Evidence map›Paper›PMID 26555245›Full record

ArticleThe ISME journal2016

Metatranscriptomic insights on gene expression and regulatory controls in Candidatus Accumulibacter phosphatis.

Ben O Oyserman, Daniel R Noguera, Tijana Glavina del Rio, Susannah G Tringe, Katherine D McMahon

Open access · bronzeAbstract read
In one paragraph

Article in The ISME journal, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

29 citing papers in PubMed, 121 citations in OpenAlex.

  1. Article
  2. Comparative transcription profiles ofFrontiers in microbiology · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. Expanding the Diversity ofApplied and environmental microbiology · 2023
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Low Global Diversity ofFrontiers in microbiology · 2021
    Article
  18. Revealing the Metabolic Flexibility of "Applied and environmental microbiology · 2020
    Article
  19. Review
  20. 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

5 authors at 2 institutions in 1 country.

Ben O OysermanDepartment of Civil and Environmental Engineering, University of Wisconsin at Madison, Madison, WI, USA.
Daniel R NogueraDepartment of Civil and Environmental Engineering, University of Wisconsin at Madison, Madison, WI, USA.
Tijana Glavina del RioUS Department of Energy Joint Genome Institute, Walnut Creek, CA, USA.
Susannah G TringeUS Department of Energy Joint Genome Institute, Walnut Creek, CA, USA.ORCID http://orcid.org/0000-0001-6479-8427
Katherine D McMahonDepartment of Civil and Environmental Engineering, University of Wisconsin at Madison, Madison, WI, USA.
University of Wisconsin–Madison · USJoint Genome Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Previous studies on enhanced biological phosphorus removal (EBPR) have focused on reconstructing genomic blueprints for the model polyphosphate-accumulating organism Candidatus Accumulibacter phosphatis. Here, a time series metatranscriptome generated from enrichment cultures of Accumulibacter was used to gain insight into anerobic/aerobic metabolism and regulatory mechanisms within an EBPR cycle. Co-expressed gene clusters were identified displaying ecologically relevant trends consistent with batch cycle phases. Transcripts displaying increased abundance during anerobic acetate contact were functionally enriched in energy production and conversion, including upregulation of both cytoplasmic and membrane-bound hydrogenases demonstrating the importance of transcriptional regulation to manage energy and electron flux during anerobic acetate contact. We hypothesized and demonstrated hydrogen production after anerobic acetate contact, a previously unknown strategy for Accumulibacter to maintain redox balance. Genes involved in anerobic glycine utilization were identified and phosphorus release after anerobic glycine contact demonstrated, suggesting that Accumulibacter routes diverse carbon sources to acetyl-CoA formation via previously unrecognized pathways. A comparative genomics analysis of sequences upstream of co-expressed genes identified two statistically significant putative regulatory motifs. One palindromic motif was identified upstream of genes involved in PHA synthesis and acetate activation and is hypothesized to be a phaR binding site, hence representing a hypothetical PHA modulon. A second motif was identified ~35 base pairs (bp) upstream of a large and diverse array of genes and hence may represent a sigma factor binding site. This analysis provides a basis and framework for further investigations into Accumulibacter metabolism and the reconstruction of regulatory networks in uncultured organisms.

Indexed as

Gene Expression ProfilingAcetyl Coenzyme ABetaproteobacteriaBioreactorsBiotechnologyGene Regulatory NetworksGlycineHydrogenMetabolic Networks and PathwaysPhosphorusAcetyl Coenzyme AGlycineHydrogenPhosphorus

Identifiers

PMID26555245
PMCPMC4796919
OpenAlexW2242576385

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.