Literature DB >> 25414492

Draft Genome Sequence of Nitrincola sp. Strain A-D6, an Arsenic-Resistant Gammaproteobacterium Isolated from a Salt Flat.

Natalia Valdés1, Javier Rivera-Araya1, Jonathan Bijman2, Lorena Escudero, Cecilia Demergasso3, Sebastián Fernández2, Alonso Ferrer1, Renato Chávez1, Gloria Levicán4.   

Abstract

We report Nitrincola sp. strain A-D6, which was characterized as an arsenic-resistant bacterium isolated from the Ascotán Salt Flat in northern Chile. The size of the genome is 3,795,776 bp, with a G+C content of 49.96%. Genes for the arsenic-resistant Ars system and arsenic oxidation have been encoded.
Copyright © 2014 Valdés et al.

Entities:  

Year:  2014        PMID: 25414492      PMCID: PMC4239347          DOI: 10.1128/genomeA.01144-14

Source DB:  PubMed          Journal:  Genome Announc


GENOME ANNOUNCEMENT

Arsenic (As) is a ubiquitous element present in the environment in different forms (1). Inorganic arsenic, most often in trivalent or pentavalent form, is the most abundant species of As in nature and is commonly present in soil, water, and food (2). This metalloid is extremely toxic to living organisms and its toxicity is primarily based on its chemical speciation. However, some microorganisms cope with arsenic toxicity in a variety of different ways (1, 3, 4). Such microorganisms therefore play an important role in the arsenic geocycle (5). Nitrincola sp. strain A-D6 was isolated from Salar de Ascotán, a circum-neutral and arsenic-containing salt flat environment in northern Chile. The Nitrincola genus comprises aerobic and Gram-negative bacteria belonging to the Gammaproteobacteria subdivision (6). This report can shed light on the molecular mechanisms involved in arsenic metabolism in this bacterium and its role in the biogeochemical cycle of arsenic in this extreme environment. The genome of strain A-D6 was sequenced using the Ion Torrent PGM platform and single-end libraries. The low-quality sequences were examined by FastQC (version 0.10.1; Babraham Institute [http://www.bioinformatics.bbsrc.ac.uk/projects/fastqc/]) and then trimmed by Trimmomatic version 0.32 (7) before assembly. The trimmed sequence were assembled de novo using a coverage assembled of 40×, with Mira assembler version 4.0.2 (8) and the CAP3 (9) program. This resulted in 117 contigs. Contig sizes range from 850 to 121,978 bp (N50, 52,683 bp). The length of the total draft genome of Nitrincola sp. strain A-D6 is 3,795,776 bp, with a G+C content of 49.96%. The annotation of the assembled genome was submitted to the RAST (Rapid Annotation using Subsystem Technology) server (10). The tRNA genes were detected by tRNAscan-SE version 1.23 (11) and the rRNA with RNAmmer (12). The draft genome was shown to encode 43 tRNA sequences, one complete 5S-16S-23S operon, and 4,401 protein-coding genes, 22.27% of which were assigned hypothetical functions. This hypothetical set was assigned to 4 clusters of orthologous groups that comprise a metabolic cluster with 662 genes, a genetic information processing cluster with 187 genes, an environmental information processing cluster with 272 genes, and a cellular process cluster with 99 genes. The genes responsible for arsenic metabolism include arsenite oxidase small subunit (aioA) and large subunit (aioB), and an azu gene encoding for the physiological electron acceptor azurin (13). The genes responsible for arsenic resistance include an Ars system (arsRDACH). ArsC from the Ars system is a cytoplasmic arsenate reductase that reduces As(V) to As(III) (1). ArsD represses upper expression levels of the ars operon in the absence of As(III). ArsA is an ATPase that converts membrane potential to ATP, which is usually hydrolyzed by ArsB, making As(III) efflux more efficient. ArsB is an integral membrane protein that pumps As(III) out of the cell (1), however a canonical arsB gene is not encoded in the genome of this bacterium. Interestingly, Nitrincola sp. has a gene that encodes for the Acr3 extrusion pump (14). Thus, Nitrincola sp. strain A-D6 possesses a complete set of genes for dissimilatory oxidation and a system for reducing and extruding arsenic.

Nucleotide sequence accession numbers.

This whole-genome shotgun project has been deposited at DDBJ/EMBL/GenBank under the accession number JRLB00000000. The version described in this paper is version JRLB01000000.
  13 in total

1.  tRNAscan-SE: a program for improved detection of transfer RNA genes in genomic sequence.

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Journal:  Nucleic Acids Res       Date:  1997-03-01       Impact factor: 16.971

Review 2.  Arsenic metabolism by microbes in nature and the impact on arsenic remediation.

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4.  Nitrincola lacisaponensis gen. nov., sp. nov., a novel alkaliphilic bacterium isolated from an alkaline, saline lake.

Authors:  Pedro A Dimitriu; Sanjay K Shukla; Jennifer Conradt; M Carmen Márquez; Antonio Ventosa; Anne Maglia; Brent M Peyton; Holly C Pinkart; Melanie R Mormile
Journal:  Int J Syst Evol Microbiol       Date:  2005-11       Impact factor: 2.747

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Review 6.  The bile/arsenite/riboflavin transporter (BART) superfamily.

Authors:  Nahla M Mansour; Mrinalini Sawhney; Dorjee G Tamang; Christian Vogl; Milton H Saier
Journal:  FEBS J       Date:  2007-02       Impact factor: 5.542

Review 7.  Microbial responses to environmental arsenic.

Authors:  David Páez-Espino; Javier Tamames; Víctor de Lorenzo; David Cánovas
Journal:  Biometals       Date:  2009-01-07       Impact factor: 2.949

8.  How prokaryotes deal with arsenic(†).

Authors:  Djamila Slyemi; Violaine Bonnefoy
Journal:  Environ Microbiol Rep       Date:  2011-11-03       Impact factor: 3.541

9.  RNAmmer: consistent and rapid annotation of ribosomal RNA genes.

Authors:  Karin Lagesen; Peter Hallin; Einar Andreas Rødland; Hans-Henrik Staerfeldt; Torbjørn Rognes; David W Ussery
Journal:  Nucleic Acids Res       Date:  2007-04-22       Impact factor: 16.971

10.  The RAST Server: rapid annotations using subsystems technology.

Authors:  Ramy K Aziz; Daniela Bartels; Aaron A Best; Matthew DeJongh; Terrence Disz; Robert A Edwards; Kevin Formsma; Svetlana Gerdes; Elizabeth M Glass; Michael Kubal; Folker Meyer; Gary J Olsen; Robert Olson; Andrei L Osterman; Ross A Overbeek; Leslie K McNeil; Daniel Paarmann; Tobias Paczian; Bruce Parrello; Gordon D Pusch; Claudia Reich; Rick Stevens; Olga Vassieva; Veronika Vonstein; Andreas Wilke; Olga Zagnitko
Journal:  BMC Genomics       Date:  2008-02-08       Impact factor: 3.969

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  1 in total

1.  First draft genome sequence of a strain from the genus Fusibacter isolated from Salar de Ascotán in Northern Chile.

Authors:  Antonio E Serrano; Lorena V Escudero; Cinthya Tebes-Cayo; Mauricio Acosta; Olga Encalada; Sebastián Fernández-Moroso; Cecilia Demergasso
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