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      Novel, Deep-Branching Heterotrophic Bacterial Populations Recovered from Thermal Spring Metagenomes

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          Abstract

          Thermal spring ecosystems are a valuable resource for the discovery of novel hyperthermophilic Bacteria and Archaea, and harbor deeply-branching lineages that provide insight regarding the nature of early microbial life. We characterized bacterial populations in two circumneutral (pH ~8) Yellowstone National Park thermal ( T ~80°C) spring filamentous “streamer” communities using random metagenomic DNA sequence to investigate the metabolic potential of these novel populations. Four de novo assemblies representing three abundant, deeply-branching bacterial phylotypes were recovered. Analysis of conserved phylogenetic marker genes indicated that two of the phylotypes represent separate groups of an uncharacterized phylum (for which we propose the candidate phylum name “Pyropristinus”). The third new phylotype falls within the proposed Calescamantes phylum. Metabolic reconstructions of the “Pyropristinus” and Calescamantes populations showed that these organisms appear to be chemoorganoheterotrophs and have the genomic potential for aerobic respiration and oxidative phosphorylation via archaeal-like V-type, and bacterial F-type ATPases, respectively. A survey of similar phylotypes (>97% nt identity) within 16S rRNA gene datasets suggest that the newly described organisms are restricted to terrestrial thermal springs ranging from 70 to 90°C and pH values of ~7–9. The characterization of these lineages is important for understanding the diversity of deeply-branching bacterial phyla, and their functional role in high-temperature circumneutral “streamer” communities.

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          Most cited references46

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          NAST: a multiple sequence alignment server for comparative analysis of 16S rRNA genes

          Microbiologists conducting surveys of bacterial and archaeal diversity often require comparative alignments of thousands of 16S rRNA genes collected from a sample. The computational resources and bioinformatics expertise required to construct such an alignment has inhibited high-throughput analysis. It was hypothesized that an online tool could be developed to efficiently align thousands of 16S rRNA genes via the NAST (Nearest Alignment Space Termination) algorithm for creating multiple sequence alignments (MSA). The tool was implemented with a web-interface at . Each user-submitted sequence is compared with Greengenes' ‘Core Set’, comprising ∼10 000 aligned non-chimeric sequences representative of the currently recognized diversity among bacteria and archaea. User sequences are oriented and paired with their closest match in the Core Set to serve as a template for inserting gap characters. Non-16S data (sequence from vector or surrounding genomic regions) are conveniently removed in the returned alignment. From the resulting MSA, distance matrices can be calculated for diversity estimates and organisms can be classified by taxonomy. The ability to align and categorize large sequence sets using a simple interface has enabled researchers with various experience levels to obtain bacterial and archaeal community profiles.
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            Evidence for lateral gene transfer between Archaea and bacteria from genome sequence of Thermotoga maritima.

            The 1,860,725-base-pair genome of Thermotoga maritima MSB8 contains 1,877 predicted coding regions, 1,014 (54%) of which have functional assignments and 863 (46%) of which are of unknown function. Genome analysis reveals numerous pathways involved in degradation of sugars and plant polysaccharides, and 108 genes that have orthologues only in the genomes of other thermophilic Eubacteria and Archaea. Of the Eubacteria sequenced to date, T. maritima has the highest percentage (24%) of genes that are most similar to archaeal genes. Eighty-one archaeal-like genes are clustered in 15 regions of the T. maritima genome that range in size from 4 to 20 kilobases. Conservation of gene order between T. maritima and Archaea in many of the clustered regions suggests that lateral gene transfer may have occurred between thermophilic Eubacteria and Archaea.
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              Alternative pathways of carbon dioxide fixation: insights into the early evolution of life?

              G Fuchs (2010)
              The fixation of inorganic carbon into organic material (autotrophy) is a prerequisite for life and sets the starting point of biological evolution. In the extant biosphere the reductive pentose phosphate (Calvin-Benson) cycle is the predominant mechanism by which many prokaryotes and all plants fix CO(2) into biomass. However, the fact that five alternative autotrophic pathways exist in prokaryotes is often neglected. This bias may lead to serious misjudgments in models of the global carbon cycle, in hypotheses on the evolution of metabolism, and in interpretations of geological records. Here, I review these alternative pathways that differ fundamentally from the Calvin-Benson cycle. Revealingly, these five alternative pathways pivot on acetyl-coenzyme A, the turntable of metabolism, demanding a gluconeogenic pathway starting from acetyl-coenzyme A and CO(2). It appears that the formation of an activated acetic acid from inorganic carbon represents the initial step toward metabolism. Consequently, biosyntheses likely started from activated acetic acid and gluconeogenesis preceded glycolysis.
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                Author and article information

                Contributors
                Journal
                Front Microbiol
                Front Microbiol
                Front. Microbiol.
                Frontiers in Microbiology
                Frontiers Media S.A.
                1664-302X
                15 March 2016
                2016
                : 7
                : 304
                Affiliations
                [1] 1Department of Biology, University of New Mexico Albuquerque, NM, USA
                [2] 2Thermal Biology Institute and Department of Land Resources and Environmental Sciences, Montana State University Bozeman, MT, USA
                [3] 3Center for Genomics and Bioinformatics, Indiana University Bloomington, IN, USA
                Author notes

                Edited by: Jesse G. Dillon, California State University, Long Beach, USA

                Reviewed by: Tim Magnuson, Idaho State University, USA; Yiran Dong, University of Illinois, Urbana-Champaign, USA

                *Correspondence: William P. Inskeep binskeep@ 123456montana.edu ;
                Cristina D. Takacs-Vesbach cvesbach@ 123456unm.edu

                This article was submitted to Extreme Microbiology, a section of the journal Frontiers in Microbiology

                †Present Address: Daniel R. Colman, Thermal Biology Institute and Department of Microbiology and Immunology, Montana State University, Bozeman, MT, USA;

                Ryan deM. Jennings, Mercer University, Macon, GA, USA;

                Kendra R. Maas, Biotechnology-Bioservices Center, University of Connecticut, Storrs, CT, USA

                Article
                10.3389/fmicb.2016.00304
                4791363
                27014227
                193fb1de-cda7-410a-9cd9-0e3c08371575
                Copyright © 2016 Colman, Jay, Inskeep, Jennings, Maas, Rusch and Takacs-Vesbach.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 07 November 2015
                : 24 February 2016
                Page count
                Figures: 8, Tables: 2, Equations: 0, References: 65, Pages: 14, Words: 9353
                Funding
                Funded by: U.S. Department of Energy 10.13039/100000015
                Award ID: CSP 787081
                Award ID: 112443
                Funded by: National Science Foundation 10.13039/100000001
                Award ID: HRD 0832947
                Funded by: Division of Graduate Education 10.13039/100000082
                Award ID: 0654336
                Award ID: 02-06773
                Categories
                Microbiology
                Original Research

                Microbiology & Virology
                aquificales,hot springs,thermotogae,calescamantes,pyropristinus,hyperthermophiles,yellowstone national park

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