Evidence map›Paper›PMID 24779863›Full record

ArticleMicrobial biotechnology2014

Construction of leaky strains and extracellular production of exogenous proteins in recombinant Escherichia coli.

Zhao-Yuan Chen, Jie Cao, Li Xie, Xiao-Fei Li, Zhen-Hai Yu, Wang-Yu Tong

Abstract read
In one paragraph

Article in Microbial biotechnology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. A molecular toolkit for heterologous protein secretion acrossbioRxiv : the preprint server for biology · 2023
    Article
  11. Article
  12. Protein Extraction and Purification by Differential Solubilization.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  13. Extracellular production of Ulp1Applied microbiology and biotechnology · 2022
    Article
  14. Article
  15. Article
  16. Repetitive Fed-Batch: A Promising Process Mode for Biomanufacturing WithFrontiers in bioengineering and biotechnology · 2020
    Article
  17. Article
  18. Reteplase: Structure, Function, and Production.Advanced biomedical research · 2019
    Review
  19. Review
  20. Secretion of recombinant proteins fromEngineering in life sciences · 2018
    Review
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

6 authors.

Zhao-Yuan ChenIntegrated Biotechnology Laboratory, School of Life Sciences, Anhui University, Hefei, 230601, China.
Jie Cao
Li Xie
Xiao-Fei Li
Zhen-Hai Yu
Wang-Yu Tong

Funding

Transgenic Mouse and Biobank CoreP01CA095616 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI DEPINHO, RONALD ANTHONY · 2003 to 2012
$20.3M
NCI NIH HHS P01 CA095616
6 · The paper itself

Abstract

In this study, a strategy of the construction of leaky strains for the extracellular production of target proteins was exploited, in which the genes mrcA, mrcB, pal and lpp (as a control) from Escherichia coli were knocked out by using single- and/or double-gene deletion methods. Then the recombinant strains for the expression of exogenous target proteins including Trx-hPTH (human parathyroid hormone 1-84 coupled with thioredoxin as a fusion partner) and reteplase were reconstructed to test the secretory efficiency of the leaky strains. Finally, the fermentation experiments of the target proteins from these recombinant leaky strains were carried out in basic media (Modified R media) and complex media (Terrific Broth media) in flasks or fermenters. The results demonstrated that the resultant leaky strains were genetically stable and had a similar growth profile in the complex media as compared with the original strain, and the secretory levels of target proteins into Modified R media from the strains with double-gene deletion (up to 88.9%/mrcA lpp-pth) are higher than the excretory levels from the strains with single-gene deletion (up to 71.1%/lpp-pth) and the host E. coli JM109 (DE3) (near zero). The highest level of extracellular production of Trx-hPTH in fermenters is up to 680 mg l(-1).

Indexed as

Metabolic EngineeringCulture MediaEscherichia coliGene DeletionGenomic InstabilityParathyroid HormoneRecombinant ProteinsThioredoxinsTissue Plasminogen ActivatorCulture MediaParathyroid HormoneRecombinant ProteinsreteplaseThioredoxinsTissue Plasminogen Activator

Identifiers

PMID24779863
PMCPMC4241728

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.