Literature DB >> 23723392

Draft Genome Sequence of the Deep-Sea Bacterium Shewanella benthica Strain KT99.

F M Lauro1, R A Chastain, S Ferriera, J Johnson, A A Yayanos, D H Bartlett.   

Abstract

We report the draft genome sequence of the obligately piezophilic Shewanella benthica strain KT99 isolated from the abyssal South Pacific Ocean. Strain KT99 is the first piezophilic isolate from the Tonga-Kermadec trench, and its genome provides many clues on high-pressure adaptation and the evolution of deep-sea piezophilic bacteria.

Entities:  

Year:  2013        PMID: 23723392      PMCID: PMC3668000          DOI: 10.1128/genomeA.00210-13

Source DB:  PubMed          Journal:  Genome Announc


GENOME ANNOUNCEMENT

Members of the genus Shewanella are Gram-negative gammaproteobacteria that are common in aquatic environments and are well known for their multifaceted respiration systems. Despite their distribution, only 2 species are found in ocean waters deeper than 2,000 m: Shewanella benthica and Shewanella violacea (1). These isolates are usually piezophilic and psychrophilic (2, 3). On 17 October 2001, an insulated trap baited with scraps of mahi-mahi was deployed as a free vehicle into the Kermadec Trench at 32° 01.07’S, 177° 20.99'W over a depth of 9,856 m for 14 h. The temperature at that depth was ~1.8°C, and recovered trapped amphipods (dead from decompression) were found at <6°C and were immediately moved to a cold room. Several amphipods were heat sealed in plastic bags and compressed to 99.7 MPa (4). One of these bags with decayed amphipods was used, after completion of the cruise, to grow bacterial colonies using methods previously described (4) at 99.7 MPa and ~2°C. One of the colonies was dubbed strain KT99. Freshly inoculated cultures (1:1,000 dilution) of S. benthica KT99 reach the stationary phase in ~160 h at 10°C and 90 MPa. No growth is observed at the same temperature at 40 MPa or 140 MPa. Genomic DNA was purified from 1.5 liters of culture grown at 90 MPa and 10°C. The cells were harvested, washed once in phosphate-buffered saline (PBS), and resuspended in 2.4 ml of nuclei lysis buffer (Promega). The extraction was completed according to the protocol of the Wizard Genomic DNA kit (Promega). The precipitated DNA pellet was further purified by resuspension in 1.2 ml of of Tris-EDTA (TE) buffer, extraction once with 1.2 ml of phenol-chloroform (pH 8.0) and once with 1.2 ml of chloroform, and precipitation by centrifugation (16,000 × g, 10 min, 4°C) with 120 µl of sodium acetate (3 M [pH 4.8]) and 4 ml of ethanol (100%). A small aliquot was used for quantification and quality control. The draft genome sequence was determined by shotgun sequencing as follows: two genomic libraries with insert sizes of 4 kb (plasmid) and 40 kb (fosmid) were constructed. The prepared plasmid and fosmid clones were sequenced from both ends to provide paired-end reads on ABI 3730xl DNA sequencers (Applied Biosystems). Successful reads were used as input values for the Celera Assembler. The whole-genome shotgun (WGS) sequence produced by the assembler was then annotated using the PGAAP at NCBI. The genome of S. benthica KT99 has 4.35 million bp encoding 4,235 predicted open reading frames (ORFs), with a G+C content of 46%. There are multiple predicted copies of the rRNA operon that carry elongated stem-loops found only in piezophilic bacteria (5). The genome contains complete pathways for a heterotrophic lifestyle, such as the complete glycolytic and tricarboxylic acid (TCA) pathways. The COG composition compared to that of the sister species Shewanella frigidimarina NCIMB400 (accession no. NC_008345) was found to be statistically enriched in the genes for DNA replication, recombination, and repair (COG category L) and, in particular, for 4 different classes of transposases (COG2826, COG3436, COG3676, COG5433). Deep-sea metagenomes are overrepresented in mobile elements (6, 7) that might have functional roles in the hadal and abyssal ocean (7). The genome also encoded a type A fatty acid synthase-polyketide synthase (FAS-PKS) system (8) for the synthesis of polyunsaturated fatty acids, such as eicosapentaenoic acid (EPA) (20:5, n-3) and docosahexaenoic acid (DHA) (22:6, n-3). S. benthica KT99 has been shown to produce EPA and traces of DHA (9), and the resulting increase in membrane unsaturation might play a role in low-temperature and high-pressure environments (10). There was no evidence for the presence of light-activated photolyases, a hallmark for autochthony in deep-sea bacteria (9).

Nucleotide sequence accession number.

The Whole-Genome Shotgun project was deposited in NCBI under the accession no. ABIC00000000.
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Authors:  Federico M Lauro; Roger A Chastain; Lesley E Blankenship; A Aristides Yayanos; Douglas H Bartlett
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2.  Community genomics among stratified microbial assemblages in the ocean's interior.

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Authors:  Federico M Lauro; Douglas H Bartlett
Journal:  Extremophiles       Date:  2007-01-17       Impact factor: 2.395

4.  Biochemical function and ecological significance of novel bacterial lipids in deep-sea procaryotes.

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5.  Extremely barophilic bacteria isolated from the Mariana Trench, Challenger Deep, at a depth of 11,000 meters.

Authors:  C Kato; L Li; Y Nogi; Y Nakamura; J Tamaoka; K Horikoshi
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6.  Isolation of extremophiles with the detection and retrieval of Shewanella strains in deep-sea sediments from the west Pacific.

Authors:  Fengping Wang; Peng Wang; Mingxia Chen; Xiang Xiao
Journal:  Extremophiles       Date:  2003-12-13       Impact factor: 2.395

7.  Taxonomic studies of deep-sea barophilic Shewanella strains and description of Shewanella violacea sp. nov.

Authors:  Y Nogi; C Kato; K Horikoshi
Journal:  Arch Microbiol       Date:  1998-10       Impact factor: 2.552

8.  Widespread occurrence of secondary lipid biosynthesis potential in microbial lineages.

Authors:  Christine N Shulse; Eric E Allen
Journal:  PLoS One       Date:  2011-05-19       Impact factor: 3.240

9.  Going deeper: metagenome of a hadopelagic microbial community.

Authors:  Emiley A Eloe; Douglas W Fadrosh; Mark Novotny; Lisa Zeigler Allen; Maria Kim; Mary-Jane Lombardo; Joyclyn Yee-Greenbaum; Shibu Yooseph; Eric E Allen; Roger Lasken; Shannon J Williamson; Douglas H Bartlett
Journal:  PLoS One       Date:  2011-05-24       Impact factor: 3.240

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1.  Microbial diversity and adaptation to high hydrostatic pressure in deep-sea hydrothermal vents prokaryotes.

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Journal:  Extremophiles       Date:  2015-06-23       Impact factor: 2.395

2.  Stability of cytochromes c' from psychrophilic and piezophilic Shewanella species: implications for complex multiple adaptation to low temperature and high hydrostatic pressure.

Authors:  Asako Suka; Hiroya Oki; Yuki Kato; Kazuki Kawahara; Tadayasu Ohkubo; Takahiro Maruno; Yuji Kobayashi; Sotaro Fujii; Satoshi Wakai; Lisa Lisdiana; Yoshihiro Sambongi
Journal:  Extremophiles       Date:  2019-01-28       Impact factor: 2.395

3.  An extracytoplasmic function sigma factor-dependent periplasmic glutathione peroxidase is involved in oxidative stress response of Shewanella oneidensis.

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4.  Laboratory investigation of high pressure survival in Shewanella oneidensis MR-1 into the gigapascal pressure range.

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5.  Genome-Wide Detection of Small Regulatory RNAs in Deep-Sea Bacterium Shewanella piezotolerans WP3.

Authors:  Muhammad Z Nawaz; Huahua Jian; Ying He; Lei Xiong; Xiang Xiao; Fengping Wang
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6.  In Vivo Water Dynamics in Shewanella oneidensis Bacteria at High Pressure.

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7.  Microbiomes of Hadal Fishes across Trench Habitats Contain Similar Taxa and Known Piezophiles.

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8.  Distinctive gene and protein characteristics of extremely piezophilic Colwellia.

Authors:  Logan M Peoples; Than S Kyaw; Juan A Ugalde; Kelli K Mullane; Roger A Chastain; A Aristides Yayanos; Masataka Kusube; Barbara A Methé; Douglas H Bartlett
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  8 in total

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