Evidence map›Paper›PMID 35037270›Full record

ArticleThe EMBO journal2022

Low membrane fluidity triggers lipid phase separation and protein segregation in living bacteria.

Marvin Gohrbandt, André Lipski, James W Grimshaw, Jessica A Buttress, Zunera Baig, Brigitte Herkenhoff, Stefan Walter, Rainer Kurre, Gabriele Deckers-Hebestreit, Henrik Strahl

Abstract read
In one paragraph

Article in The EMBO journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing 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

69 citing papers in PubMed.

  1. The phenotypic landscape of the model firmicuteProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. InJournal of bacteriology · 2026
    Article
  3. Article
  4. Article
  5. mLife · 2026
    Article
  6. Article
  7. Article
  8. Article
  9. InbioRxiv : the preprint server for biology · 2026
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. FFoods (Basel, Switzerland) · 2026
    Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article

9 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Marvin GohrbandtMikrobiologie, Fachbereich Biologie/Chemie, Universität Osnabrück, Osnabrück, Germany.ORCID 0000-0002-2470-3232
André LipskiLebensmittelmikrobiologie und -hygiene, Institut für Ernährungs- und Lebensmittelwissenschaften, Rheinische Friedrich-Wilhelms-Universität Bonn, Bonn, Germany.
James W GrimshawCentre for Bacterial Cell Biology, Biosciences Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK.ORCID 0000-0002-1276-9912
Jessica A ButtressCentre for Bacterial Cell Biology, Biosciences Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK.ORCID 0000-0001-8822-6917
Zunera BaigCentre for Bacterial Cell Biology, Biosciences Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK.
Brigitte HerkenhoffMikrobiologie, Fachbereich Biologie/Chemie, Universität Osnabrück, Osnabrück, Germany.
Stefan WalterMikrobiologie, Fachbereich Biologie/Chemie, Universität Osnabrück, Osnabrück, Germany.
Rainer KurreCenter of Cellular Nanoanalytics, Integrated Bioimaging Facility, Universität Osnabrück, Osnabrück, Germany.
Gabriele Deckers-HebestreitMikrobiologie, Fachbereich Biologie/Chemie, Universität Osnabrück, Osnabrück, Germany.ORCID 0000-0002-7369-8310
Henrik StrahlCentre for Bacterial Cell Biology, Biosciences Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK.ORCID 0000-0003-4416-2178

Funding

Biotechnology and Biological Sciences Research Council BB/M011186/1Biotechnology and Biological Sciences Research Council BB/S00257X/1Medical Research Council MR/N013840/1
6 · The paper itself

Abstract

All living organisms adapt their membrane lipid composition in response to changes in their environment or diet. These conserved membrane-adaptive processes have been studied extensively. However, key concepts of membrane biology linked to regulation of lipid composition including homeoviscous adaptation maintaining stable levels of membrane fluidity, and gel-fluid phase separation resulting in domain formation, heavily rely upon in vitro studies with model membranes or lipid extracts. Using the bacterial model organisms Escherichia coli and Bacillus subtilis, we now show that inadequate in vivo membrane fluidity interferes with essential complex cellular processes including cytokinesis, envelope expansion, chromosome replication/segregation and maintenance of membrane potential. Furthermore, we demonstrate that very low membrane fluidity is indeed capable of triggering large-scale lipid phase separation and protein segregation in intact, protein-crowded membranes of living cells; a process that coincides with the minimal level of fluidity capable of supporting growth. Importantly, the in vivo lipid phase separation is not associated with a breakdown of the membrane diffusion barrier function, thus explaining why the phase separation process induced by low fluidity is biologically reversible.

Indexed as

Bacillus subtilisCell MembraneEscherichia coliMembrane FluidityMembrane LipidsProteinsMembrane LipidsProteinshomeoviscous adaptationlipid domainslipid phase separationmembrane fluidityprotein partitioning

Identifiers

PMID35037270
PMCPMC8886542

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.