Glycobiology Advance Access originally published online on May 5, 2008
Glycobiology 2008 18(7):549-558; doi:10.1093/glycob/cwn037
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1,4GlcNAc-capped mucin-type O-glycan inhibits cholesterol -glucosyltransferase from Helicobacter pylori and suppresses H. pylori growth
5 Tumor Microenvironment Program, Glycobiology Unit, Cancer Center, Burnham Institute for Medical Research, La Jolla, CA 92037, USA
6 Department of Pathology, Shinshu University School of Medicine, Matsumoto 390-8621, Japan
1 To whom correspondence should be addressed: Tel: +81-858-646-3144; Fax: +81-858-646-3193; e-mail: minoru{at}burnham.org
Received on January 29, 2008; revised on April 23, 2008; accepted on April 29, 2008
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Abstract |
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Helicobacter pylori infects over half of the world's population and is thought to be a leading cause of gastric ulcer, gastric carcinoma, and gastric malignant lymphoma of mucosa-associated lymphoid tissue type. Previously, we reported that a gland mucin (MUC6) present in the lower portion of the gastric mucosa containing
1,4-N-acetylglucosamine (1,4GlcNAc)-capped core 2-branched O-glycans suppresses H. pylori growth by inhibiting the synthesis of -glucosyl cholesterol, a major constituent of the H. pylori cell wall (Kawakubo et al. 2004. Science. 305:1003-1006). Therefore, we cloned the genomic DNA encoding cholesterol -glucosyltransferase (HP0421) and expressed its soluble form in Escherichia coli. Using this soluble HP0421, we show herein that HP0421 sequentially acts on uridine diphosphoglucose and cholesterol in an ordered Bi-Bi manner. We found that competitive inhibition of HP0421 by 1,4GlcNAc-capped core 2-branched O-glycan is much more efficient than noncompetitive inhibition by newly synthesized -glucosyl cholesterol. Utilizing synthetic oligosaccharides, -glucosyl cholesterol, and monosaccharides, we found that 1,4GlcNAc-capped core 2-branched O-glycan most efficiently inhibits H. pylori growth. These findings together indicate that 1,4GlcNAc-capped O-glycans suppress H. pylori growth by inhibiting HP0421, and that 1,4GlcNAc-capped core 2 O-glycans may be useful to treat patients infected with H. pylori.
Key words:
4GlcNAc-capped core 2-branched O-glycan
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cholesterol -glucosyltransferase
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growth inhibition
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Helicobacter pylori
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novel antibiotics
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Introduction |
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TopAbstractIntroductionResultsDiscussionMaterials and methodsFundingConflict of interest statementReferences |
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Helicobacter pylori infects over half of the world's population and is a leading cause of gastric ulcer, gastric carcinoma, and mucosa-associated lymphoid tissue-type malignant lymphoma (Marshall and Warren 1984
; Peek and Blaser 2002). This infection is ubiquitous among human population, and recent studies show that an association of H. pylori with humans took place before modern humans spread out from Africa. H. pylori apparently spread from East Africa around 58,000 years ago (Linz et al. 2007). Before then, the prototypic microbe apparently jumped from humans to wild cats such as the cheetah approximately 200,000 years ago (Eppinger et al. 2006).
In H. pylori infection, bacteria first attach to surface mucous cells of the gastric mucosa, an attachment facilitated by binding of the H. pylori adhesion molecule Bab A to blood group antigens expressed on mucous cells (Ilver et al. 1998). The human population of South American Amerindians dominantly express blood group O antigen (Mourant et al. 1976). Interestingly, Bab A from this population binds blood group O antigen more efficiently than other blood group antigens (Aspholm-Hurtig et al. 2004).
Once H. pylori infects the stomach, the microbe preferentially colonizes the surface mucous cell-derived mucins (Hidaka et al. 2001). This infection initiates an inflammatory response in infected epithelia and is associated with mucosal infiltration of neutrophils, monocytes, and lymphocytes, causing gastritis (Rauws et al. 1988). If untreated, the disease further progresses to gastric ulcer, carcinoma, and malignant lymphoma.
The second phase of the disease progression, however, occurs in 3–6% of infected individuals (Peek and Blaser 2002). In this population, surface mucous cells are targeted by infection, but H. pylori are only rarely found in gland mucous cells in the deeper portion of the gastric mucosa (Hidaka et al. 2001; Matsuzawa et al. 2003), suggesting the presence of a defense mechanism in these cells.
Indeed, gland mucous cells secrete mucins containing 1,4-N-acetylglucosamine (4GlcNAc)-capped core 2-branched O-glycans (Ishihara et al. 1996), and our recent studies indicate that 4GlcNAc-capped core 2-branched O-glycans expressed on soluble CD43, prepared by utilizing 1,4-N-acetylglucosaminyltransferase (4GnT) cDNA (Nakayama et al. 1999; Zhang et al. 2001), inhibit H. pylori growth in a dose-dependent manner (Kawakubo et al. 2004). We also showed that gland mucins containing 4GlcNAc-capped O-glycans isolated from human gastric mucosa, such as MUC6 (Zhang et al. 2001; Nordman et al. 2002), inhibit H. pylori growth (Kawakubo et al. 2004). By contrast, surface mucins lacking 4GlcNAc-capped core 2-branched O-glycans, such as MUC5AC (Zhang et al. 2001; Nordman et al. 2002), facilitate H. pylori growth, suggesting the presence of factors stimulating H. pylori growth in the surface mucins (Kawakubo et al. 2004). Growth inhibition by 4GlcNAc-capped core 2-branched O-glycans is apparently due to inhibition of cholesterol -glucosyltransferase (HP0421), which synthesizes -glucosyl cholesterol (Kawakubo et al. 2004; Fukuda et al. 2006). -Glucosyl cholesterol and its derivatives are major components of the cell walls of Helicobacter species and constitute more than 25% of total cell wall lipids of H. pylori, reaching almost 130 µM (Hirai et al. 1995; Haque et al. 1996). In addition, it has been reported recently that -glucosyl cholesterol abrogates phagocytosis of H. pylori and compromises subsequent T cell activation directed toward H. pylori (Wunder et al. 2006). Conversely, the increased amount of cholesterol resulted in increased phagocytosis of H. pylori and increased T cell responses toward H. pylori. These results demonstrate that -glucosylation of cholesterol in H. pylori facilitates both infectivity and pathogenicity of H. pylori.
We recently cloned genomic DNA encoding HP0421 from H. pylori and related Helicobacter species and expressed it in Escherichia coli (Lee et al. 2006). We found that HP0421 activity was inhibited by core 2-branched mucin-type O-glycans containing 1,4GlcNAc residues (4GlcNAc-core 2) (Lee et al. 2006). However, it is unclear how HP0421 acts on substrates and whether oligosaccharides inhibit H. pylori growth (Lebrun et al. 2006; Lee et al. 2006). Here, we first measured kinetics of HP0421 activity on acceptor and donor substrates. We found that UDP displays competitive inhibition toward HP0421 when the concentration of uridine diphosphoglucose (UDP-Glc) is varied. When we analyzed the effect of chemically synthesized -glucosyl cholesterol on HP0421, we found that it displays mixed-type inhibition. We also showed that 1,4GlcNAc-capped core 2-branched O-glycan exhibits a competitive inhibition toward HP0421. Finally, we showed that 4GlcNAc-capped core 2-branched O-glycan efficiently inhibits H. pylori growth, while core 2-branched O-glycan devoid of an 4GlcNAc-capping structure exhibits no inhibitory effect. These results combined indicate that derivatives of 4GlcNAc-capping core 2 O-glycan may be useful to treat patients infected with H. pylori.
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Results |
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TopAbstractIntroductionResultsDiscussionMaterials and methodsFundingConflict of interest statementReferences |
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Synthesis of
-glucosyl cholesterol by HP0421We previously cloned genomic DNA encoding HP0421 from H. pylori and other Helicobacter species and produced soluble His-tagged HP0421 (Lee et al. 2006
). After the expression in E. coli, the enzyme was isolated from solubilized E. coli periplasm on a Ni-NTA column and dialyzed against a Hepes-NaOH buffer (pH 7.5) to remove imidazole. This preparation resulted in a single protein band of an apparent molecular weight of 
39 kDa based on SDS–gel electrophoresis (Lee et al. 2006). Since the calculated molecular weight is 46,030 Da, this protein has an anomalous electrophoretic mobility. Because cholesterol is barely soluble without detergent, 0.1% Triton X-100 was added to the incubation mixture.
Inhibition of HP0421 activity by UDP and cholesterol
To determine how HP0421 acts on acceptor and donor substrates, enzyme activity was measured at various UDP-Glc concentrations, while fixed amounts of UDP or cholesterol were added as inhibitors. The Lineweaver–Burk plot of the inhibition profile of UDP in the presence of UDP-Glc intersected at the Y-axis, indicating competitive inhibition (Figure 1A). In contrast, cholesterol did not exhibit competitive inhibition in the presence of UDP-Glc and showed mixed-type inhibition (Figure 1B). These results suggest that cholesterol is likely utilized after UDP-Glc complexes with the enzyme. We then measured HP0421 activity at different fixed concentrations of cholesterol. Cholesterol affected HP0421activity in a mixed-type manner, consistent with the above results (Figure 1C). Using the data in Figure 1C, we first obtained the Km for cholesterol (2.5 µM) and for UDP-Glc (64 µM) using a nonlinear regression analysis program, DNRPEASY (Duggleby 1984), as follows (see also Ly et al. 2002; Zhang et al. 2003):
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- Ka is the Michaelis constant for substrate A (in this case, A = UDP-Glc)
- Kb is the Michaelis constant for substrate B (in this case, B = cholesterol)
- Kia is the inhibition constant for substrate A
- kcat = Vmax/[E] = 2.61 ± 0.18 min–1
- Ka: (6.40 ± 0.69) x 10 µM (the Michaelis constant for UDP-Glc)
- Kb: 2.47 ± 1.21 µM (the Michaelis constant for cholesterol)
- Kia: (2.32 ± 1.14) x 102 µM (the inhibition constant for UDP-Glc).
- Kb is the Michaelis constant for substrate B (in this case, B = cholesterol)
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-Glucosyl cholesterol inhibits HP0421 noncompetitivelyTo delineate further how the enzyme acts on donor and acceptor substrates, inhibition of HP0421 by
-glucosyl cholesterol was examined. First, we synthesized -glucosyl cholesterol using a new method. While a procedure for the synthesis of -glucosyl cholesterol had been reported (Schene and Waldman 1998), in our hands this method provided a poor yield. Therefore, we established a novel synthetic procedure (Figure 2). Glucose (Compound 1 in Figure 2) was per-O-acetylated and converted to the corresponding thioethyl glycoside (step a). Following benzylidene acetal formation (step b), O-acetyl groups were replaced by TBSOTf (step c), since TBS derivatization facilitates -glycosylation. After glycosylation (step d), benzylidene and acetyl protective groups were removed to yield -glucosyl cholesterol (Compound 6 in Figure 2). Mass spectrometric analysis showed the major peak at m/z 571.37, which corresponds to [M + Na]+, and signals at m/z 566.43 and 587.37 corresponding to [M + NH4]+ and [M + K]+, respectively (Figure 3). The [1H]-NMR spectrum indicates that glucose is -linked to cholesterol (Figure 4). This was confirmed by the detection of a signal at 99.14 ppm by [13C]-NMR (data not shown).
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HP0421 activity was measured at various UDP-Glc concentrations in the presence of 5 µM cholesterol.
-Glucosyl cholesterol was then added as an inhibitor. The Lineweaver–Burk plot showed that -glucosyl cholesterol inhibited HP0421 in a noncompetitive, mixed-type manner (Figure 5A). Similarly, -glucosyl cholesterol inhibited HP0421 activity in a mixed-type manner when the cholesterol concentration was varied (Figure 5B). These results combined indicate that HP0421 acts in an ordered Bi-Bi manner (Figure 6).
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Inhibition of HP0421 by
4GlcNAc-capped oligosaccharidePreviously, we demonstrated that HP0421 can be inhibited by mucin-type O-glycans (Lee et al. 2006
). The oligosaccharides tested are 4GlcNAc-core 2 [GlcNAc1
4Galβ14GlcNAcβ16(Galβ13)GalNAc1octyl], sialylated core 2 [NeuAc23Galβ14GlcNAcβ16(Galβ1 3)GalNAc1octyl], sialylated core 1 (NeuAc23Galβ1 3GalNAc1octyl), core 2 backbone [GlcNAcβ16(Galβ 13)GalNAc1p-nitrophenol], and core 1 backbone (Galβ13GalNAc1p-nitrophenol) (Lee et al. 2006). Among these mucin-type O-glycans, we found that 4GlcNAc-capped core 2-branched O-glycan, 4GlcNAc-core 2 was the best inhibitor. To determine how this oligosaccharide inhibits HP0421, HP0421 was incubated with varying UDP-Glc concentrations in the presence of 5 µM cholesterol, and then 4GlcNAc-core 2 oligosaccharide was added. Lineweaver– Burk analysis shows that 4GlcNAc-core 2 oligosaccharide inhibits HP0421 in a competitive manner (Figure 7). Using the DNRPEASY program, we found that Ki for 4GlcNAc-core 2 is 418 ± 60 µM while Ki for UDP is 22.9 ± 1.1 µM. This value is almost identical to that obtained previously (Lee et al. 2006), whereas IC50 is 0.75 mM for monosialylated and disialylated core 2 O-glycan (Lee et al. 2006).
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Since the Ki value for
GlcNAc-core 2 is 0.42 mM and GlcNAc-core 2 is a competitive inhibitor, we can deduce the relationship between Ki and IC50 as follows: |
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where
- 420 µM is the Ki value calculated above
- 3.6 µM is the S value for UDP-Glc used to get the IC50 value (Lee et al. 2006)
- 64 µM is the Km value for UDP-Glc.
- 3.6 µM is the S value for UDP-Glc used to get the IC50 value (Lee et al. 2006)
4GlcNAc-core 2 O-glycan inhibits H. pylori growth
Previously, we reported that recombinant CD43 expressing 4GlcNAc residues inhibits H. pylori growth (Kawakubo et al. 2004). However, we had not determined whether oligosaccharides containing 4GlcNAc residues inhibit H. pylori growth. Other structural requirements were not known. We thus evaluated the effect of 4GlcNAc-core 2 O-glycan, sialylated core 2 O-glycan (disialo-core 2), monosaccharides, or -glucosyl cholesterol on H. pylori growth. Monosaccharide N-acetylglucosamine had no effect on H. pylori growth, but higher concentrations of p-nitrophenyl -N-acetylglucosamine inhibited microbial growth (Figure 8B and C). H. pylori growth was significantly inhibited by 0.5 mM core 2 O-glycan containing an 4GlcNAc-capping structure (Figure 8E). Inhibition by 4GlcNAc-core 2 O-glycan was more robust than that by -glucosyl cholesterol, the product of HP0421 (Figure 8F). We also tested sialylated core 2 O-glycan, since this O-glycan is the second best inhibitor for HP0421 in vitro among the oligosaccharides tested (Lee et al. 2006), and represents a major O-glycan in mucins (Capon et al. 1992; Lloyd et al. 1996). Interestingly, sialylated core 2 O-glycan without an 4GlcNAc-capping structure had no inhibitory activity (Figure 8D). These combined results indicate that an 4GlcNAc-capped core 2-branched O-glycan most efficiently inhibits H. pylori growth, and an 1,4GlcNAc residue is essential for that inhibition (see also Discussion).
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Incubation of mono- and oligosaccharides in the H. pylori culture medium did not modify the oligosaccharides
To determine whether monosaccharides and oligosaccharides are modified during the incubation with H. pylori, these saccharides were isolated from the medium incubated with or without H. pylori. Thin layer chromatography of the medium itself showed several molybdenum sulfuric-positive compounds derived from the medium. In addition, a spot migrated at the same position as a control (M) was detected and the migration of the spot was essentially identical to that obtained in the medium cultured with H. pylori (Figure 9). These results indicate that the monosaccharides and oligosaccharides were not modified after incubation with H. pylori.
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Discussion |
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TopAbstractIntroductionResultsDiscussionMaterials and methodsFundingConflict of interest statementReferences |
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The present study demonstrates that HP0421 acts in an ordered Bi-Bi manner, as shown for many other glycosyltransferases (Qasba et al. 2005
). If the enzyme acts in an unordered Ping-Pong manner, neither UDP nor cholesterol should competitively inhibit its activity. The present study also demonstrates that a product like -glucosyl cholesterol does not competitively inhibit HP0421. By contrast, 4GlcNAc-core 2 O-glycan apparently inhibits HP0421 in a competitive manner. These results strongly suggest that cholesterol is added to the enzyme/substrate complex after a complex between the enzyme and UDP-Glc forms (Figure 6). By this mechanism, the enzyme/UDP-Glc complex presumably induces a conformational change such that flexible loops form to accommodate more favorable binding to an acceptor substrate.
HP0421 utilizes UDP-Glc and then produces -linked glucose attached to cholesterol. The HP0421 and -1,4-galactosyltransferase from Neisseria meningitidis have a common property to contain -linked sugar residue. Indeed -1,4-galactosyltransferase also acts in an ordered Bi-Bi kinetic mechanism (Ly et al. 2002). Moreover, crystal structural studies show that -1,3-galactosyltransferase from N. meningitides displays a conformation change in the COOH-terminal region of the enzyme as UDP and C-1 of the galactose is cleaved and the enzyme is bound with UDP (Zhang et al. 2003). These findings suggest that HP0421 also likely displays a similar conformational change during the enzymatic reaction.
As shown previously, inflammation associated with H. pylori infection is marked by an appearance of HEV-like vessels in the gastric mucosa, which likely recruit lymphocytes and aggravate the inflammatory response. However, HEV-like vessels disappear once H. pylori in the stomach is eradicated by antibiotics (Kobayashi et al. 2004). Individuals free of H. pylori recover normal gastric mucosa morphology and show only residual lymphocyte recruitment. Using a transgenic mouse model in which gastrin overexpression is driven by the insulin promoter (Wang et al. 2000), the inflammation–carcinoma sequence in the stomach was facilitated by H. felis infection. Gene microarray analysis showed that the pathological sequence is characterized by initial upregulation of inflammation-related genes such as the chemokine receptor CXCR4 and later CD74 and CXCL-5 (Kobayashi et al. 2007). Thus specific genes are upregulated sequentially during the inflammation–carcinoma progression in the stomachs of mice infected by H. felis.
The present study demonstrates that 4GlcNAc-capped core 2-branched O-glycan inhibits H. pylori growth much more efficiently than sialylated core 2 O-glycan. The minimum concentration of 4GlcNAc-core 2 required for growth inhibition is 0.25 mM, similar to IC50 (0.44 mM) for the inhibition of HP0421 activity. These results are consistent with our conclusion that 4GlcNAc-core 2 inhibits H. pylori growth by inhibiting HP0421 activity, and thus most likely inhibits H. pylori-directed inflammation.
H. pylori does not synthesize cholesterol and thus needs to take up exogenous cholesterol (Kawakubo et al. 2004; Wunder et al. 2006). Recent studies showed that H. pylori incorporates cholesterol from the cholesterol-rich lipid-raft of epithelial cells (Wunder et al. 2006). Cholesterol in the medium, which most likely forms micelle with other lipids, must be also incorporated into H. pylori though its efficiency is very low (Wunder et al. 2006). During its incorporation, most cholesterol is -glucosylated by HP0421 (Wunder et al. 2006). Although HP0421 apparently does not have a transmembrane domain, the enzyme is loosely associated with the membrane (Lebrun et al. 2006; Lee et al. 2006). The catalytic domain of HP0421 should face the cytoplasm to utilize UDP-Glc present in the cytoplasm, as suggested previously (Lebrun et al. 2006). 4GlcNAc-core 2 oligosaccharides have their hydrophobic N-acetyl groups, which may be associated with micelle containing cholesterol and thus incorporated together with cholesterol into H. pylori. Since sialylated O-glycans are highly hydrophilic, they are unlikely associated with lipid micelle, thus unable to incorporate into H. pylori. These findings are consistent with previous findings that Galβ14GlcNAc can be incorporated into cells only after making it hydrophobic by full acetylation (Sarkar et al. 1995), and GalNAc can be incorporated into cells by having hydrophobic benzyl aglycon (Kuan et al. 1989). Future studies will be of significance to determine if 4GlcNAc-capped core 2 O-glycan is enriched into cholesterol-rich raft in stomach, thus allowing their efficient incorporation into H. pylori.
While H. pylori can be eradicated from most patients by amoxicillin and erythromycin plus acid-lowering drugs, in a minority of patients H. pylori is resistant to those treatments. Moreover, this treatment exerts an effect on intestinal bacterial flora that can lead to unwanted side effects such as diarrhea (Rauws et al. 1988). The discovery of HP0421 inhibitors will be important because of their function as antibiotics against H. pylori. Since HP0421 is present only in Helicobacter species (Lee et al. 2006), inhibition of this enzyme acts as a Helicobacter-specific antibiotic, therefore, with minimal side effects. Future studies are important to develop 4GlcNAc-core 2 O-glycan-based drug for the treatment of H. pylori infection.
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Materials and methods |
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Expression of HP0421
Genomic DNA encoding HP0421 was cloned from H. pylori ATCC 700392, whose entire genome has been sequenced (Tomb et al. 1997
), as described (Lee et al. 2006). Genomic DNA encoding HP0421, originally subcloned into pBluescript SK (–) was amplified by PCR using primers containing NdeI (5') and XhoI (3') sites. The PCR product was subcloned into NdeI and XhoI sites of pTKNd6XH, which harbors a 6X Histidine tag at the C-terminus (Kim et al. 2003). The pTKNd6XH vector was obtained through the courtesy of Dr. Kwan-Hwa Park, Department of Food Science and Biotechnology, Seoul National University, Korea. In this vector, HP0421 expression is driven by the Bacillus licheniformis amylotic enzyme promoter (Kim et al. 1992). E. coli was transformed with pTKHd6XH-HP0421 by nucleoporation and cultured in an LB medium. Bacteria were precipitated by a brief centrifugation and suspended in 100 mM Tris–HCl (pH 7.5) containing 15% glycerol and 5 mM dithiothreitol (DTT). After treatment with 20 µg mL–1 lysozyme at 20°C for 5 min, samples were sonicated briefly and centrifuged at 20,000 g for 10 min. Supernatants were applied to a Ni-NTA column (GE Healthcare, Little Chalfont, United Kingdom) and washed with a 50 mM Tris–HCl buffer (pH 7.5) containing 0.3 M NaCl and 20 mM imidazole. Soluble HP0421-6XH was eluted with the same buffer containing 0.3 M NaCl and 250 mM imidazole. The eluate was dialyzed at 4°C using an ultrafiltration kit (Millipore, Billeria, MA) against a 50 mM Hepes-NaOH buffer (pH 7.5) containing 15% glycerol and 5 mM DTT. The enzyme obtained was kept at 4°C.
Enzyme assay
The enzyme solution was incubated in a 50 mM Hepes-NaOH buffer (pH 7.5) containing 20 µM UDP-Glc (50,000 cpm), 5 µM cholesterol, and 0.1% Triton X-100. After 10–30 min of incubation, the reaction was stopped by the addition of 80 mM HCl (final concentration) and then 10 volumes of ethyl acetate. After brief centrifugation, radioactivity in the ethyl acetate (upper) layer was measured. As shown previously, -glucosyl cholesterol can be extracted into the ethyl acetate layer (Hirai et al. 1995). To analyze kinetic properties of HP0421, the concentration of UDP-Glc or cholesterol was varied. In many experiments, different fixed amounts of UDP, cholesterol, -glucosyl cholesterol, or 4GlcNAc-core 2-branched O-glycan were added.
Synthesis of -glucosyl cholesterol and 4GlcNAc-core 2 O-glycan
Glucose was peracetylated overnight in pyridine and acetic anhydride (eight glucose equivalents) at room temperature. After it was dried by evaporation, ethyl sulfide (1.05 eq) and BF3·OEt2 (1.1 eq) were added in CH2Cl2 at 0°C. After gradual warming to room temperature, the product (Compound 2) was obtained at a 92% yield. Compound 2 was treated in CH3ONa (0.1 eq) in methanol at room temperature for deacetylation and then reacted with benzaldehyde dimethyl acetal (1.2 eq) in the presence of a small amount of TSOH·H2O catalyst at room temperature (yield 89%). The benzylidene acetal compound was then treated with t-butyldimethyl silyl ethers (TBSOTf, 3.0 eq) in the presence of pyridine (4.0 eq) and CH2Cl2 at –20°C (yield 95% of Compound 4). After thioglycoside 4 was in situ activated with bromine, the product was conjugated to cholesterol (2.0 eq) in the presence of AgOTf (2.0 eq) sym-collidine (1.8 eq) in CH2Cl2 at 0°C (yield 75%). Although the product was a mixture of - and β-linked compounds (1:1), isomers were separated by silica gel column chromatography (Compound 5). Finally, TBS was removed by TBAF (2.0 eq) in tetrahydrofuran, and benzylidene groups were removed by 80% acetic acid treatment at 70°C (yield 86%) yielding the desired product (Compound 6). Product identification was confirmed by mass spectrometric and NMR analyses.
GlcNAc14Galβ14GlcNAcβ16(Galβ13)GalNAc 1octyl, 4GlcNAc-core 2 O-glycan was newly synthesized by a two-step glycosylation strategy as reported (Wang et al. 2007). Briefly, GlcNAc14Gal was conjugated to GlcNAc, forming ethylthio-glycosylated GlcNAc1 4Galβ14GlcNAc, using a modification of the published procedure (Buskas and Konradsson 2000). This compound was conjugated in situ with Galβ13GalNAcoctyl, resulting in GlcNAc14Galβ14GlcNAcβ16(Galβ1 3)GalNAc1octyl. The obtained compound exhibited NMR and mass spectra consistent with the desired compound (Wang et al. 2007). Disialylated core 2 O-glycan was synthesized as described previously (Sengupta et al. 2003). N-Acetylglucosamine and p-nitrophenyl -N-acetylglucosamine were purchased from Sigma.
To determine the effect of these oligosaccharides on HP0421activity, oligosaccharides were dissolved in a minimal amount of dimethyl sulfoxide (DMSO) and added to the reaction mixture described above to assay HP0421. A reaction mixture containing only DMSO served as a control. The enzyme assay was carried out in triplicate.
Bacterial growth assay
H. pylori (ATCC 43504; American Type Culture Collection, Manassas, VA) was cultured as described with minor modifications (Kawakubo et al. 2004). Briefly, H. pylori was cultured in Brucella broth supplemented with 10% horse serum at 35°C in 15% CO2, followed by a second culture with Mueller–Hinton broth (Eiken Chemical, Tokyo, Japan) supplemented with 5.5% horse serum at 35°C in 15% CO2. Diluted bacteria (1 x 107 cells mL–1) were then cultured further in Mueller–Hinton broth supplemented with 5.5% horse serum containing various amounts of synthetic oligosaccharides and monosaccharides. Oligosaccharides and monosaccharides were dissolved in DMSO and added to the culture medium to a final concentration of 1% DMSO. Control culture was carried out in the presence of 1% DMSO. Growth of bacteria cultured at 35°C in 15% CO2 was determined by measuring the OD 600 nm every day.
TLC of monosaccharides and oligosaccharides
Synthetic oligosaccharides and monosaccharides in DMSO were cultured in Brucella broth containing 10% fetal bovine serum for 5 days at 35°C in 12% CO2 atmosphere with or without H. pylori (1 x 107 cells mL–1). Final concentration of oligosaccharides and monosaccharides was 1 mM or 2 mM. Control culture was performed in the presence of 1% DMSO. After incubation, sugar compounds were extracted from the culture media by adding 1.5 volumes of ethanol at –20°C for 1 h. After centrifugation, the supernatant was diluted with 5 volumes of water and then applied to a high-capacity C18 column (Alltech, Deerfield, IL). The fraction eluted with methanol was dried in a Speed Vac concentrator and dissolved in 90% methanol for TLC. TLC was developed in CH2Cl2/methanol (2:1 for GlcNAc, 3:1 for GlcNAc -PNP, or 5:1 for -glucosyl cholesterol and control) and chloroform/methanol/water (3:3:1 for disialo-core 2 and 4GlcNAc-core 2). Separated saccharides were visualized by heating at 80°C for 30 min after dipping in the molybdate reagent. The molybdate reagent was prepared by first dissolving 7.5 g of ammonium molybdate in water and then 5 g of cerium sulfate tetrahydrate was added. After dissolving both compounds by adding 29 mL of sulfuric acid, the final volume was brought to 500 mL by slowly adding water.
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Funding |
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TopAbstractIntroductionResultsDiscussionMaterials and methodsFundingConflict of interest statementReferences |
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National Institutes of Health (CA71932 to M.F. and P.H.S., CA33000 to M.F.); Ministry of Education, Culture, Sports, Science and Technology of Japan (14082201 to J.N., B-18790240 to M.K.); Toyobo Biotechnology Foundation (fellowship to Y.I.).
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Conflict of interest statement |
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TopAbstractIntroductionResultsDiscussionMaterials and methodsFundingConflict of interest statementReferences |
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We declare no conflict of interest.
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Acknowledgements |
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The authors thank Drs. Kiyohiko Angata, Misa Suzuki, Tomoya O. Akama, Masatomo Kawakubo and Yukata Takano for useful discussion, Dr. Elise Lamar for critical reading of the manuscript, and Ms. Aleli Morse for organizing the manuscript.
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Footnotes |
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2 Present address: Department of Food Science and Nutrition, Pusan National University, Busan 609-735, Korea.
3 Alternate address: Laboratory for Organic Chemistry, Swiss Federal Institute of Technology (ETH) Zurich, Wolfgang-Pauli Str. 10, 8093 Zurich, Switzerland.
4 These authors equally contributed to this work.
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Abbreviations |
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4GlcNAc-core 2 O-glycan, GlcNAc14Galβ14GlcNAcβ 16(Galβ13)GalNAc1octyl; DMSO, dimethyl sulfoxide; HEV, high endothelial venules; TLC, thin layer chromatography; UDC, uridine diphosphoglucose |
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TopAbstractIntroductionResultsDiscussionMaterials and methodsFundingConflict of interest statementReferences |
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