Evidence map›Paper›PMID 21130896›Full record

ArticleMetabolic engineering2011

Comprehensive engineering of Escherichia coli for enhanced expression of IgG antibodies.

Tomohiro Makino, Georgios Skretas, Tae-Hyun Kang, George Georgiou

Abstract read
In one paragraph

Article in Metabolic engineering, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

26 citing papers in PubMed.

  1. Article
  2. Strategies to Enhance Periplasmic Recombinant Protein Production Yields inFrontiers in bioengineering and biotechnology · 2021
    Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Isolating Escherichia coli strains for recombinant protein production.Cellular and molecular life sciences : CMLS · 2017
    Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Combinatorial approaches for inverse metabolic engineering applications.Computational and structural biotechnology journal · 2012
    Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Tomohiro MakinoDepartment of Chemical Engineering, The University of Texas at Austin, Austin, TX 78712-0231, USA.
Georgios Skretas
Tae-Hyun Kang
George Georgiou

Funding

PROTEIN DISULFIDE BOND ISOMERIZATION IN E COLIR01GM055090 · NIGMS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI BECKWITH, JONATHAN · 1998 to 2009
$4.3M
NIGMS NIH HHS GM55090NIGMS NIH HHS R01 GM055090
6 · The paper itself

Abstract

The expression of IgG antibodies in Escherichia coli is of increasing interest for analytical and therapeutic applications. In this work, we describe a comprehensive and systematic approach to the development of a dicistronic expression system for enhanced IgG expression in E. coli encompassing: (i) random mutagenesis and high-throughput screening for the isolation of over-expressing strains using flow cytometry and (ii) optimization of translation initiation via the screening of libraries of synonymous codons in the 5' region of the second cistron (heavy chain). The effects of different promoters and co-expression of molecular chaperones on full-length IgG production were also investigated. The optimized system resulted in reliable expression of fully assembled IgG at yields between 1 and 4 mg/L of shake flask culture for different antibodies.

Indexed as

Escherichia coliEscherichia coli ProteinsGenetic EngineeringHigh-Throughput Screening AssaysImmunoglobulin GMutagenesisProtein EngineeringEscherichia coli ProteinsImmunoglobulin G

Identifiers

PMID21130896
PMCPMC3057344

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.