glu residue found in the acceptor-binding domain of the protein. First identified in the solved three-dimensional structure of Bacillus subtilis SpsA as Asp191 , this residue and its equivalents in other GTs are thought to serve as the base catalyst in the direct displacement mechanism apparently employed by these enzymes [11, 20]. To identify the Hfx. volcanii AglD equivalent of B. subtilis SpsA Asp191, the sequence of the soluble region of AglD (residues 1–259) was aligned with the sequence of B. subtilis SpsA, as well as with those of the other GT2 enzymes where the functional equivalent of B. subtilis SpsA Asp191 is known, namely, Sinorhizobium meliloti ExoM and Salmonella enterica WbbE. Earlier site-directed mutagenesis efforts had revealed ExoM Asp187 and WbbE Glu180 to serve the same role as SpsA Asp191 [21, 22]. Tcoffee (http://tcoffee.vital-it.ch/cgi-bin/Tcoffee/tcoffee_cgi/index.cgi?stage1=1anddaction=TCOFFEE::Regular) aligned AglD Asp201 with SpsA Asp191, ExoM Asp187 and WbbE Glu180. The MAFFT program (v6.531b; http://www.ebi.ac.uk/Tools/mafft/index.html) also aligned AglD Asp201 with the same SpsA, ExoM and WbbE residues. On the other hand, alignment of archaeal homologues of Hfx. volcanii AglD using the ClustalW (Figure 2), Tcoffee or MAFFT programs revealed that AglD Asp173 but not Asp201 is conserved. In all cases, the programs consulted were used with their default settings.
As a next step towards identifying the AglD equivalent of SpsA Asp191, the importance of Asp173, Asp195, and Asp201 for AglD activity was considered by site-directed mutagenesis.
Transformation of Hfx. volcanii ΔaglD cells with a plasmid encoding AglD D173E (Figure 4) did not restore the SDS-PAGE migration or glycostaining of the S-layer glycoprotein. However, as these S-layer glycoprotein traits were fully restored in cells expressing AglD D173N, it would appear that the conserved Asp173 does not serve as the catalytic base of the enzyme but is likely important for AglD structure. This idea may be supported by the observation that the D173A mutant could not be expressed (not shown). The importance of Asp195, another somewhat conserved Asp residue in this region, was also considered. Hfx. volcanii ΔaglD cells transformed to express AglD D195A (Figure 4) or D195E (not shown) readily replaced the actions of the missing enzyme, showing that the Asp at this position is not necessary for AglD activity. By contrast, if the aglD-deleted strain was transformed to express AglD D201A or D201N, SDS-PAGE migration and glycostaining of the S-layer glycoprotein were as observed in cells lacking native AglD (Figure 4). When, however, Hfx. volcanii ΔaglD cells were transformed to express the D201E mutant, the S-layer glycoprotein behaved as in the background strain (Figure 4). These results thus point to Asp201 as being the catalytic base of AglD and the functional equivalent of SpsA Asp191. Furthermore, as is the case with other GT2 family members , Asp201 can be replaced by Glu.
Homology modeling of Hfx. volcanii AglD residues Asp110-Asp112, Asp173, Asp195, and Asp201, based on the available three-dimensional structural of B. subtilis SpsA , further supports the assignment of AglD D201 as being equivalent to subtilis SpsA Asp191. As reflected in Figure 5, considerable overlap in term of both position and orientation exists between AglD D201 and B. subtilis SpsA Asp191. The same cannot be said for either AglD Asp173 or Asp195.
Hfx. volcanii AglD and its archaeal homologues also contain several other fully conserved residues in that part of the soluble N-terminal region under consideration in this study. The contribution of these residues, as well as that of their neighbors, was next considered. Complementation of ΔaglD Hfx. volcanii cells with plasmid-encoded AglD R139A failed to restore either S-layer glycoprotein migration in SDS-PAGE or the ability of PAS glycostain to label this reporter (Figure 6). The same was true in cells expressing AglD R139E, R139K or R139M (not shown). Thus, AglD Arg139 is apparently essential for enzyme activity. By contrast, complementation of AglD-lacking Hfx. volcanii cells with plasmid-encoded AglD D133A or G177A restored S-layer glycoprotein SDS-PAGE migration to that observed for the native protein, although less S-layer glycoprotein is detected in the cells expressing AglD D133A. The significance of this observation is not clear. In addition, the S-layer glycoprotein in both AglD D133A- and G177A-expressing cells could be glycostained (Figure 6). As such, although conserved in Hfx. volcanii AglD and its archaeal homologues, Asp133 and Gly177 do not appear to be essential for the catalytic workings of the enzyme. Similarly, the introduction of CBD-tagged AglD G137A, S138A, Q175A, C176A, F178A or K179A mutants into Hfx. volcanii ΔaglD cells led to a restoration of AglD activity, indicating that none of these residues contribute to the reaction catalyzed by the enzyme (not shown).
Finally, to eliminate the possibility that the inability of certain plasmid-encoded versions of the protein to restore absent AglD activity was due to poor or no expression, the level of each CBD-AglD considered in this study was assessed by immunoblot using antiCBD antibodies (Figure 7).
When one considers that Nanoarchaeum equitans, the archaeon containing the smallest genome identified to date [31, 32], encodes only 3 GTs, namely, one member of the GT2 family and two members of the GT4 family , it is fair to say that analysis of archaeal GTs can provide unique insight into the evolution of such enzymes, as well as adding to our comprehension of protein processing in extreme conditions. Despite such promise, only limited experimental data on archaeal GTs involved in protein glycosylation is presently available. The crystal structure of Stt3/AglB from Pyrococcus furiosus, the sole component of the archaeal oligosaccharyltransferase [5, 6], has been solved , shedding new light on the workings of this central component of the N-glycosylation machinery. Still, although P. furiosus has been reported to contain glycoproteins , the oligosaccharyltransferase in this species has been thus far only demonstrated to modify an artificial substrate [7, 35]. Similarly, while both Thermoplasma acidophilum  and Pyrococcus horikoshii  have been reported to contain glycoproteins, the participation of biochemically characterized dolichyl phosphomannose synthases from these species [37, 38] in protein glycosylation has yet to be demonstrated. As such, the present analysis of Hfx. volcanii AglD represents the first examination of a glycosyltransferase experimentally verified as participating in the modification of an identified archaeal glycoprotein, namely, the S-layer glycoprotein.
In the present study, sequence alignment was combined with site-directed mutagenesis to identify AglD residues important for the function of the enzyme, as reflected in AglD-mediated modulation of the SDS-PAGE migration and glycostaining of a reporter glycoprotein, the S-layer glycoprotein. This approach assigned AglD Asp110, Thr111, and Asp112 as the DXD motif typical of inverting GT-A fold-bearing GTs. AglD Asp110 was shown to be essential for catalytic activity, while a negative charge at position 112 was deemed necessary. In the case of the AglD D112E mutant, recovery of S-layer glycoprotein SDS-PAGE migration was noted, yet the loss of PAS glycostaining associated with the deletion strain was largely not restored. This could reflect the generation of an enzyme possessing different activity than that of the native protein, one that adds a different sugar to the final position of S-layer glycoprotein-bound pentasaccharide. Indeed, the failure of PAS glycostain to label the tetrasaccharide N-linked to the S-layer glycoprotein in cells lacking AglD points to inability of this labeling reagent to interact with certain sugar subunits. Moreover, within the GT2 family (whose members include Hfx. volcanii AglD), differences in the organization and importance of DXD motif constituents exist. In the case of S. meliloti ExoM, where the DXD motif includes Asp96 and Asp98, it was shown that replacing the former with Ala completely eliminated enzymatic activity, whereas the same replacement at position 98 only led to a 70% loss of activity . In S. enterica WbbE, where the DXD motif is expanded to include Asp93, Asp95, and Asp96, it was shown that exchanging either Asp93 or Asp96 with Ala abolished enzyme activity, while the same replacement at Asp95 only reduced that activity .
The site-directed mutagenesis approach developed here, along with sequence alignment and homology modeling, also indicate Asp201 as likely serving as the AglD catalytic base. Just as the corresponding residue in S. enterica WbbE, that is, Glu180, could be functionally replaced by Asp , AglD D201E was also active. By contrast, replacing the Asp187 catalytic base in S. mililoti ExoM led to a complete loss of function . Such nuances may be indicative of differences in the donors and/or acceptors employed by each enzyme or point to unique mechanistic traits. In addition, although conserved in the archaeal AglD homologues examined in this study, Hfx. volcanii AglD Asp173 was not assigned as the catalytic base of the enzyme, given its functional replacement by a similarly sized Asn but not a similarly charged Glu. Hence, it would appear that Asp173 is of structural, rather than catalytic, importance to AglD activity. In addition to these residues, at least another Hfx. volcanii AglD amino acid seems to be needed for enzyme function, that is, Arg139. The AglD counterparts of other residues shown to be important for the catalytic activity of GT2 family members, such as S. meliloti ExoM Asp44 and Asp96 , may also play a role in the activity of the archaeal enzyme.
In conclusion, this paper describes an in vivo assay designed to consider the contribution of various AglD residues to the activity of the enzyme. In the assay, the ability of plasmid-encoded versions of AglD, selectively mutated at positions suspected of being important for enzyme function, to restore both S-layer glycoprotein SDS-PAGE migration and glycostaining affected in ΔaglD cells is assessed. In this manner, Asp110, Asp112, and Asp201 were all determined as being important for AglD activity, as was Asp139.
Supplementary Table 1—Primers used for site-directed mutagenesis of aglD.
The authors thank Dr. Raz Zarivach for assistance with the homology modeling. Support came from the Israel Science Foundation (Grant 30/07) and the US Army Research Office (Grant W911NF-07-1-0260).