Evidence map›Paper›PMID 28659875›Full record

ArticleFrontiers in microbiology2017

Predicting Species-Resolved Macronutrient Acquisition during Succession in a Model Phototrophic Biofilm Using an Integrated 'Omics Approach.

Stephen R Lindemann, Jennifer M Mobberley, Jessica K Cole, L M Markillie, Ronald C Taylor, Eric Huang, William B Chrisler, H S Wiley, Mary S Lipton, William C Nelson and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in microbiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
22.6field-weighted citation impact, top 1% 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

7 citing papers in PubMed, 346 citations in OpenAlex.

  1. Article
  2. Article
  3. Comparative genomics of the genusMicrobial genomics · 2020
    Article
  4. Article
  5. Review
  6. Article
  7. 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

12 authors at 2 institutions in 1 country.

Stephen R LindemannBiological Sciences Division, Pacific Northwest National Laboratory, RichlandWA, United States.
Jennifer M MobberleyBiological Sciences Division, Pacific Northwest National Laboratory, RichlandWA, United States.
Jessica K ColeBiological Sciences Division, Pacific Northwest National Laboratory, RichlandWA, United States.
L M MarkillieWhistler Center for Carbohydrate Research, Department of Food Science, Purdue University, West LafayetteIN, United States.
Ronald C TaylorBiological Sciences Division, Pacific Northwest National Laboratory, RichlandWA, United States.
Eric HuangBiological Sciences Division, Pacific Northwest National Laboratory, RichlandWA, United States.
William B ChrislerBiological Sciences Division, Pacific Northwest National Laboratory, RichlandWA, United States.
H S WileyEnvironmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, RichlandWA, United States.
Mary S LiptonEnvironmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, RichlandWA, United States.
William C NelsonBiological Sciences Division, Pacific Northwest National Laboratory, RichlandWA, United States.
James K FredricksonBiological Sciences Division, Pacific Northwest National Laboratory, RichlandWA, United States.
Margaret F RomineBiological Sciences Division, Pacific Northwest National Laboratory, RichlandWA, United States.
Pacific Northwest National Laboratory · USPurdue University West Lafayette · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The principles governing acquisition and interspecies exchange of nutrients in microbial communities and how those exchanges impact community productivity are poorly understood. Here, we examine energy and macronutrient acquisition in unicyanobacterial consortia for which species-resolved genome information exists for all members, allowing us to use multi-omic approaches to predict species' abilities to acquire resources and examine expression of resource-acquisition genes during succession. Metabolic reconstruction indicated that a majority of heterotrophic community members lacked the genes required to directly acquire the inorganic nutrients provided in culture medium, suggesting high metabolic interdependency. The sole primary producer in consortium UCC-O, cyanobacterium

Indexed as

carbon fixationmetagenomicsmetaproteomicsmetatranscriptomicsnitrate reductionperiphytonphosphate transportsulfate reduction

Identifiers

PMID28659875
PMCPMC5468372
OpenAlexW2624701244

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.