Evidence map›Paper›PMID 32973704›Full record

ArticleFrontiers in microbiology2020

Super-Resolution Microscopy and Single-Molecule Tracking Reveal Distinct Adaptive Dynamics of MreB and of Cell Wall-Synthesis Enzymes.

Simon Dersch, Johanna Mehl, Lisa Stuckenschneider, Benjamin Mayer, Julian Roth, Alexander Rohrbach, Peter L Graumann

Open access · goldAbstract read
In one paragraph

Article in Frontiers in microbiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.2field-weighted citation impact, top 12% of its field
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

15 citing papers in PubMed, 21 citations in OpenAlex.

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  14. Real-Time Messenger RNA Dynamics inFrontiers in microbiology · 2021
    Article
  15. 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

7 authors at 2 institutions in 1 country.

Simon DerschSYNMIKRO, LOEWE-Zentrum für Synthetische Mikrobiologie, Philipps-Univetsität Marburg, Marburg, Germany.
Johanna MehlLaboratory for Bio- and Nano-Photonics, Department of Microsystems Engineering-IMTEK, BIOSS Centre for Biological Signalling Studies, University of Freiburg, Freiburg, Germany.
Lisa StuckenschneiderSYNMIKRO, LOEWE-Zentrum für Synthetische Mikrobiologie, Philipps-Univetsität Marburg, Marburg, Germany.
Benjamin MayerSYNMIKRO, LOEWE-Zentrum für Synthetische Mikrobiologie, Philipps-Univetsität Marburg, Marburg, Germany.
Julian RothLaboratory for Bio- and Nano-Photonics, Department of Microsystems Engineering-IMTEK, BIOSS Centre for Biological Signalling Studies, University of Freiburg, Freiburg, Germany.
Alexander RohrbachLaboratory for Bio- and Nano-Photonics, Department of Microsystems Engineering-IMTEK, BIOSS Centre for Biological Signalling Studies, University of Freiburg, Freiburg, Germany.
Peter L GraumannSYNMIKRO, LOEWE-Zentrum für Synthetische Mikrobiologie, Philipps-Univetsität Marburg, Marburg, Germany.
Loewe Center for Synthetic Microbiology · DEUniversity of Freiburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The movement of filamentous, actin-like MreB and of enzymes synthesizing the bacterial cell wall has been proposed to be highly coordinated. We have investigated the motion of MreB and of RodA and PbpH cell wall synthesis enzymes at 500 ms and at 20 ms time scales, allowing us to compare the motion of entire MreB filaments as well as of single molecules with that of the two synthesis proteins. While all three proteins formed assemblies that move with very similar trajectory orientation and with similar velocities, their trajectory lengths differed considerably, with PbpH showing shortest and MreB longest trajectories. These experiments suggest different on/off rates for RodA and PbpH at the putative peptidoglycan-extending machinery (PGEM), and during interaction with MreB filaments. Single molecule tracking revealed distinct slow-moving and freely diffusing populations of PbpH and RodA, indicating that they change between free diffusion and slow motion, indicating a dynamic interaction with the PGEM complex. Dynamics of MreB molecules and the orientation and speed of filaments changed markedly after induction of salt stress, while there was little change for RodA and PbpH single molecule dynamics. During the stress adaptation phase, cells continued to grow and extended the cell wall, while MreB formed fewer and more static filaments. Our results show that cell wall synthesis during stress adaptation occurs in a mode involving adaptation of MreB dynamics, and indicate that

Indexed as

Bacillus subtiliscell shape maintenanceMreB cytoskeletonRodAsingle molecule dynamics

Identifiers

PMID32973704
PMCPMC7468405
OpenAlexW3081398164

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.