Literature DB >> 27795267

High-Quality Draft Genome Sequence of Thermocrinis jamiesonii GBS1T Isolated from Great Boiling Spring, Nevada.

Rakesh Ganji1, Senthil K Murugapiran1, John C Ong1, Namritha Manoharan1, Marcel Huntemann2, Alicia Clum2, Manoj Pillay2, Krishnaveni Palaniappan2, Neha Varghese2, Natalia Mikhailova2, Dimitrios Stamatis2, T B K Reddy2, Chew Yee Ngan2, Chris Daum2, Kecia Duffy2, Nicole Shapiro2, Victor Markowitz2, Natalia Ivanova2, Nikos Kyrpides2, Tanja Woyke2, Jeremy A Dodsworth3, Brian P Hedlund4,5.   

Abstract

The draft genome of Thermocrinis jamiesonii GBS1T is 1,315,625 bp in 10 contigs and encodes 1,463 predicted genes. The presence of sox genes and various glycoside hydrolases and the absence of uptake NiFe hydrogenases (hyaB) are consistent with a requirement for thiosulfate and suggest the ability to use carbohydrate polymers.
Copyright © 2016 Ganji et al.

Entities:  

Year:  2016        PMID: 27795267      PMCID: PMC5073254          DOI: 10.1128/genomeA.01112-16

Source DB:  PubMed          Journal:  Genome Announc


GENOME ANNOUNCEMENT

Strain GBS1T was isolated from the water column of Great Boiling Spring (GBS), Nevada, and described as a novel species, Thermocrinis jamiesonii, belonging to the family Aquificaceae (1). It is thermophilic, autotrophic, obligately microaerophilic, and grows chemolithoheterotrophically on peptone, casamino acids, or acetate with thiosulfate as the electron donor (1). It is different from other species of Thermocrinis in its use of thiosulfate as the sole electron donor and its high tolerance for NaCl (1). The draft genome of strain GBS1T was generated at the U.S. Department of Energy (DOE) Joint Genome Institute (JGI) using Illumina HiSeq 2000 sequencing technology yielding 18,071,694 filtered reads totaling 2.7 Gbp. Details of library construction and sequencing performed at JGI can be found at http://www.jgi.doe.gov. Filtered reads were assembled using Velvet (ver. 1.2.07) and Allpaths–LG (ver. r46652) (2, 3). The genome was annotated using Prodigal ver. 2.5 (4), as part of the JGI microbial annotation pipeline (5). The T. jamiesonii GBS1T draft genome is 1,315,625 bp in 10 contigs, and encodes 1,463 predicted genes, including 1,415 protein-coding genes, 43 tRNA genes, and a single rRNA operon. Analysis of the genome for carbohydrate-active enzymes (CAZymes) (6) revealed 36 CAZymes, 6 of which are glycoside hydrolases (GHs) probably involved in degradation of chitodextrins/peptidoglycans (3 genes belonging to the GH23 family) and starch (GH13, GH57, GH77). These genes suggest GBS1T might be capable of growth on some polymers, such as starch, as has been shown for Thermocrinis minervae (7). These cultivation and genomic data, along with in situ experiments, suggest some Aquificales to be mixotrophic or heterotrophic, rather than strictly autotrophic (8). Consistent with the previous report (1), the GBS1T genome encodes a sox gene cluster (soxABXYZ) required for thiosulfate oxidation (9). The genome lacks an NiFe hydrogenase (hyaB) and a canonical formate dehydrogenase (fdhA), which is consistent with the inability of GBS1T to grow with H2 or formate as electron donors. However, the GBS water metagenome (JGI taxon identification number 2084038020; hyaB: GBSWBa_00119800; fdhA: GBSWBa_00059550) and a fraction of the Thermocrinis population in GBS has hyaB and/or fdhA (10). A variety of Aquificales fix CO2 via the reverse tricarboxylic acid (rTCA) cycle, including other Thermocrinis species, Aquifex, and Hydrogenobacter (11). The GBS1T draft genome lacks 2-oxoglutarate-ferredoxin oxidoreductase, which is required for the rTCA cycle, but possesses other key enzymes, such as citryl-CoA lyase, citryl-CoA synthetase, and fumarate reductase (11). GBS1T is capable of autotrophic growth, and the GBS water metagenome contains genes with high nucleotide identity to the Thermocrinis albus 2-oxoglutarate-ferredoxin oxidoreductase (GBSWBa_00110880), so it seems likely that GBS1T possesses this gene but it is not present in the assembly. Though neither motility nor flagella was observed in cultures of GBS1T (1), its genome has all the genes required for flagellar assembly, L rings, and P rings. The GBS1T genome encodes capacity to synthesize C16:0, C18:0, and C18:1ω9c fatty acids, which were abundant cellular fatty acids along with the Aquificales C20–22 signature lipids (12) under standard growth conditions.

Accession number(s).

The T. jamiesonii GBS1T genome sequence is available in GenBank under the accession numbers JNIE01000001 to JNIE01000010. The data are also available from GenBank (NZ_JNIE00000000.1; GI: 657836485) and from the Joint Genome Institute (JGI) Integrated Microbial Genomes (IMG) system (2562617198) (13).
  13 in total

1.  High-quality draft assemblies of mammalian genomes from massively parallel sequence data.

Authors:  Sante Gnerre; Iain Maccallum; Dariusz Przybylski; Filipe J Ribeiro; Joshua N Burton; Bruce J Walker; Ted Sharpe; Giles Hall; Terrance P Shea; Sean Sykes; Aaron M Berlin; Daniel Aird; Maura Costello; Riza Daza; Louise Williams; Robert Nicol; Andreas Gnirke; Chad Nusbaum; Eric S Lander; David B Jaffe
Journal:  Proc Natl Acad Sci U S A       Date:  2010-12-27       Impact factor: 11.205

2.  Velvet: algorithms for de novo short read assembly using de Bruijn graphs.

Authors:  Daniel R Zerbino; Ewan Birney
Journal:  Genome Res       Date:  2008-03-18       Impact factor: 9.043

3.  Community microrespirometry and molecular analyses reveal a diverse energy economy in Great Boiling Spring and Sandy's Spring West in the U.S. Great Basin.

Authors:  Caitlin N Murphy; Jeremy A Dodsworth; Aaron B Babbitt; Brian P Hedlund
Journal:  Appl Environ Microbiol       Date:  2013-03-08       Impact factor: 4.792

Review 4.  Ecological aspects of the distribution of different autotrophic CO2 fixation pathways.

Authors:  Ivan A Berg
Journal:  Appl Environ Microbiol       Date:  2011-01-07       Impact factor: 4.792

5.  Prodigal: prokaryotic gene recognition and translation initiation site identification.

Authors:  Doug Hyatt; Gwo-Liang Chen; Philip F Locascio; Miriam L Land; Frank W Larimer; Loren J Hauser
Journal:  BMC Bioinformatics       Date:  2010-03-08       Impact factor: 3.169

6.  Thermocrinis minervae sp. nov., a hydrogen- and sulfur-oxidizing, thermophilic member of the Aquificales from a Costa Rican terrestrial hot spring.

Authors:  Sara L Caldwell; Yitai Liu; Isabel Ferrera; Terry Beveridge; Anna-Louise Reysenbach
Journal:  Int J Syst Evol Microbiol       Date:  2009-08-03       Impact factor: 2.747

7.  Spatial and temporal variability of biomarkers and microbial diversity reveal metabolic and community flexibility in Streamer Biofilm Communities in the Lower Geyser Basin, Yellowstone National Park.

Authors:  F Schubotz; D R Meyer-Dombard; A S Bradley; H F Fredricks; K-U Hinrichs; E L Shock; R E Summons
Journal:  Geobiology       Date:  2013-08-28       Impact factor: 4.407

8.  Thermocrinis jamiesonii sp. nov., a thiosulfate-oxidizing, autotropic thermophile isolated from a geothermal spring.

Authors:  Jeremy A Dodsworth; John C Ong; Amanda J Williams; Alice C Dohnalkova; Brian P Hedlund
Journal:  Int J Syst Evol Microbiol       Date:  2015-09-29       Impact factor: 2.747

9.  dbCAN: a web resource for automated carbohydrate-active enzyme annotation.

Authors:  Yanbin Yin; Xizeng Mao; Jincai Yang; Xin Chen; Fenglou Mao; Ying Xu
Journal:  Nucleic Acids Res       Date:  2012-05-29       Impact factor: 16.971

10.  The standard operating procedure of the DOE-JGI Microbial Genome Annotation Pipeline (MGAP v.4).

Authors:  Marcel Huntemann; Natalia N Ivanova; Konstantinos Mavromatis; H James Tripp; David Paez-Espino; Krishnaveni Palaniappan; Ernest Szeto; Manoj Pillay; I-Min A Chen; Amrita Pati; Torben Nielsen; Victor M Markowitz; Nikos C Kyrpides
Journal:  Stand Genomic Sci       Date:  2015-10-26
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