Evidence map›Paper›PMID 23417485›Full record

ArticleJournal of bacteriology2013

High hydrostatic pressure induces counterclockwise to clockwise reversals of the Escherichia coli flagellar motor.

Masayoshi Nishiyama, Yoshiyuki Sowa, Yoshifumi Kimura, Michio Homma, Akihiko Ishijima, Masahide Terazima

Abstract read
In one paragraph

Article in Journal of bacteriology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Osmotaxis inProceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  7. Article
  8. Article
  9. Review
  10. 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

6 authors.

Masayoshi NishiyamaThe Hakubi Center for Advanced Research, Kyoto University, Kyoto, Japan. mnishiyama@icems.kyoto-u.ac.jp
Yoshiyuki Sowa
Yoshifumi Kimura
Michio Homma
Akihiko Ishijima
Masahide Terazima

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The bacterial flagellar motor is a reversible rotary machine that rotates a left-handed helical filament, allowing bacteria to swim toward a more favorable environment. The direction of rotation reverses from counterclockwise (CCW) to clockwise (CW), and vice versa, in response to input from the chemotaxis signaling circuit. CW rotation is normally caused by binding of the phosphorylated response regulator CheY (CheY-P), and strains lacking CheY are typically locked in CCW rotation. The detailed mechanism of switching remains unresolved because it is technically difficult to regulate the level of CheY-P within the concentration range that produces flagellar reversals. Here, we demonstrate that high hydrostatic pressure can induce CW rotation even in the absence of CheY-P. The rotation of single flagellar motors in Escherichia coli cells with the cheY gene deleted was monitored at various pressures and temperatures. Application of >120 MPa pressure induced a reversal from CCW to CW at 20°C, although at that temperature, no motor rotated CW at ambient pressure (0.1 MPa). At lower temperatures, pressure-induced changes in direction were observed at pressures of <120 MPa. CW rotation increased with pressure in a sigmoidal fashion, as it does in response to increasing concentrations of CheY-P. Application of pressure generally promotes the formation of clusters of ordered water molecules on the surfaces of proteins. It is possible that hydration of the switch complex at high pressure induces structural changes similar to those caused by the binding of CheY-P.

Indexed as

Bacterial ProteinsBiomechanical PhenomenaEscherichia coliEscherichia coli ProteinsFlagellaGene Expression Regulation, BacterialHydrostatic PressureMembrane ProteinsMethyl-Accepting Chemotaxis ProteinsMolecular Motor ProteinsMovementProtein BindingRotationTemperatureThermodynamicsBacterial ProteinscheY protein, E coliEscherichia coli ProteinsMembrane ProteinsMethyl-Accepting Chemotaxis ProteinsMolecular Motor Proteins

Identifiers

PMID23417485
PMCPMC3624566

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.