Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K39/00—Medicinal preparations containing antigens or antibodies
  • A61K39/02—Bacterial antigens
  • A61K39/09—Lactobacillales, e.g. aerococcus, enterococcus, lactobacillus, lactococcus, streptococcus
  • A61K39/092—Streptococcus
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
  • A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
  • A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
  • A61K47/62—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being a protein, peptide or polyamino acid
  • A61K47/64—Drug-peptide, drug-protein or drug-polyamino acid conjugates, i.e. the modifying agent being a peptide, protein or polyamino acid which is covalently bonded or complexed to a therapeutically active agent
  • A61K47/646—Drug-peptide, drug-protein or drug-polyamino acid conjugates, i.e. the modifying agent being a peptide, protein or polyamino acid which is covalently bonded or complexed to a therapeutically active agent the entire peptide or protein drug conjugate elicits an immune response, e.g. conjugate vaccines
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P11/00—Drugs for disorders of the respiratory system
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
  • A61P31/04—Antibacterial agents
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P37/00—Drugs for immunological or allergic disorders
  • A61P37/02—Immunomodulators
  • A61P37/04—Immunostimulants
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
  • C07H1/00—Processes for the preparation of sugar derivatives
  • C07H1/06—Separation; Purification
  • C07H1/08—Separation; Purification from natural products
• • C—CHEMISTRY; METALLURGY
  • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
  • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
  • C12P19/00—Preparation of compounds containing saccharide radicals
  • C12P19/04—Polysaccharides, i.e. compounds containing more than five saccharide radicals attached to each other by glycosidic bonds
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K39/00—Medicinal preparations containing antigens or antibodies
  • A61K2039/60—Medicinal preparations containing antigens or antibodies characteristics by the carrier linked to the antigen
  • A61K2039/6087—Polysaccharides; Lipopolysaccharides [LPS]
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K39/00—Medicinal preparations containing antigens or antibodies
  • A61K2039/62—Medicinal preparations containing antigens or antibodies characterised by the link between antigen and carrier
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K39/00—Medicinal preparations containing antigens or antibodies
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
  • C08B37/00—Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
  • C08B37/00—Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
  • C08B37/0003—General processes for their isolation or fractionation, e.g. purification or extraction from biomass

Definitions

• This invention relates to methods for removing excess soluble protein and other impurities from cellular lysates of Streptococcus pneumoniae (S. pneumoniae) serotypes used in the production of purified pneumococcal polysaccharides.
• Streptococcus pneumoniae are Gram-positive, lancet shaped cocci that are usually seen in pairs (diplococci), but also in short chains or as single cells. They grow readily on blood agar plates with glistening colonies and display alpha hemolysis unless grown anaerobically where they show beta hemolysis. They are sensitive to bile salts that can break down the cell wall with the presence of the cells' own enzyme, autolysin.
• the organism is an aerotolerant anaerobe and is fastidious in that it has complex nutritional requirements.
• the cells of most pneumococcal serotypes have a capsule which is a polysaccharide coating surrounding each cell. This capsule is a determinant of virulence in humans because it interferes with phagocytosis by preventing antibodies from attaching to the bacterial cells.
• capsular serotypes There are currently 90 capsular serotypes identified, with 23 serotypes responsible for about 90% of invasive disease.
• the polysaccharide can confer a reasonable degree of immunity to S. pneumoniae in individuals with developed or unimpaired immune systems.
• the polysaccharide when the polysaccharide is conjugated with a high molecular weight protein such as CRMi97 and formulated into a vaccine containing conjugates of multiple serotypes, such conjugate vaccines allow for an immune response in infants and elderly who are also most at risk for pneumococcal infections.
• the capsular polysaccharide for each S. pneumoniae serotype utilized for vaccine products is produced by growing the organism in liquid medium. The population of the organism is often scaled up from a seed vial to seed bottles and passed through one or more seed fermentors of increasing volume until production scale fermentation volumes are reached.
• the end of the growth cycle can be determined by one of several means, at which point the cells are lysed through the addition of a detergent or other reagent which aids in the cell wall breakdown and release of autolysin which causes cellular lysis when the cells reach stationary phase.
• the broth is then harvested for downstream (purification) processing.
• the major contaminants are cellular proteins, nucleic acids, C-polysaccharide and medium components.
• the present invention relates to a process for producing substantially purified capsular polysaccharides from a Streptococcus pneumoniae cell lysate.
• This process comprises the steps of: (a) providing a fermentation broth comprising bacterial cells that produce a selected Streptococcus pneumoniae serotype;
• step (b) lysing the bacterial cells in step (a) with a lytic agent, thereby producing a cell lysate comprising cell debris, soluble proteins, nucleic acids, and polysaccharides;
• step (c) clarifying the cell lysate of step (b) using centrifugation or filtration to remove cell debris, thereby producing a clarified cell lysate;
• step (d) ultraf ⁇ ltering and diaf ⁇ ltering the clarified cell lysate of step (c) to remove low molecular weight impurities and increase polysaccharide concentration, thereby producing a retentate;
• step (e) lowering the pH of the retentate of step (d) to less than 4.5 to precipitate protein and nucleic acids, thereby forming an acidified retentate solution;
• step (f) holding the acidified retentate solution formed in step (e) for a time sufficient to allow settling of the precipitate, followed by filtration or centrifugation of the acidified retentate solution, thereby producing a clarified polysaccharide solution; (g) filtering the clarified polysaccharide solution of step (f) through an activated carbon filter;
• step (h) ultraf ⁇ ltering and diaf ⁇ ltering the filtered solution produced by step (g), thereby producing a concentrated purified polysaccharide solution
• step (i) filtering the concentrated purified polysaccharide solution produced by step (h) using a sterile filter; whereby substantially purified capsular polysaccharides in the form of a solution are produced.
• Exemplary, non-limiting S. pneumoniae serotypes selected for this embodiment of the invention are 1, 4, 5, 6A, 6B, 7F, 9V, 14, 18C, 19A, 19F, and 23F.
• the pH of step (e) is lowered to about 3.5.
• the diaf ⁇ ltration of step (h) comprises a pH adjustment to between about 5.5 to about 7.5.
• the diaf ⁇ ltration of step (h) comprises a pH adjustment to between about 7.0 to about 7.5.
• the diafiltration of step (h) comprises a pH adjustment to about 7.4.
• step (e) removes at least 98% of protein from the retentate of step (d).
• step (g) removes at least 90% of the protein from the clarified polysaccharide solution of step (f).
• the activated carbon filter of step (g) comprises wood-based phosphoric acid-activated carbon.
• step (f) comprises holding the acidified retentate solution formed in step (e) for at least 2 hours.
• the lytic agent of step (b) is deoxycholate sodium (DOC).
• the lytic agent of step (b) is a non-animal derived lytic agent.
• the lytic agent of step (b) is the non-animal derived lytic agent N-lauryl sarcosine sodium (NLS).
• the substantially purified capsular polysaccharide produced by a process of the invention from a Streptococcus pneumoniae cell lysate may be used in the manufacture of a pneumococcal vaccine, preferably a pneumococcal vaccine containing polysaccharide conjugated with a protein carrier.
• the present invention also relates to a process for producing substantially purified capsular polysaccharides from a Streptococcus pneumoniae cell lysate comprising serotype 1, 4, 5, 6A, 6B, 7F, 9V, 14, 18C, 19F, or 23F. This process comprises the steps of:
• step (b) lysing the bacterial cells in step (a) with a lytic agent, thereby producing a cell lysate comprising cell debris, soluble proteins, nucleic acids, and polysaccharides;
• step (c) clarifying the cell lysate of step (b) using centrifugation or filtration to remove cell debris, thereby producing a clarified cell lysate;
• step (d) ultraf ⁇ ltering and diaf ⁇ ltering the clarified cell lysate of step (c) at room temperature at neutral pH in salt free media to remove low molecular weight impurities and increase polysaccharide concentration, thereby producing a salt free retentate;
• step (e) lowering the pH of the salt free retentate of step (d) to less than 4.5 to precipitate protein and nucleic acids, thereby forming an acidified retentate solution;
• step (f) filtering the clarified polysaccharide solution of step (f) through an activated carbon filter;
• step (h) ultrafiltering and diafiltering the filtered solution produced by step (g), thereby producing a concentrated purified polysaccharide solution
• step (i) filtering the concentrated purified polysaccharide solution produced by step (h) using a sterile filter; whereby substantially purified capsular polysaccharides comprising serotype 1, 4, 5, 6A, 6B, 7F, 9V, 14, 18C, 19F, or 23F in the form of a solution are produced.
• the pH of step (e) is lowered to about 3.5.
• the diafiltration of step (h) comprises a pH adjustment to between about 5.5 to about 7.5.
• the diafiltration of step (h) comprises a pH adjustment to between about 7.0 to about 7.5.
• the diafiltration of step (h) comprises a pH adjustment to about 7.4.
• step (e) removes at least 98% of protein from the salt free retentate of step (d).
• step (g) removes at least 90% of the protein from the clarified polysaccharide solution of step (f).
• the activated carbon filter of step (g) comprises wood-based phosphoric acid-activated carbon.
• the lytic agent of step (b) is deoxycholate sodium (DOC).
• the lytic agent of step (b) is a non-animal derived lytic agent.
• the lytic agent of step (b) is the non-animal derived lytic agent N-lauryl sarcosine sodium (NLS).
• the present invention also relates to a process for producing substantially purified capsular polysaccharides from a Streptococcus pneumoniae cell lysate comprising serotype 19A. This process comprises the steps of:
• step (a) providing a fermentation broth comprising bacterial cells that produce Streptococcus pneumoniae serotype 19A; (b) lysing the bacterial cells in step (a) with a lytic agent, thereby producing a cell lysate comprising cell debris, soluble proteins, nucleic acids, and polysaccharides;
• step (c) clarifying the cell lysate of step (b) using centrifugation or filtration to remove cell debris, thereby producing a clarified cell lysate;
• step (d) ultrafiltering and diafiltering the clarified cell lysate of step (c) at about 4 0 C at a pH of about 6 in sodium phosphate buffer to remove low molecular weight impurities and increase polysaccharide concentration, thereby producing a retentate;
• step (e) lowering the pH of the retentate of step (d) to less than 4.5 to precipitate protein and nucleic acids, thereby forming an acidified retentate solution;
• step (f) holding the acidified retentate solution formed in step (e) for at least 2 hours at about 4 0 C to allow settling of the precipitate, followed by filtration or centrifugation of the acidified retentate solution, thereby producing a clarified polysaccharide solution; (g) adjusting the pH of the clarified polysaccharide solution of step (f) to about 6, thereby producing a pH-adjusted clarified polysaccharide solution;
• step (h) filtering the pH-adjusted clarified polysaccharide solution of step (g) through an activated carbon filter;
• step (i) ultrafiltering and diafiltering the filtered solution produced by step (h), thereby producing a concentrated purified polysaccharide solution
• step (j) filtering the concentrated purified polysaccharide solution produced by step (i) using a sterile filter; whereby substantially purified capsular polysaccharides comprising serotype 19A in the form of a solution are produced.
• the pH of step (e) is lowered to about 3.5.
• the diaf ⁇ ltration of step (i) comprises a pH adjustment to between about 5.5 to about 7.5.
• the diaf ⁇ ltration of step (i) comprises a pH adjustment to between about 7.0 to about 7.5.
• the diaf ⁇ ltration of step (i) comprises a pH adjustment to about 7.4.
• step (e) removes at least 98% of protein from the retentate of step (d).
• step (h) removes at least 90% of the protein from the pH-adjusted clarified polysaccharide solution of step (g).
• the activated carbon filter of step (h) comprises wood-based phosphoric acid-activated carbon.
• the sodium phosphate buffer of step (d) is 25 mM sodium phosphate.
• the lytic agent of step (b) is deoxycholate sodium (DOC).
• the lytic agent of step (b) is a non-animal derived lytic agent.
• the lytic agent of step (b) is the non-animal derived lytic agent N-lauryl sarcosine sodium (NLS).
• Figure 1 shows average in-process polysaccharide (PS) yield, protein/PS ratio, and nucleic acid (NA)/PS ratio for serotype 5 using the shortened purification process of the invention. Results are shown for each purification step.
• PS polysaccharide
• NA nucleic acid
• Figure 2 shows NMR spectra for serotype 4 PS from the current purification process (A) compared to serotype 4 PS from the shortened purification process (B). No significant differences between the two spectra were observed.
• the second peak from the right in both spectra was pyruvate, and the pyruvate group peak height was comparable in both spectra.
• Figure 3 shows average in-process PS yield, protein/PS ratio, and NA/PS ratio for serotype 4 using the shortened purification process of the invention. Results are shown for each purification step.
• Figure 4 shows average in-process PS yield, protein/PS ratio, and NA/PS ratio for serotype 19A using the shortened purification process of the invention. Results are shown for each purification step.
• Figure 5 shows average in-process PS yield, protein/PS ratio, and NA/PS ratio for serotype 7F using the shortened purification process of the invention. Results are shown for each purification step.
• Figure 6 shows average in-process PS yield, protein/PS ratio, and NA/PS ratio for serotype 6B using the shortened purification process of the invention. Results are shown for each purification step.
• Figure 7 shows average in-process PS yield, protein/PS ratio, and NA/PS ratio for serotype 6A using the shortened purification process of the invention. Results are shown for each purification step.
• Figure 8 shows average in-process PS yield, protein/PS ratio, and NA/PS ratio for serotype 1 using the shortened purification process of the invention. Results are shown for each purification step.
• Figure 9 shows average in-process PS yield, protein/PS ratio, and NA/PS ratio for serotype 14 using the shortened purification process of the invention. Results are shown for each purification step.
• Figure 10 shows a comparison of PS in -process yields for serotypes 1, 4, 5, 6A, 6B, 7F, 9V, 14, 18C, 19 A, and 19F purified using the shortened purification process of the invention.
• Figure 11 shows a comparison of protein/PS ratios for serotypes 1, 4, 5, 6A,
• Figure 12 shows a comparison of NA/PS ratios for serotypes 1, 4, 5, 6A, 6B, 7F, 9V, 14, 18C, 19A, and 19F purified using the shortened purification process of the invention. Results are compared for each purification step.
• Figure 13 shows protein removal efficiency attributable to the acidification step of the shortened purification process of the invention.
• the difference in protein concentration (SDS-PAGE) before and after acidification is plotted against initial protein concentration before acidification for batches of serotypes 1, 4, 5, 6A, 6B, 7F, 9V, 14, 18C, 19A, and 19F.
• the protein concentration difference divided by the initial protein concentration reflected the protein removal rate by the acidification step.
• Figure 14 shows protein removal efficiency attributable to the carbon adsorption step of the shortened purification process of the invention.
• the amount of protein removed (adsorbed on carbon) was plotted against initial protein loading amounts for batches of serotypes 1, 4, 5, 6A, 6B, 7F, 9V, 14, 18C, 19A, and 19F.
• the amount of protein removed divided by the initial protein loading amounts reflected the protein removal rate by the carbon adsorption step.
• the present invention relates to a shortened purification process to reduce the soluble protein levels in cellular Streptococcus pneumoniae lysates to produce substantially purified capsular polysaccharides suitable for incorporation into pneumococcal conjugate vaccines.
• 7vPnC 7-valent pneumococcal conjugate
• 13vPnC 13-valent pneumococcal conjugate
• the process of the present invention eliminates up to eight of these steps while accomplishing the same purification and eliminates the need for chromatography.
• the present invention relates to a more efficient purification process that is less expensive, takes less time, and involves fewer steps.
• the shortened purification process of the present invention relates to the discovery that ultrafiltering and diafiltering a clarified cellular S. pneumoniae lysate broth, followed by acidification of the concentrated lysate broth to a pH of less than 4.5, preferably about 3.5, precipitates at least 98% of the protein in the solution without seriously affecting polysaccharide yield.
• ultrafiltration and diafiltration of the clarified lysate broth makes it possible to use any low molecular weight pH titrant such as sodium carbonate during 5 * . pneumoniae serotype fermentation and prevents foaming of the clarified lysate broth when acidified to a pH of less than 4.5.
• “Clarified lysate broth” refers to a lysate broth that has undergone centrifugation or filtration to remove cell debris.
• “Diafiltering,” “diafiltration,” “DF,” and like terms refer to, for example, using semi-permeable membranes with appropriate physical and chemical properties to remove small molecules from a solution.
• Ultrafiltering refers to, for example, using semi-permeable membranes with appropriate physical and chemical properties to discriminate between molecules in a solution and concentrate like molecules into a smaller volume of solution.
• ultrafiltration and diafiltration typically comprise "cross-flow” or "tangential-flow” filtration in order to avoid clogging of the filter membranes.
• cross-flow the solution to be filtered is passed across the surface of the membrane. Materials which pass through the membrane are referred to as the permeate. The materials which do not pass through the membrane are referred to as the retentate. The retentate is recycled to a feed reservoir to be refiltered.
• any acid may be used to lower the pH of the ultrafiltered and diafiltered lysate broth so long as a pH of less than 4.5, particularly about 3.5, is achieved. Accordingly, both organic and mineral acids may be used within the methods of the invention.
• mineral acid refers to an acid derived from inorganic mineral by chemical reaction as opposed to organic acids.
• mineral acids that may be used within the methods of the present invention include hydrochloric acid, nitric acid, phosphoric acid, and sulphuric acid.
• the pH of the concentrated lysate broth is lowered to less than 4.4, 4.3, 4.2, 4.1, 4.0, 3.9, 3.8, 3.7, 3.6, 3.5, 3.4, 3.3, 3.2, 3.1, or 3.0.
• the pH of the concentrated lysate broth is lowered to about 4.4, about 4.3, about 4.2, about 4.1, about 4.0, about 3.9, about 3.8, about 3.7, about 3.6, about 3.5, about 3.4, about 3.3, about 3.2, about 3.1, about 3.0, about 2.9, about 2.8, about 2.7, about 2.6, about 2.5, about 2.4, about 2.3, about 2.2, about 2.1, or about 2.0.
• the shortened purification process of the present invention also relates to the discovery that, in combination with the concentration and low pH steps described above, filtration using activated carbon precipitates at least 90% of remaining protein without seriously affecting polysaccharide yield.
• carbon filtration using carbon derived from sawdust or other wood products and activated with phosphoric acid was found to be more effective at reducing or removing protein impurities than carbons used within current carbon filtration methods.
• the present invention relates to a process for producing substantially purified capsular polysaccharides from a Streptococcus pneumoniae cell lysate comprising the steps of:
• step (b) lysing the bacterial cells in step (a) with a lytic agent, thereby producing a cell lysate comprising cell debris, soluble proteins, nucleic acids, and polysaccharides;
• step (c) clarifying the cell lysate of step (b) using centrifugation or filtration to remove cell debris, thereby producing a clarified cell lysate;
• step (d) ultrafiltering and diafiltering the clarified cell lysate of step (c) to remove low molecular weight impurities and increase polysaccharide concentration, thereby producing a retentate;
• step (e) lowering the pH of the retentate of step (d) to less than 4.5, particularly about 3.5, to precipitate protein and nucleic acids, thereby forming an acidified retentate solution; (f) holding the acidified retentate solution formed in step (e) for a time sufficient to allow settling of the precipitate, particularly for at least 2 hours with or without agitation, followed by filtration or centrifugation of the acidified retentate solution, thereby producing a clarified polysaccharide solution;
• step (g) filtering the clarified polysaccharide solution of step (f) through an activated carbon filter, particularly an activated carbon filter comprising wood-based phosphoric acid-activated carbon;
• step (h) ultrafiltering and diafiltering the filtered solution produced by step (g), thereby producing a concentrated purified polysaccharide solution
• step (i) filtering the concentrated purified polysaccharide solution produced by step (h) using a sterile filter; whereby substantially purified capsular polysaccharides in the form of a solution are produced.
• the sterile filtration of step (i) is useful to remove bacteria and particles from the concentrated purified polysaccharide solution.
• Exemplary, non-limiting S. pneumoniae serotypes selected for this embodiment of the invention are 1, 4, 5, 6A, 6B, 7F, 9V, 14, 18C, 19A, 19F, and 23F.
• step (e) removes at least 98% of protein from the retentate of step (d).
• step (g) removes at least 90% of the protein from the clarified polysaccharide solution of step (f).
• the diaf ⁇ ltration of step (h) comprises a pH adjustment to between about 5.5 to about 7.5.
• the diaf ⁇ ltration of step (h) comprises a pH adjustment to between about 7.0 to about 7.5, and more particularly to about 7.4.
• substantially purified capsular polysaccharide- containing lysate or “solution containing substantially purified capsular polysaccharides” refers to a cellular Streptococcus pneumoniae lysate or solution from which protein has been removed such that the percent ratio of protein to polysaccharide (protein/PS) is less than 10%, less than 9%, less than 8%, less than 7%, less than 6%, less than 5%, less than 4%, less than 3%, less than 2%, or less than 1% and the percent ratio of nucleic acid to polysaccharide (NA/PS) is less than 5%, less than 4%, less than 3%, less than 2%, or less than 1%.
• protein/PS percent ratio of protein to polysaccharide
• NA/PS nucleic acid to polysaccharide
• the percent ratios of protein/PS and NA/PS for substantially purified capsular polys accharide-containing lysates or solutions comprising specific serotypes are as follows: for serotype 1 the ratio of protein/PS is less than 2% and the ratio of NA/PS is less than 2%, for serotype 4 the ratio of protein/PS is less than 3% and the ratio of NA/PS is less than 2%, for serotype 5 the ratio of protein/PS is less than or equal to 7.5% and the ratio of NA/PS is less than or equal to 2%, for serotype 6A the ratio of protein/PS is less than 2% and the ratio of NA/PS is less than 2%, for serotype 6B the ratio of protein/PS is less than 4% and the ratio of NA/PS is less than 1%, for serotype 7F the ratio of protein/PS is less than 5% and the ratio of NA/PS is less than 2%, for serotype 9V the ratio of protein/PS is less than 2% and the ratio of NA/PS
• Methods for the quantification of protein, polysaccharide, and nucleic acid concentrations in a cellular lysate or solution are well known in the art and include, for example, SDS-PAGE (Sodium Dodecyl Sulfate Polyacrylamide Gel Electrophoresis) analysis, HPLC (High Performance Liquid Chromatography) and SEC (Size Exclusion Chromatography), modified Lowry assays, spectrophotometry, SEC-MALLS (Size-Exclusion Chromatography/Multi-Angle Laser Light Scattering), and NMR (Nuclear Magnetic Resonance).
• the bacterial cells may be lysed using any lytic agent.
• a “lytic agent” is any agent that aids in cell wall breakdown and release of autolysin which causes cellular lysis including, for example, detergents.
• detergent refers to any anionic or cationic detergent capable of inducing lysis of bacterial cells.
• Representative examples of such detergents for use within the methods of the present invention include deoxycholate sodium (DOC), N-lauryl sarcosine (NLS), chenodeoxycholic acid sodium, and saponins.
• the lytic agent used for lysing bacterial cells is DOC.
• DOC is the sodium salt of the bile acid deoxycholic acid, which is commonly derived from biological sources such as cows or oxen.
• DOC activates the LytA protein, which is an autolysin that is involved in cell wall growth and division in Streptococcus pneumoniae .
• the LytA protein has choline binding domains in its C-terminal portion, and mutations of the lytA gene are known to produce LytA mutants that are resistant to lysis with DOC.
• the lytic agent used for lysing bacterial cells is a non-animal derived lytic agent.
• Non-animal derived lytic agents for use within the methods of the present invention include agents from non-animal sources with modes of action similar to that of DOC (i.e. , that affect LytA function and result in lysis of Streptococcus pneumoniae cells).
• non-animal derived lytic agents include, but are not limited to, analogs of DOC, surfactants, detergents, and structural analogs of choline, and may be determined using procedures as described in the Experimental section herein below.
• the non-animal derived lytic agent is selected from the group consisting of decanesulfonic acid, tert-octylphenoxy poly(oxyethylene)ethanols (e.g. Igepal® CA-630, CAS #: 9002-93-1, available from Sigma Aldrich, St. Louis, MO), octylphenol ethylene oxide condensates (e.g. Triton® X-IOO, available from Sigma Aldrich, St.
• NLS N-lauryl sarcosine sodium
• lauryl iminodipropionate sodium dodecyl sulfate, chenodeoxycholate, hyodeoxycholate, glycodeoxycholate, taurodeoxycholate, taurochenodeoxycholate, and cholate.
• the non-animal derived lytic agent is NLS.
• the present invention also relates to serotype-specif ⁇ c modifications to the process described above.
• serotype-specif ⁇ c modifications to the process described above.
• modifications to the process described were useful in stabilizing the 19A polysaccharide. These modifications included carrying out the ultrafiltration and diaf ⁇ ltration step prior to acidification at about 4 0 C at a pH of about 6 in sodium phosphate buffer, holding the acidified retentate solution for at least 2 hours at about 4 0 C to allow settling of the precipitate, and adjusting the pH of the clarified polysaccharide solution to 6 prior to the activated carbon filtration step.
• the present invention also relates to a process for producing substantially purified capsular polysaccharides from a Streptococcus pneumoniae cell lysate comprising serotype 1, 4, 5, 6A, 6B, 7F, 9V, 14, 18C, 19F, or 23F comprising the steps of:
• step (a) providing a fermentation broth comprising bacterial cells that produce Streptococcus pneumoniae serotype 1, 4, 5, 6A, 6B, 7F, 9V, 14, 18C, 19F, or 23F; (b) lysing the bacterial cells in step (a) with a detergent, thereby producing a cell lysate comprising cell debris, soluble proteins, nucleic acids, and polysaccharides;
• step (c) clarifying the cell lysate of step (b) using centrifugation or filtration to remove cell debris, thereby producing a clarified cell lysate;
• step (d) ultrafiltering and diafiltering the clarified cell lysate of step (c) at room temperature at neutral pH in salt free media to remove low molecular weight impurities and increase polysaccharide concentration, thereby producing a salt free retentate; (e) lowering the pH of the salt free retentate of step (d) to less than 4.5, particularly about 3.5, to precipitate protein and nucleic acids, thereby forming an acidified retentate solution;
• step (f) holding the acidified retentate solution formed in step (e) for at least 2 hours at room temperature with or without agitation to allow settling of the precipitate, followed by filtration or centrifugation of the acidified retentate solution, thereby producing a clarified polysaccharide solution;
• step (g) filtering the clarified polysaccharide solution of step (f) through an activated carbon filter, particularly an activated carbon filter comprising wood-based phosphoric acid-activated carbon; (h) ultrafiltering and diafiltering the filtered solution produced by step (g), thereby producing a concentrated purified polysaccharide solution; and
• step (i) filtering the concentrated purified polysaccharide solution produced by step (h) using a sterile filter; whereby substantially purified capsular polysaccharides comprising serotype 1, 4, 5, 6A, 6B, 7F, 9V, 14, 18C, 19F, or 23F in the form of a solution are produced.
• step (e) removes at least 98% of protein from the salt free retentate of step (d).
• step (g) removes at least 90% of the protein from the clarified polysaccharide solution of step (f).
• the diaf ⁇ ltration of step (h) comprises a pH adjustment to between about 5.5 to about 7.5.
• the diaf ⁇ ltration of step (h) comprises a pH adjustment to between about 7.0 to about 7.5, and more particularly to about 7.4.
• the present invention also relates to a process for producing substantially purified capsular polysaccharides from a Streptococcus pneumoniae cell lysate comprising serotype 19A comprising the steps of
• step (b) lysing the bacterial cells in step (a) with a detergent, thereby producing a cell lysate comprising cell debris, soluble proteins, nucleic acids, and polysaccharides;
• step (c) clarifying the cell lysate of step (b) using centrifugation or filtration to remove cell debris, thereby producing a clarified cell lysate;
• step (d) ultrafiltering and diafiltering the clarified cell lysate of step (c) at about 4 0 C at a pH of about 6 in sodium phosphate buffer, 25 mM sodium phosphate, to remove low molecular weight impurities and increase polysaccharide concentration, thereby producing a retentate; (e) lowering the pH of the retentate of step (d) to less than 4.5, particularly about 3.5, to precipitate protein and nucleic acids, thereby forming an acidified retentate solution;
• step (f) holding the acidified retentate solution formed in step (e) for at least 2 hours at about 4 0 C with or without agitation to allow settling of the precipitate, followed by filtration or centrifugation of the acidified retentate solution, thereby producing a clarified polysaccharide solution;
• step (g) adjusting the pH of the clarified polysaccharide solution of step (f) to about 6, thereby producing a pH-adjusted clarified polysaccharide solution;
• step (h) filtering the pH-adjusted clarified polysaccharide solution of step (g) through an activated carbon filter, particularly an activated carbon filter comprising wood-based phosphoric acid-activated carbon;
• step (i) ultrafiltering and diafiltering the filtered solution produced by step (h), thereby producing a concentrated purified polysaccharide solution
• step (j) filtering the concentrated purified polysaccharide solution produced by step (i) using a sterile filter; whereby substantially purified capsular polysaccharides comprising serotype 19A in the form of a solution are produced.
• step (e) removes at least 98% of protein from the retentate of step (d).
• step (h) removes at least 90% of the protein from the pH-adjusted clarified polysaccharide solution of step (g).
• the diaf ⁇ ltration of step (i) comprises a pH adjustment to between about 5.5 to about 7.5.
• the diaf ⁇ ltration of step (i) comprises a pH adjustment to between about 7.0 to about 7.5, and more particularly to about 7.4.
• Example 1 Shortened Purification Process for S. pneumoniae Polysaccharide Serotypes 1. 4. 5. 6A. 6B. 7F. 14 and 19A.
• S. pneumoniae fermentation broths lysed with deoxycholate sodium (DOC) were obtained either within two days following their harvest or stored in 4°C and processed within the following week.
• the present purification process included the following changes compared to the existing purification process: 1) the acidification step was moved from the beginning to after the first ultrafiltration/diafiltration (UF/DF) step, and the pH was adjusted to 3.5 instead of 5; 2) the diafiltration buffer was changed from 0.025 M phosphate to de-ionized (DI) water; 3) carbon adsorption was changed to 2 CUNO R32SP carbon disks (CUNO Inc., Wayne, NJ) using wood-based phosphoric acid-activated carbon, and the adsorption time was extended from 4 to 12 turnovers (each turnover was 22 minutes); and 4) pH was adjusted to 7.4 during the last 3OK diafiltration step when diafiltered about 5 times.
• the same purification procedure was applied to serotypes 1, 4, 5, 6A, 6B, or 7F.
• Clarification of the lysate The purpose of this step was to remove cell debris and clarify the broth. This was accomplished either by centrifugation or filtration. The broth was centrifuged at 10,000 g for 30 min or until the broth was clear at 20 0 C (4°C for type 19A), or filtered with a Millipore Prefilter (Millipore Corp., Billerica, MA) with the addition of Celpure ® filter aids (Advanced Minerals, Santa Barbara, CA). The clarified lysate was collected for further processing and the pellets were discarded.
• First UF/DF Ultrafiltration/Diafiltration
• Diafiltration was performed using about 10 volumes DI water (pH 6, 25 mM phosphate for 19A). Acidification: More than 98% of the proteins were removed in this step. While stirring, concentrated phosphoric acid was added carefully to the retentate. The pH of the retentate was adjusted to a target value of pH 3.5. The acidified retentate was stirred for half an hour and aged in room temperature to age overnight (2 hours at 4°C for 19A), resulting in the precipitation of protein and nucleic acids.
• Clarification of Acidified Retentate This was the clarification step to remove the precipitates after acidification.
• the slurry of acidified solution was centrifuged in a rotor at 10,000 rpm (17,000 Relative Centrifugal Force or RCF) for one hour at 20 0 C (except for 6B, in which case the centrifugation was 6 hours at 37°C).
• the supernatant was collected and the pellet was discarded.
• Depth filtration with a Millipore Prefilter Millipore Corp., Billerica, MA
• Celpure ® filter aids Advanced Minerals, Santa Barbara, CA
• Type 5 Shortened Purification Batches The comparison of final PS yield, PS molecular weight and major impurity levels of three purification batches using the shortened process and those using the current process for Type 5 are shown in Table 1. All the starting broths were DOC lysed high cell density fermentation batches, which had a higher polysaccharide concentration ( ⁇ 0.5 g/L) than the standard SOP fermentation broth (-0.3 g/L). A 30K or 50K membrane was used for the first UF/DF step. The impurity levels were calculated using impurity/PS ratios. The same approach was used for all other serotypes described herein.
• the protein ratios of all three batches using the shortened purification process met the specification of ⁇ 7.5%, and were also comparable to that of the current process.
• the nucleic acid (NA) as well as C- polysaccharide (C-PS) ratios were also well below the specifications of ⁇ 2.0% and ⁇ 35%, respectively and were comparable to that of the current process.
• the results of the final PS yield and impurity levels of the three batches shown in Table 1 demonstrate the reproducibility and robustness of the shortened process.
• PS loss occurred mostly in the first UF/DF step and the acidification step.
• the loss of PS at the first UF/DF step was due to adsorption of PS or PS-protein complex to the surface of the membrane. This loss was minimized by rinsing the retentate side of the membrane with DI water after the diafiltration and combining the rinse with the original retentate.
• the loss of PS at the acidification step could be due to two reasons: physical adsorption of PS to the precipitation solids, and polysaccharide binding to the protein with co-precipitation during acidification. This second possibility was further investigated and results showed evidence of PS/protein binding.
• Figure 1 shows the reduction of protein/PS ratio at each purification step.
• the centrifugation step removed a small percentage of proteins, the majority of protein was removed at the acidification step. Only a trace amount of protein was detected after pH 3.5 treatment even for the highest protein potency batch. Similar to protein/PS ratio, the nucleic acid/PS ratio showed variability of impurity levels among batches.
• the 30/50K UF/DF step removed a significant amount of nucleic acid as compared to protein removal in the same processing step. Without being bound by theory, this may have been due to the molecular size of nucleic acids being smaller than that of proteins, making them relatively easier to be removed via the 30/50K UF/DF step.
• the first centrifugation and acidification step also removed a considerable amount of nucleic acid.
• Table 2 shows that the activated carbon adsorption step also reduces protein/PS and NA/PS level. The percentage reduction was not as significant as the first two steps, but this step was important for removing the color of the solution and ensured that the impurity level met the specification.
• Type 4 Shortened Purification Batches A summary of three shortened purification batches for Type 4 is shown in Table 3. The feed broths for all three batches were DOC-lysed.
• the type 4 PS yield was also between 50-60%. Protein/PS ratio and nucleic acid/PS ratio were well within their specifications. C-PS ratio was also well within the specification. The molecular weight of all of the three batches were close to -300 kg/mol. Serotype 4 PS purified by the current purification process using the similar fermentation broth also gave a lower molecular weight 285 kg/mol. Comparison of the HPLC chromatographs of the PS from fermentation broth and the final purified solution showed that there were no differences in the PS retention time. This suggested that the difference in molecular weight difference was not caused by the process change, but rather due to intrinsic nature of the fermentation process.
• the Type 4 PS contains a pyruvate group in the purified molecule, and this pyruvate was important for conjugation for use in a pneumococcal conjugate vaccine.
• NMR analysis was conducted.
• Figure 2 shows the NMR spectra for standard type 4 PS and that from batch L29276-47. No significant differences between the two spectra were observed.
• the second peak from the right in both spectra was pyruvate, and the pyruvate group peak height was comparable in both spectra.
• the pyruvate ratios for all three shortened process batches were 0.8 mol/mol, and met the specification of >0.7 mol/mol.
• Figure 3 shows average PS yield, protein/PS and NA/PS ratio change at each of the purification steps for the three batches in Table 4.
• the protein removal occurred mostly at the acidification step as expected.
• the first centrifugation and UF/DF steps also collectively removed a certain amount of protein, but the protein reduction was less than the acidification step.
• the activated carbon step removed a certain amount of protein and NA and brought the impurity levels below the specifications. It also removed the color of the solution as well.
• Type 19A Shortened Purification Batches Type 19A polysaccharide is unstable and the molecular weight changes during purification. The shortened purification process was modified slightly in order to stabilize the 19A polysaccharide. These modifications are summarized as follows: 1) the purification steps were mostly conducted at 4°C in the chill room; 2) the first IOOK diafiltration was chilled using 25 mM phosphate buffer (4°C) with a pH of 6 instead of using room temperature water; 3) the acidification holding time was reduced from overnight to 2 hours; and 4) after clarifying the acidified IOOK retentate, the pH was adjusted to 6 and activated carbon adsorption was conducted at pH 6 instead of 3.5.
• the PS yields of the two shortened purification batches were 62 and 76% respectively.
• Final protein/PS ratio, nucleic acid ratio, and C-PS ratio all met their respective specifications.
• the final molecular weights of polysaccharides from the two batches were 525 kg/mol and 488 kg/mol, respectively, and were close to that of the PS of 19A used in phase III clinical trials (486kg/mol).
• the PS yield, protein and NA reduction at each of the purification steps are shown in Table 6 and Figure 4.
• the results showed PS loss at each of the purification steps except the first centrifugation step.
• protein and NA removal mostly took place at the first three steps, and there was hardly any detectable protein and NA left after acidification.
• the activated carbon adsorption step did not remove a significant amount of protein and NA, possibly due to very low protein and NA concentration after the acidification, the step was still needed for color removal.
• Type 7F Shortened Purification Batches: Type 7F is a non-ionic polysaccharide, which typically requires change in steps during purification using the existing process compared to the serotypes described above ). However, the shortened purification process of the present invention was successfully applied to serotype 7F without the need for process deviation.
• Two batches of type 7F broth were purified using the shortened process. One was a standard fermentation broth (L29276-107) and one was a high cell density broth (L29276-157). The results of the two batches are summarized in Table 7.
• the PS yield of type 7F was actually higher than the other serotypes, possibly due to less binding of the non -ionic polymer to the charged protein molecules.
• Final protein, NA and C-PS ratios were all well within their specifications.
• Molecular weight of type 7F was comparable to that of standard batches and even though the 7F molecular weight was quite high, the PS solution was not very viscous due to smaller excluded volume of the nonionic polymer.
• Type 7F PS yield, protein and NA ratio at each of the purification steps are shown in Table 8 and the average of the two batches was plotted in Figure 5.
• PS loss was less than that of serotypes 5 and 4. Protein and NA ratio reduction was mostly by the first centrifugation, IOOK UF/DF, and acidification steps. Similar to other serotypes, the IOOK UF/DF was more efficient in removing NA than proteins. Although the activated carbon adsorption step did not remove a significant amount of protein and NA due to very low impurity levels after acidification, the step was still needed for color removal.
• Type 6B Shortened Purification Batches Two batches of 6B were purified using the shortened purification process. It was found the clarification of the acidified IOOK retentate took a longer time than the other serotypes (6 hours instead of 1 hour). Except for this difference, the purification process was similar to that of the serotypes. The results of the two batches are summarized in Table 9.
• Type 6A Shortened Purification Batches Two batches of type 6A were purified using the shortened purification process. The PS yield, impurity levels and molecular weight of the final solutions are summarized in Table 11.
• the final PS yields of the two 6A batches were both >70%, which were the highest among the serotypes processed using the shortened process. Protein, NA, and C-PS ratios were all within specifications.
• Table 12 and Figure 7 show in-process PS yield, protein and NA ratio change at each of the purification steps.
• the acidification was the most efficient step, while for NA, IOOK UF/DF reduced the most NA/PS ratio.
• the activated carbon adsorption step did not remove a significant amount of protein and NA due to very low impurity levels after acidification, the step was still needed for color removal.
• Type 1 Shortened Purification Batches Two batches of type 1 purified by the shortened process are summarized in Table 13. Batch L29276-170 was purified from high cell density fermentation broth and L29276-173 was from standard fermentation broth.
• the PS yields of both batches were about 50%, and the impurity levels for protein, NA and C-PS were all within their specifications.
• the in-process PS yield, protein and NA ratios after each of the purification steps are shown in Table 14 and Figure 8.
• the trends were similar to other serotypes purified. PS loss occurred mostly at the acidification and activated carbon adsorption steps, and most of protein and NA removal occurred at the first three steps. More NA was removed at the IOOK UF/DF step than proteins. Although the activated carbon adsorption step did not remove a significant amount of protein and NA due to very low impurity levels after acidification, the step was still needed for color removal.
• Type 14 Shortened Purification Batches Two batches of serotype 14 were purified using the shortened purification process with no process deviations. The final PS yield, and impurity levels are summarized in Table 15.
• serotype 14 is a non-ionic polysaccharide, and its current purification process is slightly different from the other serotypes.
• the shortened purification process of the present invention was successfully applied to serotype 14 without the need for such additional steps.
• the PS yields of the two shortened purification process batches were 50-60%, and protein and NA ratios were within their specifications.
• the molecular weights of the purified PS also met the specification.
• In-process PS yield, protein and NA ratios are summarized in Table 16 and Figure 9. Similar trends of PS loss, protein and NA removal were observed as for the other tested serotypes described above.
• PS removal for all the serotypes described in Example 1 plus serotypes 9V, 18C, and 19F were plotted in one graph in Figure 10. Most of the serotypes followed a similar trend with PS loss at each of the purification steps. There was an increase of PS yield for type 6B at the first centrifugation step and type 14 at the acidification step. PS percentage loss varied from serotype to serotype. Type 5 seemed to lose most PS at the acidification step and type 4 at the activated carbon adsorption step. Protein/PS ratios for each purification step for each of the serotypes are shown in Figure 11.
• the figure shows that there was a difference in initial protein/PS ratios for different serotypes, with types 1, 4, 5, 9V, 19F, and 18C having the highest initial protein/PS ratios. Even though the protein/PS ratios were much higher for types 1, 4, 5, 9V, 19F, and 18C compared to the other serotypes even after the first UF/DF step, the acidification step greatly reduced the protein/PS ratio and not much protein was left after this step.
• NA/PS ratios also varied from serotype to serotype.
• Types 1 and 5 had the highest NA/PS ratio, followed by types 18C and 4.
• the first centrifugation and UF/DF step removed a significant amount of NA for these serotypes and type 1 seemed to be the most efficient. There was very little NA left after the acidification step.
• FIG. 13 shows the slope of the linear fit of protein concentration difference with respect to initial protein concentration (by SDS-PAGE assay). A very good linear relationship was observed between the protein concentration change and the initial concentration, with the R close to 1. The slope was 0.9876, which corresponds to a 98.76% protein removal (assuming negligible solution volume change). Therefore, for all serotypes studied, the acidification step was very efficient and on average it removed more than 98% protein.
• the present example investigated whether non-animal derived lytic agents could be used as a substitute for deoxycholate sodium (DOC) within the process described above for the production of substantially purified capsular Streptococcus pneumoniae polysaccharides.
• DOC deoxycholate sodium
• LytA protein which is an autolysin that is involved in cell wall growth and division in Streptococcus pneumoniae.
• the LytA protein has choline binding domains in its C- terminal portion, and mutations of the lytA gene are known to produce LytA mutants that are resistant to lysis with DOC.
• a rapid microtiter plate assay was developed to identify compounds that cause cell lysis by a mechanism similar to that of DOC.
• Several non-animal derived alternatives to DOC were identified which were equally effective as DOC at killing Streptococcus pneumoniae cells and releasing polysaccharide.
• the size and purity of the polysaccharides produced with the non-animal derived compounds were identical to those produced with DOC.
• Cell Lysis Compounds to be tested were added to fermentation broth at a final concentration of 0.1 to 0.01% (v/v) and the solution was allowed to incubate at 37°C for one hour. The solution was then stored at 2-8°C overnight. The following morning the solution was centrifuged to remove all cell debris. The cell-free broth was analyzed by SEC-HPLC to determine the concentration of released polysaccharide. The lysis could be performed at any temperature between 2-37°C, preferably at a pH range of 6.0-7.5. The concentration of the detergent was typically between 0.05-0.2% depending on the particular detergent.
• Mitrotiter Assay A rapid microtiter plate assay was devised for examining /j ⁇ 4 -dependent lysis of pneumococci by different detergents or surfactants. Two pairs of isogenic strains of S. pneumoniae were used in the assay; one member of each pair was wild type for the lytA gene while the other strain carried a deletion in the lytA gene Thus, if lysis were dependent on an active lytA function, that detergent would not lyse the mutant strains.
• the four strains, R6X, R6X ⁇ lytA, D39 and D39 ⁇ lytA, were cultivated in HySoy medium to approximately mid-log phase (OD 6 oo -0.2-0.8; OD ⁇ oo Optical Density at 600 nm). Cells were then centrifuged and cell pellets were resuspended in HySoy medium. To each well of the microtiter plate, 100 ⁇ L of cell suspension was added, along with 10 ⁇ L of detergent stocks or water as a control. After about 15 minutes at 36°C, the OD ⁇ oo of the samples was measured with a Spectramax® spectrophotometer (Molecular Devices, Sunnyvale, CA).
• the PS content of the lysate was determined using SEC-HPLC coupled to a refractive index (RI) detector.
• S. pneumoniae serotypes 1 and 6B were separately grown in Hy-Soy based media. The cultures were separately harvested and separately dispensed into tubes.
• the non-animal derived compounds to be screened for lytic activity comparable to
• DOC were prepared as stock solutions (in suitable solvents) and added to the cultures. After overnight incubation, the tubes were centrifuged and the PS content of the lysates for each serotype were determined by SEC-HPLC and compared to DOC. Screening for Non- Animal Derived Lytic Agents Using lytA Mutants
• Isogenic pairs of strains containing the lytA mutation were grown in a Hy-Soy based medium. The cells were harvested and dispensed into wells in a microttiter plate. The test compound was added and the culture was incubated. After 15 min at 36 0 C, the optical density (OD ⁇ oo) of each well was determined using a SpectraMax® plate reader (Molecular Devices, Sunnyvale, CA)(see Tables 17 and 18, which summarize results from two separate tests for exemplary compounds).
• decanesulfonic acid decanesulfonic acid
• Igepal® CA-630 tert-octylphenoxy poly(oxyethylene)ethanol
• CAS #: 9002-93-1 available from Sigma Aldrich, St. Louis, MO
• N-lauryl sarcosine sodium NLS
• lauryl iminodipropionate sodium dodecyl sulfate
• Triton® X-IOO chenodeoxycholate, hyodeoxycholate, glycodeoxycholate, taurodeoxycholate, taurochenodeoxycholate, and cholate.
• S. pneumoniae polysaccharide serotypes 1, 4, 5, 6A, 6B, and 7F were purified at the 1OL scale as described above in Examples 1 and 2 using the improved process of the present invention.
• NLS 0.1%) was used as the lytic agent while in another group DOC (0.12%) was used as the lytic agent.
• PS yield, protein/PS ratios, NA/PS ratios, and PS molecular weight were measured as described above, and results are summarized in Table 19.

Landscapes

• Health & Medical Sciences (AREA)
• Life Sciences & Earth Sciences (AREA)
• Chemical & Material Sciences (AREA)
• Engineering & Computer Science (AREA)
• Organic Chemistry (AREA)
• General Health & Medical Sciences (AREA)
• Medicinal Chemistry (AREA)
• Molecular Biology (AREA)
• Bioinformatics & Cheminformatics (AREA)
• Biochemistry (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Pharmacology & Pharmacy (AREA)
• Animal Behavior & Ethology (AREA)
• Immunology (AREA)
• Public Health (AREA)
• Veterinary Medicine (AREA)
• Microbiology (AREA)
• Epidemiology (AREA)
• Biotechnology (AREA)
• Genetics & Genomics (AREA)
• Wood Science & Technology (AREA)
• Zoology (AREA)
• General Chemical & Material Sciences (AREA)
• Proteomics, Peptides & Aminoacids (AREA)
• Materials Engineering (AREA)
• Polymers & Plastics (AREA)
• Mycology (AREA)
• General Engineering & Computer Science (AREA)
• Sustainable Development (AREA)
• Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
• Virology (AREA)
• Oncology (AREA)
• Pulmonology (AREA)
• Communicable Diseases (AREA)
• Polysaccharides And Polysaccharide Derivatives (AREA)
• Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
• Preparation Of Compounds By Using Micro-Organisms (AREA)
• Peptides Or Proteins (AREA)

Priority Applications (19)

Applications Claiming Priority (2)

Publications (2)

Family

ID=39712482

Family Applications (1)

Country Status (29)

Cited By (69)

Families Citing this family (37)

Family Cites Families (19)

• 2008
  • 2008-03-20 HU HUE08732592A patent/HUE031567T2/hu unknown
  • 2008-03-20 KR KR1020097021976A patent/KR101500771B1/ko active Active
  • 2008-03-20 DK DK18177128.8T patent/DK3406635T3/da active
  • 2008-03-20 NZ NZ580134A patent/NZ580134A/en unknown
  • 2008-03-20 PT PT181771288T patent/PT3406635T/pt unknown
  • 2008-03-20 MY MYPI20093908 patent/MY150927A/en unknown
  • 2008-03-20 AU AU2008231041A patent/AU2008231041B2/en active Active
  • 2008-03-20 PL PL08732592T patent/PL2129693T3/pl unknown
  • 2008-03-20 WO PCT/US2008/057688 patent/WO2008118752A2/en not_active Ceased
  • 2008-03-20 KR KR1020157002150A patent/KR20150021127A/ko not_active Ceased
  • 2008-03-20 US US12/052,525 patent/US8652480B2/en active Active
  • 2008-03-20 DK DK08732592.4T patent/DK2129693T3/en active
  • 2008-03-20 SI SI200832196T patent/SI3406635T1/sl unknown
  • 2008-03-20 PT PT87325924T patent/PT2129693T/pt unknown
  • 2008-03-20 RU RU2009135485/10A patent/RU2516340C2/ru active
  • 2008-03-20 CL CL200800831A patent/CL2008000831A1/es unknown
  • 2008-03-20 CA CA2681570A patent/CA2681570C/en active Active
  • 2008-03-20 EP EP11194173.8A patent/EP2436700B8/en active Active
  • 2008-03-20 HU HUE11194173A patent/HUE039169T2/hu unknown
  • 2008-03-20 MX MX2009010221A patent/MX2009010221A/es active IP Right Grant
  • 2008-03-20 PL PL18177128.8T patent/PL3406635T3/pl unknown
  • 2008-03-20 HU HUE18177128A patent/HUE059085T2/hu unknown
  • 2008-03-20 SI SI200831741A patent/SI2129693T1/sl unknown
  • 2008-03-20 BR BRPI0809212A patent/BRPI0809212B8/pt active IP Right Grant
  • 2008-03-20 JP JP2009554744A patent/JP5688902B2/ja active Active
  • 2008-03-20 EP EP18177128.8A patent/EP3406635B1/en active Active
  • 2008-03-20 ES ES18177128T patent/ES2922132T3/es active Active
  • 2008-03-20 SI SI200831984T patent/SI2436700T1/sl unknown
  • 2008-03-20 PL PL11194173T patent/PL2436700T3/pl unknown
  • 2008-03-20 DK DK11194173.8T patent/DK2436700T5/en active
  • 2008-03-20 UA UAA200909741A patent/UA99278C2/ru unknown
  • 2008-03-20 EP EP08732592.4A patent/EP2129693B1/en active Active
  • 2008-03-20 ES ES08732592.4T patent/ES2614249T3/es active Active
  • 2008-03-20 CN CN200880012946.2A patent/CN101663327B/zh active Active
  • 2008-03-20 PT PT111941738T patent/PT2436700T/pt unknown
  • 2008-03-20 ES ES11194173.8T patent/ES2677353T3/es active Active
• 2009
  • 2009-09-17 HN HN2009001965A patent/HN2009001965A/es unknown
  • 2009-09-21 GT GT200900249A patent/GT200900249A/es unknown
  • 2009-09-21 NI NI200900172A patent/NI200900172A/es unknown
  • 2009-09-22 ZA ZA200906625A patent/ZA200906625B/xx unknown
  • 2009-09-22 IL IL201106A patent/IL201106A/en active IP Right Grant
  • 2009-09-23 EC EC2009009652A patent/ECSP099652A/es unknown
  • 2009-09-23 CR CR11041A patent/CR11041A/es unknown
  • 2009-10-20 CO CO09117278A patent/CO6251324A2/es active IP Right Grant
• 2014
  • 2014-01-24 US US14/163,863 patent/US8999697B2/en active Active
• 2015
  • 2015-01-27 JP JP2015013167A patent/JP2015143225A/ja not_active Withdrawn
  • 2015-02-27 US US14/633,141 patent/US9675681B2/en active Active
• 2017
  • 2017-03-23 JP JP2017056848A patent/JP6825950B2/ja active Active
  • 2017-08-08 CL CL2017002029A patent/CL2017002029A1/es unknown
• 2018
  • 2018-11-06 JP JP2018208647A patent/JP2019048844A/ja not_active Withdrawn
• 2020
  • 2020-01-31 JP JP2020014532A patent/JP6872649B2/ja active Active

Also Published As

Similar Documents

Legal Events