Evidence map›Paper›PMID 30402373›Full record

ArticleChemistryOpen2018

Direct Observation of Bacterial Growth in Giant Unilamellar Vesicles: A Novel Tool for Bacterial Cultures.

Masamune Morita, Kaoru Katoh, Naohiro Noda

Abstract read
In one paragraph

Article in ChemistryOpen, 2018. 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. Article
  2. Article
  3. Article
  4. Encapsulated bacteria deform lipid vesicles into flagellated swimmers.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  5. Article
  6. Review
  7. Bacterial Behavior in Confined Spaces.Frontiers in cell and developmental biology · 2021
    Review
  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

3 authors.

Masamune MoritaBiomedical Research Institute National Institute of Advanced Industrial Science and Technology (AIST), Center 6 1-1-1 Higashi Tsukuba Ibaraki 305-8566 Japan.ORCID 0000-0003-0219-2467
Kaoru KatohBiomedical Research Institute National Institute of Advanced Industrial Science and Technology (AIST), Center 6 1-1-1 Higashi Tsukuba Ibaraki 305-8566 Japan.ORCID 0000-0001-6590-413X
Naohiro NodaBiomedical Research Institute National Institute of Advanced Industrial Science and Technology (AIST), Center 6 1-1-1 Higashi Tsukuba Ibaraki 305-8566 Japan.ORCID 0000-0001-7592-5495

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bacterial cultivation techniques are classic, basic, and common processes used to characterize the physiological activity of bacteria in their environment. Owing to recent advances in bacterial cultivation techniques, the physiological activity of bacteria can be elucidated at the single-cell culture level. Here, we report a novel method to monitor the real-time activity of bacterial growth at the single-cell level inside giant unilamellar vesicles (GUVs). This method consists of two steps: 1) encapsulation of single bacteria in 1-33 pL scale GUVs and 2) immobilization of the GUVs on a planar lipid bilayer membrane on a glass surface. We directly observed single

Indexed as

artificial cell-based incubatorsbacterial cultivationbioreactorsgiant unilamellar vesiclessingle-cell cultures

Identifiers

PMID30402373
PMCPMC6208190

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.