Abstracts - faqs.org

Abstracts

Biological sciences

Search abstracts:
Abstracts » Biological sciences

Overexpression of trigger factor prevents aggregation of recombinant proteins in Escherichia coli

Article Abstract:

Overexpression of the chaperonelike trigger factor of E. coli can prevent recombinant proteins from aggregating. Trigger factor correctly folded three recombinant proteins known to be susceptible to aggregation: mouse endostatin, human oxygen-regulated protein ORP150, and human lysozyme.

Author: Nishihara, Kazuyo, Kanemori, Masaaki, Yanagi, Hideki, Yura, Takashi
Publisher: American Society for Microbiology
Publication Name: Applied and Environmental Microbiology
Subject: Biological sciences
ISSN: 0099-2240
Year: 2000
Protein folding

User Contributions:

Comment about this article or add new information about this topic:

CAPTCHA


Overexpression of protein disulfide isomerase DsbC stabilizes multiple-disulfide-bonded recombinant protein produced and trnsported to the periplasm in Escherichia coli

Article Abstract:

Results show that periplasmic production and stabilization of horseradish peroxidase is influenced by Dsb proteins and calcium. Data indicate that total enzyme production increases severalfold by the overexpression of disulfide-bonded isomerase DsbC.

Author: Yanagi, Hideki, Kurokawa, Yoichi, Yura,Takashi
Publisher: American Society for Microbiology
Publication Name: Applied and Environmental Microbiology
Subject: Biological sciences
ISSN: 0099-2240
Year: 2000
United States, Japan, Analysis, Enzymes, Gene expression, Enzyme synthesis, Peroxidase

User Contributions:

Comment about this article or add new information about this topic:

CAPTCHA


Chaperone coexpression plasmids: differential and synergistic roles of DnaK-DnaJ-GrpE and GroEl-GroES in assisting folding of an allergen of Japanese cedar pollen, Cryj2, in Escherichia coli

Article Abstract:

DnaK-DnaJ-GrpE and GroEl-GroES containing chaperone coexpression plasmids were constructed and used to stabilize the assembly of recombinant proteins synthesized in the heterologous expression system of Escherichia coli. The plasmids were able to promote the synthesis of stable Cryj2, a Japanese cedar pollen allergen, in Escherichia coli. The functions of DnaK-DnaJ-GrpE and GroEl-GroES are distinct and synergistic.

Author: Nishihara, Kazuyo, Kanemori, Masaaki, Yanagi, Hideki, Yura, Takashi, Kitagawa, Masanari
Publisher: American Society for Microbiology
Publication Name: Applied and Environmental Microbiology
Subject: Biological sciences
ISSN: 0099-2240
Year: 1998
Genetic aspects, Genetic engineering, Plasmids

User Contributions:

Comment about this article or add new information about this topic:

CAPTCHA


Subjects list: Research, Escherichia coli, Recombinant proteins
Similar abstracts:
  • Abstracts: The pioneer translation initiation complex is functionally distinct from but structurally overlaps with the steady-state translation initiation complex
  • Abstracts: The ShcA phosphotyrosine docking protein sensitizes cardiovascular signaling in the mouse embryo. Protein-protein interactions define specificity in signal transduction
  • Abstracts: Chromatin-specific regulation of LEF-1-beta-catenin transcription activation and inhibition in vitro
  • Abstracts: Quantitative detection of Escherichia coli O157 in surface waters by using immunomagnetic electrochemiluminescence
This website is not affiliated with document authors or copyright owners. This page is provided for informational purposes only. Unintentional errors are possible.
Some parts © 2025 Advameg, Inc.