Evidence map›Paper›PMID 31344304›Full record

ArticleChembiochem : a European journal of chemical biology2019

Reconstitution and Coupling of DNA Replication and Segregation in a Biomimetic System.

Daniel Hürtgen, Judita Mascarenhas, Michael Heymann, Seán M Murray, Petra Schwille, Victor Sourjik

Open access · hybridAbstract read
In one paragraph

Article in Chembiochem : a European journal of chemical biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

5 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Towards a synthetic cell cycle.Nature communications · 2021
    Review
  4. Review
  5. Reconstitution and Coupling of DNA Replication and Segregation in a Biomimetic System.Chembiochem : a European journal of chemical biology · 2019
    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 at 2 institutions in 1 country.

Daniel HürtgenMax Planck Institute for Terrestrial Microbiology &, LOEWE Center for Synthetic Microbiology (Synmikro), Karl-von-Frisch Strasse 16, 35043, Marburg, Germany.ORCID 0000-0002-9558-4103
Judita MascarenhasMax Planck Institute for Terrestrial Microbiology &, LOEWE Center for Synthetic Microbiology (Synmikro), Karl-von-Frisch Strasse 16, 35043, Marburg, Germany.
Michael HeymannMax Planck Institute of Biochemistry, Am Klopferspitz 18, 82152, Martinsried, Germany.
Seán M MurrayMax Planck Institute for Terrestrial Microbiology &, LOEWE Center for Synthetic Microbiology (Synmikro), Karl-von-Frisch Strasse 16, 35043, Marburg, Germany.
Petra SchwilleMax Planck Institute of Biochemistry, Am Klopferspitz 18, 82152, Martinsried, Germany.
Victor SourjikMax Planck Institute for Terrestrial Microbiology &, LOEWE Center for Synthetic Microbiology (Synmikro), Karl-von-Frisch Strasse 16, 35043, Marburg, Germany.
Loewe Center for Synthetic Microbiology · DEMax Planck Institute of Biochemistry · DE

Funding

Bundesministerium für Bildung und ForschungMax Planck GesellschaftMaxSynBio
6 · The paper itself

Abstract

A biomimetic system capable of replication and segregation of genetic material constitutes an essential component for the future design of a minimal synthetic cell. Here we have used the simple T7 bacteriophage system and the plasmid-derived ParMRC system to establish in vitro DNA replication and DNA segregation, respectively. These processes were incorporated into biomimetic compartments providing an enclosed reaction space. The functional lifetime of the encapsulated segregation system could be prolonged by equipping it with ATP-regenerating and oxygen-scavenging systems. Finally, we showed that DNA replication and segregation processes could be coupled in vitro by using condensed DNA nanoparticles resulting from DNA replication. ParM spindles extended over tens of micrometers and could thus be used for segregation in compartments that are significantly longer than bacterial cell size. Overall, this work demonstrates the successful bottom-up assembly and coupling of molecular machines that mediate replication and segregation, thus providing an important step towards the development of a fully functional minimal cell.

Indexed as

Artificial CellsBiomimeticsDNA-Directed DNA PolymeraseDNA ReplicationEscherichia coliEscherichia coli ProteinsNanoparticlesPlasmidsSynthetic Biologybacteriophage T7 induced DNA polymeraseDNA-Directed DNA PolymeraseEscherichia coli ProteinsDNA nanoparticlesDNA replicationDNA segregationminimal cellParMT7

Identifiers

PMID31344304
PMCPMC6899551
OpenAlexW2963320290

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.