Draft genome sequence data and analysis of Brachybacterium sp. strain EE-P12 isolated from a laboratory-scale anaerobic reactor

The species of the genus Brachybacterium belonging to the family Dermabacteraceae within the phylum Actinobacteria are gram-positive, facultatively anaerobic or aerobic, nonmotile and nonsporeforming bacteria. Cells of Brachybacterium spp. vary in shape from coccoid forms (stationary phase) to rods (exponential phase). Brachybacterium species can be isolated from numerous sources such as poultry deep litter, human gut, soil, food products. Here we describe the draft genome sequence of Brachybacterium sp. EE-P12 that was isolated from a laboratory-scale anaerobic digester. The genome sequencing generated 3,964,988 bp, with a G+C content of 72.2%. This draft genome data has been deposited at DDBJ/ENA/GenBank under the accession number QXCP00000000 (https://www.ncbi.nlm.nih.gov/nuccore/QXCP00000000).


Value of the data
Draft genome assembly of Brachybacterium sp. will increase the knowledge of its ecology and genetics and create an opportunity for comparative studies with other bacteria.
Draft genome data can be useful for the scientific community working in the field of application of brachybacteria in several biotechnological processes.
The draft genome will accelerate functional genomics research.

Data
In the present work, we describe the draft genome sequence data and genome annotation of Brachybacterium sp. strain EE-P12 isolated from a laboratory-scale mesophilic biogas reactor fed with chicken manure as monosubstrate. In addition, we included the 16S rRNA gene sequence data of the strain EE-P12. The 16S rRNA gene sequence of the strain EE-P12 determined in this study had a 1376 bp-length. Fig. 1 demonstrates the neighbor-joining phylogenetic tree derived from 16S rRNA gene sequences of the strain EE-P12 and its taxonomic neighbors. The assembly of the draft genome sequence of Brachybacterium sp. strain EE-P12 generated 21 contigs (4 500 bp) with an N 50 of 412,638, a total length of 3,964,988 bp and G þC content of 72.2%. The RAST server predicted 3600 coding sequences. The pie chart demonstrating the counts for each subsystem feature and the subsystem coverage is shown in Fig. 2. In addition, the genome of Brachybacterium sp. strain EE-P12 was demonstrated to encode at least 3 rRNAs and 55 tRNAs. Table 1 shows the comparison of the genomic feature of Brachybacterium sp. strain EE-P12 with some other Brachybacterium species. The strain Brachybacterium sp. strain EE-P12 possesses several genes responsible for monosaccharides and proteins degradation and fermentation processes (such as mixed acid fermentation, lactate fermentation and acetyl-CoA fermentation to butyrate). Several genes responsible for resistance to toxic compounds (such as mercury, cobalt, zinc and cadmium) and several fluoroquinolones were also observed.

Experimental design, materials and methods
The Brachybacterium sp. strain EE-P12 was isolated from a laboratory-scale mesophilic biogas reactor fed with chicken manure as monosubstrate and operated at high ammonia loads (4 5.0 NH 4 -N g L À 1 ) [1]. The bacterial strain Brachybacterium sp. EE-P12 was cultured on LB agar at þ37°C for 2 days of incubation. Genomic DNA from the bacterial strain EE-P12 was extracted using a FastDNA spin kit (MP Biomedicals, USA) as previously described [2] and stored at -20°C until processing. The quality of the obtained DNA was estimated by agarose gel electrophoresis, concentration and purity were measured by spectrophotometric analysis, confirming the ratio of absorbance at 260 nm and 280 nm of between 1.8 and 2.0. Next, the identification of the species affiliation was performed using morphological characteristics and biochemical tests followed by sequencing of its 16 S rRNA gene with an ABI PRISM 3130xl Genetic Analyzer (Thermo Fisher Scientific, USA). In addition, we constructed the phylogenetic tree based on the 16 S rRNA gene sequences using MEGA 7 software [3]. A library for whole genome sequencing was prepared from genomic DNA as described previously [2]. Finally, whole genome sequencing was performed at Joint KFU-Riken Laboratory, Kazan Federal University (Kazan, Russia) with the HiSeq. 2500 Sequencing System (Illumina, USA), HiSeq PE Rapid Cluster Kit v2 (Illumina, USA) and HiSeq Rapid SBS Kit v2 (500 cycles) (Illumina, USA). Sequence read quality was assessed using FastQC v0.11.5 [4], the filtered reads were then assembled using Velvet version 1.2.10 [5], and the contigs dataset was ordered using Mauve version 2.4.0 [6] with default parameters. The genome sequence of Brachybacterium sp. was annotated using the RAST server (annotation scheme: RASTtk) [7]. The rRNA and tRNA genes numbers were identified using RNAmmer 1.2 [8] and tRNA scan-SE 1.23 [9], respectively.

Acknowledgements
The reported study was funded by the Russian Foundation for Basic Research (Russia) [Grant no. 16-34-60093 mol_a_dk].

Transparency document. Supporting information
Transparency data associated with this article can be found in the online version at https://doi.org/ 10.1016/j.dib.2018.11.104.