Nanopore Long-Read Guided Complete Genome Assembly of Hydrogenophaga intermedia , and Genomic Insights into 4-Aminobenzenesulfonate, p -Aminobenzoic Acid and Hydrogen Metabolism in the Genus Hydrogenophaga
We improved upon the previously reported draft genome of strain PBC, a 4-aminobenzenesulfonate-degrading bacterium, by supplementing the assembly with Nanopore long reads which enabled the reconstruction of the genome as a single contig. From the complete genome, major genes responsible for the cata...
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Published in: | Frontiers in microbiology Vol. 8; p. 1880 |
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Abstract | We improved upon the previously reported draft genome of
strain PBC, a 4-aminobenzenesulfonate-degrading bacterium, by supplementing the assembly with Nanopore long reads which enabled the reconstruction of the genome as a single contig. From the complete genome, major genes responsible for the catabolism of 4-aminobenzenesulfonate in strain PBC are clustered in two distinct genomic regions. Although the catabolic genes for 4-sulfocatechol, the deaminated product of 4-aminobenzenesulfonate, are only found in
, the
operon responsible for the first deamination step of 4-aminobenzenesulfonate is conserved in various
strains. The absence of
gene in the complete genome of
PBC is consistent with its
-aminobenzoic acid (pABA) auxotrophy but surprisingly comparative genomics analysis of 14
genomes indicate that pABA auxotrophy is not an uncommon feature among members of this genus. Of even more interest, several
strains do not possess the genomic potential for hydrogen oxidation, calling for a revision to the taxonomic description of
as "hydrogen eating bacteria." |
---|---|
AbstractList | We improved upon the previously reported draft genome of Hydrogenophaga intermedia strain PBC, a 4-aminobenzenesulfonate-degrading bacterium, by supplementing the assembly with Nanopore long reads which enabled the reconstruction of the genome as a single contig. From the complete genome, major genes responsible for the catabolism of 4-aminobenzenesulfonate in strain PBC are clustered in two distinct genomic regions. Although the catabolic genes for 4-sulfocatechol, the deaminated product of 4-aminobenzenesulfonate, are only found in H. intermedia, the sad operon responsible for the first deamination step of 4-aminobenzenesulfonate is conserved in various Hydrogenophaga strains. The absence of pabB gene in the complete genome of H. intermedia PBC is consistent with its p-aminobenzoic acid (pABA) auxotrophy but surprisingly comparative genomics analysis of 14 Hydrogenophaga genomes indicate that pABA auxotrophy is not an uncommon feature among members of this genus. Of even more interest, several Hydrogenophaga strains do not possess the genomic potential for hydrogen oxidation, calling for a revision to the taxonomic description of Hydrogenophaga as “hydrogen eating bacteria.” We improved upon the previously reported draft genome of strain PBC, a 4-aminobenzenesulfonate-degrading bacterium, by supplementing the assembly with Nanopore long reads which enabled the reconstruction of the genome as a single contig. From the complete genome, major genes responsible for the catabolism of 4-aminobenzenesulfonate in strain PBC are clustered in two distinct genomic regions. Although the catabolic genes for 4-sulfocatechol, the deaminated product of 4-aminobenzenesulfonate, are only found in , the operon responsible for the first deamination step of 4-aminobenzenesulfonate is conserved in various strains. The absence of gene in the complete genome of PBC is consistent with its -aminobenzoic acid (pABA) auxotrophy but surprisingly comparative genomics analysis of 14 genomes indicate that pABA auxotrophy is not an uncommon feature among members of this genus. Of even more interest, several strains do not possess the genomic potential for hydrogen oxidation, calling for a revision to the taxonomic description of as "hydrogen eating bacteria." We improved upon the previously reported draft genome of Hydrogenophaga intermedia strain PBC, a 4-aminobenzenesulfonate-degrading bacterium, by supplementing the assembly with Nanopore long reads which enabled the reconstruction of the genome as a single contig. From the complete genome, major genes responsible for the catabolism of 4-aminobenzenesulfonate in strain PBC are clustered in two distinct genomic regions. Although the catabolic genes for 4-sulfocatechol, the deaminated product of 4-aminobenzenesulfonate, are only found in H. intermedia , the sad operon responsible for the first deamination step of 4-aminobenzenesulfonate is conserved in various Hydrogenophaga strains. The absence of pabB gene in the complete genome of H. intermedia PBC is consistent with its p -aminobenzoic acid (pABA) auxotrophy but surprisingly comparative genomics analysis of 14 Hydrogenophaga genomes indicate that pABA auxotrophy is not an uncommon feature among members of this genus. Of even more interest, several Hydrogenophaga strains do not possess the genomic potential for hydrogen oxidation, calling for a revision to the taxonomic description of Hydrogenophaga as “hydrogen eating bacteria.” |
Author | Gan, Han M Lee, Yin P Austin, Christopher M |
AuthorAffiliation | 2 Genomics Facility, Tropical Medicine and Biology Platform, Monash University Malaysia , Bandar Sunway , Malaysia 3 School of Science, Monash University Malaysia , Bandar Sunway , Malaysia 1 Centre for Integrative Ecology, School of Life and Environmental Sciences, Deakin University , Geelong, VIC , Australia |
AuthorAffiliation_xml | – name: 1 Centre for Integrative Ecology, School of Life and Environmental Sciences, Deakin University , Geelong, VIC , Australia – name: 3 School of Science, Monash University Malaysia , Bandar Sunway , Malaysia – name: 2 Genomics Facility, Tropical Medicine and Biology Platform, Monash University Malaysia , Bandar Sunway , Malaysia |
Author_xml | – sequence: 1 givenname: Han M surname: Gan fullname: Gan, Han M organization: School of Science, Monash University Malaysia, Bandar Sunway, Malaysia – sequence: 2 givenname: Yin P surname: Lee fullname: Lee, Yin P organization: School of Science, Monash University Malaysia, Bandar Sunway, Malaysia – sequence: 3 givenname: Christopher M surname: Austin fullname: Austin, Christopher M organization: School of Science, Monash University Malaysia, Bandar Sunway, Malaysia |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29046667$$D View this record in MEDLINE/PubMed |
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Keywords | Hydrogenophaga phylogeny hydrogen metabolism Nanopore comparative genomics |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Edited by: John R. Battista, Louisiana State University, United States This article was submitted to Evolutionary and Genomic Microbiology, a section of the journal Frontiers in Microbiology Reviewed by: Nikolai Ravin, Research Center for Biotechnology (RAS), Russia; Rommel Thiago Juca Ramos, Federal University of Pará, Brazil |
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strain PBC, a 4-aminobenzenesulfonate-degrading bacterium, by supplementing the assembly with Nanopore... We improved upon the previously reported draft genome of Hydrogenophaga intermedia strain PBC, a 4-aminobenzenesulfonate-degrading bacterium, by supplementing... We improved upon the previously reported draft genome of Hydrogenophaga intermedia strain PBC, a 4-aminobenzenesulfonate-degrading bacterium, by supplementing... |
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SubjectTerms | comparative genomics hydrogen metabolism Hydrogenophaga Microbiology Nanopore phylogeny |
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Title | Nanopore Long-Read Guided Complete Genome Assembly of Hydrogenophaga intermedia , and Genomic Insights into 4-Aminobenzenesulfonate, p -Aminobenzoic Acid and Hydrogen Metabolism in the Genus Hydrogenophaga |
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