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

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Comparison of 26 sphingomonad genomes reveals diverse environmental adaptations and biodegradative capabilities. / Aylward, Frank O.; McDonald, Bradon R.; Adams, Sandra M.; Valenzuela, Alejandra; Schmidt, Rebeccah A.; Goodwin, Lynne A.; Woyke, Tanja; Currie, Cameron R.; Suen, Garret; Poulsen, Michael.

In: Applied and Environmental Microbiology, Vol. 79, No. 12, 2013, p. 3724-3733.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Aylward, FO, McDonald, BR, Adams, SM, Valenzuela, A, Schmidt, RA, Goodwin, LA, Woyke, T, Currie, CR, Suen, G & Poulsen, M 2013, 'Comparison of 26 sphingomonad genomes reveals diverse environmental adaptations and biodegradative capabilities', Applied and Environmental Microbiology, vol. 79, no. 12, pp. 3724-3733. https://doi.org/10.1128/AEM.00518-13

APA

Aylward, F. O., McDonald, B. R., Adams, S. M., Valenzuela, A., Schmidt, R. A., Goodwin, L. A., Woyke, T., Currie, C. R., Suen, G., & Poulsen, M. (2013). Comparison of 26 sphingomonad genomes reveals diverse environmental adaptations and biodegradative capabilities. Applied and Environmental Microbiology, 79(12), 3724-3733. https://doi.org/10.1128/AEM.00518-13

Vancouver

Aylward FO, McDonald BR, Adams SM, Valenzuela A, Schmidt RA, Goodwin LA et al. Comparison of 26 sphingomonad genomes reveals diverse environmental adaptations and biodegradative capabilities. Applied and Environmental Microbiology. 2013;79(12):3724-3733. https://doi.org/10.1128/AEM.00518-13

Author

Aylward, Frank O. ; McDonald, Bradon R. ; Adams, Sandra M. ; Valenzuela, Alejandra ; Schmidt, Rebeccah A. ; Goodwin, Lynne A. ; Woyke, Tanja ; Currie, Cameron R. ; Suen, Garret ; Poulsen, Michael. / Comparison of 26 sphingomonad genomes reveals diverse environmental adaptations and biodegradative capabilities. In: Applied and Environmental Microbiology. 2013 ; Vol. 79, No. 12. pp. 3724-3733.

Bibtex

@article{8783e4b4cfb2451ba24487fec021d3ef,
title = "Comparison of 26 sphingomonad genomes reveals diverse environmental adaptations and biodegradative capabilities",
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.",
author = "Aylward, {Frank O.} and McDonald, {Bradon R.} and Adams, {Sandra M.} and Alejandra Valenzuela and Schmidt, {Rebeccah A.} and Goodwin, {Lynne A.} and Tanja Woyke and Currie, {Cameron R.} and Garret Suen and Michael Poulsen",
year = "2013",
doi = "10.1128/AEM.00518-13",
language = "English",
volume = "79",
pages = "3724--3733",
journal = "Applied and Environmental Microbiology",
issn = "0099-2240",
publisher = "American Society for Microbiology",
number = "12",

}

RIS

TY - JOUR

T1 - Comparison of 26 sphingomonad genomes reveals diverse environmental adaptations and biodegradative capabilities

AU - Aylward, Frank O.

AU - McDonald, Bradon R.

AU - Adams, Sandra M.

AU - Valenzuela, Alejandra

AU - Schmidt, Rebeccah A.

AU - Goodwin, Lynne A.

AU - Woyke, Tanja

AU - Currie, Cameron R.

AU - Suen, Garret

AU - Poulsen, Michael

PY - 2013

Y1 - 2013

N2 - 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.

AB - 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.

U2 - 10.1128/AEM.00518-13

DO - 10.1128/AEM.00518-13

M3 - Journal article

C2 - 23563954

VL - 79

SP - 3724

EP - 3733

JO - Applied and Environmental Microbiology

JF - Applied and Environmental Microbiology

SN - 0099-2240

IS - 12

ER -

ID: 46076456