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• W2111015751 abstract "The type 3 synthase catalyzes the formation of the Streptococcus pneumoniae type 3 capsular polysaccharide [-3)-β-d-GlcUA-(1, 4)-β-d-Glc-(1-]n. Synthesis is comprised of two distinct catalytic phases separated by a transition step whereby an oligosaccharylphosphatidylglycerol primer becomes tightly bound to the carbohydrate acceptor recognition site of the synthase. Using the recombinant synthase in Escherichia coli membranes, we determined that a critical oligosaccharide length of ∼8 monosaccharides was required for recognition of the growing chain by the synthase. Upon binding of the oligosaccharide-lipid to the carbohydrate recognition site, the polymerization reaction entered a highly processive phase to produce polymer of high molecular weight. The initial oligosaccharide-synthetic phase also appeared to be processive, the duration of which was enhanced by the concentration of UDP-GlcUA and diminished by an increase in temperature. The overall reaction approached a steady state equilibrium between the polymer- and oligosaccharide-forming phases that was shifted toward the former by higher UDP-GlcUA levels or lower temperatures and toward the latter by lower concentrations of UDP-GlcUA or higher temperatures. The transition step between the two enzymatic phases demonstrated cooperative kinetics, which is predicted to reflect a possible reorientation of the oligosaccharide-lipid in conjunction with the formation of a tight binding complex. The type 3 synthase catalyzes the formation of the Streptococcus pneumoniae type 3 capsular polysaccharide [-3)-β-d-GlcUA-(1, 4)-β-d-Glc-(1-]n. Synthesis is comprised of two distinct catalytic phases separated by a transition step whereby an oligosaccharylphosphatidylglycerol primer becomes tightly bound to the carbohydrate acceptor recognition site of the synthase. Using the recombinant synthase in Escherichia coli membranes, we determined that a critical oligosaccharide length of ∼8 monosaccharides was required for recognition of the growing chain by the synthase. Upon binding of the oligosaccharide-lipid to the carbohydrate recognition site, the polymerization reaction entered a highly processive phase to produce polymer of high molecular weight. The initial oligosaccharide-synthetic phase also appeared to be processive, the duration of which was enhanced by the concentration of UDP-GlcUA and diminished by an increase in temperature. The overall reaction approached a steady state equilibrium between the polymer- and oligosaccharide-forming phases that was shifted toward the former by higher UDP-GlcUA levels or lower temperatures and toward the latter by lower concentrations of UDP-GlcUA or higher temperatures. The transition step between the two enzymatic phases demonstrated cooperative kinetics, which is predicted to reflect a possible reorientation of the oligosaccharide-lipid in conjunction with the formation of a tight binding complex. The Streptococcus pneumoniae type 3 capsule is a high molecular weight polysaccharide that grows at the nonreducing end by the alternate addition of Glc and GlcUA 2The abbreviations used are: GlcUA, glucuronic acid; PLD, phospholipase D. (1Cartee R.T. Forsee W.T. Yother J. J. Biol. Chem. 2000; 275: 3907-3914Abstract Full Text Full Text PDF PubMed Scopus (54) Google Scholar). Its synthesis is mediated by the type 3 synthase, which is a processive glycosyltransferase in the GT-2 family that includes other members that synthesize cellulose, hyaluronan, chitin, and related β-glycans (2Saxena I.M. Brown R.M.J. Fevere M. Geremia R.A. Henrissat B. J. Bacteriol. 1995; 177: 1419-1424Crossref PubMed Google Scholar, 3Campbell J.A. Davies G.J. Bulone V. Henrissat B. Biochem. J. 1997; 326: 929-942Crossref PubMed Scopus (630) Google Scholar, 4Keenleyside W.J. Whitfield C. J. Biol. Chem. 1996; 271: 28581-28592Abstract Full Text Full Text PDF PubMed Scopus (115) Google Scholar). Similar to other members of this class, the type 3 synthase contains a carbohydrate recognition site that binds the growing polysaccharide and is an integral part of the complex catalytic mechanism (5Forsee W.T. Cartee R.T. Yother J. J. Biol. Chem. 2000; 275: 25972-25978Abstract Full Text Full Text PDF PubMed Scopus (31) Google Scholar). In both S. pneumoniae type 3 and Escherichia coli expressing the recombinant synthase, a novel lipid determined to be glucosylphosphatidylglycerol accumulates in the membranes and serves as a primer for polysaccharide synthesis (6Cartee R.T. Forsee W.T. Yother J. J. Bacteriol. 2005; 187: 4470-4479Crossref PubMed Scopus (32) Google Scholar). The first reaction catalyzed by the type 3 synthase is the transfer of Glc from UDP-Glc to phosphatidylglycerol. Glucosylphosphatidylglycerol is present at low concentrations in synthase-containing cells and serves as an acceptor for GlcUA from UDP-GlcUA to form the disaccharide lipid, glucuronyl-glucosyl-phosphatidylglycerol. When both UDP-sugars are present at very low concentrations, the synthase catalyzes a short lived processive reaction that results in the formation of a glycolipid fraction consisting of a mixture of short oligosaccharides (7Cartee R.T. Forsee W.T. Jensen J.W. Yother J. J. Biol. Chem. 2001; 276: 48831-48839Abstract Full Text Full Text PDF PubMed Scopus (30) Google Scholar). As the concentrations of the UDP-sugars increase, the reaction abruptly becomes highly processive, and the products are rapidly extended into polymers of dramatically increased chain length. Presumably, a critical step in the initiation and elongation of high molecular weight polymer is the binding of the oligosaccharide-lipid to the carbohydrate acceptor recognition site of the synthase. Although much is known about carbohydrate acceptor recognition sequences among glycoside hydrolases, there is very little information on this aspect of catalysis by most polysaccharide biosynthetic systems. Several hundred glycoside hydrolases have been grouped into over 40 different families based on the sequences of their carbohydrate binding domains (8Boraston A.B. Bolam D.N. Gilbert H.J. Davies G.J. Biochem. J. 2004; 382: 769-781Crossref PubMed Scopus (1537) Google Scholar). In general, these binding domains are noncatalytic and serve to bring the biocatalytic domains into close proximity with their polysaccharide substrates (9Flint J. Bolam D.N. Nurizzo D. Taylor E.J. Williamson M.P. Walters C. Davies G.J. Gilbert H.J. J. Biol. Chem. 2005; 280: 23718-23726Abstract Full Text Full Text PDF PubMed Scopus (33) Google Scholar). In contrast, structural studies of glycosyltransferases have not revealed significant sequence motifs that would provide for an interaction with carbohydrate acceptors. Based on hydrophobic cluster analysis, sequence homology, and x-ray crystallographic data, a fairly detailed picture is emerging of the binding and catalytic interaction of some glycosyltransferases with their nucleotide diphosphate sugar donor (10Charnock S.J. Davies G.J. Biochemistry. 1999; 38: 6380-6385Crossref PubMed Scopus (310) Google Scholar, 11Davies, G. J., Charnock, S. J., and Henrissat, B., (201) Trends Glycosci. Glycotechnol. 13, 105–120Google Scholar, 12Unligil U.M. Zhou S. Yuwaraj S. Sarkar M. Schachter H. Rini J.M. EMBO J. 2000; 19: 5269-5280Crossref PubMed Scopus (239) Google Scholar). This information has led to the development of a rather strong argument for the existence of only a single nucleotide-sugar binding site in polymerases, such as type 3 synthase, that require two distinct nucleotide sugar donors (11Davies, G. J., Charnock, S. J., and Henrissat, B., (201) Trends Glycosci. Glycotechnol. 13, 105–120Google Scholar). The polymerization reaction catalyzed by many processive glycosyltransferases is thought to involve a cyclical translocation process wherein the polymer chain detaches, slides forward, and then reattaches to the enzyme to allow another round of sugar additions. Enzymes similar to the type 3 synthase have been postulated to undergo a translocation step after the addition of every two sugars to avoid the necessity of rotating either the polymer or the synthase (2Saxena I.M. Brown R.M.J. Fevere M. Geremia R.A. Henrissat B. J. Bacteriol. 1995; 177: 1419-1424Crossref PubMed Google Scholar, 13Koyama M. Helbert W. Imai T. Sugiyama J. Henrissat B. Proc. Natl. Acad. Sci. U. S. A. 1997; 94: 9091-9095Crossref PubMed Scopus (236) Google Scholar). Previous work from this laboratory has shown that polysaccharide chains are ejected from the type 3 synthase when one UDP-sugar is present at high concentration and the other is limiting or absent, suggesting that an abortive translocation process might serve to terminate chain growth (5Forsee W.T. Cartee R.T. Yother J. J. Biol. Chem. 2000; 275: 25972-25978Abstract Full Text Full Text PDF PubMed Scopus (31) Google Scholar). The current investigation indicates that the carbohydrate recognition site may form a complex with an approximate eight-sugar segment of the growing polysaccharide chain, and that this interaction may provide for the high degree of processivity of chain assembly as well as for controlling the ultimate size of the polymer. Materials—Econo-safe scintillation mixture was obtained from Research Products International Corp. and Biogel P-4 was from Bio-Rad Laboratories. Lysozyme, UDP-Glc, UDP-GlcUA, and Streptomyces chromofuscus phospholipase D (PLD) were from Sigma. Chromatography paper (3MM Chr) and DEAE-cellulose (DE-52) were from Whatman. UDP-[14C]GlcUA (175 mCi/mmol) was purchased from ICN, and Nonidet P-40 was from Calbiochem. Todd Hewitt broth, yeast extract, and tryptone were from Difco. Preparation of Type 3 Oligosaccharide Standards—[14C]GlcUA-labeled type 3 polymer was digested with Bacillus circulans type 3-specific depolymerase as previously described (5Forsee W.T. Cartee R.T. Yother J. J. Biol. Chem. 2000; 275: 25972-25978Abstract Full Text Full Text PDF PubMed Scopus (31) Google Scholar, 14Campbell J.H. Pappenheimer A.M. Immunochemistry. 1966; 3: 195-212Crossref PubMed Scopus (27) Google Scholar, 15Torriani A. Pappenheimer A. J. Biol. Chem. 1962; 237: 3-13Abstract Full Text PDF PubMed Google Scholar). The released oligosaccharides were fractionated and purified by DEAE-cellulose chromatography and gel filtration on Biogel P-4, as described below. Growth Conditions and Membrane Preparation—Recombinant E. coli strain JD424 containing the type 3 synthase (Cps3S) has been described (16Dillard J.P. Vandersea M.W. Yother J. J. Exp. Med. 1995; 181: 973-983Crossref PubMed Scopus (119) Google Scholar). The clone contains a 2.1-kb Sau3AI fragment from S. pneumoniae WU2 consisting of the 3′-end of cps3D and the complete cps3S. The growth of strain JD424, induction of synthase expression, and harvesting of the cells was performed as described previously (5Forsee W.T. Cartee R.T. Yother J. J. Biol. Chem. 2000; 275: 25972-25978Abstract Full Text Full Text PDF PubMed Scopus (31) Google Scholar). Spheroplasts and membranes were obtained following lysozyme digestion and sonication, as described previously except that leupeptin and pepstatin were omitted from the spheroplasting reaction (7Cartee R.T. Forsee W.T. Jensen J.W. Yother J. J. Biol. Chem. 2001; 276: 48831-48839Abstract Full Text Full Text PDF PubMed Scopus (30) Google Scholar). Assay of Synthase Activity—Type 3 synthase activity was determined in 100-μl reaction mixtures consisting of 100 mm Hepes (pH 7.5), 10 mm MgCl2, 1 mm UDP-Glc, 0.01 μCi of UDP-[14C]GlcUA, and E. coli membranes (3–15 μg of protein). Standard reactions were incubated at 35 °C for 10 min and terminated by the addition of 5 μl of 12.5 m acetic acid. The reaction components were separated by ascending paper chromatography on Whatman 3MM paper with a solvent mixture of butanol:acetic acid:water (44:16:40). The chromatograms were cut into 1-cm strips, and polymer (origin product) and oligo-lipid (migrating slightly faster than Glc) were quantified by liquid scintillation counting. Enzyme activity was determined by calculating the nmol of hexuronic acid incorporated per mg of protein. All experiments were repeated multiple times and/or under varying conditions. The results shown are representative of these experiments. Preparation of Preloaded Synthase—The carbohydrate acceptor binding site of the type 3 synthase was preloaded with unlabeled growing polymer in a 3-ml reaction mixture consisting of E. coli membranes (2 mg of protein), 100 mm Hepes (pH 7.5), 10 mm MgCl2, 0.1 mm UDP-Glc, and 0.1 mm UDP-GlcUA. The reaction was incubated for 2 min at 25 °C and terminated by placing on ice. The membrane-enzyme-polysaccharide complexes were collected by centrifugation at 100,000 × g for 30 min, and suspended in 2.5 ml of a wash solution consisting of 100 mm Hepes (pH 7.5) and 10% glycerol. The washed membranes were collected by centrifugation, as above. The membrane pellet was washed two more times as described above. Preparation of Products for Chromatography—Oligosaccharide-lipid and polymer products were synthesized in scaled-up standard enzyme assay mixtures under the conditions indicated in the figure legends. The reactions were terminated by placing on ice, and the labeled membranes were washed three times by centrifugation as described above. The washed membranes were suspended in 200 μl of 5 mm EDTA (pH 7.5), heated at 100 °C for 4 min, and solubilized by the addition of 0.25% Nonidet P-40. The solubilized products were digested with PLD (10 units/100 μl) for 1 h at 30°C in a mixture containing 50 mm Tris (pH 8) and 10 mm CaCl2. The digests were heated at 100 °C for 5 min, and the precipitate was removed by centrifugation at 10,000 × g for 5 min. Analytical Methods—The length of the type 3 polysaccharide was determined using the lipid anchor as a marker for the reducing end oligosaccharide fragment following hydrolysis of the polymer with type 3-specific depolymerase. 3W. T. Forsee, R. T. Cartee, and J. Yother, manuscript in preparation. The size of the residual hydrophobic oligosaccharide was determined, and polymer size was calculated based on the proportions of radioisotope in the hydrophilic and hydrophobic oligosaccharide fractions. Protein was determined as described with a Coomassie Blue dye using bovine serum albumin as the standard (17Bradford M.M. Anal. Biochem. 1976; 72: 248-254Crossref PubMed Scopus (217548) Google Scholar). Ion exchange chromatography was carried out on 0.6 × 2.5-cm columns of DEAE-cellulose (OH–) following removal of the lipid component from samples by PLD digestion. The columns were equilibrated with 5 ml of 20 mm ammonium acetate (pH 7.4) and washed with 3 volumes of H2O prior to application of the sample in 2 ml of H2O. The columns were washed with 2 ml of H2O, and the products were eluted by one of two ionic gradient methods. Optimum oligosaccharide separation was achieved with a 40-ml linear gradient of 0–0.2 m ammonium acetate (pH 7.4) at a flow rate of 0.8 ml/min. Fractions (1.2 ml) were collected and monitored for radioactivity by liquid scintillation counting and for ionic strength by conductivity. Oligosaccharide and polymer mixtures were fractionated with a 2-step gradient at a flow rate of 0.4 ml/min. The first step consisted of a 30-ml gradient of 0–0.3 m ammonium acetate (pH 7.4) and was followed by a second step of 0.3–1.5 m ammonium acetate (pH 7.4). Fractions (0.65 ml) were monitored as above. Gel filtration chromatography was carried out on 1.5 × 88-cm columns of Biogel P-4 irrigated with a solution consisting of 0.2 m NaCl, 0.1 m ammonium acetate (pH 7.4), 0.04% Nonidet P-40, and 0.02% sodium azide at a flow rate of 10 ml/h. Prior to application to the column, samples were digested with PLD as described above. Column fractions of 0.9 ml were collected and monitored for radioactivity. Effect of UDP-sugar Concentrations and Temperature on the Processivity of the Synthase Reaction—When equimolar concentrations of UDP-Glc and UDP-GlcUA are present in reactions with E. coli membranes containing type 3 synthase, a rapid transition from oligosaccharide-lipid to polymer synthesis occurs in the UDP-sugar concentration range of 1–10 μm (7Cartee R.T. Forsee W.T. Jensen J.W. Yother J. J. Biol. Chem. 2001; 276: 48831-48839Abstract Full Text Full Text PDF PubMed Scopus (30) Google Scholar). By maintaining the UDP-Glc at the more physiological concentration of 1000 μm (18Ramos A. Boels I.C. de Vos W.M. Santos H. Appl. Environ. Microbiol. 2001; 67: 33-41Crossref PubMed Scopus (88) Google Scholar) and varying the UDP-GlcUA concentration, the rate of formation of oligosaccharide-lipids was found to be hyperbolic, whereas the corresponding values of polymer formation generated a concave curve at low concentrations of UDP-GlcUA (Fig. 1A). As the temperature was increased from 40 to 54 °C, the concavity of the rate curve for polymer formation was strikingly accentuated (Fig. 1B). The synthase was stable at these temperatures, and the Vmax at 54 °C was greater than twice that at 35 °C (data not shown). We previously suggested that these concave rate curves might be due to polysaccharide ejection from the carbohydrate acceptor binding site of the synthase (5Forsee W.T. Cartee R.T. Yother J. J. Biol. Chem. 2000; 275: 25972-25978Abstract Full Text Full Text PDF PubMed Scopus (31) Google Scholar), since the highest rates of ejection occur at low concentrations of UDP-GlcUA and high levels of UDP-Glc. However, a similar effect was observed when the concentration of UDP-Glc was reduced 10-fold (data not shown), and under these conditions, the rate of ejection would be greatly reduced. Likewise, ejection is relatively low under conditions of high UDP-GlcUA and low UDP-Glc (5Forsee W.T. Cartee R.T. Yother J. J. Biol. Chem. 2000; 275: 25972-25978Abstract Full Text Full Text PDF PubMed Scopus (31) Google Scholar), but temperature enhancement of concavity was also observed when UDP-GlcUA was maintained at 1 mm while varying the UDP-Glc concentration (Fig. 1C). We therefore further explored the basis for this sigmoid-like behavior. At equimolar concentrations of the two UDP-sugars, polymer synthesis occurs subsequent to that of the oligosaccharide-lipid precursor, indicating a precursor-product relationship (7Cartee R.T. Forsee W.T. Jensen J.W. Yother J. J. Biol. Chem. 2001; 276: 48831-48839Abstract Full Text Full Text PDF PubMed Scopus (30) Google Scholar). A time lag in the onset of polymer formation was also apparent at 35 °C in reactions containing 1000 μm UDP-Glc and 1.5 μm UDP-GlcUA, whereas the oligosaccharide-lipid began to accumulate immediately (Fig. 2A). Even if this lag were taken into account, the concavity shown in Fig. 1A would be only marginally reduced. At 45 °C and at a UDP-GlcUA concentration of 7.5 μm, which is well within the concave region of the 45 °C rate curve in Fig. 1B, there was only a slight lag in the initiation of polymer formation (Fig. 2B). Accentuation of the concave rate curves with increasing temperature as seen in Fig. 1B is therefore not explained by the time lag in polymer formation. Effect of UDP-sugar Concentrations on Oligosaccharide-lipid Formation—When S. pneumoniae membranes are incubated with labeled UDP-GlcUA in the absence of UDP-Glc, the reaction catalyzed by the type 3 synthase is completely nonprocessive and only a single glucuronosyl unit is transferred to the oligosaccharide-lipid. Digestion of this product with PLD yields a water-soluble product slightly larger than a disaccharide (presumably disaccharyl-glycerol) (6Cartee R.T. Forsee W.T. Yother J. J. Bacteriol. 2005; 187: 4470-4479Crossref PubMed Scopus (32) Google Scholar). Incubation of the recombinant E. coli membranes in the presence of labeled UDP-GlcUA (1 μm) but in the absence of UDP-Glc similarly resulted in the addition of only a single glucuronosyl unit to the oligosaccharide-lipid. The PLD-digested product of this reaction eluted from DEAE-cellulose at the same ionic strength as a disaccharide Glc-β1,3-GlcUA standard (Fig. 3A, left). Increasing the concentration of UDP-Glc to 0.3 μm resulted in two additional oligosaccharide components that eluted at positions suggesting charges similar to the di- and triuronosyl standards (Fig. 3B, left). When both UDP-sugars were present at 1 μm, the major oligosaccharide corresponded to the charge of the triuronosyl elution position, and an additional minor peak corresponding to the expected charge of a tetrauronosyl constituent was also visible (Fig. 3C, left). At 1 mm UDP-Glc, the triuronosyl oligosaccharide was the predominant constituent, and a small but significant tetrauronosyl oligosaccharide was again evident (Fig. 3D, left). The single anionic product in reaction A (Fig. 3A, left) was resolved into two components by gel filtration on Biogel P-4 (Fig. 3A, right). Based on charge and size, the more rapidly migrating product appears to be glucuronosyl-glycerol, whereas the slower moving product appears to be consistent with GlcUA-Glc-glycerol. The mono-, di-, and triuronosyl components shown in Fig. 3, B and C (right), eluted from the Biogel P-4 column slightly later than the respective type 3 di-, tetra-, and hexasaccharide standards (Glc-GlcUA)n, which were previously characterized (14Campbell J.H. Pappenheimer A.M. Immunochemistry. 1966; 3: 195-212Crossref PubMed Scopus (27) Google Scholar). These positions are consistent with the retention of glycerol at their reducing termini following PLD hydrolysis of the respective oligosaccharide-lipids, suggestive of the homologous series (GlcUA-Glc)n-glycerol.3 The oligosaccharides represented by the peaks in the right panel of Fig. 3D were synthesized at a very high concentration of UDP-Glc, and they appear to be slightly larger than their respective homologs in Fig. 3, B and C, which were synthesized at a 1000-fold lower concentration of UDP-Glc. Presumably, the products formed at the high UDP-Glc concentration would have Glc at their nonreducing termini, resulting in the formation of the alternate series, Glc-(GlcUA-Glc)n-glycerol. At the 1 μm UDP-Glc concentration, 5–10% of the incorporated label was in polymer, as demonstrated by gel filtration (Fig. 3C, right), indicating that a low percentage of the oligosaccharide-lipids had attained a size sufficient for recognition by the carbohydrate binding site and had been extended into a high molecular weight polysaccharide. At 1 mm UDP-Glc, ∼20% of the incorporated label was in polymer (Fig. 3D, right). When the concentration of UDP-Glc was maintained at 1 mm and UDP-GlcUA was increased to 5 μm, there was a dramatic shift from oligo-lipid formation to polymer formation, with 82% of the incorporation occurring in polymer (data not shown). Coincident to this shift was an increase in polymer size from ∼200 sugars at 1 μm UDP-GlcUA to ∼4000 sugars at 5 μm UDP-GlcUA. The rapid transition to polymer formation was comparable to that observed at equimolar concentrations of the UDP-sugars (7Cartee R.T. Forsee W.T. Jensen J.W. Yother J. J. Biol. Chem. 2001; 276: 48831-48839Abstract Full Text Full Text PDF PubMed Scopus (30) Google Scholar). Particularly significant under these conditions, as seen in the left and right panels of Fig. 3D, are the very prominent size of the triuronosyl oligosaccharide, a very small amount of a tetrauronosyl oligosaccharide, and then a very large gap lacking any larger intermediate size components prior to high molecular weight polysaccharide. These data are consistent with the carbohydrate binding site of the type 3 synthase requiring an approximate octasaccharide-(i.e. tetrauronosyl-)lipid primer for recognition and the ensuing highly processive polymer formation reaction. Effect of Temperature on the Transition from Oligosaccharide-lipid to Polymer Formation—In reactions containing 2 μm UDP-GlcUA and 1 mm UDP-Glc, incubation at 25 °C resulted in ∼50% of the incorporated label in polymer and 50% in oligosaccharides (Fig. 4A). At 45 °C, the formation of polymer was reduced to ∼15% (Fig. 4B), and only negligible polymer was synthesized in the 54 °C reaction (Fig. 4C). There was also a marked effect on the size profile of the oligosaccharides, with a steady reduction in size occurring with increasing temperature. Thus, binding of the oligosaccharide-lipid at the carbohydrate recognition site and the cooperativity of the series of reactions preceding the recognition step are quite sensitive to changes in temperature. Effect of Preformed Polysaccharide on the Rate of Polymer Formation— When the type 3 synthase contained preformed polysaccharide, the rate curves for polymer formation were no longer concave but were typically hyperbolic (compare Fig. 5 with Fig. 1B). These data clearly demonstrate that the cooperativity occurred either before or during the binding of the oligosaccharide-lipid primer to the carbohydrate binding site of the synthase. It should also be noted that polymer formation rates in Fig. 5 were greater at the higher temperature, as expected, and in contrast to Fig. 1B. In reactions conducted with 2.5 μm UDP-GlcUA and 1 mm UDP-Glc, the activity with enzyme preloaded with polysaccharide was linear for only a short duration, particularly at the higher temperature (Fig. 6). These data are in agreement with previous observations (5Forsee W.T. Cartee R.T. Yother J. J. Biol. Chem. 2000; 275: 25972-25978Abstract Full Text Full Text PDF PubMed Scopus (31) Google Scholar) demonstrating that the rate of polymer ejection increases with increasing temperature and with decreasing UDP-GlcUA concentrations. These data also illustrate why the rate of polymer formation shown in Fig. 1B is lower at the higher temperature, which is contrary to the expected norm. When insufficient UDP-GlcUA is present to saturate the synthase, the percent of enzyme engaged in polymer synthesis decreases as the temperature increases. The high and low processive states of the synthase appear to exist in a reciprocal steady state, with polymer formation favored by higher UDP-GlcUA concentrations and lower temperature, although oligosaccharide-lipid formation is favored by lower nucleotide sugar levels and higher temperatures (see Fig. 8 and “Discussion”). In agreement with this, polymer formation with preloaded synthase was increasingly linear with time as the concentration of UDP-GlcUA was increased (data not shown). This is consistent with the decreased rate of ejection from S. pneumoniae membranes as the concentration of the conjugate UDP-sugar was increased (5Forsee W.T. Cartee R.T. Yother J. J. Biol. Chem. 2000; 275: 25972-25978Abstract Full Text Full Text PDF PubMed Scopus (31) Google Scholar). As would be expected, the initial rate of oligosaccharide-lipid formation by preloaded membranes was greatly reduced as compared with polymer formation (compare Fig. 7 with Fig. 2).FIGURE 8Effect of the concentration of UDP-GlcUA and temperature on the steady state relationship of the biosynthetic modes of the type 3 synthase. The concentration of UDP-Glc is assumed to be much higher than that of UDP-GlcUA, as under normal biological conditions. The membrane-bound type 3 synthase initiates synthesis on a lipid acceptor (▵) and alternately adds Glc (•) and GlcUA (○). At low UDP-GlcUA concentrations or at higher temperatures, oligosaccharide-lipid continuously dissociates from the synthase and accumulates in the membrane. As the concentration of UDP-GlcUA increases a greater percentage of the enzyme transitions into a complex with the tetrauronosyl oligosaccharide-lipid, initiating the elaboration of high molecular weight polysaccharide.View Large Image Figure ViewerDownload Hi-res image Download (PPT)FIGURE 7Time course of oligosaccharide-lipid and polymer formation with preloaded synthase at 45 °C. The reaction mixtures were identical to those in Fig. 6 and contained 2.5 μm UDP-GlcUA and 1 mm UDP-Glc. Following incubations for the indicated times, the products were analyzed for polymer (○) and oligosaccharide-lipid (•) by paper chromatography.View Large Image Figure ViewerDownload Hi-res image Download (PPT) Carbohydrate acceptor binding sites are thought to play an important role in the biosynthesis of numerous polysaccharides, but very little data is available on this part of the assembly process. Type 3 synthase in S. pneumoniae membranes is tightly bound to preformed nascent polysaccharide chains (5Forsee W.T. Cartee R.T. Yother J. J. Biol. Chem. 2000; 275: 25972-25978Abstract Full Text Full Text PDF PubMed Scopus (31) Google Scholar). Under most conditions the polysaccharide chain remains tightly associated with the enzyme, and virtually no dissociation occurs during various experimental manipulations, including centrifugation, freezing, and thawing, and incubation at room temperature. These isolated complexes are able to catalyze the addition of Glc and GlcUA to extend the length of the preformed chains, indicating that the catalytic integrity has been maintained during the isolation. The type 3 synthase in recombinant E. coli, which is unable to synthesize polymer in vivo because it lacks UDP-GlcUA, can be obtained in a polysaccharide-free form and is ideal for studying the initiation of polymer synthesis. The first step in the assembly of type 3 polymer appears to be the transfer of glucose to phosphatidylglycerol to build up a pool of glucosylphosphatidylglycerol in the membrane, which serves as a readily available primer for polymer synthesis when adequate levels of the two nucleotide sugars, UDP-Glc and UDP-GlcUA, are provided (6Cartee R.T. Forsee W.T. Yother J. J. Bacteriol. 2005; 187: 4470-4479Crossref PubMed Scopus (32) Google Scholar). The second phase consists of the alternate addition of GlcUA and Glc to the oligosaccharyl-lipid primer, which initially is only loosely associated with the synthase and is free to dissociate from the enzyme. Here we showed that when UDP-sugar concentrations were low, the oligosaccharide-lipids failed to achieve a critical binding length and accumulated in the membrane. When successive transfers of GlcUA and Glc occurred with sufficient rapidity to produce an oligosaccharide of sufficient length for recognition (approximately four repeating disaccharides), the growing chain became tightly associated with the synthase. No product intermediate in size between an octasaccharide and high molecular weight polymer was observed, indicating that the nascent chain was rapidly extended by a highly processive reaction subsequent to binding. We previously reported on the tendency of the type 3 synthase to generate sigmoid-like kinetics at low concentrations of the nucleotide sugar substrates, but also noted that the enhanced rate of chain ejection under these same conditions complicated further evaluation (5Forsee W.T. Cartee R.T. Yother J. J. Biol. Chem. 2000; 275: 25972-25978Abstract Full Text Full Text PDF PubMed Scopus (31) Google Scholar). The marked concavity observed here occurs in the absence of bound polysaccharide and is primarily related to an event(s) during the initial sequence of reactions leading to the binding of the oligosaccharide-lipid primer to the carbohydrate recognition site of the synthase. Sigmoid kinetic behavior is also displayed by hyaluronan synthase in Streptococcus pyogenes (19Tlapak-Simmons V.L. Baggenstoss B.A. Kumari K. Heldermon C. Weigel P.H. J. Biol. Chem. 1999; 274: 4246-4253Abstract Full Text Full Text PDF PubMed Scopus (62) Google Scholar), and indirect evidence of a possible conformational change in this enzyme in Streptococcus equisimilis has been presented (20Tlapak-Simmons V.L. Baron C.A. Weigel P.H. Biochemistry. 2004; 43: 9234-9242Crossref PubMed Scopus (46) Google Scholar). Based on these studies a “pendulum model” of chain elongation at the reducing end has been proposed in which two functional synthase domains would each contain a separate binding site for the two distinct UDP-sugars required for synthesis (21Tlapak-Simmons V.L. Baron C.A. Gotschall R. Haque D. Canfield W.M. Wiegel P.H. J. Biol. Chem. 2005; 280: 13012-13018Abstract Full Text Full Text PDF PubMed Scopus (49) Google Scholar). Another model has also been proposed to explain how a processive β-glycosyltransferase with only a single catalytic center could provide for the elaboration of a polysaccharide composed of alternating sugars (22Charnock S.J. Henrissat B. Davies G.J. Plant Physiol. 2001; 125: 527-531Crossref PubMed Scopus (58) Google Scholar). It was suggested that the last sugar residue added to the nonreducing end of the bound acceptor in the catalytic center might redefine the affinity of the site for the alternate nucleotide donor. We have previously noted that the type 3 synthase ejects any bound polysaccharide from the carbohydrate binding site when only one UDP-sugar is present, and this ejection is inhibited as the concentration of the second UDP-sugar increases (5Forsee W.T. Cartee R.T. Yother J. J. Biol. Chem. 2000; 275: 25972-25978Abstract Full Text Full Text PDF PubMed Scopus (31) Google Scholar). Although the available information concerning the complexity of these interactions is scant, the best evidence suggests that ejection of the polysaccharide occurs during an abortive attempt to translocate the chain. Of special interest were the ejection Km values of 0.004 and 880 μm for UDP-GlcUA and UDP-Glc, respectively, compared with their respective Ki values of 2 and 5 μm. These values indicate a marked change in affinity of the synthase for each of the UDP-sugars in reactions containing both nucleotides in contrast to reactions where only a single UDP-sugar is present. Because both the formation of oligosaccharide-lipid in reactions with membranes lacking preformed polysaccharide and polymer synthesis using membranes containing preformed polysaccharide demonstrated typical substrate concentration dependence, it is a reasonable assumption that the primary cooperativity in the overall reaction was manifest in a transitional event(s) linking these two reaction sequences. In particular, the buildup of the triuronosyl product as shown in Fig. 3D, indicates that a synergism supplied by increasing levels of UDP-GlcUA was necessary to provide the momentum enabling the synthase to transition into the highly processive tetrauronosyl primer-enzyme complex. Additional evidence that the primary catalytic barrier is situated at this point in the overall reaction sequence is provided in Fig. 4B, which shows that a moderate reduction in the level of the triuronosyl oligosaccharide due to increasing the temperature to 45 °C was accompanied by a dramatic reduction in polysaccharide synthesis. It would also appear that the heightened concavity in polymer formation observed at the higher temperatures reflected, at least in part, the cooperative action of an elevated nucleotide-sugar level required to counter the temperature-induced higher rate of dissociation of oligosaccharide-lipid from the synthase. The polymer formation rate curves presented here represent a composite of a series of reactions and do not lend themselves to standard kinetic analysis. If the transition step could be studied in isolation from the hyperbolic reactions on either side, it can be speculated that purely sigmoid kinetics would be observed that could be further analyzed. Based on the current knowledge of the biosynthesis of type 3 polysaccharide, the most probable explanation of these results may be a conformational change in the synthase. Because the type 3 synthase and related β-glycosyltransferases are known to simultaneously transport their polysaccharides during synthesis, the initiation of polymerization by the type 3 synthase may involve a reorientation of the growing oligosaccharide and possibly the transport of the lipid anchor from the inner to the outer membrane leaflet. Here, it serves as an anchor for the capsule following ejection of the completed chain from the enzyme catalytic site (6Cartee R.T. Forsee W.T. Yother J. J. Bacteriol. 2005; 187: 4470-4479Crossref PubMed Scopus (32) Google Scholar). The transition event is also thought to lock the oligosaccharide-lipid in a tight binding complex with the synthase, whereupon the highly processive polymerization phase ensues. In theory, the addition of each sugar would now fine tune the affinity of the binding site for the appropriate nucleotide sugar to donate the succeeding glycosidic addition (22Charnock S.J. Henrissat B. Davies G.J. Plant Physiol. 2001; 125: 527-531Crossref PubMed Scopus (58) Google Scholar), providing for a stable alternating catalytic center enabling the repetitive addition of Glc and GlcUA to the growing polymer. Just how the synthase provides for the integrity of glycosidic addition in the initial reaction sequence to produce the oligosaccharide-lipid is less apparent. The processive nature of the initial reaction sequence indicates at least a transient association of the oligosaccharide-lipid with the synthase that presumably provides for the appropriate sugar addition. However, prior to the addition of the first sugar residue, there would be no apparent way to provide for catalytic specificity. This may explain the unusual ability of the type 3 synthase to utilize phosphatidylglycerol as an acceptor both for Glc (6Cartee R.T. Forsee W.T. Yother J. J. Bacteriol. 2005; 187: 4470-4479Crossref PubMed Scopus (32) Google Scholar) and also for GlcUA to form the smaller GlcUA-lipid product in Fig. 3A, right. This latter product appeared primarily in the absence of UDP-Glc and may not occur in vivo at greatly elevated levels of UDP-Glc. In the absence of a bound oligosaccharide substrate to act as a cofactor, the synthase demonstrates a decreased fidelity in recognizing the appropriate acceptor substrate. It is significant that polymer formation rate curves were concave as a function of the concentrations of both UDP-Glc and UDP-GlcUA and that the concavity of both of these curves was thermally enhanced. This suggests a possible chain of protein-mediated catalytic events initiating at the nucleotide-sugar binding site and translated through the carbohydrate binding site to modulate binding, translocation, and ejection of the elongating polysaccharide chain, resulting in a steady state equilibrium among the various modes of synthase activity, as depicted in Fig. 8. The presence of high concentrations of UDP-GlcUA or low temperature favors a steady state with a high proportion of the synthase in the polymer-forming, highly processive state. At lower concentrations of UDP-GlcUA or higher temperatures, the steady state concentration of synthase in the polymer-forming mode is reduced because of an increased rate of ejection of polysaccharide from the carbohydrate binding site. In the latter case, there is also an increased rate of dissociation of the oligosaccharide-lipid from the synthase resulting in the accumulation of oligosaccharide-lipid consisting of mostly three or less repeating disaccharides. It is through this intricate sequence of interactions that slight fluctuations in the concentration of UDP-GlcUA are able to modulate the chain length of type 3 polymer over a large range. The size of the polymer is a function of both the rate of the polymerization reaction, and the length of time the growing chain remains bound to the synthase. Both of these parameters behave in a convex curvilinear manner with respect to the concentration of UDP-GlcUA, providing for a large increase in polymer size with only a minimal increase in UDP-GlcUA.3" @default.
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• W2111015751 title "Role of the Carbohydrate Binding Site of the Streptococcus pneumoniae Capsular Polysaccharide Type 3 Synthase in the Transition from Oligosaccharide to Polysaccharide Synthesis" @default.
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