Literature DB >> 30533623

Draft Genome Sequences of the Nitrate-Dependent Iron-Oxidizing Proteobacteria Acidovorax sp. Strain BoFeN1 and Paracoccus pantotrophus Strain KS1.

A Price1, M C Macey1, J Miot2, K Olsson-Francis1.   

Abstract

The draft genomes of the nitrate-dependent iron-oxidizing bacteria Acidovorax sp. strain BoFeN1 and Paracoccus pantotrophus strain KS1 are presented. These genomes supply supporting data to investigations of the mechanisms underlying this anaerobic form of microbial biogeochemical iron cycling.

Entities:  

Year:  2018        PMID: 30533623      PMCID: PMC6256601          DOI: 10.1128/MRA.01050-18

Source DB:  PubMed          Journal:  Microbiol Resour Announc        ISSN: 2576-098X


ANNOUNCEMENT

Acidovorax sp. strain BoFeN1 and Paracoccus pantotrophus strain KS1 have both demonstrated the capability to perform nitrate-dependent Fe2+ oxidation (NDFO), whereby Fe3+ precipitates are formed during microbial nitrate reduction (1, 2). NDFO is a geomicrobiological process which has been recognized for the past 2 decades (3) and is responsible for the production of Fe3+-bearing minerals in anaerobic, circumneutral, reducing environments under conditions similar to those that were prevalent on the early Earth and ancient Mars (1, 4–6). Despite this potential importance in the early history of life, the putative underlying mechanisms are largely unconfirmed experimentally (7), despite some advances (8, 9). Acidovorax sp. strain BoFeN1 is a Gram-negative, rod-shaped bacterium belonging to the family Comamonadaceae in the order Burkholderiales of the class Betaproteobacteria. Acidovorax sp. strain BoFeN1 was isolated from littoral sediments of Lake Constance on the Germany-Switzerland border and assigned to the genus Acidovorax based on 16S rRNA gene sequence analysis (1). This isolate was donated by Jennyfer Miot of the Mineralogy, Material Physics and Cosmochemistry Institute (IMPMC) in Paris, France. Paracoccus pantotrophus strain KS1 is a Gram-negative, motile coccoid bacterium belonging to the family Rhodobacteraceae in the order Rhodobacterales, in the class Alphaproteobacteria. Paracoccus pantotrophus strain KS1 was isolated from soil at Kew Gardens in the United Kingdom and was originally reported as a member of the genus Thiobacillus but was later reclassified to the genus Paracoccus based on the 16S rRNA gene sequence (10, 11). This strain was purchased as a live culture (DSM 11072) from the German Collection of Microorganisms and Cell Cultures (DSMZ) in Leibniz, Germany. The two strains were maintained in pure culture in aerobic nutrient medium (5.0 g liter−1 peptone and 3.0 g liter−1 meat extract) at 30°C prior to DNA extraction and genome sequencing, which was performed by MicrobesNG (https://microbesng.uk/) using the Illumina MiSeq platform with 2 × 250-bp paired-end reads. Trimmed reads were produced using Trimmomatic version 0.30 (http://www.usadellab.org/cms/?page=trimmomatic) with a sliding window quality cutoff of Q15, and de novo assembly was performed using SPAdes version 3.7 (http://cab.spbu.ru/software/spades/) (12, 13). Coverage of 30× was achieved during sequencing, and genome annotation was performed using the RAST annotation server version 2.0 (http://rast.nmpdr.org/rast.cgi) via the classic RAST pipeline (14). The draft genome of strain Acidovorax sp. strain BoFeN1 consisted of 4.06 Mb in 184 contigs (N50 = 37,384), with a GC content of 63.77%. A total of 3,794 protein-coding sequences were predicted from the annotated genome, with 50 tRNAs identified using the ARAGORN version 1.1 tRNA detection program (http://mbio-serv2.mbioekol.lu.se/ARAGORN/) (15). The closest match for the 16S rRNA gene was identified in the GenBank database, by using the BLASTN program (https://blast.ncbi.nlm.nih.gov/Blast.cgi), as Acidovorax defluvii strain BSB411 (99% similarity; GenBank accession number NR_026506). The draft genome of Paracoccus pantotrophus strain KS1 consisted of 4.16 Mb in 227 contigs (N50 = 36,889), with a GC content of 67.69%. A total of 3,941 protein-coding sequences and 54 tRNAs were predicted from the annotated genome. The nearest 16S rRNA gene sequence was identified using BLASTN, with a best match as Paracoccus pantotrophus (100%; accession number AB098590). Neither genome contained a dedicated ferroxidase, suggesting that NDFO in these strains is not a direct enzymatic process to acquire electrons. Full denitrification pathways were confirmed in both strains by the presence of nitrogen species reductase genes (nar, nir, nor, and nos), with additional genes for a periplasmic nitrate reductase (Nap) in the Paracoccus pantotrophus strain KS1 genome.

Data availability.

DDBJ/ENA/GenBank accession numbers have been assigned for Acidovorax sp. strain BoFeN1 (QOZT00000000) and Paracoccus pantotrophus strain KS1 (QOZU00000000). Raw sequencing reads for Acidovorax sp. strain BoFeN1 (SRP157586) and Paracoccus pantotrophus strain KS1 (SRP157588) are available in the NCBI Sequence Read Archive.
  12 in total

1.  ARAGORN, a program to detect tRNA genes and tmRNA genes in nucleotide sequences.

Authors:  Dean Laslett; Bjorn Canback
Journal:  Nucleic Acids Res       Date:  2004-01-02       Impact factor: 16.971

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3.  Nitrate-dependent [Fe(II)EDTA]2- oxidation by Paracoccus ferrooxidans sp. nov., isolated from a denitrifying bioreactor.

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Journal:  Syst Appl Microbiol       Date:  2005-09-01       Impact factor: 4.022

4.  Autotrophic growth on carbon disulfide is a property of novel strains of Paracoccus denitrificans.

Authors:  S L Jordan; I R McDonald; A J Kraczkiewicz-Dowjat; D P Kelly; F A Rainey; J C Murrell; A P Wood
Journal:  Arch Microbiol       Date:  1997-09       Impact factor: 2.552

Review 5.  Insight into the evolution of the iron oxidation pathways.

Authors:  Marianne Ilbert; Violaine Bonnefoy
Journal:  Biochim Biophys Acta       Date:  2012-10-06

6.  Fe(II) oxidation is an innate capability of nitrate-reducing bacteria that involves abiotic and biotic reactions.

Authors:  Hans K Carlson; Iain C Clark; Steven J Blazewicz; Anthony T Iavarone; John D Coates
Journal:  J Bacteriol       Date:  2013-05-17       Impact factor: 3.490

7.  Toward a mechanistic understanding of anaerobic nitrate-dependent iron oxidation: balancing electron uptake and detoxification.

Authors:  Hans K Carlson; Iain C Clark; Ryan A Melnyk; John D Coates
Journal:  Front Microbiol       Date:  2012-02-20       Impact factor: 5.640

8.  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

9.  Fe biomineralization mirrors individual metabolic activity in a nitrate-dependent Fe(II)-oxidizer.

Authors:  Jennyfer Miot; Laurent Remusat; Elodie Duprat; Adriana Gonzalez; Sylvain Pont; Mélanie Poinsot
Journal:  Front Microbiol       Date:  2015-09-08       Impact factor: 5.640

10.  Trimmomatic: a flexible trimmer for Illumina sequence data.

Authors:  Anthony M Bolger; Marc Lohse; Bjoern Usadel
Journal:  Bioinformatics       Date:  2014-04-01       Impact factor: 6.937

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2.  Interactions of Vallisneria natans and Iron-Oxidizing Bacteria Enhance Iron-Bound Phosphorus Formation in Eutrophic Lake Sediments.

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4.  Unchanged nitrate and nitrite isotope fractionation during heterotrophic and Fe(II)-mixotrophic denitrification suggest a non-enzymatic link between denitrification and Fe(II) oxidation.

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