Production of Capsular Polysaccharide ofStreptococcus pneumoniae Type 14 and Its Purification by Affinity Chromatography

Production and purification of CPS-14.CPS-14 was prepared from S. pneumoniae strains obtained from The National Centre for Streptococcus (Alberta, Canada) as described by Lund and Henrichsen (7) in 5-liter flasks containing 2 liters of tryptic soy broth (Difco Laboratories, Detroit, Mich.) and incubated at 37°C for 18 to 24 h. Growth was stopped by adding formaldehyde to a final concentration of 0.2% (wt/vol); the cells were lysed with sodium deoxycholate (0.1%, wt/vol) and then centrifuged. The supernatant was concentrated by ultrafiltration (using a hollow fiber cartridge with a molecular mass cutoff of 10 kDa) to 1/10 the original volume, and it was extensively dialyzed against distilled water and lyophilized.

In a typical experiment, 165 mg of lyophilized powder was suspended in 5 ml of 50 mM sodium phosphate buffer (pH 7.4) containing 0.15 M NaCl (PBS buffer). The suspension was centrifuged at 4°C for 15 min at 4,000 × g . A 4-ml portion of the clear supernatant was applied to a column packed with 2 ml of commercial soybean lectin-agarose (Sigma Chemical Co., St. Louis, Mo.). According to the manufacturer, the ligand content was approximately 2 mg of lectin per ml of packed gel. Nonbound material was recycled three times, and the column was then washed with 16 ml of PBS buffer. Elution was performed with 0.1 M d-galactose in PBS buffer. Two 4-ml fractions were collected, and each fraction was dialyzed against distilled water or gel filtered by using prepacked PD-10 columns (Pharmacia Amersham, Uppsala, Sweden) with distilled water and finally lyophilized. For a small laboratory bench scale up of the procedure, a column was packed with 9.0 ml of soybean lectin-agarose and the protocol described above was used with appropriately scaled volumes.

Specific latex reagent.Rabbits were immunized with serotype 14 aldehyde-inactivated S. pneumoniae bacterial cells by using the immunization protocol of Lund and Henrichsen (7). Peripheral blood was collected, and the immunoglobulin fraction was purified from the serum by salt precipitation with 30% saturated ammonium sulfate. To avoid cross-reactions with the C polysaccharide produced by all serotypes, anti-C antibodies were eliminated by adsorption with a suspension of inactivated cells of a noncapsulated rugose C-mutant S. pneumoniae strain. The antisera were adsorbed onto latex reagent by the method of Battistoni (1). Agglutination of the samples was quantified by a twofold serial dilution assay. The titer was defined as the reciprocal of the highest dilution able to produce visible agglutination.

Protein content.The protein content was determined both spectrophotometrically by using the relationship between absorbance at 280 nm and absorbance at 260 nm (5) and by the bicinchoninic acid (Pierce, Rockford, Ill.) method (10).

¹H-NMR analysis.The ¹H nuclear magnetic resonance (¹H-NMR) spectrum of a sample dissolved in D₂O was determined with a Brucker DPX-400 spectrometer by using standard pulse sequences. Sodium 3-trimethylsilylpropionate-d₄ (δ_H0.00) was used as an internal reference.

Sugar analysis.Purified polysaccharide (0.5 mg) was hydrolyzed with 2 M trifluoroacetic acid at 120°C for 1 h. The resulting monosaccharides were analyzed as their alditol acetates by gas-liquid chromatography on an SE-54 fused-silica capillary column by using the following temperature program: 140°C for 3 min, followed by an increase to 240°C at a rate of 3°C min⁻¹. Gas chromatography-mass spectrometry was performed by using the column and conditions mentioned above with a Shimadzu QP-5050 gas chromatograph-mass spectrometer.

Production and affinity purification of CPS-14.The latex reagent was calibrated with a pure sample of S. pneumoniaeCPS-14, and the detection limit was found to be 60 ng/ml. This value was used to estimate the amounts of CPS-14 in the culture medium and the culture supernatant after cell lysis, and the data indicated that almost all of the CPS-14 was released into the medium.

Table 1 summarizes the data regarding affinity purification of CPS-14 from culture medium supernatant. Although the estimated amount of CPS-14 in the starting material was very small (3.9 mg), our one-step procedure resulted in a polysaccharide preparation that was virtually free of protein (Table1). The soluble protein content represented 50% of the starting dry weight. In the purified polysaccharide, the protein content was 0.15% (wt/wt) (spectrophotometric method) or zero (bicinchoninic acid method). The results for the eluted material in Table 1 are the results for the first elution fraction. The polysaccharide content of the second elution fraction was very low, as indicated by the latex technique (titer, 64). Furthermore, the protein content was 4.5%, and so the second elution fraction was discarded. The maximum capacity of the column was found to be approximately 1.5 mg of polysaccharide per ml of soybean lectin-agarose-packed gel (Table 1).

The process was scaled up to a 9.0-ml packed gel column. In this case the capacity of the column was 1.2 mg of polysaccharide per ml of packed gel, and after three cycles the capacity was 1.1 mg of polysaccharide per ml of packed gel.

Identity and quality of the product.The polysaccharide obtained reacted positively with CPS-14-specific latex reagent, giving a high titer, as indicated in Table 1. Sugar analysis of the product revealed the presence of d-glucose,N-acetyl-d-glucosamine, andd-galactose at relative proportions of 1:1:2, which corresponded to the reported composition of the polysaccharide (6). The ¹H-NMR spectra (Fig.2) showed the tetrasaccharide repetitive unit having all of the monosaccharides in the anomeric β-configuration and the presence of an N-acetyl group, as expected. No leakage of lectin from the column was observed, as indicated by negative hemagglutination (9) performed with the eluted material.

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Fig. 2.

¹H-NMR spectrum of CPS-14 obtained by affinity chromatography.

The one-step purification procedure described here is easy to perform and faster than traditional multistep methods that include fractional precipitation, protease and DNase treatments, and/or ion-exchange chromatography, among other procedures (1a, 3a). In contrast, a good yield of high-purity CPS-14 is produced by our one-step method, and our procedure may be easily scaled up.