DNA was used for 300-bp paired-end library preparation with Nextera XT DNA Sample Preparation Kit. The genome sequences were obtained by using MiSeq sequencer (Illumina). Sequences obtained were pre-processed using Prinseq software (v.0.20.4) to remove reads smaller than 35 bp and low-score sequences (Phred 30). Sequence reads were assembled using A5-Miseq software (v.20160825). The software CheckM was used to check for completeness and contamination. Gene prediction and functional annotation were performed using the Rapid Annotation using Subsystem Technology (RAST) program.