Structural and Biochemical Characterization of Glycoside Hydrolase Family 79 β-Glucuronidase from Acidobacterium capsulatum

Background: The three-dimensional structures of β-glucuronidase have been solved only for the GH2 enzymes. Results: AcGlcA79A is composed of a (β/α)8-barrel domain and a β-domain. Conclusion: The substrate binding site of AcGlcA79A is adapted for recognition of GlcA as a substrate. Significance: This is the first report describing the crystal structure, mechanism, and catalytic residues of a GH79 enzyme. We present the first structure of a glycoside hydrolase family 79 β-glucuronidase from Acidobacterium capsulatum, both as a product complex with β-d-glucuronic acid (GlcA) and as its trapped covalent 2-fluoroglucuronyl intermediate. This enzyme consists of a catalytic (β/α)8-barrel domain and a β-domain with irregular Greek key motifs that is of unknown function. The enzyme showed β-glucuronidase activity and trace levels of β-glucosidase and β-xylosidase activities. In conjunction with mutagenesis studies, these structures identify the catalytic residues as Glu173 (acid base) and Glu287 (nucleophile), consistent with the retaining mechanism demonstrated by 1H NMR analysis. Glu45, Tyr243, Tyr292–Gly294, and Tyr334 form the catalytic pocket and provide substrate discrimination. Consistent with this, the Y292A mutation, which affects the interaction between the main chains of Gln293 and Gly294 and the GlcA carboxyl group, resulted in significant loss of β-glucuronidase activity while retaining the side activities at wild-type levels. Likewise, although the β-glucuronidase activity of the Y334F mutant is ∼200-fold lower (kcat/Km) than that of the wild-type enzyme, the β-glucosidase activity is actually 3 times higher and the β-xylosidase activity is only 2.5-fold lower than the equivalent parameters for wild type, consistent with a role for Tyr334 in recognition of the C6 position of GlcA. The involvement of Glu45 in discriminating against binding of the O-methyl group at the C4 position of GlcA is revealed in the fact that the E45D mutant hydrolyzes PNP-β-GlcA approximately 300-fold slower (kcat/Km) than does the wild-type enzyme, whereas 4-O-methyl-GlcA-containing oligosaccharides are hydrolyzed only 7-fold slower.

enzymes, such as ␤-galactosidases, ␤-mannosidases, and ␤-glucuronidases, whereas the GH79 family consists of both exo-acting (␤-glucuronidase) and endo-acting (heparanase) enzymes. Human heparanase plays a decisive role in diseaserelated processes, such as cell invasion, angiogenesis, and cancer metastasis. Several structural models of heparanase have been generated by computer programs using known clan GH-A structures as templates (10 -12). However, to date, no experimental structure or even a preliminary crystallization report of a GH79 enzyme is available; the three-dimensional structure of a GH79 enzyme is eagerly anticipated.
For many years, bacterial ␤-glucuronidases were believed to be restricted to E. coli and closely related Enterobacteriaceae. Recently, however, the enzyme activity has been found among non-enterobacterial, anaerobic residents of the digestive tract, such as Bacteroides and Clostridium (13)(14)(15). Although these species exhibit lower ␤-glucuronidase activity than E. coli, they are ϳ100-fold more abundant. Hence, it is suggested that they make a significant overall contribution to the enterohepatic circulation. Other bacterial genera with ␤-glucuronidase activity are Streptococcus, Staphylococcus, Corynebacterium, Alcaligenes, and many soil bacteria (16). In these bacteria, the enzyme is involved in carbohydrate and energy metabolism and may contribute to invasion during bacterial pathogenesis.
In contrast, GH79 ␤-glucuronidases from Arabidopsis thaliana, Aspergillus niger, and Neurospora crassa have been reported to act on plant proteoglycans (5)(6)(7). The A. niger and N. crassa enzymes have been shown to release both GlcA and 4-O-methyl-GlcA (MeGlcA) from arabinogalactan proteins (6,7). No GH2 ␤-glucuronidases are known in plants, and no GH2 ␤-glucuronidase homologous sequences have been found in plants (17). Therefore, GH79 enzymes appear to play important roles in the metabolism of plant proteoglycans.
Thus, ␤-glucuronidases play an important role in plants, animals, and probably microorganisms. In this study, we present the three-dimensional structure of ␤-glucuronidase from Acidobacterium capsulatum (AcGlcA79A); this is the first structure of a GH79 enzyme. We also performed mutagenesis studies based on the structure of the enzyme-GlcA complex. Our results clearly demonstrate the structure-function relationship of GH79 ␤-glucuronidase and will help guide studies of other GH79 enzyme systems.
Expression of AcGlcA79A and Mutant Generation-A. capsulatum NBRC15755 was obtained from the National Institute of Technology and Evaluation (Kazusa, Japan). The gene encoding a putative ␤-glucuronidase (ACP_2665; GenBank TM accession number ACO32043) was amplified from A. capsulatum genomic DNA by PCR using Phusion DNA polymerase (Finnzymes, Espoo, Finland) and the following primers: for-

␤-Glucuronidase from A. capsulatum
ward, 5Ј-CAT ATG GCT TTT GCC CGC GGC GGA CTG GCT-3Ј; reverse, 5Ј-AAG CTT AGC GAA TTC GAG CAA TGC GCC GGA-3Ј. The amplified DNA was cloned into pET30(ϩ) (Novagen, Darmstadt, Germany) at NdeI and HindIII restriction enzyme sites (underlined). Recombinant enzymes were expressed using the T7 expression system in E. coli BL21-Gold(DE3) (Novagen) and purified with a C-terminal histidine tag (supplemental Fig. S1). Amino acid substitutions in AcGlcA79A were generated by inverse PCR using the expression vector pET30/AcGlcA79A as template DNA and the appropriate primers. Expression of mutants and their purification were performed in the same way as for wild-type AcGlcA79A. Further details can be found in the supplemental Experimental Procedures.
Crystallization, Data Collection, and Structural Determination-Initial crystallization screening of AcGlcA79A was conducted by the sitting drop, vapor diffusion method at 20°C, mixing 0.3 l of the protein solution (4.6 mg ml Ϫ1 ) and an equal volume of precipitant against 50 l of reservoir solution using the following commercially available kits: JCSGϩ Suite (Qiagen, Düsseldorf, Germany), Crystal Screen HT, and Index HT (Hampton Research, Aliso Viejo, CA). After refinement of the crystallization conditions, AcGlcA79A was crystallized by the sitting drop, vapor diffusion method with a precipitant solution composed of 2.0 M sodium phosphate monobasic monohydrate/potassium phosphate dibasic (0.5:9.5 (v/v), pH not adjusted) and with a protein concentration of 2.5 mg ml Ϫ1 . Crystals with maximum dimensions of 200 ϫ 200 ϫ 500 m were consistently obtained within a few days at 20°C. Selenomethionine (Se-Met)-labeled AcGlcA79A was produced using the E. coli B834(DE3) methionine auxotroph and was crystallized under the same conditions as for the native enzyme. The GlcA complex was prepared by soaking the AcGlcA79A crystals in crystallization liquor containing GlcA powder for 5 min. The fluorinated glucuronide (2FGlcA) intermediate complex was prepared by adding the crystallization liquor containing 0.3% (w/v) DNP-2FGlcA into the AcGlcA79A crystallization drop and incubating for 5 min.
Diffraction experiments were conducted at the Photon Factory (PF) or the PF-Advanced Ring (PF-AR), High Energy

Activity of wild type (WT) and mutants of AcGlcA79A against PNP-␤-GlcA
Each set of results is based on the average of three independent measurements. Results are means Ϯ S.E.
a The enzyme (0.1 M) was incubated with PNP-␤-GlcA at a concentration of 1.5 M. Kinetic parameters were not determined because mutants were too inactive to obtain individual kinetic constants. The activity of the rest of mutants such as E173Q, E287A, E287Q, Y334W, Y292A, H327K, H327T, and E45Q was not detected under this condition.

TABLE 3
Activities of AcGlcA79A wild type and mutants for PNP-␤-GlcA,

PNP-␤-Glc, and PNP-␤-Xyl
Each set of results is based on the average of three independent measurements. Results are means Ϯ S.E. ND, not detectable.

PNP-␤-Xyl
Research Organization, Tsukuba, Japan. The crystals were moved into the mother liquor containing 20% (v/v) glycerol as a cryoprotectant, and a single crystal was scooped in a nylon loop and flash frozen in a nitrogen gas stream at Ϫ178°C. Diffraction data were collected with the Quantum 270 CCD detector (Area Detector Systems Corp., Poway, CA). Data were integrated and scaled using the programs DENZO and Scalepack in the HKL2000 program suite (19). AcGlcA79A crystals diffracted to ϳ1.4-Å resolution (space group I4 1 22). Assuming that the asymmetric unit of the crystal contained one AcGlcA79A molecule, the Matthews coefficient was calculated to be 2.7 Å 3 Da Ϫ1 (20); this corresponded to the 55% solvent content of the crystals. Structural analysis of AcGlcA79A was conducted through the multiwavelength anomalous dispersion method using Se-Met-labeled AcGlcA79A crystals. Seven selenium atom positions were determined, and initial phases were calculated using the AutoSol and AutoBuild wizards in the PHENIX program suite (21). The obtained initial model was further improved using the program ARP/wARP (22). Manual model rebuilding, introduction of water molecules, and molecular refinement were conducted using Coot and Refmac5 (23,24). One phosphate ion and several glycerol molecules were added into the model. For the analyses of GlcA-and 2FGlcA-binding structures of AcGlcA79A, structural determination was conducted using the ligand-free structure as the starting model, and the bound ligand was observed in the difference electron density map. Refinement parameters for the ligands were generated by the GlycoBioChem PRODRG2 Server (25). Data collection and structure refinement statistics are given in Table 1. Stereochemistry of the models was analyzed with the program Rampage (26) in the CCP4 program suite (27). Structural drawings were prepared by the program PyMOL (Schrödinger, LLC, New York).
Enzyme Assays-␤-Glucuronidase activity was assayed using PNP-␤-GlcA at 37°C in McIlvaine buffer (pH 3.0) as described in the supplemental Experimental Procedures. The amount of PNP released was detected at A 400 (extinction coefficient ϭ 7284 M Ϫ1 ⅐cm Ϫ1 ). One unit of enzyme activity was defined as the amount of enzyme that released 1 mol of PNP/min. The effects of pH and temperature on enzyme activity were investigated as described previously (28). The effect of pH on enzyme activity was examined with or without 90 mM formic acid or 90 mM acetic acid as described above.
The substrate specificity of AcGlcA79A toward various PNPglycosides was determined. The assay method was identical to that described for PNP-␤-GlcA. The kinetic parameters of the wild type and mutants of AcGlcA79A for PNP-␤-GlcA, PNP-␤-Glc, and PNP-␤-Xyl were determined as follows. The reac-tions were performed in McIlvaine buffer (pH 3.5) containing 0.01-10 mM substrates, 0.1% (w/v) bovine serum albumin, and 0.9 nM-10.0 mM enzyme at 37°C for up to 10 min. The amount of PNP released was determined from the A 400 data. The kinetic parameters k cat and K m were determined by Lineweaver-Burk plot from three independent experiments and at five substrate concentrations. The substrate specificity and the catalytic efficiency of the wild type and mutants of AcGlcA79A were analyzed using MeGlcA-␤-1,6-Gal 2 . Briefly, the enzyme (5 M) was incubated with the substrate (10 M) in McIlvaine buffer (pH 3.5) at 37°C. At regular time intervals, the amount of degradation of each substrate was quantified by high performance anion exchange chromatography with pulsed amperometric detection (29). The assay was performed in duplicate.
Determination of Stereochemistry of Hydrolysis by 1 H NMR-The substrates and recombinant enzymes were lyophilized twice from D 2 O before use. A solution of 15 mM PNP-␤-GlcA (Koch-Light, UK) in 0.04 M deuterated sodium acetate buffer (pH 3.7) was incubated with 0.5 mg of AcGlcA79A. This enzyme concentration was needed to achieve a rapid substrate hydrolysis to minimize the effect of mutarotation on determination of the anomeric configuration of the primary product of hydrolysis. 1 H NMR spectra were recorded at different time intervals on a Varian 400-MR (400-MHz) spectrometer.

RESULTS AND DISCUSSION
Expression and Characterization of AcGlcA79A-The cloning and expression of AcGlcA79A are described in the supplemental Experimental Procedures. Recombinant AcGlcA79A activities were tested using various PNP-glycosides as substrates. AcGlcA79A showed significant activity only for PNP-␤-GlcA with negligibly weak or no activity for other substrates. Using PNP-␤-GlcA as the substrate, maximal enzyme activity was detected at pH 3.0 and 50°C. The enzyme was stable between pH 2.8 and 4.5 at 30°C for 1 h and at pH 3.0 at Ͻ55°C for 1 h. The K m and k cat values of AcGlcA79A for PNP-␤-GlcA were 0.015 Ϯ 0.001 mM and 34 Ϯ 1 s Ϫ1 , respectively (Tables 2  and 3). These values of AcGlcA79A are similar to the previously reported values of GH79 enzymes (7). The K m values of the A. niger and N. crassa recombinant GH79 enzymes were 0.030 and 0.038 mM, respectively, and the k cat values were 26.9 and 13.5 s Ϫ1 , respectively (7). Because the A. niger and N. crassa enzymes showed 4-O-methyl-␤-glucuronidase activity, the activity of AcGlcA79A for the MeGlcA-containing oligosaccharide MeGlcA-␤-1,6-Gal 2 was tested. AcGlcA79A barely hydrolyzed MeGlcA-␤-1,6-Gal 2 , and its activity for MeGlcA-␤-1,6-Gal 2 was 10 3 times lower than that for PNP-␤-GlcA (Table 4). These results suggest that AcGlcA79A is a genuine ␤-glucuronidase.

␤-Glucuronidase from A. capsulatum
Three-dimensional Structure of AcGlcA79A-The crystal structure of AcGlcA79A was determined by the multiwavelength anomalous dispersion method using Se-Met derivative data. Native and GlcA complex structures were determined successively. Structure refinement statistics are summarized in Table 1. The quality and accuracy of the final structures were further demonstrated to show that all residues fall within the common regions of the Ramachandran stereochemistry plot.
Recombinant AcGlcA79A is composed of a single polypeptide chain of 488 amino acids with the additional C-terminal residues ( 476 KLAAALEHHHHHH 488 ) derived from the expression vector and purification tag. Seventeen N-terminal residues (Met 1 -Ser 17 ) and five C-terminal residues (His 484 -His 488 ) were not identified because of a lack of electron density. Three cis-peptide bonds were found at Gly 214 -Pro 215 , Gly 246 -Pro 247 , and Ser 457 -Gly 458 . The final model consists of one AcGlcA79A molecule with one or two phosphate ions and one or four glycerol molecules. The overall structures of the ligand-free and GlcA complexes were almost the same, and the calculated root mean square difference was 0.2 Å for the C␣ atom pairs.
The protein consists of domains A and C (Fig. 1). The N-terminal ␤-strand (Val 20 -Ile 35 ) is inserted into the domain C, and the peptide folds into the (␤/␣) 8 -barrel of domain A (Gly 41 -Ala 360 ) and finally enfolds the ␤-domain of domain C. The secondary structure elements of AcGlcA79A are numbered in Fig.  1B.
Domain A consists of a (␤/␣) 8 -barrel, which is the catalytic domain in many glycoside hydrolases. The GlcA binding site is located at the C-terminal end of the central ␤-barrel and was designated as the catalytic pocket. GH79 and GH2 enzymes are classified into the same GH-A clan, and the overall folding of their structures shows certain similarities. The root mean square difference for the core C␣ atoms between the catalytic domains of AcGlcA79A and E. coli GH2 ␤-glucuronidase was calculated to be 2.6 Å. In addition to the core secondary structures of the (␤/␣) 8 -barrel, several loops fold into some small substructures and contribute to the formation of the catalytic pocket (Fig. 1).
Domain C consists of nine ␤-strands with strands C␤0 and C␤4 aligned parallel and the others in interacting antiparallel configurations (Fig. 1B). The eight strands other than C␤0 comprise a typical antiparallel ␤-domain structure containing Greek key motifs (Fig. 1). This C-terminal domain structure is observed in many glycoside hydrolases, although in many cases its function remains unknown.
Active Site and Catalytic Mechanism-The active site of AcGlcA79A is located at the C-terminal end in the central (␤/␣) 8 -barrel and is represented by a pocket shape (Fig. 1). In the GlcA complex structure, Glu 173 is located near the O1 atom of GlcA (2.3-2.4 Å), and Glu 287 is located close to the C1 atom (3.0 Å). The distance between Glu 173 and Glu 287 of AcGlcA79A is 5.25 Å. The location of these acidic amino acids suggests that Glu 173 and Glu 287 are the catalytic residues of AcGlcA79A, functioning as acid/base and nucleophile, respectively, consistent with the expected retaining mechanism (Fig. 2). It has been reported that the distance between two catalytic residues is 7-10 Å in inverting glycosyl hydrolases and 5-6 Å in retaining glycosyl hydrolases (30). This is also apparent from the rule of the clan GH-A (4/7 superfamily) catalytic module in which the two catalytic residues are located posteriorly in A␤4 and A␤7 (31). The locations of Glu 173 and Glu 287 of AcGlcA79A are the same as those of the catalytic residues of GH2 enzymes and correspond to the 4/7 superfamily rule.
To verify the identities of the catalytic residues of AcGlcA79A, Gly, Ala, and Gln mutants of Glu 173 and Glu 287 were constructed. As expected, the activities of all mutants were at least 10 4 times lower than those of the wild-type enzyme ( Table 2). The k cat /K m values of E173G, E173A, and E287G mutants were 0.5, 0.1, and 0.2 mM Ϫ1 ⅐s Ϫ1 , respectively. Chemical rescue experiments were subsequently performed for E173G, E173A, E287G, and E287A using formic acid and acetic acid as exogenous nucleophiles (see supplemental Experimental Procedures). The ␤-glucuronidase activities of the mutants were measured in McIlvaine buffers (0.1 M citric acid and 0.2 M Na 2 HPO 4 ) of various pH values with or without 90 mM formic acid and 90 mM acetic acid (supplemental Fig. S2). The pH activity profiles of E173G and E173A were the same with or without the chemicals, and the enzyme activities of the mutants remained significantly lower than that of the wild type. However, the pH activity profiles of E287G and E287A with formic acid were different in the pH range 2-5. The enzyme activity of E287G with formic acid near the optimum pH (2.6 -3.5) recovered completely to the same level as that of the wild type. For E287A, 25% of the enzyme activity was recovered. In contrast, acetic acid did not affect the enzyme activities of E287G and E287A most likely because acetic acid is too large to enter the pocket created by the mutation. These data further suggest that Glu 287 is the nucleophile.
Because the catalytic mechanism of GH79 enzymes had not been verified experimentally, the anomeric configuration of the hydrolysis product was determined (Fig. 3). The hydrolysis of PNP-␤-GlcA with AcGlcA79A in D 2 O was followed by 1 H NMR analysis. The enzyme load was sufficient to complete the hydrolysis of 15 mM substrate in about 4 min. As shown in Fig.  3, the disappearance of the H1 signal of the glucuronide at 5.3 ppm was accompanied by parallel changes of the PNP aglycone signals into PNP signals (signals between 6.8 and 8.3 ppm). Free uronic acid was generated as the ␤-anomer as evidenced by the rapid appearance of the H1␤ resonance at 4.7 ppm. The ␣-anomer signal only appeared later as a result of mutarotation ( Fig. 4 and supplemental Fig. S3). These results show that AcGlcA79A is a retaining enzyme utilizing a double displacement mechanism of hydrolysis. It is very probable that all enzymes belonging to this family will prove to be retaining. Consistent with this mechanism, we detected transglycosylation products generated by AcGlcA79A (data not shown). Similar transglycosylation reactions catalyzed by GH79 ␤-glucuronidase from A. niger have been reported previously (6, 7). Ligand-binding Structure-The catalytic center of AcGlcA79A is pocket-shaped as is typically found in exo-acting enzymes (Figs. 2, A and B, and 4). In the GlcA complex structure, the aromatic ring of Tyr 243 lies parallel to the pyranosyl ring of GlcA, providing stabilizing hydrophobic interactions. The O2 and O3 atoms of GlcA are recognized by hydrogen bonds, such as those between the O2 and Asn 172 -N␦2 atoms and between the O3 and both Glu 45 -O⑀2 and Asn 80 -N atoms. The O4 atom of GlcA is surrounded by Pro 104 and His 327 and forms a hydrogen bond with Asp 105 . Recognition of the GlcA carboxyl group is achieved by hydrogen bonds between O6A and Gln 293 -N and between O6B and both Gly 294 -N and Tyr 334 -O (Fig. 2). Fig. 4C shows a crosssectional view of the active site pocket of the GlcA complex structure and clearly indicates that there is no extra space around the substrate. This was also indicated by a sugar soaking experiment in which no residual sugar was observed when the AcGlcA79A crystals were soaked with Glc, Xyl, or GalA.
2-Deoxy-2-fluoroglycosides, which act as mechanismbased inhibitors to form covalent intermediates, are powerful chemical tools for identifying the active site nucleophile in retaining glycosidases as reported by Withers and Aebersold (18). By adding DNP-2FGlcA to the AcGlcA79A crystal, the fluorinated glucuronide residue (2FGlcA) was observed to be covalently bound to Glu 287 (Fig. 2C) through an ␣-con-  figured linkage. The positions of the O2 and O3 atoms of 2FGlcA are almost the same as with GlcA, but the C1 atom is shifted by 1.3 Å toward Glu 287 because of covalent bond formation (Fig. 2D).
Mutagenesis Study of AcGlcA79A-To investigate the basis of substrate specificity of AcGlcA79A, appropriate mutations were introduced at the residues that interact with GlcA, and the properties of the constructed mutants were characterized (Tables 2 and 3). Although GlcA and Glc are structurally different only at the C6 position (-COOH for GlcA and -CH 2 OH for Glc), AcGlcA79A discriminates greatly between GlcA and Glc. To address this discrimination, a Y334F mutant was constructed along with Y334W and Y292A mutants to alter the space around the C6 position of GlcA and change the position of the main chain of Gln 293 and Gly 294 . Around the C6 position of GlcA, the main chain atoms of Gln 293 and Gly 294 and Tyr 334 -O interact with the carboxyl group of GlcA (Fig. 2).
As shown in Table 3, the catalytic efficiency of the Y334F mutant for hydrolysis of PNP-␤-GlcA is lower than that of the wild type due to an increased K m value. In contrast, the activity for PNP-␤-Glc is close to that of the wild type. Consequently, the activity ratio for PNP-␤-Glc to PNP-␤-GlcA (Glc/GlcA ratio) is 567 times higher than that of the wild type, suggesting that the para-OH of Tyr 334 is necessary for recognizing the carboxyl group of GlcA. Tyr 334 enables AcGlcA79A to interact predominantly with GlcA and exhibit higher ␤-glucuronidase activity. The Y334W mutant could not cleave PNP-␤-GlcA at all presumably due to steric hindrance. When Tyr 334 was substituted with tryptophan, the space around the C6 position of GlcA appeared to be filled with the aromatic ring of tryptophan so that GlcA could not possibly bind. The Y292A mutant also lost all activity for PNP-␤-GlcA, whereas its catalytic efficiency with PNP-␤-Glc was close to that of the wild-type enzyme. The positions of Gln 293 and Gly 294 may be influenced by the substitution of Tyr 292 with alanine so that GlcA is unable to bind in the catalytic pocket. The catalytic efficiencies of Y334F and Y292A for PNP-␤-Xyl were 0.37 and 0.65 times lower, respectively, than that of the wild type. However, the activity ratio of PNP-␤-Xyl to PNP-␤-GlcA (Xyl/GlcA ratio) was higher for both mutants. Y334F had a 72 times higher activity ratio than the wild-type enzyme. Although the mutants showed broader substrate specificity than the wild type, none of the activities for GlcA reached the level of the wild type. AcGlcA79A appears to discriminate GlcA through the residues around C6, including Tyr 334 , Tyr 292 , Gln 293 , and Gly 294 , while maintaining high enzyme activity toward GlcA.
Although some GH79 enzymes exhibit 4-O-methyl-␤-glucuronidase activity, AcGlcA79A barely hydrolyzes the MeGlcAcontaining oligosaccharide ( Table 4). As shown in Fig. 4C, there is no extra space for a methyl group around the C4 position of GlcA in the GlcA complex structure. To investigate the discrimination mechanism for the 4-O-methyl group of MeGlcA, mutations at Glu 45 and His 327 , which surround the C4 hydroxyl group of GlcA, were designed to make space for the 4-O-methyl group. The enzyme activities of His 327 mutants for PNP-␤-GlcA were eliminated or drastically reduced by 10 Ϫ4 -10 Ϫ3 times relative to the wild-type AcGlcA79A with similar results being seen for Glu 45 mutants ( Table 2). In the case of the E45D mutation, the k cat and the K m values for PNP-␤-GlcA were 36 Ϯ 3 s Ϫ1 and 4.8 Ϯ 0.6 mM, respectively, resulting in a 3.3 ϫ 10 3 times reduction in activity relative to that of the wild-type enzyme (Tables 3 and 4). The carboxyl group of Glu 45 is close to the O4 atom of GlcA at a distance of 3.2 Å and is hydrogenbonded with the Thr 81 -O␥1, Thr 81 -N, Asp 85 -N, and His 327 -N⑀2 atoms. E45D might cause a structural distortion of the hydrogen-bonding network around the C4 position of GlcA and change the surrounding environment of C4. By contrast, the catalytic efficiency of the E45D mutant for MeGlcA-␤-1,6-Gal 2 was only 7 times lower than the wild type. As a result, the activity ratio for MeGlcA-␤-1,6-Gal 2 to PNP-␤-GlcA (MeGlcA/GlcA ratio) of the E45D mutant was 43 times higher than that of the wild type, strongly suggesting that Glu 45 is one of the key residues by which AcGlcA79A distinguishes the 4-Omethyl group of GlcA.
The substrate binding site of AcGlcA79A is specialized for recognition of GlcA as a substrate. A mutagenesis study revealed that Tyr 334 and Tyr 292 interact with the C6 position of GlcA and that Glu 45 recognizes the C4 position of GlcA. Single amino acid mutations did not drastically change the substrate specificity because part of the substrate binding site was formed by the main chain atoms of the protein. These results will help guide studies of other GH79 enzyme systems.