SK13492002A3 - Lipopolylsacharidy z E. coli, spôsob ich získania a ich použitie - Google Patents

Lipopolylsacharidy z E. coli, spôsob ich získania a ich použitie Download PDF

Info

Publication number: SK13492002A3
Authority: SK; Slovakia
Prior art keywords: lps; coli; lipoid; dsm; lipopolysaccharides
Prior art date: 2000-03-20

Application number

SK1349-2002A

Other languages

English (en)

Slovak (sk)

Inventor

Hans Proppert

Jrgen Malinka

J�Rgen Schulze

Ulrich Sonnenborn

Ulrich Z�Hringer

Artur Ulmer

Ernst Theodor Rietschel

Original Assignee

Pharma-Zentrale Gmbh

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2000-03-20

Filing date

2001-03-20

Publication date

2003-03-04

2001-03-20 Application filed by Pharma-Zentrale Gmbh filed Critical Pharma-Zentrale Gmbh

2003-03-04 Publication of SK13492002A3 publication Critical patent/SK13492002A3/sk

Links

239000002158 endotoxin Substances 0.000 title claims abstract description 73
229920006008 lipopolysaccharide Polymers 0.000 title claims abstract description 67
241000588724 Escherichia coli Species 0.000 title claims abstract description 47
238000000034 method Methods 0.000 claims description 10
125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 claims description 5
239000000284 extract Substances 0.000 claims description 3
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 2
230000002906 microbiologic effect Effects 0.000 claims description 2
238000003809 water extraction Methods 0.000 claims description 2
102000035195 Peptidases Human genes 0.000 claims 1
108091005804 Peptidases Proteins 0.000 claims 1
235000019833 protease Nutrition 0.000 claims 1
235000000346 sugar Nutrition 0.000 abstract description 8
230000002519 immonomodulatory effect Effects 0.000 abstract description 2
230000001717 pathogenic effect Effects 0.000 abstract description 2
238000006116 polymerization reaction Methods 0.000 abstract description 2
229920001542 oligosaccharide Polymers 0.000 description 25
150000002482 oligosaccharides Chemical class 0.000 description 24
MSWZFWKMSRAUBD-UHFFFAOYSA-N beta-D-galactosamine Natural products NC1C(O)OC(CO)C(O)C1O MSWZFWKMSRAUBD-UHFFFAOYSA-N 0.000 description 16
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 12
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
238000004458 analytical method Methods 0.000 description 10
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
MSWZFWKMSRAUBD-IVMDWMLBSA-N 2-amino-2-deoxy-D-glucopyranose Chemical compound N[C@H]1C(O)O[C@H](CO)[C@@H](O)[C@@H]1O MSWZFWKMSRAUBD-IVMDWMLBSA-N 0.000 description 9
102000000589 Interleukin-1 Human genes 0.000 description 9
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230000000694 effects Effects 0.000 description 9
108060008682 Tumor Necrosis Factor Proteins 0.000 description 7
FZHXIRIBWMQPQF-UHFFFAOYSA-N Glc-NH2 Natural products O=CC(N)C(O)C(O)C(O)CO FZHXIRIBWMQPQF-UHFFFAOYSA-N 0.000 description 6
WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 6
238000005481 NMR spectroscopy Methods 0.000 description 6
102000000852 Tumor Necrosis Factor-alpha Human genes 0.000 description 6
230000001580 bacterial effect Effects 0.000 description 6
239000012153 distilled water Substances 0.000 description 6
239000000203 mixture Substances 0.000 description 6
235000014113 dietary fatty acids Nutrition 0.000 description 5
238000000605 extraction Methods 0.000 description 5
239000000194 fatty acid Substances 0.000 description 5
229930195729 fatty acid Natural products 0.000 description 5
150000004665 fatty acids Chemical class 0.000 description 5
238000001840 matrix-assisted laser desorption--ionisation time-of-flight mass spectrometry Methods 0.000 description 5
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MSWZFWKMSRAUBD-GASJEMHNSA-N 2-amino-2-deoxy-D-galactopyranose Chemical compound N[C@H]1C(O)O[C@H](CO)[C@H](O)[C@@H]1O MSWZFWKMSRAUBD-GASJEMHNSA-N 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 4
229910019142 PO4 Inorganic materials 0.000 description 4
230000004071 biological effect Effects 0.000 description 4
239000012228 culture supernatant Substances 0.000 description 4
231100000284 endotoxic Toxicity 0.000 description 4
230000002346 endotoxic effect Effects 0.000 description 4
238000002290 gas chromatography-mass spectrometry Methods 0.000 description 4
238000001030 gas--liquid chromatography Methods 0.000 description 4
238000002360 preparation method Methods 0.000 description 4
230000000405 serological effect Effects 0.000 description 4
238000012360 testing method Methods 0.000 description 4
241000894006 Bacteria Species 0.000 description 3
108010067770 Endopeptidase K Proteins 0.000 description 3
241000607142 Salmonella Species 0.000 description 3
VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 3
210000002950 fibroblast Anatomy 0.000 description 3
GZQKNULLWNGMCW-PWQABINMSA-N lipid A (E. coli) Chemical compound O1[C@H](CO)[C@@H](OP(O)(O)=O)[C@H](OC(=O)C[C@@H](CCCCCCCCCCC)OC(=O)CCCCCCCCCCCCC)[C@@H](NC(=O)C[C@@H](CCCCCCCCCCC)OC(=O)CCCCCCCCCCC)[C@@H]1OC[C@@H]1[C@@H](O)[C@H](OC(=O)C[C@H](O)CCCCCCCCCCC)[C@@H](NC(=O)C[C@H](O)CCCCCCCCCCC)[C@@H](OP(O)(O)=O)O1 GZQKNULLWNGMCW-PWQABINMSA-N 0.000 description 3
235000021317 phosphate Nutrition 0.000 description 3
239000010452 phosphate Substances 0.000 description 3
239000013641 positive control Substances 0.000 description 3
108090000623 proteins and genes Proteins 0.000 description 3
238000011160 research Methods 0.000 description 3
150000003839 salts Chemical class 0.000 description 3
150000008163 sugars Chemical class 0.000 description 3
HNSDLXPSAYFUHK-UHFFFAOYSA-N 1,4-bis(2-ethylhexyl) sulfosuccinate Chemical compound CCCCC(CC)COC(=O)CC(S(O)(=O)=O)C(=O)OCC(CC)CCCC HNSDLXPSAYFUHK-UHFFFAOYSA-N 0.000 description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
102000016911 Deoxyribonucleases Human genes 0.000 description 2
108010053770 Deoxyribonucleases Proteins 0.000 description 2
108090000790 Enzymes Proteins 0.000 description 2
102000004190 Enzymes Human genes 0.000 description 2
241000283973 Oryctolagus cuniculus Species 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
239000008346 aqueous phase Substances 0.000 description 2
238000003556 assay Methods 0.000 description 2
244000052616 bacterial pathogen Species 0.000 description 2
150000001720 carbohydrates Chemical group 0.000 description 2
210000004027 cell Anatomy 0.000 description 2
238000001516 cell proliferation assay Methods 0.000 description 2
231100000673 dose–response relationship Toxicity 0.000 description 2
239000000499 gel Substances 0.000 description 2
239000008103 glucose Substances 0.000 description 2
238000004128 high performance liquid chromatography Methods 0.000 description 2
150000002500 ions Chemical class 0.000 description 2
238000004949 mass spectrometry Methods 0.000 description 2
239000011159 matrix material Substances 0.000 description 2
MYWUZJCMWCOHBA-VIFPVBQESA-N methamphetamine Chemical compound CN[C@@H](C)CC1=CC=CC=C1 MYWUZJCMWCOHBA-VIFPVBQESA-N 0.000 description 2
238000005016 nuclear Overhauser enhanced spectroscopy Methods 0.000 description 2
229920002401 polyacrylamide Polymers 0.000 description 2
102000004169 proteins and genes Human genes 0.000 description 2
-1 sialic acid oligosaccharides Chemical class 0.000 description 2
229910052709 silver Inorganic materials 0.000 description 2
239000004332 silver Substances 0.000 description 2
238000002415 sodium dodecyl sulfate polyacrylamide gel electrophoresis Methods 0.000 description 2
238000006467 substitution reaction Methods 0.000 description 2
239000006228 supernatant Substances 0.000 description 2
239000000725 suspension Substances 0.000 description 2
238000001551 total correlation spectroscopy Methods 0.000 description 2
XLEYFDVVXLMULC-UHFFFAOYSA-N 2',4',6'-trihydroxyacetophenone Chemical compound CC(=O)C1=C(O)C=C(O)C=C1O XLEYFDVVXLMULC-UHFFFAOYSA-N 0.000 description 1
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
VOBNSQKMDIOJTQ-UHFFFAOYSA-N 2-aminoethyl phosphono hydrogen phosphate Chemical compound NCCOP(O)(=O)OP(O)(O)=O VOBNSQKMDIOJTQ-UHFFFAOYSA-N 0.000 description 1
RVBUGGBMJDPOST-UHFFFAOYSA-N 2-thiobarbituric acid Chemical compound O=C1CC(=O)NC(=S)N1 RVBUGGBMJDPOST-UHFFFAOYSA-N 0.000 description 1
208000035404 Autolysis Diseases 0.000 description 1
241000283690 Bos taurus Species 0.000 description 1
241000589876 Campylobacter Species 0.000 description 1
206010057248 Cell death Diseases 0.000 description 1
102000004127 Cytokines Human genes 0.000 description 1
108090000695 Cytokines Proteins 0.000 description 1
BGWQRWREUZVRGI-OLLRPPRZSA-N D-glucoheptopyranose Chemical compound OC[C@H](O)[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O BGWQRWREUZVRGI-OLLRPPRZSA-N 0.000 description 1
102000007260 Deoxyribonuclease I Human genes 0.000 description 1
108010008532 Deoxyribonuclease I Proteins 0.000 description 1
241000305071 Enterobacterales Species 0.000 description 1
229930186217 Glycolipid Natural products 0.000 description 1
102000003886 Glycoproteins Human genes 0.000 description 1
108090000288 Glycoproteins Proteins 0.000 description 1
229910004373 HOAc Inorganic materials 0.000 description 1
XLYOFNOQVPJJNP-ZSJDYOACSA-N Heavy water Chemical compound [2H]O[2H] XLYOFNOQVPJJNP-ZSJDYOACSA-N 0.000 description 1
241000589989 Helicobacter Species 0.000 description 1
YPZMPEPLWKRVLD-UHFFFAOYSA-N L-glycero-D-manno-heptose Natural products OCC(O)C(O)C(O)C(O)C(O)C=O YPZMPEPLWKRVLD-UHFFFAOYSA-N 0.000 description 1
OVRNDRQMDRJTHS-UHFFFAOYSA-N N-acelyl-D-glucosamine Natural products CC(=O)NC1C(O)OC(CO)C(O)C1O OVRNDRQMDRJTHS-UHFFFAOYSA-N 0.000 description 1
OVRNDRQMDRJTHS-KEWYIRBNSA-N N-acetyl-D-galactosamine Chemical compound CC(=O)N[C@H]1C(O)O[C@H](CO)[C@H](O)[C@@H]1O OVRNDRQMDRJTHS-KEWYIRBNSA-N 0.000 description 1
MBLBDJOUHNCFQT-UHFFFAOYSA-N N-acetyl-D-galactosamine Natural products CC(=O)NC(C=O)C(O)C(O)C(O)CO MBLBDJOUHNCFQT-UHFFFAOYSA-N 0.000 description 1
OVRNDRQMDRJTHS-RTRLPJTCSA-N N-acetyl-D-glucosamine Chemical compound CC(=O)N[C@H]1C(O)O[C@H](CO)[C@@H](O)[C@@H]1O OVRNDRQMDRJTHS-RTRLPJTCSA-N 0.000 description 1
MBLBDJOUHNCFQT-LXGUWJNJSA-N N-acetylglucosamine Natural products CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O)[C@H](O)CO MBLBDJOUHNCFQT-LXGUWJNJSA-N 0.000 description 1
241000588653 Neisseria Species 0.000 description 1
241001523956 Parengyodontium album Species 0.000 description 1
102000006382 Ribonucleases Human genes 0.000 description 1
108010083644 Ribonucleases Proteins 0.000 description 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
102100040247 Tumor necrosis factor Human genes 0.000 description 1
241000607598 Vibrio Species 0.000 description 1
239000002253 acid Substances 0.000 description 1
238000005903 acid hydrolysis reaction Methods 0.000 description 1
150000001413 amino acids Chemical class 0.000 description 1
238000005571 anion exchange chromatography Methods 0.000 description 1
239000000427 antigen Substances 0.000 description 1
239000006286 aqueous extract Substances 0.000 description 1
SQVRNKJHWKZAKO-UHFFFAOYSA-N beta-N-Acetyl-D-neuraminic acid Natural products CC(=O)NC1C(O)CC(O)(C(O)=O)OC1C(O)C(O)CO SQVRNKJHWKZAKO-UHFFFAOYSA-N 0.000 description 1
235000014633 carbohydrates Nutrition 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
238000001460 carbon-13 nuclear magnetic resonance spectrum Methods 0.000 description 1
210000000170 cell membrane Anatomy 0.000 description 1
229920001429 chelating resin Polymers 0.000 description 1
238000004587 chromatography analysis Methods 0.000 description 1
238000003776 cleavage reaction Methods 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
235000021310 complex sugar Nutrition 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
238000002784 cytotoxicity assay Methods 0.000 description 1
231100000263 cytotoxicity test Toxicity 0.000 description 1
230000002950 deficient Effects 0.000 description 1
230000003111 delayed effect Effects 0.000 description 1
238000003795 desorption Methods 0.000 description 1
IJKVHSBPTUYDLN-UHFFFAOYSA-N dihydroxy(oxo)silane Chemical compound O[Si](O)=O IJKVHSBPTUYDLN-UHFFFAOYSA-N 0.000 description 1
238000001962 electrophoresis Methods 0.000 description 1
239000002095 exotoxin Substances 0.000 description 1
231100000776 exotoxin Toxicity 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
210000003953 foreskin Anatomy 0.000 description 1
239000005350 fused silica glass Substances 0.000 description 1
238000004817 gas chromatography Methods 0.000 description 1
239000011521 glass Substances 0.000 description 1
229960002442 glucosamine Drugs 0.000 description 1
125000002791 glucosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)* 0.000 description 1
150000002386 heptoses Chemical class 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
238000007654 immersion Methods 0.000 description 1
210000000987 immune system Anatomy 0.000 description 1
230000003053 immunization Effects 0.000 description 1
238000002649 immunization Methods 0.000 description 1
238000000338 in vitro Methods 0.000 description 1
238000011534 incubation Methods 0.000 description 1
230000000968 intestinal effect Effects 0.000 description 1
238000011835 investigation Methods 0.000 description 1
150000002596 lactones Chemical class 0.000 description 1
239000007788 liquid Substances 0.000 description 1
238000011068 loading method Methods 0.000 description 1
230000014759 maintenance of location Effects 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
238000005259 measurement Methods 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
238000006140 methanolysis reaction Methods 0.000 description 1
150000004702 methyl esters Chemical class 0.000 description 1
230000003278 mimic effect Effects 0.000 description 1
238000002156 mixing Methods 0.000 description 1
238000012986 modification Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
150000002772 monosaccharides Chemical class 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
239000012074 organic phase Substances 0.000 description 1
210000000496 pancreas Anatomy 0.000 description 1
230000007918 pathogenicity Effects 0.000 description 1
210000005259 peripheral blood Anatomy 0.000 description 1
239000011886 peripheral blood Substances 0.000 description 1
KSSNXJHPEFVKHY-UHFFFAOYSA-N phenol;hydrate Chemical compound O.OC1=CC=CC=C1 KSSNXJHPEFVKHY-UHFFFAOYSA-N 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
238000002264 polyacrylamide gel electrophoresis Methods 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
230000000379 polymerizing effect Effects 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
230000035755 proliferation Effects 0.000 description 1
238000000746 purification Methods 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
238000011002 quantification Methods 0.000 description 1
230000007017 scission Effects 0.000 description 1
239000013049 sediment Substances 0.000 description 1
230000028043 self proteolysis Effects 0.000 description 1
238000000926 separation method Methods 0.000 description 1
238000004611 spectroscopical analysis Methods 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1
102000003390 tumor necrosis factor Human genes 0.000 description 1
241001515965 unidentified phage Species 0.000 description 1
239000003643 water by type Substances 0.000 description 1
238000001262 western blot Methods 0.000 description 1

Classifications

- 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
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic 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
- 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
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
General Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Biochemistry (AREA)
Medicinal Chemistry (AREA)
General Chemical & Material Sciences (AREA)
Zoology (AREA)
Wood Science & Technology (AREA)
Materials Engineering (AREA)
Polymers & Plastics (AREA)
Bioinformatics & Cheminformatics (AREA)
Molecular Biology (AREA)
Veterinary Medicine (AREA)
General Engineering & Computer Science (AREA)
Biotechnology (AREA)
Microbiology (AREA)
Public Health (AREA)
Animal Behavior & Ethology (AREA)
Pharmacology & Pharmacy (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Genetics & Genomics (AREA)
Immunology (AREA)
Polysaccharides And Polysaccharide Derivatives (AREA)
Preparation Of Compounds By Using Micro-Organisms (AREA)
Saccharide Compounds (AREA)
Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

SK1349-2002A 2000-03-20 2001-03-20 Lipopolylsacharidy z E. coli, spôsob ich získania a ich použitie SK13492002A3 (sk)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE10013539A DE10013539B4 (de)	2000-03-20	2000-03-20	Lipopolysaccharide aus Escherichia coli, Verfahren zu deren Herstellung und deren Verwendungen
PCT/EP2001/003153 WO2001070756A2 (de)	2000-03-20	2001-03-20	Lipopolysaccharide aus escherichia coli

Publications (1)

Publication Number	Publication Date
SK13492002A3 true SK13492002A3 (sk)	2003-03-04

Family

ID=7635468

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK1349-2002A SK13492002A3 (sk)	2000-03-20	2001-03-20	Lipopolylsacharidy z E. coli, spôsob ich získania a ich použitie

Country Status (28)

Country	Link
US (1)	US6833451B2 (et)
EP (1)	EP1266023A2 (et)
JP (1)	JP2003528175A (et)
KR (1)	KR20030047878A (et)
CN (1)	CN1436245A (et)
AP (1)	AP2002002622A0 (et)
AU (2)	AU2001273899B2 (et)
BG (1)	BG107115A (et)
BR (1)	BR0109392A (et)
CA (1)	CA2402544A1 (et)
CZ (1)	CZ20023469A3 (et)
DE (1)	DE10013539B4 (et)
EA (1)	EA005217B1 (et)
EE (1)	EE200200537A (et)
HK (1)	HK1053148A1 (et)
HR (1)	HRP20020682A2 (et)
HU (1)	HUP0204540A3 (et)
IL (1)	IL151785A0 (et)
IS (1)	IS6517A (et)
MX (1)	MXPA02009215A (et)
NO (1)	NO20024480L (et)
NZ (1)	NZ520968A (et)
PL (1)	PL368447A1 (et)
SK (1)	SK13492002A3 (et)
UA (1)	UA75068C2 (et)
WO (1)	WO2001070756A2 (et)
YU (1)	YU71202A (et)
ZA (1)	ZA200207408B (et)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US20030031684A1 (en)	2001-03-30	2003-02-13	Corixa Corporation	Methods for the production of 3-O-deactivated-4'-monophosphoryl lipid a (3D-MLA)
DE10328669B4 (de) *	2003-06-26	2005-12-01	Pharma-Zentrale Gmbh	Plasmidfreier Klon des E. coli Stammes DSM 6601
WO2005051321A2 (en) *	2003-11-25	2005-06-09	Washington University	Treatment of inflammatory bowel disease through induction of indoleamine 2,3-dioxygenase
US20050238651A1 (en) *	2003-11-25	2005-10-27	Gurtner Gregory J	Treatment of inflammatory bowel disease
WO2006025995A2 (en) *	2004-07-27	2006-03-09	The Regents Of The University Of California	Compositions and methods using md-2 mutants and chimeric proteins
CN100354428C (zh) *	2005-01-13	2007-12-12	丁友玲	隧道式干热灭菌设备测试用内毒素指示剂的制备方法
EP1961823B1 (en)	2005-11-28	2024-06-12	Biomedical Research Group Inc.	Method for producing lipopolysaccharide and lipopolysaccharide
US9664677B2 (en)	2010-04-19	2017-05-30	Massachusetts Institute Of Technology	Polymer-nanostructure composition for selective molecular recognition
US20130066064A1 (en) *	2010-05-20	2013-03-14	Glaxosmithkline Biologicals S.A,	Novel process
CN105137073A (zh) *	2015-08-06	2015-12-09	中国兽医药品监察所	牛布鲁氏菌胶体金抗体检测试纸条
PL432842A1 (pl) *	2020-02-10	2021-08-16	Uniwersytet Warszawski	LPS do zastosowania w indukowaniu u osobnika tolerancji na alergeny pokarmowe wywołujące alergie pokarmowe zależne od IgE
AU2021235152B2 (en) *	2020-03-13	2026-02-05	Hephaistos-Pharma	Detoxified lipopolysaccharides (IPS), naturally non-toxic lps, and uses thereof

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DE19844191A1 (de) *	1998-09-28	2000-03-30	Pharma Zentrale Gmbh	Lipopolysaccharide aus Escherichia coli

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2001
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Publication number	Publication date
BG107115A (bg)	2003-05-30
ZA200207408B (en)	2003-01-02
EA005217B1 (ru)	2004-12-30
CA2402544A1 (en)	2002-09-10
AP2002002622A0 (en)	2002-09-30
HUP0204540A3 (en)	2003-12-29
CZ20023469A3 (cs)	2003-04-16
NO20024480L (no)	2002-11-20
WO2001070756A3 (de)	2002-05-02
HK1053148A1 (zh)	2003-10-10
HRP20020682A2 (en)	2004-12-31
US6833451B2 (en)	2004-12-21
EE200200537A (et)	2004-04-15
NZ520968A (en)	2005-07-29
NO20024480D0 (no)	2002-09-19
AU7389901A (en)	2001-10-03
HUP0204540A2 (hu)	2003-04-28
US20030108573A1 (en)	2003-06-12
JP2003528175A (ja)	2003-09-24
MXPA02009215A (es)	2004-09-10
YU71202A (sh)	2006-01-16
DE10013539A1 (de)	2001-10-18
WO2001070756A2 (de)	2001-09-27
KR20030047878A (ko)	2003-06-18
AU2001273899B2 (en)	2005-10-06
EA200200997A1 (ru)	2003-04-24
EP1266023A2 (de)	2002-12-18
PL368447A1 (en)	2005-03-21
CN1436245A (zh)	2003-08-13
UA75068C2 (en)	2006-03-15
DE10013539B4 (de)	2006-07-13
BR0109392A (pt)	2003-06-03
IL151785A0 (en)	2003-04-10
IS6517A (is)	2002-08-21

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