Evidence map›Paper›PMID 22041895›Full record

ArticleThe Journal of biological chemistry2011

Salt sensitivity of minimal twin arginine translocases.

René van der Ploeg, James P Barnett, Nishi Vasisht, Vivianne J Goosens, Dierk C Pöther, Colin Robinson, Jan Maarten van Dijl

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

9 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. 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 3 institutions in 2 countries.

René van der PloegDepartment of Medical Microbiology, University Medical Center Groningen and University of Groningen, 9700 RB Groningen, The Netherlands.
James P BarnettSchool of Life Sciences, University of Warwick, Coventry, CV4 7AL, United Kingdom.
Nishi VasishtSchool of Life Sciences, University of Warwick, Coventry, CV4 7AL, United Kingdom.
Vivianne J GoosensDepartment of Medical Microbiology, University Medical Center Groningen and University of Groningen, 9700 RB Groningen, The Netherlands.
Dierk C PötherDepartment of Medical Microbiology, University Medical Center Groningen and University of Groningen, 9700 RB Groningen, The Netherlands.
Colin RobinsonSchool of Life Sciences, University of Warwick, Coventry, CV4 7AL, United Kingdom.
Jan Maarten van DijlDepartment of Medical Microbiology, University Medical Center Groningen and University of Groningen, 9700 RB Groningen, The Netherlands. Electronic address: J.M.van.Dijl@med.umcg.nl.
University of Warwick · GBUniversity Medical Center Groningen · NLUniversity of Groningen · NL

Funding

Biotechnology and Biological Sciences Research Council
6 · The paper itself

Abstract

Bacterial twin arginine translocation (Tat) pathways have evolved to facilitate transport of folded proteins across membranes. Gram-negative bacteria contain a TatABC translocase composed of three subunits named TatA, TatB, and TatC. In contrast, the Tat translocases of most Gram-positive bacteria consist of only TatA and TatC subunits. In these minimal TatAC translocases, a bifunctional TatA subunit fulfils the roles of both TatA and TatB. Here we have probed the importance of conserved residues in the bifunctional TatAy subunit of Bacillus subtilis by site-specific mutagenesis. A set of engineered TatAy proteins with mutations in the cytoplasmic hinge and amphipathic helix regions were found to be inactive in protein translocation under standard growth conditions for B. subtilis or when heterologously expressed in Escherichia coli. Nevertheless, these mutated TatAy proteins did assemble into TatAy and TatAyCy complexes, and they facilitated membrane association of twin arginine precursor proteins in E. coli. Interestingly, most of the mutated TatAyCy translocases were salt-sensitive in B. subtilis. Similarly, the TatAC translocases of Bacillus cereus and Staphylococcus aureus were salt-sensitive when expressed in B. subtilis. Taken together, our present observations imply that salt-sensitive electrostatic interactions have critical roles in the preprotein translocation activity of certain TatAC type translocases from Gram-positive bacteria.

Indexed as

Amino Acid SequenceAnti-Bacterial AgentsArginineBacillus cereusBacillus subtilisEscherichia coliEscherichia coli ProteinsGenetic Complementation TestListeria monocytogenesMembrane Transport ProteinsMolecular Sequence DataMutagenesis, Site-DirectedMutationPlasmidsSaltsStaphylococcusAnti-Bacterial AgentsArginineEscherichia coli ProteinsMembrane Transport ProteinsSaltsTatA protein, E coliTatC protein, E coli

Identifiers

PMID22041895
PMCPMC3243503
OpenAlexW2150952759

What OpenQuestion holds

Textmetadata
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.