MX343356B - Toxinas proteicas recombinantes de alto nivel de expresion. - Google Patents
Toxinas proteicas recombinantes de alto nivel de expresion.Info
- Publication number
- MX343356B MX343356B MX2012011103A MX2012011103A MX343356B MX 343356 B MX343356 B MX 343356B MX 2012011103 A MX2012011103 A MX 2012011103A MX 2012011103 A MX2012011103 A MX 2012011103A MX 343356 B MX343356 B MX 343356B
- Authority
- MX
- Mexico
- Prior art keywords
- high level
- toxin
- level expression
- recombinant toxin
- toxin proteins
- Prior art date
Links
- 108700012359 toxins Proteins 0.000 title abstract 2
- 230000001580 bacterial effect Effects 0.000 abstract 2
- 108010071134 CRM197 (non-toxic variant of diphtheria toxin) Proteins 0.000 abstract 1
- 206010008631 Cholera Diseases 0.000 abstract 1
- 108010049048 Cholera Toxin Proteins 0.000 abstract 1
- 102000009016 Cholera Toxin Human genes 0.000 abstract 1
- 108010053187 Diphtheria Toxin Proteins 0.000 abstract 1
- 102000016607 Diphtheria Toxin Human genes 0.000 abstract 1
- 108010081690 Pertussis Toxin Proteins 0.000 abstract 1
- 108700033844 Pseudomonas aeruginosa toxA Proteins 0.000 abstract 1
- 239000012634 fragment Substances 0.000 abstract 1
- 229930186900 holotoxin Natural products 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 229960000814 tetanus toxoid Drugs 0.000 abstract 1
- 239000003053 toxin Substances 0.000 abstract 1
- 231100000765 toxin Toxicity 0.000 abstract 1
- 230000014616 translation Effects 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/10—Transferases (2.)
- C12N9/1048—Glycosyltransferases (2.4)
- C12N9/1051—Hexosyltransferases (2.4.1)
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/195—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria
- C07K14/21—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria from Pseudomonadaceae (F)
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/195—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria
- C07K14/235—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria from Bordetella (G)
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/195—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria
- C07K14/28—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria from Vibrionaceae (F)
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/195—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria
- C07K14/34—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria from Corynebacterium (G)
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K19/00—Hybrid peptides, i.e. peptides covalently bound to nucleic acids, or non-covalently bound protein-protein complexes
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
- C12N15/74—Vectors or expression systems specially adapted for prokaryotic hosts other than E. coli, e.g. Lactobacillus, Micromonospora
- C12N15/78—Vectors or expression systems specially adapted for prokaryotic hosts other than E. coli, e.g. Lactobacillus, Micromonospora for Pseudomonas
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/10—Transferases (2.)
- C12N9/1048—Glycosyltransferases (2.4)
- C12N9/1077—Pentosyltransferases (2.4.2)
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- 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
- C12P21/00—Preparation of peptides or proteins
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- 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
- C12P21/00—Preparation of peptides or proteins
- C12P21/02—Preparation of peptides or proteins having a known sequence of two or more amino acids, e.g. glutathione
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
- G01N33/573—Immunoassay; Biospecific binding assay; Materials therefor for enzymes or isoenzymes
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2319/00—Fusion polypeptide
- C07K2319/01—Fusion polypeptide containing a localisation/targetting motif
- C07K2319/036—Fusion polypeptide containing a localisation/targetting motif targeting to the medium outside of the cell, e.g. type III secretion
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Y—ENZYMES
- C12Y204/00—Glycosyltransferases (2.4)
- C12Y204/01—Hexosyltransferases (2.4.1)
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Y—ENZYMES
- C12Y204/00—Glycosyltransferases (2.4)
- C12Y204/02—Pentosyltransferases (2.4.2)
- C12Y204/02036—NAD(+)--diphthamide ADP-ribosyltransferase (2.4.2.36)
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Y—ENZYMES
- C12Y304/00—Hydrolases acting on peptide bonds, i.e. peptidases (3.4)
- C12Y304/24—Metalloendopeptidases (3.4.24)
- C12Y304/24068—Tentoxilysin (3.4.24.68), i.e. tetanus neurotoxin
Abstract
La presente invención se refiere a un método para producir una toxina protéica recombinante en una célula hospedera de Pseudomonas, dicho método que comprende: ligar en un vector de expresión una secuencia de nucleótidos que codifica una toxina protéica, en donde la secuencia de nucleótidos que codifica la toxina proteína se fusiona a una secuencia que codifica la señal de secreción que es Azu, IbpS31A, o Cupa2, y que CupA2, y que cuando se expresa dirige la transferencia de la toxina protéica al periplasma transformar la célula hospedera de Pseudomonas con el vector de expresión; y cultivar la célula hospedera de Pseudomonas transformada en un medio de cultivo adecuado para la expresión de la toxina protéica recombinante; en donde la toxina protéica recombinante es CRM197, producida a un rendimiento de toxina protéica soluble CRM197 y/o activa de 0.2 gramos por litro a 12 gramos por litro.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US31915210P | 2010-03-30 | 2010-03-30 | |
PCT/US2010/030573 WO2011123139A1 (en) | 2010-03-30 | 2010-04-09 | High level expression of recombinant crm197 |
US32523510P | 2010-04-16 | 2010-04-16 | |
PCT/US2011/030227 WO2011126811A2 (en) | 2010-03-30 | 2011-03-28 | High level expression of recombinant toxin proteins |
Publications (2)
Publication Number | Publication Date |
---|---|
MX2012011103A MX2012011103A (es) | 2015-05-15 |
MX343356B true MX343356B (es) | 2016-11-03 |
Family
ID=44763483
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2012011103A MX343356B (es) | 2010-03-30 | 2011-03-28 | Toxinas proteicas recombinantes de alto nivel de expresion. |
Country Status (11)
Country | Link |
---|---|
US (3) | US8530171B2 (es) |
EP (1) | EP2553102B1 (es) |
JP (1) | JP5839411B2 (es) |
KR (1) | KR20130072201A (es) |
CN (1) | CN102869778B (es) |
AU (1) | AU2011238711B2 (es) |
BR (1) | BR112012024898A2 (es) |
CA (1) | CA2793978C (es) |
MX (1) | MX343356B (es) |
NZ (1) | NZ602958A (es) |
WO (1) | WO2011126811A2 (es) |
Families Citing this family (29)
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WO2002020059A2 (en) | 2000-09-01 | 2002-03-14 | The Government Of The United States Of America As Represented By The Secretary, Department Of Health And Human Services | Vibrio cholerae o139 conjugate vaccines |
KR20130072201A (ko) | 2010-03-30 | 2013-07-01 | 피페넥스 인크. | 재조합 독소 단백질의 고수준 발현 |
RU2754446C2 (ru) | 2011-04-22 | 2021-09-02 | ВАЙЕТ ЭлЭлСи | Композиции, относящиеся к мутантному токсину CLOSTRIDIUM DIFFICILE, и способы их применения |
WO2013084071A2 (en) | 2011-12-08 | 2013-06-13 | Novartis Ag | Clostridium difficile toxin-based vaccine |
US9169304B2 (en) | 2012-05-01 | 2015-10-27 | Pfenex Inc. | Process for purifying recombinant Plasmodium falciparum circumsporozoite protein |
EP2869838B1 (en) * | 2012-07-05 | 2020-09-02 | Children's Medical Center Corporation | The bacterial biofilm matrix as a platform for protein delivery |
BR122016023101B1 (pt) | 2012-10-21 | 2022-03-22 | Pfizer Inc | Polipeptídeo, composição imunogênica que o compreende, bem como célula recombinante derivada de clostridium difficile |
CN104140972B (zh) * | 2013-05-07 | 2018-01-23 | 上海惠盾生物技术有限公司 | 白喉毒素突变体crm197的制备方法 |
US9321834B2 (en) | 2013-12-05 | 2016-04-26 | Leidos, Inc. | Anti-malarial compositions |
WO2015117093A1 (en) * | 2014-01-31 | 2015-08-06 | Fina Biosolutions, Llc | Expression and purification of crm197 and related proteins |
US10597664B2 (en) * | 2014-01-31 | 2020-03-24 | Fina Biosolutions, Llc | Expression and purification of CRM proteins and related proteins, and protein domains |
US11060123B2 (en) | 2014-01-31 | 2021-07-13 | Fina Biosolutions, Llc | Production of soluble recombinant protein without n-terminal methionine |
EP3221339A1 (en) | 2014-11-20 | 2017-09-27 | Biological E Limited | Codon optimized polynucleotide for high level expression of crm197 |
BR112018069945A2 (pt) * | 2016-04-06 | 2019-02-05 | Plant Health Care Inc | micróbios benéficos para distribuição de peptídeos ou proteínas efetoras e uso dos mesmos |
US11071779B2 (en) | 2016-06-17 | 2021-07-27 | Children's Medical Center Corporation | Biofilm matrix-boosted vaccine |
RU2636346C1 (ru) * | 2016-07-01 | 2017-11-22 | Федеральное бюджетное учреждение науки Государственный научный центр прикладной микробиологии и биотехнологии (ФБУН ГНЦ ПМБ) | Способ получения рекомбинантного экзопротеина А Pseudomonas aeruginosa |
KR101908590B1 (ko) | 2017-02-01 | 2018-10-16 | (주)포바이오코리아 | Crm197의 용해성 단백질 발현 및 정제 방법 |
EP3444269A1 (en) | 2017-08-17 | 2019-02-20 | National Research Council of Canada | Systems and methods for the production of diphtheria toxin polypeptides |
US10787671B2 (en) | 2017-10-27 | 2020-09-29 | Pfenex Inc. | Method for production of recombinant Erwinia asparaginase |
AU2018354069A1 (en) * | 2017-10-27 | 2020-06-11 | Pelican Technology Holdings, Inc. | Bacterial leader sequences for periplasmic protein expression |
US10662433B2 (en) | 2017-10-27 | 2020-05-26 | Pfenex Inc. | Method for production of recombinant E. coli asparaginase |
CN112513066A (zh) * | 2018-01-19 | 2021-03-16 | 台湾浩鼎生技股份有限公司 | Crm197蛋白质表达 |
US10829731B2 (en) * | 2018-01-25 | 2020-11-10 | Alliance For Sustainable Energy, Llc | Biocatalysts for conversion of thermochemical waste streams |
KR102475419B1 (ko) * | 2018-07-16 | 2022-12-07 | 주식회사 유바이오로직스 | Crm197을 고농도로 발현하는 코리네박테리움 균주 |
EP3893870A1 (en) | 2018-12-13 | 2021-10-20 | Huya Bioscience International LLC | Sulcardine administration for treatment of acute atrial fibrillation |
BR112022006851A2 (pt) * | 2019-10-14 | 2022-07-05 | Syngenta Crop Protection Ag | Proteínas inseticidas |
BE1029145B1 (fr) * | 2021-02-26 | 2022-09-27 | Curavac Europe | Methode de production d'une forme periplasmique de la proteine crm197 |
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CN113201473B (zh) * | 2021-04-22 | 2022-06-07 | 广东省科学院微生物研究所(广东省微生物分析检测中心) | 香茅醇在制备促进铜绿假单胞菌毒力基因toxA表达的制剂中的应用 |
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CN101500581B (zh) | 2006-06-08 | 2013-10-30 | 科内尔研究基金会 | 编码艰难梭菌毒素a和毒素b受体结合域的密码子优化dna分子及其使用方法 |
BRPI0807834A2 (pt) | 2007-01-31 | 2014-07-22 | Dow Global Technologies Inc | " sequências-líder bacterianas para expressão aumentada ". |
US9580719B2 (en) | 2007-04-27 | 2017-02-28 | Pfenex, Inc. | Method for rapidly screening microbial hosts to identify certain strains with improved yield and/or quality in the expression of heterologous proteins |
CN101688213A (zh) * | 2007-04-27 | 2010-03-31 | 陶氏环球技术公司 | 用于快速筛选微生物宿主以鉴定某些在表达异源蛋白质方面具有改善的产量和/或质量的菌株的方法 |
WO2010008764A1 (en) * | 2008-06-23 | 2010-01-21 | Dow Global Technologies Inc. | Pseudomonas fluorescens strains for production of extracellular recombinant protein |
GB0917647D0 (en) | 2009-10-08 | 2009-11-25 | Glaxosmithkline Biolog Sa | Expression system |
KR20130072201A (ko) | 2010-03-30 | 2013-07-01 | 피페넥스 인크. | 재조합 독소 단백질의 고수준 발현 |
-
2011
- 2011-03-28 KR KR1020127027780A patent/KR20130072201A/ko not_active Application Discontinuation
- 2011-03-28 CN CN201180018149.7A patent/CN102869778B/zh active Active
- 2011-03-28 MX MX2012011103A patent/MX343356B/es active IP Right Grant
- 2011-03-28 NZ NZ602958A patent/NZ602958A/en unknown
- 2011-03-28 CA CA2793978A patent/CA2793978C/en active Active
- 2011-03-28 WO PCT/US2011/030227 patent/WO2011126811A2/en active Application Filing
- 2011-03-28 JP JP2013502705A patent/JP5839411B2/ja active Active
- 2011-03-28 BR BR112012024898A patent/BR112012024898A2/pt not_active Application Discontinuation
- 2011-03-28 AU AU2011238711A patent/AU2011238711B2/en active Active
- 2011-03-28 EP EP11766437.5A patent/EP2553102B1/en active Active
- 2011-03-28 US US13/073,955 patent/US8530171B2/en active Active
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2013
- 2013-07-26 US US13/952,484 patent/US8906636B2/en active Active
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JP2013529064A (ja) | 2013-07-18 |
AU2011238711B2 (en) | 2015-06-18 |
US8906636B2 (en) | 2014-12-09 |
WO2011126811A2 (en) | 2011-10-13 |
EP2553102A2 (en) | 2013-02-06 |
US20140051093A1 (en) | 2014-02-20 |
EP2553102A4 (en) | 2013-10-23 |
WO2011126811A3 (en) | 2012-03-08 |
EP2553102B1 (en) | 2015-12-09 |
US20110287443A1 (en) | 2011-11-24 |
JP5839411B2 (ja) | 2016-01-06 |
CA2793978C (en) | 2021-08-03 |
CN102869778B (zh) | 2015-05-20 |
NZ602958A (en) | 2014-07-25 |
MX2012011103A (es) | 2015-05-15 |
CN102869778A (zh) | 2013-01-09 |
AU2011238711A1 (en) | 2012-11-08 |
KR20130072201A (ko) | 2013-07-01 |
US8530171B2 (en) | 2013-09-10 |
US20150361405A1 (en) | 2015-12-17 |
CA2793978A1 (en) | 2011-10-13 |
BR112012024898A2 (pt) | 2015-10-06 |
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