J Genomics 2016; 4:16-18. doi:10.7150/jgen.15063
Short Research Communication
Draft Genome Sequence of Kocuria rhizophila strain TPW45, an Actinobacterium Isolated from Freshwater
Division of Genetics and Molecular Biology, Institute of Biological Sciences, Faculty of Science, University of Malaya, Kuala Lumpur, Malaysia
Adrian TGS, Tan PW, Chen JW, Yin WF, Chan KG. Draft Genome Sequence of Kocuria rhizophila strain TPW45, an Actinobacterium Isolated from Freshwater. J Genomics 2016; 4:16-18. doi:10.7150/jgen.15063. Available from http://www.jgenomics.com/v04p0016.htm
Kocuria rhizophila is a ubiquitous bacterium which is well known for its industrial value. Here, we present the draft genome of Kocuria rhizophila strain TPW45 which was isolated from Sungai Gabai, Selangor, Malaysia. The assembled genome comprised of 46 contigs and the estimated genome size is 2.7 Mb. Based on the RAST annotation, a gene cluster responsible for aromatic compound degradation was identified in this strain.
Keywords: Kocuria rhizophila, Phenylacetate degradation, Whole genome sequencing
Kocuria rhizophila is a Gram-positive, coccoid, and spherical bacterium belonging to the family Micrococcaceae in the phylum Actinobacteria, and was designated as a new species by Kovács and coworkers (1). Members of the genus Kocuria have been isolated from a wide variety of natural sources, and K. rhizophila in particular, was found to have important industrial applications. K. rhizophila has been utilised as the standard quality control strain for antimicrobial susceptibility testing (2) and also as a decolorizing agent of industrial dyes (3). Our strain was isolated from Sungai Gabai, Selangor, Malaysia and analysis of the genome revealed the presence of an aromatic compound degradation pathway.
Initially, the genomic DNA of K. rhizophila TPW45 was extracted using MasterPure™ Complete DNA and RNA Purification Kit (Epicentre, Inc., Madison, WI, USA) according to the manufacturer's recommended protocol. Subsequently, the quality of DNA was examined using the NanoDrop 2000 spectrophotometer (Thermo Scientific) and quantified using Qubit 2.0 fluorometer (Life Technologies). For whole-genome sequencing of K. rhizophila TPW45, the library was prepared using Illumina Nextera DNA Sample Preparation Kit as per manufacturer's guidelines. The sequencing of this strain was then performed on the Illumina HiSeq 2500 (Illumina, Inc., CA) using a paired-end library with an average insert size of 702 bp, obtaining 3,407,419 raw reads of 100 bp in length. After trimming, de novo assembly of the genome was performed using CLC Genomics Workbench 7.0 (4) while the genome annotation was performed using Rapid Annotation using Subsystem Technology (RAST) (5).
The assembled genome consists of 2,701,701 bases across 46 contigs with an N50 contig length of 114,097 bases. The average genome coverage was found to be 202.76×. The assembled genome was found to have a G + C content of 70.6%, falling within the range of known K. rhizophila genomes (Table 1). There were 2,349 predicted coding DNA sequences (CDS), whereas a total of 50 tRNAs were predicted using tRNAscan-SE (6), and 4 rRNAs was identified by using RNAmmer (7). This draft genome revealed a putative gene cluster involved in aromatic compound degradation that encodes a phenylacetatic acid (PAA) pathway. This PAA gene cluster was found in contig 17 of our strain and the gene arrangement was found to be similar to that of K. rhizophila strain DC2201, which is a closely related strain (Figure 1). Phenylacetate or phenylacetyl-coenzyme A (CoA) can be found as a derivative product from many substrates namely phenylalanine, 2-phenylethylamine, some phenylalkanoic acids, and also pollutants such as styrene and ethylbenzene. (8) The PAA pathway proceeds via phenylacetyl-coA and ring fission is hydrolysed via a multicomponent oxygenase encoded by paaGHIJK. (9)
In summary, phenylacetate degradation has been more widely studied in Proteobacteria such as Escherichia spp. and Pseudomonas spp. compared to Gram-positive bacteria. (8) We hope that this genome sequence of strain TPW45 will provide more insight into the phenylacetate degradation pathway by K. rhizophila. Further analysis of this genome and supporting experimental evidence will be needed to support this prediction and further understand the process of aromatic compound degradation by bacteria via PAA catabolism.
Genome features of Kocuria rhizophila strain TPW45 and K. rhizophila reference sequences from RAST.
|Strain||Source||Size (Mb)||No. of Contig(s)||G+C (%)||No. of CDS||No. of rRNA||No. of tRNA|
|P7-4||Intestine of rabbitfish (Siganus doliatus)||2.82||75||70.4||2,370||5||46|
|14ASP||Endophyte of Oxalis corniculata||2.70||183||70.8||1,900||8||46|
Orientation and annotation of phenylacetic acid (PAA) gene cluster involved in K. rhizophila strain TPW45 and DC2201 as identified from RAST server. (1) Phenylacetate-CoA oxygenase/reductase, PaaK subunit; (2) Phenylacetate-CoA oxygenase, PaaJ subunit; (4) Phenylacetate-CoA oxygenase, PaaI subunit; (5) Phenylacetate-CoA oxygenase, PaaH subunit; (7) Phenylacetate-CoA oxygenase, PaaG subunit; (8) Phenylacetic acid degradation protein PaaD, thioesterase; (10) Phenylacetate-coenzyme A ligase, PaaF; (12) Transcriptional regulator, TetR family; (15) Aldehyde dehydrogenase , PaaZ(Click on the image to enlarge.)
Nucleotide sequence accession number
The whole genome shotgun project has been deposited in DDBJ/EMBL/GenBank under accession number JWTC00000000.1.
This work was supported by the University of Malaya for High Impact Research Grant (UM-MOHE HIR Nature Microbiome Grant No. H-50001-A000027) awarded to Kok-Gan Chan.
The authors have declared that no competing interest exists.
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Corresponding author: Division of Genetics and Molecular Biology, Institute of Biological Sciences, Faculty of Science, University of Malaya, Kuala Lumpur 50603, Malaysia; E-mail: kokganedu.my