MX353243B - Metodo para incrementar la secrecion de proteinas recombinantes. - Google Patents

Metodo para incrementar la secrecion de proteinas recombinantes.

Info

Publication number
MX353243B
MX353243B MX2014012407A MX2014012407A MX353243B MX 353243 B MX353243 B MX 353243B MX 2014012407 A MX2014012407 A MX 2014012407A MX 2014012407 A MX2014012407 A MX 2014012407A MX 353243 B MX353243 B MX 353243B
Authority
MX
Mexico
Prior art keywords
secretion
increasing
recombinant proteins
cells
cell wall
Prior art date
Application number
MX2014012407A
Other languages
English (en)
Other versions
MX2014012407A (es
Inventor
Jost Wolfgang
Knappenberger Mathias
Claussnitzer Doreen
Schaaf Andreas
Original Assignee
Greenovation Biotech 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.)
Filing date
Publication date
Application filed by Greenovation Biotech Gmbh filed Critical Greenovation Biotech Gmbh
Publication of MX2014012407A publication Critical patent/MX2014012407A/es
Publication of MX353243B publication Critical patent/MX353243B/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P21/00Preparation of peptides or proteins
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N1/00Microorganisms, e.g. protozoa; Compositions thereof; Processes of propagating, maintaining or preserving microorganisms or compositions thereof; Processes of preparing or isolating a composition containing a microorganism; Culture media therefor
    • C12N1/12Unicellular algae; Culture media therefor
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N1/00Microorganisms, e.g. protozoa; Compositions thereof; Processes of propagating, maintaining or preserving microorganisms or compositions thereof; Processes of preparing or isolating a composition containing a microorganism; Culture media therefor
    • C12N1/14Fungi; Culture media therefor
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N5/00Undifferentiated human, animal or plant cells, e.g. cell lines; Tissues; Cultivation or maintenance thereof; Culture media therefor
    • C12N5/0018Culture media for cell or tissue culture
    • C12N5/0025Culture media for plant cell or plant tissue culture
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P21/00Preparation of peptides or proteins
    • C12P21/02Preparation of peptides or proteins having a known sequence of two or more amino acids, e.g. glutathione
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2500/00Specific components of cell culture medium
    • C12N2500/60Buffer, e.g. pH regulation, osmotic pressure

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Biotechnology (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Genetics & Genomics (AREA)
  • Biomedical Technology (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Microbiology (AREA)
  • Biochemistry (AREA)
  • Botany (AREA)
  • Cell Biology (AREA)
  • Medicinal Chemistry (AREA)
  • Virology (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Molecular Biology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Mycology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Peptides Or Proteins (AREA)

Abstract

La presente invención se refiere a un método para producir una proteína recombinante en células de plantas, caracterizado porque comprende las etapas de: (a) desarrollar células que tienen una pared celular en un primer medio de cultivo que tiene una osmolaridad de menos de 0.1 osmol/L, en donde el medio no comprende un polímero de superficie activa no iónico o comprende el polímero de superficie activa no iónico en una concentración máxima, por lo que la proteína se acumula en el interior de la célula o en el espacio apoplástico de la célula (b) desarrollar luego las células en un segundo medio de cultivo que contiene una combinación de un polímero de superficie activa no iónico en una concentración mínima y iones de metal monovalente y que tiene una osmolaridad de al menos 0.32 osmol/L, en donde la proteína recombinante es expresada en las células y por lo que la proteína recombinante es secretada a través de la pared celular en el medio, en donde la etapa (a) se lleva a cabo durante un período de al menos 2 días, en donde para el polímero también (i) la concentración máxima de la etapa (a) es 0.08% en peso y la concentración mínima de la etapa (b) es 0.5% en peso, o (ii) la concentración máxima de la etapa (a) es 0.01% en peso y la concentración mínima de la etapa (b) es 0.1% en peso.
MX2014012407A 2012-04-17 2013-04-17 Metodo para incrementar la secrecion de proteinas recombinantes. MX353243B (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP12164458.7A EP2653548A1 (de) 2012-04-17 2012-04-17 Verfahren zur Erhöhung der Sekretion rekombinanter Proteine
PCT/EP2013/057956 WO2013156504A1 (de) 2012-04-17 2013-04-17 Verfahren zur erhöhung der sekretion rekombinanter proteine

Publications (2)

Publication Number Publication Date
MX2014012407A MX2014012407A (es) 2015-04-09
MX353243B true MX353243B (es) 2018-01-05

Family

ID=48143287

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2014012407A MX353243B (es) 2012-04-17 2013-04-17 Metodo para incrementar la secrecion de proteinas recombinantes.

Country Status (19)

Country Link
US (1) US9850513B2 (es)
EP (2) EP2653548A1 (es)
JP (1) JP6215305B2 (es)
KR (1) KR102028738B1 (es)
CN (1) CN104379750A (es)
AU (1) AU2013248312B2 (es)
BR (1) BR112014025306B1 (es)
CA (1) CA2870587A1 (es)
DK (1) DK2839012T3 (es)
ES (1) ES2755973T3 (es)
HR (1) HRP20191876T1 (es)
IL (1) IL235052B (es)
IN (1) IN2014DN08664A (es)
LT (1) LT2839012T (es)
MX (1) MX353243B (es)
PL (1) PL2839012T3 (es)
PT (1) PT2839012T (es)
SI (1) SI2839012T1 (es)
WO (1) WO2013156504A1 (es)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2729732B2 (ja) 1992-10-05 1998-03-18 新日本製鐵株式会社 底つき容器の製造方法
EP3808854A1 (de) 2019-10-17 2021-04-21 eleva GmbH Verfahren zur gewinnung von material von pflanzenzelloberflächen
AU2021213606A1 (en) * 2020-01-31 2022-07-21 Chugai Seiyaku Kabushiki Kaisha Method for producing composition containing polypeptide with suppressed coloring

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63226281A (ja) * 1986-12-26 1988-09-20 Seitai Kinou Riyou Kagakuhin Shinseizou Gijutsu Kenkyu Kumiai 組織培養方法
JP2000245470A (ja) * 1999-02-26 2000-09-12 Noda Inst For Scient Res 植物細胞間液による外来ポリペプチドの製造方法
DE19947290A1 (de) 1999-10-01 2001-04-19 Greenovation Pflanzenbiotechno Verfahren zur Herstellung proteinöser Substanzen
CN1109750C (zh) * 2000-08-15 2003-05-28 中国水产科学研究院黄海水产研究所 一种新型低温碱性蛋白酶、制造方法、应用和产生该蛋白酶的微生物
MXPA04009381A (es) 2002-03-27 2005-01-25 Immunex Corp Metodos para incrementar la produccion de polipeptidos.
EP2154252B1 (en) * 2008-07-16 2014-12-24 Sumitomo Chemical Company, Limited Methods for producing secreted proteins
US20100035327A1 (en) * 2008-08-11 2010-02-11 Ann Marie Steele Use of rice-derived products in a universal cell culture medium

Also Published As

Publication number Publication date
AU2013248312B2 (en) 2018-08-30
HRP20191876T1 (hr) 2019-12-27
WO2013156504A1 (de) 2013-10-24
JP6215305B2 (ja) 2017-10-18
EP2839012B1 (de) 2019-08-28
LT2839012T (lt) 2019-11-25
KR102028738B1 (ko) 2019-10-04
KR20150014454A (ko) 2015-02-06
US20150079632A1 (en) 2015-03-19
MX2014012407A (es) 2015-04-09
AU2013248312A1 (en) 2014-10-23
PL2839012T3 (pl) 2020-05-18
IL235052B (en) 2019-12-31
BR112014025306B1 (pt) 2021-11-30
ES2755973T3 (es) 2020-04-24
JP2015514408A (ja) 2015-05-21
DK2839012T3 (da) 2019-10-21
US9850513B2 (en) 2017-12-26
CN104379750A (zh) 2015-02-25
PT2839012T (pt) 2019-12-05
IL235052A0 (en) 2014-12-31
EP2653548A1 (de) 2013-10-23
SI2839012T1 (sl) 2019-12-31
EP2839012A1 (de) 2015-02-25
BR112014025306A2 (pt) 2017-06-20
IN2014DN08664A (es) 2015-05-22
CA2870587A1 (en) 2013-10-24

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