Evidence map›Paper›PMID 23563954›Full record

ArticleApplied and environmental microbiology2013

Comparison of 26 sphingomonad genomes reveals diverse environmental adaptations and biodegradative capabilities.

Frank O Aylward, Bradon R McDonald, Sandra M Adams, Alejandra Valenzuela, Rebeccah A Schmidt, Lynne A Goodwin, Tanja Woyke, Cameron R Currie, Garret Suen, Michael Poulsen

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Applied and environmental microbiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed
16.0field-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

75 citing papers in PubMed, 187 citations in OpenAlex.

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  11. Effects of simulated low-temperature thermal remediation on the microbial community of a tropical creosote contaminated soil.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2024
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  12. International journal of systematic and evolutionary microbiology · 2024
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  20. Contrasting patterns of microbial dominance in theProceedings of the National Academy of Sciences of the United States of America · 2022
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15 more citing papers are in PubMed but not listed here.

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

10 authors at 3 institutions in 2 countries.

Frank O AylwardDOE Great Lakes Bioenergy Research Center, University of Wisconsin-Madison, Madison, WI, USA.
Bradon R McDonald
Sandra M Adams
Alejandra Valenzuela
Rebeccah A Schmidt
Lynne A Goodwin
Tanja Woyke
Cameron R Currie
Garret Suen
Michael Poulsen
University of Wisconsin–Madison · USGreat Lakes Bioenergy Research Center · USJoint Genome Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sphingomonads comprise a physiologically versatile group within the Alphaproteobacteria that includes strains of interest for biotechnology, human health, and environmental nutrient cycling. In this study, we compared 26 sphingomonad genome sequences to gain insight into their ecology, metabolic versatility, and environmental adaptations. Our multilocus phylogenetic and average amino acid identity (AAI) analyses confirm that Sphingomonas, Sphingobium, Sphingopyxis, and Novosphingobium are well-resolved monophyletic groups with the exception of Sphingomonas sp. strain SKA58, which we propose belongs to the genus Sphingobium. Our pan-genomic analysis of sphingomonads reveals numerous species-specific open reading frames (ORFs) but few signatures of genus-specific cores. The organization and coding potential of the sphingomonad genomes appear to be highly variable, and plasmid-mediated gene transfer and chromosome-plasmid recombination, together with prophage- and transposon-mediated rearrangements, appear to play prominent roles in the genome evolution of this group. We find that many of the sphingomonad genomes encode numerous oxygenases and glycoside hydrolases, which are likely responsible for their ability to degrade various recalcitrant aromatic compounds and polysaccharides, respectively. Many of these enzymes are encoded on megaplasmids, suggesting that they may be readily transferred between species. We also identified enzymes putatively used for the catabolism of sulfonate and nitroaromatic compounds in many of the genomes, suggesting that plant-based compounds or chemical contaminants may be sources of nitrogen and sulfur. Many of these sphingomonads appear to be adapted to oligotrophic environments, but several contain genomic features indicative of host associations. Our work provides a basis for understanding the ecological strategies employed by sphingomonads and their role in environmental nutrient cycling.

Indexed as

EnvironmentPhylogenyAdaptation, BiologicalAmino Acid SequenceAnimalsBase SequenceBiodegradation, EnvironmentalCluster AnalysisGenome, BacterialIsopteraModels, GeneticMolecular Sequence AnnotationMolecular Sequence DataOpen Reading FramesPuerto RicoSequence Analysis, DNA

Identifiers

PMID23563954
PMCPMC3675938
OpenAlexW2117054393

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.