J Genomics 2018; 6:122-126. doi:10.7150/jgen.27741
Genomic Analysis of Rhodococcus sp. Br-6, a Bromate Reducing Bacterium Isolated From Soil in Chiba, Japan
1. Institute for Advanced Biosciences, Keio University, Tsuruoka, Yamagata, Japan
2. Faculty of Environment and Information Studies, Keio University, Fujisawa, Kanagawa, Japan
3. Center for Environmental Biology and Ecosystem Studies, National Institute for Environmental Studies, Tsukuba, Ibaraki, Japan
4. Center for Regional Environmental Research, National Institute for Environmental Studies, Tsukuba, Ibaraki, Japan
5. Graduate School of Horticulture, Chiba University, Matsudo City, Chiba, Japan
Ito K, Harada M, Nakajima N, Yamamura S, Tomita M, Suzuki H, Amachi S. Genomic Analysis of Rhodococcus sp. Br-6, a Bromate Reducing Bacterium Isolated From Soil in Chiba, Japan. J Genomics 2018; 6:122-126. doi:10.7150/jgen.27741. Available from http://www.jgenomics.com/v06p0122.htm
Bromate is a byproduct of the ozone disinfection of drinking water. It is a genotoxic carcinogen and causes renal cell tumors in rats. Physicochemical removal of bromate is very difficult, making microbial reduction of bromate to bromide a promising approach to eliminate bromate from water. Rhodococcus sp. Br-6, isolated from soil, can efficiently reduce bromate by using acetate as an electron donor. We determined the draft genome sequence of Rhodococcus sp. Br-6 for the potential practical application of the bromate-reducing bacterium. Core genome phylogeny suggests that the Br-6 strain is most closely related to R. equi. The Br-6 genome contains genes encoding multiple isoforms of diaphorase, previously found to be involved in Br-6-mediated bromate reduction. The genes identified in the present study could be effective targets for experimental studies of microbial bromate reduction in the future.
Keywords: Bromate reducing bacterium, Rhodococcus sp. Br-6, Genome, Phylogeny, Diaphorase.
Chemical compounds are purified by multiple treatment steps at water treatment plants. Common filtration treatments do not remove fungal odor and agricultural chemicals so ozone treatment is commonly used. Bromate is a disinfection byproduct of ozone treatment and is formed from the bromide ion . Bromate is a genotoxic carcinogen that causes renal cell tumors in rats. However, as long as ozone treatment is carried out, it is very difficult to completely remove bromate from the water. The microbial reduction of bromate to bromide is a promising way to remove bromate from drinking water and bromate reduction in biologically activated carbon (BAC) filters can reduce bromate . Several studies have indicated that bacterial communities catalyze bromate reduction. However, to date, few bacteria from such communities have been isolated as pure cultures, and the mechanism of bacterial bromate reduction has not been elucidated. A soil bacterium Rhodococcus sp. Br-6 was previously isolated from soil in Matsudo-city, Chiba, Japan . Strain Br-6 completely reduced 250 μM bromate within 4 days in the presence of acetate as an electron donor under microaerophilic conditions. Interestingly, the bromate reduction rate of strain Br-6 was much faster than that described for other bromate-reducing bacteria .
The genus Rhodococcus comprises more than 40 species, and is widely distributed in the environment . Rhodococcus species have been used for various biotechnological applications including the production of acrylates and bioactive steroids, and fossil fuel desulfurization due to their biodegradative abilities . We determined the draft genome sequence of Rhodococcus sp. Br-6 to understand its detailed metabolism and for the future practical application of bromate-reducing bacteria. We used multiple databases to identify genes involved in bromate reduction by strain Br-6 and assigned functional protein annotations. We also compared the genome sequence of Br-6 with that of sequenced Rhodococcus strains to reconstruct the genome-based phylogenetic tree and to assess the conservation of Br-6 genes in other Rhodococcus genomes.
Materials and Methods
Genome sequencing and assembly
Rhodococcus sp. Br-6 was grown aerobically in a minimal salt medium containing acetate as the carbon source , and DNA was extracted using a DNeasy blood and tissue kit (Qiagen, Hilden, Germany). Whole-genome sequencing was performed using the Illumina MiSeq sequencing platform as per manufacturer's instructions. The sequencer produced 300-bp paired-end reads that were obtained from 550-bp inserts. Quality control and genome assembly were performed as described previously .
The genome was annotated using Prokka v1.11 . A total of 5,186 protein coding DNA sequences (CDSs) were predicted using Prokka for the Br-6 strain. We performed similarity searches of the 5,186 Br-6 proteins against the UniProt Reference Clusters UniRef90 (Release: 07-Sep-2016; Number of clusters: 44,448,796)  using BLASTP  with the E value cutoff of 1e-05 and assigned the most similar (best hit) protein sequence information. The genome was also annotated using KAAS (KEGG Automatic Annotation Server)  for which gene data sets from three Rhodococcus spp. (R. jostii, R. erythropolis PR4, and R. opacus B4) and the default set of organisms (abbreviated as “hsa, dme, cel, ath, sce, cho, eco, nme, hpy, rpr, bsu, lla, cac, mge, mtu, ctr, bbu, syn, bth, dra, aae, mja, ape, rha, rer, and rop” at http://www.genome.jp/tools/kaas/) were selected.
Comparative genomic analysis
For comparative analysis with Rhodococcus sp. Br-6, RefSeq data for the genome sequences of Rhodococcus species including R. defluvii and R. equi  (Table 1) were downloaded from NCBI FTP Site (ftp://ftp.ncbi.nlm.nih.gov/genomes/)  in December 2016.
Homologous groups of genes (representing “protein families”) from multiple Rhodococcus genomes were built using the pan-genome analysis pipeline Roary with the minimum BLASTP percentage identity of 80 . Nucleotide sequence alignments for genes present in a single copy in every genome (“core-genome”) were produced using MAFFT . A phylogenetic tree for the concatenated core gene alignment was reconstructed using the GTR+CAT model of FastTree version 2.1.9 . Based on previous phylogenetic studies , R. triatomae, R. jostii, R. opacus, and R. erythropolis were used as an outgroup for tree rooting. The “drop.tip” function of the package APE (version 5.0) in R (version 3.4.3) was used to remove the outgroup of the phylogenetic tree. The phylogenetic tree was drawn using FigTree version 1.4.3 (http://tree.bio.ed.ac.uk/software/figtree/).
To assess the conservation of the protein-encoding genes of strain Br-6 in other Rhodococcus strains, we performed TBLASTN searches with the E-value cutoff of 1e-5  to compare strain Br-6 protein sequences with whole nucleotide sequences of 13 Rhodococcus strains. This approach can detect genes that were missed due to differences in gene finding algorithms.
Genomic features of the Rhodococcus strains analyzed
|Accession No.||Organism||% GC||Size (bp)||CDS|
|GCF_000196695.1||R. equi 103S||68.8||5,043,170||4,512|
|GCF_000738775.1||R. defluvii strain Ca11||68.7||5,134,337||4,791|
|GCF_002094305.1||R. equi strain DSM 20307||68.8||5,199,710||4,803|
|This study||Rhodococcus sp. Br-6||68.7||5,496,476||5,186|
|GCF_000341795.1||R. triatomae BKS 15-14||69.0||5,824,349||5,269|
|GCF_000454045.1||R. erythropolis CCM2595||62.5||6,371,421||5,828|
|GCF_000696675.2||R. erythropolis R138||62.3||6,806,506||6,130|
|GCF_000975175.1||R. erythropolis strain BG43||62.3||6,865,205||6,158|
|GCF_000010105.1||R. erythropolis PR4||62.3||6,895,538||6,437|
|GCF_001685605.1||R. opacus strain 1CP||67.1||8,637,535||7,921|
|GCF_000010805.1||R. opacus B4||67.6||8,834,939||8,203|
|GCF_000599545.1||R. opacus PD630||67.2||9,169,032||8,942|
|GCF_000014565.1||R. jostii RHA1||67.0||9,702,737||9,145|
% GC: G+C content defined as 100 × (G+C)/(A+T+G+C).
CDS: the number of protein-coding DNA sequences.
Results and Discussion
The draft genome sequence of Rhodococcus sp. Br-6 contains 23 contigs consisting of 5,496,476 bp, with a G+C content of 68.66 % (Table 1). Among the 13 Rhodococcus strains analyzed, genome size (Mb) and G+C content (%) varied from 5.0 (R. equi 103S) to 9.7 (R. jostii), and 62 (R. erythropolis) to 69 (R. triatomae), respectively. The genome size and G+C content of strain Br-6 were similar to those of the ingroup taxa (R. equi and R. defluvii).
Previously, based on the 16S rRNA gene sequence analysis, the Br-6 strain was reported to be most closely related to R. equi . In the present study, 839 core genes were used to infer the phylogenetic relationships between the 13 Rhodococcus strains. The phylogenetic tree, inferred from concatenation of the core genes (Figure 1), demonstrated that strain Br-6 and R. equi strains 103S and DSM 20307T formed a clade to which R. defluvii is the sister species. The core genome phylogeny suggests that strain Br-6 belongs to the species R. equi.
We performed TBLASTN searches  to assess the conservation of Br-6 genes in other Rhodococcus genomes. Of the 5,167 protein-coding genes detected in the Br-6 genome, 4,716 were conserved in all R. equi strains (103S and DSM 20307T), and 3,671 were conserved in all the Rhodococcus strains examined. The largest numbers of Br-6 genes were conserved in the R. equi strains, ranging from 4,753 to 4,763, followed by R. defluvii with 4,452, and finally the outgroup, ranging from 4,178 (R. triatomae) to 4,295 (R. jostii). Thus, the conservation of Br-6 genes in the Rhodococcus strains roughly follows the pattern of their phylogenetic relationships (Figure 1).
The draft genome sequence of strain Br-6 contained 5,186 protein coding DNA sequences (CDS), of which 1,452 were functionally unknown, with a product name of “hypothetical protein” (Table S1). Of the 5,186 proteins, 4,947 (95.4%) matched with 4,894 unique records in the UniRef90 database, and 2,044 (39.4%) matched with 1,481 unique KEGG orthology (KO) identifiers.
We searched for genes involved in various biological functions of strain Br-6. The Br-6 genome contained at least 13 genes coding for c-type cytochromes and at least 19 genes putatively involved in arsenic resistance or arsenic metabolism: several genes encoding HTH-type, ArsR family transcriptional regulators, arsB encoding the membrane arsenic pump protein (locus_tag: Br6_00718), aioB encoding the arsenite oxidase subunit AioB precursor (locus_tag: Br6_00766), arsA encoding the arsenic pump-driving ATPase (locus_tag: Br6_00780 and Br6_04451), arsC encoding the arsenate reductase (locus_tag: Br6_01479), and a cluster of three genes (locus_tag: Br6_04407, Br6_04408, and Br6_04409; UniProt: E4WCD3, E4WCD4, and E4WCD5) which appear to form the arsRBC operon . The draft genome contains a nitrate reductase gene cluster (locus_tag: Br6_04375, Br6_04376, Br6_04377, and Br6_04378) and denitrification regulatory proteins (locus_tag: Br6_04870 and Br6_04921), but does not contain nitrogenase genes. As expected by the fact that Rhodococcus is non-motile, the Br-6 genome did not contain any genes involved in motility.
Phylogenetic tree obtained from a concatenated nucleotide sequence alignment of the 868 core genes of 13 Rhodococcus strains. The horizontal bar at the base of the figure represents 0.008 substitutions per nucleotide site. All the internodes exhibited highest local support values of 1.0.(Click on the image to enlarge.)
Br-6 strain lpdC gene homologues identified by BLASTP search.
|BLAST search statistics|
|locus_tag||Gene||Product||Alignment length||% Identity||E-value|
|Br6_00125||cdr||coenzyme A disulfide reductase||347||28.0||1.E-21|
|Br6_00870||ahpF||alkyl hydroperoxide reductase subunit F||201||29.4||3.E-08|
|Br6_03025||yumC||ferredoxin--NADP reductase 2||320||25.0||2.E-06|
Tamai et al. (2016) suggested that diaphorase is involved in bromate reduction by strain Br-6, and that strain Br-6 has multiple isoforms of diaphorase . Some dihydrolipoyl dehydrogenase (DLD) enzymes have NADH-dependent diaphorase activity . The Br-6 genome contains the lpdC gene, which encodes DLD (locus_tag: Br6_03586; UniProt: E4W8R5). The DLD protein sequence was used as a query in a BLASTP search (E-value < 1e-5) against all the strain Br-6 predicted protein sequences to identify DLD homologues. The lpdC protein has low percentage identity (ranging from 25% to 31%) with all 10 reductase encoding homologs (Table 2), including the lpdA gene, annotated as “NAD(P)H dehydrogenase” (locus_tag: Br6_00169) or “flavoprotein disulfide reductase” (UniProt: E9T344), and the merA gene, annotated as "mercuric reductase" (Br6_01549) or "putative dihydrolipoyl dehydrogenase" (UniProt: E4WE66). The lpdC, lpdA, and merA genes were also annotated as “dihydrolipoamide dehydrogenase [EC:220.127.116.11]” (KEGG: K00382). These results suggest that these homologous genes encode multiple diaphorase isoforms. The genes identified here could be effective targets for future experimental studies.
Nucleotide sequence accession number
The whole Rhodococcus sp. Br-6 genome shotgun sequence has been deposited at DDBJ/EMBL/GenBank under the accession number BDGK00000000. The version described in this paper is the second version, BDGK02000000.
Table S1. Rhodococcus sp. strain Br-6 genes. The columns are as follows: locus_tag, length in amino acids (Laa), KEGG orthology identifiers (ko), gene and product names, and the most similar sequence annotation in the UniRef90 database (FASTA header and organism name).
We thank Nao Takeuchi for providing helpful comments about the manuscript. This work was supported in part by research funding from Keio University, Yamagata Prefecture and Tsuruoka City. Computational resources were provided by the Data Integration and Analysis Facility, National Institute for Basic Biology.
Conflicts of Interest
The authors declare that there are no conflicts of interest.
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Corresponding author: Haruo Suzuki, phone/fax number: +81-466-47-5099, email: haruokeio.ac.jp