Evidence map›Paper›PMID 23247769›Full record

ArticleCurrent microbiology2013

A novel endogenous induction of ColE7 expression in a csrA mutant of Escherichia coli.

Hao-Wei Chang, Tsung-Yeh Yang, Guang-Sheng Lei, Kin-Fu Chak

Abstract read
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In one paragraph

Article in Current microbiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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.

Hao-Wei ChangInstitute of Biochemistry and Molecular Biology, National Yang-Ming University, Taipei, 11221, Taiwan.
Tsung-Yeh Yang
Guang-Sheng Lei
Kin-Fu Chak

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Carbon storage regulator A (CsrA) is an important regulator that controls central metabolic pathways and a variety of physiological functions. We found that disruption of csrA in cells containing the ColE7 operon caused a 12-fold increase in colicin E7 production. Moreover, real-time RT-PCR demonstrated a decrease of around 50 % in the lexA mRNA of the csrA mutant. However, the cellular level of RecA protein and its mRNA were not significantly different from the wild type strain. Our results suggest that a novel induction mechanism might exist in E. coli that allows the expression of ColE7 operon in response to a metabolic shift. Proteomic analysis suggested that csrA deficient mutant may adapt PEP-glyoxylate cycle for energy production. Thus, the physiological changes in the csrA mutant may be similar to carbon source limitation for initiating the expression of ColE7 operon in response to stringent environmental conditions.

Indexed as

Gene Expression Regulation, BacterialBacterial ProteinsCarbonColicinsEnergy MetabolismEscherichia coliEscherichia coli ProteinsGene Expression ProfilingGene Knockout TechniquesLexA Repressor ProteinProteomeReal-Time Polymerase Chain ReactionRec A RecombinasesRepressor ProteinsRNA-Binding ProteinsSerine EndopeptidasesBacterial ProteinsCarbonColE7 protein, E coliColicinsCsrA protein, E coliEscherichia coli ProteinsLexA Repressor ProteinProteomeRec A RecombinasesRepressor ProteinsRNA-Binding ProteinsSerine Endopeptidases

Identifiers

What OpenQuestion holds

Textmetadata
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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.