Glycoside phosphorylases catalyze the phosphorolysis of oligosaccharides into sugar phosphates. Recently, we found a novel phosphorylase acting on β-1,2-glucooligosaccharides with degrees of polymerization of 3 or more (1,2-β-oligoglucan phosphorylase, SOGP) in glycoside hydrolase family (GH) 94. Here, we characterized SOGP from Lachnoclostridium phytofermentans (LpSOGP) and determined its crystal structure. LpSOGP is a monomeric enzyme that contains a unique β-sandwich domain (Ndom1) at its N-terminus. Unlike the dimeric GH94 enzymes possessing catalytic pockets at their dimer interface, LpSOGP has a catalytic pocket between Ndom1 and the catalytic domain. In the complex structure of LpSOGP with sophorose, sophorose binds at subsites +1 to +2. Notably, the Glc moiety at subsite +1 is flipped compared with the corresponding ligands in other GH94 enzymes. This inversion suggests the great distortion of the glycosidic bond between subsites −1 and +1, which is likely unfavorable for substrate binding. Compensation for this disadvantage at subsite +2 can be accounted for by the small distortion of the glycosidic bond in the sophorose molecule. Therefore, the binding mode at subsites +1 and +2 defines the substrate specificity of LpSOGP, which provides mechanistic insights into the substrate specificity of a phosphorylase acting on β-1,2-glucooligosaccharides.
Glycoside phosphorylases catalyze the phosphorolysis of oligosaccharides into sugar phosphates in the metabolism of specific sugars1,2. Phosphorylation of sugars without an energy source such as ATP is advantageous for saving energy physiologically3. In the application area, the reversibility of reactions and strict regioselectivity of glycoside phosphorylases are of great use for oligosaccharide synthesis4. The combination of two glycoside phosphorylases sharing a common donor substrate enhances the use of this type of enzymes, since the use of an expensive sugar 1-phosphate as a starting material can be avoided5,6. Despite several recent findings regarding new glycoside phosphorylases7, the repertoire of glycoside phosphorylases is still much smaller than that of glycoside hydrolases. In addition, the distribution of glycoside phosphorylases is limited to glycoside hydrolase (GH13, GH65, GH94, GH112, and GH130) and glycosyltransferase (GT4 and GT35) families7,8,9 (In the GH3 family, only one glycoside phosphorylase has been reported in subgroup NagZ10). Determination of the structural basis for glycoside phosphorylases is important for protein engineering to expand the variety of reactions along with exploration of glycoside phosphorylases.
GH94 along with GH112 exclusively comprises glycoside phosphorylases unlike GH13, GH65, and GH130 and follows inverting mechanism. Cellobiose phosphorylase (CBP)11,12, cellodextrin phosphorylase13, laminaribiose phosphorylase14, and 1,2-β-oligoglucan phosphorylase (SOGP, “S” means the initial letter of “sophoro-”oligosaccharide representing “β-1,2-gluco-”oligosaccharide.)15, which are members of the GH94 family, share α-d-glucose-1-phosphate (G1P) as a common donor substrate for the synthetic reaction. Recently, cellobionic acid phosphorylase (CBAP), which utilizes gluconic acid as an acceptor substrate, has been reported16. The family also contains chitobiose phosphorylase (ChBP) that acts on an chitobiose (GlcNAc-β-1,4-GlcNAc) and produces α-N-acetyl-d-glucosamine-1-phosphate through phosphorolysis17. CBP, ChBP and CBAP each form a dimer and show a similar overall quaternary structure, though the amino acid sequence identities between them are relatively low (<30%). They also share the position of the catalytic pocket, which is formed at the dimer interface between the N-terminal domain (Ndom) and the catalytic domain of another subunit, although their acceptor recognition sites are diverse18,19,20. In contrast to these glycoside phosphorylases acting on β-1,4-linked glycosides, no structure of a glycoside phosphorylase acting on β-1,2-glucan and β-1,3-glucan is available.
SOGP is an enzyme given a new EC number (EC 22.214.171.1243) according to our recent study on SOGP from Listeria innocua (LiSOGP)15. LiSOGP phosphorolyzes β-1,2-glucooligosaccharides (alternatively sophorooligosaccharides, Sops) with degrees of polymerization (DP) of 3 or more. The high specificity of LiSOGP to SopNs (N denotes DP) suggests involvement of the enzyme in β-1,2-glucan metabolism together with a β-glucosidase encoded by an adjacent gene21,22. One of the most remarkable features of LiSOGP homologs is the approximately 250 additional amino acid residues at their N-terminus. This region is supposed to be important for substrate specificity, since it is fully conserved among LiSOGP homologs. However, no LiSOGP homolog has been characterized to date.
Lachnoclostridium phytofermentans (formerly, Clostridium phytofermentans) is an anaerobic bacterium that is able to metabolize various kinds of plant polysaccharides23. The bacterium possesses many genes encoding glycoside phosphorylases including five genes belonging to the GH94 family. One of these genes is an SOGP gene homolog (Cphy_0694, LpSOGP). In this study, we characterized the enzymatic properties of LpSOGP to clarify the features of the SOGP group. Furthermore, we also determined the crystal structure of LpSOGP to understand the structure-function relationship and factors relevant to differences in substrate specificity between other enzymes in the GH94 family.
Biochemical characterization of LpSOGP
In the GH94 family, classification based on substrate specificity is almost consistent with phylogenetic grouping15. LpSOGP shows 39% amino acid sequence identity with LiSOGP and belongs to the same group as it. We evaluated the general properties of LpSOGP using Sop2 as a substrate for the synthetic reaction. The optimum temperature and pH of LpSOGP were 40 °C and pH 7, respectively. LpSOGP was stable in the pH range of 6.5–8.0 (more than 80% residual activity) and up to 37 °C. LpSOGP showed similar Km and kcat values for Sop2, Sop3, and Sop4, but no significant activity toward Glc in the synthetic reaction (Table 1). Regarding phosphorolytic activity, LpSOGP showed equivalent Km and kcat values for Sop3, Sop4, and Sop5 to those in the synthetic reaction and showed no activity toward Sop2. This kinetic analysis indicates that LpSOGP has essentially the same chain length specificity as to SopNs as LiSOGP. LpSOGP showed sufficiently high kcat/Km values for G1P and inorganic phosphate (Pi) as a GH family enzyme, though the Km value for Pi was a little higher than that on LiSOGP. A double reciprocal plot for phosphorolysis of Sop3 suggests that LpSOGP follows a sequential Bi Bi mechanism (Fig. S1). LpSOGP showed very weak activity against laminaribiose and no activity toward other disaccharides such as cellobiose or monosaccharides in the synthetic reaction on TLC analysis (Fig. S2A–C). In addition, LpSOGP did not show phosphorolytic activity toward cellobiose or laminaribiose (Fig. S2D). These results indicate that LpSOGP is highly specific to SopNs, as LiSOGP is15, and is completely different from other GH94 enzymes in substrate specificity.
The crystal structure of apo LpSOGP was determined at 2.0 Å resolution (Table S1). The crystals contain two identical molecules in an asymmetric unit. The tertiary structure consists of four domains: two N-terminal β-sandwich domains (residues 1–257, yellow, Ndom1; and 295–553, light blue, Ndom2), a catalytic (α/α)6 barrel domain (593–1020, green), and a β sheet domain (magenta). The β sheet domain consists of a middle segment (581–592) and a C-terminal segment (1021–1113). Ndom2 and the catalytic domain are connected through a helical linker region (554–580, orange), and Ndom1 and Ndom2 are connected through a linker composed of a helix and a long loop (258–294, red) (Fig. 1A). The helix is included in the linker region due to the alignment with CBAP, ChBP, and CBP. The two molecules in the asymmetric unit are in contact with each other mostly in the Ndom1 region (Fig. 1B). The contact area is only 2.5% (935.5 Å2) of the monomer surface area. The estimated ΔGdiss is a negative value (−11.2 kcal/mol), which suggests that the dissociated state is more stable, based on analysis using the protein-protein interaction interface server (PISA, http://www.ebi.ac.uk/msd-srv/prot_int/pistart.html)24. In addition, LpSOGP was eluted at the retention time of 100 kDa on size-exclusion chromatography. These results indicate that LpSOGP is a monomeric enzyme, as LiSOGP is15.
The overall structure of LpSOGP besides Ndom1 is basically similar to those of GH94 CBAP from Saccharophagus degradans (SdCBAP), ChBP from Vibrio proteolyticus (VpChBP), and CBP from Cellvibrio gilvus (CgCBP) (the RMSD values are 4.11, 3.53, and 3.29 Å, respectively). Ndom1 is unique to LpSOGP, being missing in CBP, ChBP, and CBAP (Fig. 1C). It is interesting that Ndom1 in LpSOGP occupies the same position as the Ndom in subunit B of CgCBP, when subunit A in the CgCBP dimer and the corresponding region of LpSOGP (all except for Ndom1, residues 295–1113) are superimposed (Fig. 1D left). This structural observation suggests that LpSOGP forms a catalytic pocket within its tertiary structure unlike the other three GH94 enzymes (Fig. 1D right). The structure of Ndom1 is similar to those of both Ndom2 and Ndoms (Fig. 2), though Ndom1 shows low sequence identity with them (<15%) (Table 2). It should be noted that Ndoms in CgCBP, VpChBP, and SdCBAP are similar to Ndom1 rather than Ndom2 in both the primary and 3D structures (Table 2, Fig. 2). On the contrary, the amino acid sequence identity of Ndom1 in LpSOGP with the corresponding region in LiSOGP (29%) is lower than that of Ndom2 (40%) (Fig. 1C). As for the substrate recognition region, two helices (α1 and α2) in Ndom1 constitute a part of the catalytic pocket as well as in Ndoms in VpChBP and CgCBP (Figs 2A,D,E and 3A). The corresponding region in Ndom2 is a short loop like that of SdCBAP, but the substrate recognition helix of SdCBAP is not conserved in Ndom2 (Figs 2B,C and 3B).
Complex structures with ligands
In order to understand the substrate recognition mechanism, the crystal structures of LpSOGP in complexes with G1P, Sop2 (with isofagomine d-tartrate (IFG) and (NH4)2SO4), and Sop3 (with (NH4)2SO4) were determined at 2.1, 2.0 and 2.2 Å resolution, respectively (Table S1). In the complex structure with G1P, the electron density of G1P was clearly observed at subsite −1. It is noteworthy that this is the first reported structure of an inverting glycoside phosphorylase complexed with a sugar-phosphate substrate. The Glc moiety in the G1P molecule undergoes direct interactions with R630, D631, W758, D760, and E917 (Figs 3 and 4A), all of which are highly conserved in GH94 enzymes. The position of the Glc moiety is well superimposed with ligands at subsite −1 in other GH94 enzymes such as GlcNAc in VpChBP (Fig. 5A). The phosphate moiety of the G1P molecule forms hydrogen bonds with Y922, S1005, and three water molecules (Figs 3 and 4A). Contrarily, the moiety does not form hydrogen bonds with H924 and S1006 (main chain) that correspond with the reported SO42−-recognizing residues (H624 and G710, respectively, in the case of VpChBP). This is because the phosphate moiety is slightly deviated from the position of SO42− in VpChBP and CgCBP (1.1 Å and 1.5 Å, respectively) (Fig. 5A).
Subsites +1 and +2 were revealed by the complex structure with IFG, Sop2, and (NH4)2SO4. IFG is located at subsite −1, since IFG is well superimposed with the Glc moiety of G1P (Fig. 5A). In addition, the position of SO42− is almost identical with that in VpChBP. Only the electron density of the α-anomer of Sop2 is observed adjacent to IFG (Fig. 4B). The 2-OH group in the non-reducing end glucoside and the 1-OH group in the reducing end glucoside of Sop2 face subsite −1 and outside the substrate pocket, respectively. Dihedral angles φ (O5-C1-O1-C’2) and ψ (C1-O1-C’2-C’1) in the Sop2 molecule are −69.7° and 146.5°, respectively. The corresponding angles of a free Sop2 structure whose energy is minimized25 are similar (−72° and 114°, respectively). The conformations of glucosides at both subsites are 4C1. These facts mean that Sop2 binds to LpSOGP with only a little distortion, suggesting that Sop2 is bound at subsites +1 to +2 productively. Sop2 forms 8 hydrogen bonds with Q621, D631, and Y1004 (for binding at subsite +2), and D760, R907, R916, and IFG (for binding at subsite +1) directly. Sop2 also undergoes interactions with R630, A626, G623, D760, N138, Q621, and E917 indirectly through the 8 hydrogen bonds with water molecules. Y141 constitutes the substrate pocket by forming a hydrogen bond with R907, though the residue forms no hydrogen bond with Sop2.
The Sop3 (with (NH4)2SO4)-soaked structure shows clear electron density for the Sop2 moiety at subsites +1 and +2 (Fig. 4C). The Glc moiety at subsite +2 is a β-anomer unlike in the case of Sop2 soaking, though two ligands at subsites +1 and +2 are well superimposed (Fig. 4C,D), suggesting that Sop3 is bound at subsites +1 to +3. However, since weak electron density was observed beyond the 1-OH group of the glucose moiety at subsite +2, Sop3 appears to be mostly disordered at subsite +3. The disorder at subsite +3 is perhaps due to fewer hydrogen bond interactions than at subsites +1 and +2. These observations are consistent with the similar kinetic parameters for Sop2–5. The electron density of glycerol was observed at subsite −1. The glycerol molecule is well superimposed with a part of IFG at subsite −1 (Fig. 4D). The SO42− ion was not observed in the catalytic pocket perhaps due to precipitation of ligands in the soaking solution. Overall the reaction mechanism of LpSOGP is proposed as shown in Fig. S3.
In this study, we identified the function of LpSOGP, determined its crystal structure, which is the first one among phosphorylases acting on β-linked glucan, and clarified the binding modes of substrates. The similarity between LpSOGP and LiSOGP in enzymatic function and the conserved substrate recognition residues among SOGP homologs (Fig. S4) imply that this group of SOGP homologs shares essentially the same substrate specificity. The structures of LpSOGP enable us to discuss the molecular mechanism of substrate specificity through comparison with those of other structurally available GH94 enzymes. Since many residues related with substrate recognition at subsite −1 and the catalytic acid (D760) are highly conserved among GH94 enzymes spatially (Fig. 5A), these residues were aligned to compare subsites +1 and +2 between LpSOGP and the other enzymes, SdCBAP, VpChBP, and CgCBP (Fig. 3).
The most remarkable difference between LpSOGP, and VpChBP and CgCBP at subsite +1 is the orientation of the ligands (Fig. 5B). Although the Glc moiety in LpSOGP at subsite +1 is located at a similar position to both the GlcNAc molecule in VpChBP and the Glc molecule in CgCBP, the Glc moiety in LpSOGP is rotated by more than 120° about its C2-O2 bond involved in its glycosidic linkage from the molecules in CgCBP and VpChBP. In LpSOGP, this rotation allows the anomeric position of the Glc moiety at subsite +1 to be oriented toward the open space in the catalytic pocket but not toward the wall of the pocket (Figs 4D and 5B). In LpSOGP, R907 protruding to subsite +1 and Y141 forming a hydrogen bond with R907 occupy a position that is able to hinder the binding of the Glc molecule in CgCBP and the GlcNAc molecule in VpChBP sterically. On the other hand, the positions of Q168 (VpChBP) and Q165 (CgCBP) can cause steric hindrance to the Sop2 in LpSOGP. The spatial positions of these residues explain the clear difference in substrate binding mode, though these residues correspond in the primary sequences (Fig. 3A). In addition, the positions of these residues depend on the orientations of helices shown in Fig. 5B.
In LpSOGP, the substrate inversion at subsite +1 is likely a key factor for substrate specificity, as described below. The dihedral angle of C1(IFG)-O’2 (Sop2)-C’2-C’1 (corresponding to ψ between subsite −1 and +1) is −46.0°, suggesting that the torsion angle of a glycosidic bond between subsites −1 and +1 is obviously different from that of energy-minimized Sop2 (114°)25 and is unfavorable for substrate binding. In addition, the dihedral angle (ψ) of Sop2 in LiBGL, a Sop2-degrading β-glucosidase, is also quite different (159.8°)22. However, binding of a Glc moiety to subsite +1 itself appears not to compensate for the disadvantage, since no electron density derived from Glc was observed even on soaking with 1 M Glc (data not shown). This is consistent with the fact that the number of direct interactions with Sop2 at subsite +1 is fewer than those in other GH94 phosphorylases (Table S2). The disadvantage for substrate binding is likely compensated for at subsite +2, since the glycosidic bond in the Sop2 molecule (between subsites +1 and +2) is distorted only a little. Considering the substrate binding of CBP, the dihedral angle of cellobiose (subsites −1 and +1) in CBP from Cellulomonas uda (CuCBP) is φ = −82.5° and ψ = 65.0° (PDB ID: 3S4A), being within the range of stable conformation of a free cellobiose molecule25. The position and the orientation of the Glc moiety at subsite +1 are similar to those of the Glc molecule in CgCBP. This is consistent with substrate specificity of the CBPs. Overall, the combination of “the inversion at subsite +1” and “the compensation at subsite +2” defines the substrate specificity of LpSOGP.
The architecture at subsite +2 is unique in LpSOGP, compared with in SdCBAP, VpChBP, and CgCBP. The small side chains of Gly and Ala residues provide LpSOGP with sufficient space as subsite +2. On the contrary, Q347 (SdCBAP), R343 (VpChBP), and R362 (CgCBP) protrude to subsite +2 to fill the space and interact with the ligands at subsites −1 and/or +1 (Figs 3D and 5C). In CuCBP, the side chain of the Arg residue corresponding to R362 (CgCBP) is flipped out despite that cellobiose binds to CuCBP26. This flipping makes a space corresponding to subsite +2 of LpSOGP, which is consistent with the fact that CuCBP allows gentiobiose (Glc-β-1,6-Glc) and melibiose (Glc-α-1,6-Glc) to be minor acceptor substrates27. These observations imply an evolutional relationship between SOGP and other GH94 enzymes.
Ndom1 appears to be generated through domain duplication according to its position and the structural similarity to Ndom2. This duplication monomerizes LpSOGP but retains the fundamental constitution of a catalytic pocket between hetero domains. Such an example is found in isocitrate dehydrogenases28. A class II ribonucleotide reductase is another example, though only a part of the domain is duplicated29. This evolutional pathway is reversed against oligomerization through swapping of duplicated domains30,31. Among carbohydrate-active enzymes, the monomeric constitution of GH55 β-1,3-glucanase from Phanerochaete chrysosporium composed of tandem β-helical domains seems to be caused by domain duplication32,33. However, the catalytic domain is located at the interface of the two structurally homologous domains unlike in the case of LpSOGP.
This study clearly provides mechanistic insights into the substrate specificity of LpSOGP, which is an important structural basis for enzymes acting on β-1,2-linked glucosidic bonds. The domain duplication found in LpSOGP is a unique example in carbohydrate-active enzymes and expands the knowledge on molecular evolution.
Materials and Methods
Preparation of recombinant LpSOGP
A gene encoding LpSOGP (cphy_0694, GenBankTM accession number ABX41081.1) was amplified by PCR from genomic DNA of L. phytofermentans as a template using KOD-plus DNA polymerase (Toyobo, Osaka, Japan) with the following oligonucleotides based on the genomic sequence (GenBankTM accession number CP000885): 5′-aaaccatgggcatactaaaaacattgtctg-3′ as the forward primer containing an NcoI site (underlined) and 5′-tttctcgaggttcttaacataaatatg-3′ as the reverse primer containing an XhoI site (underlined). The amplified PCR product was purified using a QIAquick PCR Purification Kit (Qiagen, Hilden, Germany), digested with NcoI and XhoI (New England Biolabs, Beverly, MA, USA), and inserted into the corresponding sites of pET28a (+) (Novagen, Madison, WI, USA) to encode a His6-tagged fusion at the C-terminus of the recombinant protein. The expression plasmid was propagated in Escherichia coli BL21(DE3) (Novagen), purified using a High Pure Plasmid Isolation Kit (Roche Diagnostics, Mannheim, Germany), and verified by sequencing (Eurofins Genomics K.K., Tokyo, Japan). The transformant was cultured in LB medium containing 30 μg/ml of kanamycin at 37 °C until OD660 reached around 0.8. After 0.1 mM IPTG (final concentration) was added to produce recombinant LpSOGP, the cells were cultured at 20 °C overnight. The cells were collected by centrifugation at 3900× g for 5 min, suspended in 50 mM MOPS-NaOH (pH 7.5) buffer containing 300 mM NaCl (buffer A), and then disrupted by sonication. The supernatant obtained on centrifugation at 27000× g for 10 min was loaded onto a HisTrap FF crude column (5 ml; GE Healthcare, Buckinghamshire, England) equilibrated with buffer A. After the column had been washed with buffer A containing 10 mM imidazole till almost unbound proteins were removed, LpSOGP was eluted with a linear gradient of imidazole (10–300 mM, 55 ml total volume) in the same buffer at a flow rate of 2 ml/min. The eluate was buffered with 20 mM MOPS-NaOH (pH 7.5) using Amicon Ultra 30,000 molecular weight cut-off (Millipore, Billerica, MA, USA) for assaying. For crystallization, the enzyme solution mixed with an equal volume of 50 mM MOPS-NaOH (pH 7.5) containing 60% saturated ammonium sulfate was loaded onto a HiTrapTM Butyl HP column (5 ml; GE Healthcare) equilibrated with 50 mM MOPS-NaOH (pH 7.5) containing 30% saturated ammonium sulfate. The enzyme was eluted with a linear gradient of 30–0% saturated ammonium sulfate (55 ml total volume) in 50 mM MOPS-NaOH (pH 7.5) at a flow rate of 2 ml/min. The eluate was buffered with 5 mM MOPS-NaOH buffer (pH 7.5) using Amicon Ultra 30,000 molecular weight cut-off to concentrate the enzyme to 10 mg/ml. An ÄKTA Prime Plus chromatography system (GE Healthcare) was used for the whole enzyme purification steps. The purity of the enzyme was analyzed by SDS-PAGE using 8% polyacrylamide gels. Protein concentrations were determined from UV absorbance at 280 nm (the extinct coefficient34 and theoretical molecular weight of LpSOGP are 167890 cm−1M−1 and 169640 Da, respectively). For expression of selenomethionine (SeMet)-labeled LpSOGP, the plasmid was introduced into E. coli B834(DE3). LeMaster medium containing 30 μg/ml kanamycin was used in place of LB medium. Protein induction and purification were performed in almost the same way as for the native protein.
The phosphorolytic activity of LpSOGP was determined by quantifying G1P produced from SopNs and 10 mM inorganic phosphate by coupling assay using phosphoglucomutase and glucose 6-phosphate dehydrogenase35. The colorization reagent and substrate solution (85 μl) comprising SopNs, inorganic phosphate, 10 μM glucose-1,6-bisphosphate (Sigma-Aldrich, St. Louis, MO, USA), 10 IU/mL glucose 6-phosphate dehydrogenase from Leuconostoc sp. (Oriental Yeast, Tokyo, Japan), 12.5 IU/mL phosphoglucomutase from rabbit muscle (Sigma-Aldrich), 1.0 mM thio-NAD+ (Oriental Yeast), 50 mM MgCl2, and 100 mM MOPS-NaOH (pH 7.5) was mixed with 85 μl of the enzyme solution in 20 mM MOPS-NaOH (pH 7.5) to start the reaction in a 96-well microplate (EIA/RIA plate, 96-well half area; Corning, NY, USA). The reaction mixture was incubated at 30 °C and the increase in absorbance at 400 nm due to thio-NADH was monitored at 1-minute interval for 10 min with a Spectramax 190 (Molecular Devices, CA, USA).
Synthetic activity was determined by measuring inorganic phosphate produced from acceptors and 10 mM G1P by the Lowry and Lopez method36. The substrate solution comprising various concentrations of SopNs and 10 mM G1P in 100 mM MOPS-NaOH (pH 7.0) (140 μl) was mixed with 20 μl of enzyme solution to start the reaction at 30 °C. Aliquots (20 μl) were taken at 2-minute intervals and was mixed with 160 μl of 0.2 M sodium phosphate (pH 4.0) and 25 mM ammonium molybdate containing 25 mM sulfuric acid to stop the reaction. The solutions were mixed with 20 μl of 1% ascorbic acid containing 0.05% potassium sulfate. After the solution had been incubated at 37 °C for 1 h, the increase in absorbance at 700 nm was measured.
For investigation of substrate specificity, the synthetic reaction was performed using a substrate solution containing 10 mM each acceptor substrate and 10 mM G1P in the presence of 100 mM MOPS-NaOH (pH 7.0). Substrates are altered to 10 mM each oligosaccharide and 10 mM inorganic phosphate for phosphorolysis. The concentration of LpSOGP was 0.1 mg/ml when Sop2 and Sop3 were used as substrates and 1.0 mg/ml for the other substrates. The reaction solution was incubated at 30 °C for 1 h and then the reaction was stopped by heat treatment at 100 °C for 5 min. The reaction products were analyzed by thin layer chromatography (TLC).
Temperature and pH profiles
The effects of temperature and pH on activity were evaluated as to the synthetic activity using 10 mM Sop2 and 10 mM G1P. The optimum temperature and pH were determined by measuring the activity at various temperatures (0–60 °C) and in various pH ranges in 20 mM buffers, respectively, as follows: sodium acetate (pH 4.0–5.5), MES-NaOH (pH 5.5–6.5), MOPS-NaOH (pH 6.5–7.5), Tris-HCl (pH 7.5–9.0), and glycine-NaOH (pH 9.0–10.0). The thermal and pH stabilities were determined from the residual synthetic activity at 30 °C after incubation of LpSOGP (0.5 mg/ml) at various temperatures (0–60 °C) in 100 mM MOPS-NaOH (pH 7.5), and at 37 °C in 20 mM various buffers as described above, respectively.
Each reaction solution (0.5 μl) was spotted onto a TLC plate (Kieselgel 60 F254; Merck, Darmstadt, Germany). The TLC plates were developed with 75% acetonitrile in water (v/v). The TLC plates were then soaked in a 5% sulfuric acid:95% ethanol (v/v) solution and heated in an oven until bands were sufficiently visible.
The initial velocities of the synthetic and phosphorolytic reactions with various concentrations of substrates were determined under the standard conditions. The kinetic parameters for SopNs were calculated by curve fitting the experimental data to the Michaelis-Menten equation (1) using GraFit version 7.0.3.
where v is reaction velocity, kcat is turnover number, Km is Michaelis constant, [E]0 is enzyme concentration, and [S] is substrate concentration.
LpSOGP (2 mg/ml) was loaded onto a SuperdexTM 200 10/300 GL column (GE Healthcare) equilibrated with 50 mM Tris-HCl (pH 7.5) containing 150 mM NaCl. Ovalbumin (44 kDa), conalbumin (75 kDa), aldolase (158 kDa), ferritin (440 kDa), and thyroglobulin (669 kDa; GE Healthcare) were used as standard proteins. Blue dextran 2000 (2000 kDa; GE Healthcare) was used to determine the void volume of the column.
All crystals (native and SeMet-labeled protein) used for data collection were obtained at 25 °C using the hanging drop vapor diffusion method by mixing 1–2.4 μl of 10 mg/ml protein solution with an equal volume of reservoir solution comprising 0.1 M Tris-HCl (pH 7.5), 0.2 M calcium acetate, and 10–15% PEG3350. Crystals completely grew in 2–3 days. Crystals were cryoprotected with the reservoir solution containing 30% glycerol for the SeMet-substituted enzyme or 25% PEG400 for the native enzyme. A cryoprotectant containing MgCl2 instead of calcium acetate was used to avoid precipitation of ligands when crystals were soaked with soaking solution containing G1P or IFG (Toronto Research Chemicals Inc., Toronto, Canada), Sop2, or (NH4)2SO4. IFG was selected as a glucose analog, since it strongly inhibited the synthetic reaction of SOGP in a preliminary experiment. Crystals were then soaked in the cryoprotectants supplemented with 50 mM Sop3 (with 50 mM (NH4)2SO4) (SeMet-labeled), 20 mM G1P (native), or 20 mM Sop2 (with 1.0 mM IFG and 100 mM (NH4)2SO4) (native). In the case of soaking in 50 mM Sop3 (with 50 mM (NH4)2SO4), precipitation in the soaking solution made the concentrations of the ligands obscure. The crystals were cooled and then kept at 100 K in a nitrogen-gas stream during data collection. A set of X-ray diffraction data for each crystal was collected using a CCD detector (ADSC Quantum 210r) on a beamline BL-5A at Photon Factory (Tsukuba, Japan). The diffraction data set was processed using iMosflm37 or HKL200038. The initial phase of the LpSOGP apo structure was determined by the single wavelength anomalous dispersion method using AutoSol in Phenix39. Automated model building was also performed using the same program. Molecular replacement was performed using MOLREP40 to determine the initial phases of complex structures. Manual model building and refinement were performed using Coot41 and Refmac542, respectively. Quality checking of the structures was performed using the wwPDB validation server (http://wwpdb-validation.wwpdb.org/validservice/). PyMOL (DeLano Scientific; http://www.pymol.org) was used for the preparation of figures. The buried surface area was calculated with PISA24.
How to cite this article: Nakajima, M. et al. Mechanistic insight into the substrate specificity of 1,2-β-oligoglucan phosphorylase from Lachnoclostridium phytofermentans .Sci. Rep. 7, 42671; doi: 10.1038/srep42671 (2017).
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This work was performed with the approval of the Photon Factory Program Advisory Committee (Proposal Nos 2012G108 and 2014G509). Dr. Motomitsu Kitaoka kindly provided the materials for crystallization and several ideas for discussion. Hiroyuki Toyoizumi, Keisuke Sudo, and Shiori Saito helped us to optimize the crystallization conditions.
The authors declare no competing financial interests.
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Nakajima, M., Tanaka, N., Furukawa, N. et al. Mechanistic insight into the substrate specificity of 1,2-β-oligoglucan phosphorylase from Lachnoclostridium phytofermentans. Sci Rep 7, 42671 (2017). https://doi.org/10.1038/srep42671
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