Evidence map›Paper›PMID 21685158›Full record

ArticleApplied and environmental microbiology2011

Identification of biofilm matrix-associated proteins from an acid mine drainage microbial community.

Yongqin Jiao, Patrik D'haeseleer, Brian D Dill, Manesh Shah, Nathan C Verberkmoes, Robert L Hettich, Jillian F Banfield, Michael P Thelen

Abstract read
In one paragraph

Article in Applied and environmental microbiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing 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

28 citing papers in PubMed.

  1. Review
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  4. OprF impactsbioRxiv : the preprint server for biology · 2023
    Article
  5. Article
  6. Article
  7. Article
  8. Microbial biofilm: formation, architecture, antibiotic resistance, and control strategies.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2021
    Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Contributions of the Biofilm Matrix toJournal of fungi (Basel, Switzerland) · 2020
    Review
  14. Article
  15. Article
  16. Article
  17. Article
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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

8 authors.

Yongqin JiaoPhysical and Life Sciences, LLNL, 7000 East Ave, L-452, Livermore, CA 94550, USA.
Patrik D'haeseleer
Brian D Dill
Manesh Shah
Nathan C Verberkmoes
Robert L Hettich
Jillian F Banfield
Michael P Thelen

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In microbial communities, extracellular polymeric substances (EPS), also called the extracellular matrix, provide the spatial organization and structural stability during biofilm development. One of the major components of EPS is protein, but it is not clear what specific functions these proteins contribute to the extracellular matrix or to microbial physiology. To investigate this in biofilms from an extremely acidic environment, we used shotgun proteomics analyses to identify proteins associated with EPS in biofilms at two developmental stages, designated DS1 and DS2. The proteome composition of the EPS was significantly different from that of the cell fraction, with more than 80% of the cellular proteins underrepresented or undetectable in EPS. In contrast, predicted periplasmic, outer membrane, and extracellular proteins were overrepresented by 3- to 7-fold in EPS. Also, EPS proteins were more basic by ∼2 pH units on average and about half the length. When categorized by predicted function, proteins involved in motility, defense, cell envelope, and unknown functions were enriched in EPS. Chaperones, such as histone-like DNA binding protein and cold shock protein, were overrepresented in EPS. Enzymes, such as protein peptidases, disulfide-isomerases, and those associated with cell wall and polysaccharide metabolism, were also detected. Two of these enzymes, identified as β-N-acetylhexosaminidase and cellulase, were confirmed in the EPS fraction by enzymatic activity assays. Compared to the differences between EPS and cellular fractions, the relative differences in the EPS proteomes between DS1 and DS2 were smaller and consistent with expected physiological changes during biofilm development.

Indexed as

BiofilmsProteomicsbeta-N-AcetylhexosaminidasesCell MembraneCellulaseCold Shock Proteins and PeptidesExtracellular Matrix ProteinsHydrogen-Ion ConcentrationMembrane ProteinsMicrobial ConsortiaMolecular ChaperonesPeptide HydrolasesPeriplasmProtein Disulfide-IsomerasesSoil Microbiologybeta-N-AcetylhexosaminidasesCellulaseCold Shock Proteins and PeptidesExtracellular Matrix ProteinsMembrane ProteinsMolecular ChaperonesPeptide HydrolasesProtein Disulfide-Isomerases

Identifiers

PMID21685158
PMCPMC3147463

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.