Literature DB >> 25093637

Comparative single-cell genomics reveals potential ecological niches for the freshwater acI Actinobacteria lineage.

Trevor W Ghylin1, Sarahi L Garcia2, Francisco Moya1, Ben O Oyserman1, Patrick Schwientek3, Katrina T Forest4, James Mutschler4, Jeffrey Dwulit-Smith4, Leong-Keat Chan3, Manuel Martinez-Garcia5, Alexander Sczyrba6, Ramunas Stepanauskas5, Hans-Peter Grossart7, Tanja Woyke3, Falk Warnecke8, Rex Malmstrom3, Stefan Bertilsson9, Katherine D McMahon10.   

Abstract

Members of the acI lineage of Actinobacteria are the most abundant microorganisms in most freshwater lakes; however, our understanding of the keys to their success and their role in carbon and nutrient cycling in freshwater systems has been hampered by the lack of pure cultures and genomes. We obtained draft genome assemblies from 11 single cells representing three acI tribes (acI-A1, acI-A7, acI-B1) from four temperate lakes in the United States and Europe. Comparative analysis of acI SAGs and other available freshwater bacterial genomes showed that acI has more gene content directed toward carbohydrate acquisition as compared to Polynucleobacter and LD12 Alphaproteobacteria, which seem to specialize more on carboxylic acids. The acI genomes contain actinorhodopsin as well as some genes involved in anaplerotic carbon fixation indicating the capacity to supplement their known heterotrophic lifestyle. Genome-level differences between the acI-A and acI-B clades suggest specialization at the clade level for carbon substrate acquisition. Overall, the acI genomes appear to be highly streamlined versions of Actinobacteria that include some genes allowing it to take advantage of sunlight and N-rich organic compounds such as polyamines, di- and oligopeptides, branched-chain amino acids and cyanophycin. This work significantly expands the known metabolic potential of the cosmopolitan freshwater acI lineage and its ecological and genetic traits.

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Year:  2014        PMID: 25093637      PMCID: PMC4260696          DOI: 10.1038/ismej.2014.135

Source DB:  PubMed          Journal:  ISME J        ISSN: 1751-7362            Impact factor:   10.302


  63 in total

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Journal:  PLoS One       Date:  2013-03-04       Impact factor: 3.240

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  44 in total

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