4.8 Article

Genomic insights to SAR86, an abundant and uncultivated marine bacterial lineage

期刊

ISME JOURNAL
卷 6, 期 6, 页码 1186-1199

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/ismej.2011.189

关键词

SAR86; SAR11; metagenomic assembly; single cell genomics; proteorhodopsin; tonB receptors

资金

  1. Gordon and Betty Moore Foundation [521]
  2. US Department of Energy, Office of Science, Office of Biological and Environmental Research [DE-FC02-02ER63453]
  3. Alfred P Sloan Foundation
  4. NASA Astrobiology Institute

向作者/读者索取更多资源

Bacteria in the 16S rRNA clade SAR86 are among the most abundant uncultivated constituents of microbial assemblages in the surface ocean for which little genomic information is currently available. Bioinformatic techniques were used to assemble two nearly complete genomes from marine metagenomes and single-cell sequencing provided two more partial genomes. Recruitment of metagenomic data shows that these SAR86 genomes substantially increase our knowledge of non-photosynthetic bacteria in the surface ocean. Phylogenomic analyses establish SAR86 as a basal and divergent lineage of gamma-proteobacteria, and the individual genomes display a temperature-dependent distribution. Modestly sized at 1.25-1.7 Mbp, the SAR86 genomes lack several pathways for amino-acid and vitamin synthesis as well as sulfate reduction, trends commonly observed in other abundant marine microbes. SAR86 appears to be an aerobic chemoheterotroph with the potential for proteorhodopsin-based ATP generation, though the apparent lack of a retinal biosynthesis pathway may require it to scavenge exogenously-derived pigments to utilize proteorhodopsin. The genomes contain an expanded capacity for the degradation of lipids and carbohydrates acquired using a wealth of tonB-dependent outer membrane receptors. Like the abundant planktonic marine bacterial clade SAR11, SAR86 exhibits metabolic streamlining, but also a distinct carbon compound specialization, possibly avoiding competition. The ISME Journal (2012) 6, 1186-1199; doi:10.1038/ismej.2011.189; published online 15 December 2011

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