Literature DB >> 27326264

Draft Genome Sequence of Kocuria rhizophila strain TPW45, an Actinobacterium Isolated from Freshwater.

Tan-Guan-Sheng Adrian1, Pui-Wan Tan1, Jian-Woon Chen1, Wai-Fong Yin1, Kok-Gan Chan1.   

Abstract

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.

Entities:  

Keywords:  Kocuria rhizophila; Phenylacetate degradation; Whole genome sequencing

Year:  2016        PMID: 27326264      PMCID: PMC4911414          DOI: 10.7150/jgen.15063

Source DB:  PubMed          Journal:  J Genomics


Introduction

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
Table 1

Genome features of Kocuria rhizophila strain TPW45 and K. rhizophila reference sequences from RAST.

StrainSourceSize (Mb)No. of Contig(s)G+C (%)No. of CDSNo. of rRNANo. of tRNA
DC2201Soil2.70171.22,357346
P7-4Intestine of rabbitfish (Siganus doliatus)2.827570.42,370546
TPW45This study2.704670.62,349450
14ASPEndophyte of Oxalis corniculata2.7018370.81,900846
Figure 1

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

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.

Nucleotide sequence accession number

The whole genome shotgun project has been deposited in DDBJ/EMBL/GenBank under accession number JWTC00000000.1.
  6 in total

1.  Complete genome sequence of the soil actinomycete Kocuria rhizophila.

Authors:  Hiromi Takarada; Mitsuo Sekine; Hiroki Kosugi; Yasunori Matsuo; Takatomo Fujisawa; Seiha Omata; Emi Kishi; Ai Shimizu; Naofumi Tsukatani; Satoshi Tanikawa; Nobuyuki Fujita; Shigeaki Harayama
Journal:  J Bacteriol       Date:  2008-04-11       Impact factor: 3.490

2.  Kocuria palustris sp. nov. and Kocuria rhizophila sp. nov., isolated from the rhizoplane of the narrow-leaved cattail (Typha angustifolia).

Authors:  G Kovács; J Burghardt; S Pradella; P Schumann; E Stackebrandt; K Màrialigeti
Journal:  Int J Syst Bacteriol       Date:  1999-01

3.  Bacterial phenylalanine and phenylacetate catabolic pathway revealed.

Authors:  R Teufel; V Mascaraque; W Ismail; M Voss; J Perera; W Eisenreich; W Haehnel; G Fuchs
Journal:  Proc Natl Acad Sci U S A       Date:  2010-07-21       Impact factor: 11.205

4.  The tRNAscan-SE, snoscan and snoGPS web servers for the detection of tRNAs and snoRNAs.

Authors:  Peter Schattner; Angela N Brooks; Todd M Lowe
Journal:  Nucleic Acids Res       Date:  2005-07-01       Impact factor: 16.971

5.  RNAmmer: consistent and rapid annotation of ribosomal RNA genes.

Authors:  Karin Lagesen; Peter Hallin; Einar Andreas Rødland; Hans-Henrik Staerfeldt; Torbjørn Rognes; David W Ussery
Journal:  Nucleic Acids Res       Date:  2007-04-22       Impact factor: 16.971

6.  The RAST Server: rapid annotations using subsystems technology.

Authors:  Ramy K Aziz; Daniela Bartels; Aaron A Best; Matthew DeJongh; Terrence Disz; Robert A Edwards; Kevin Formsma; Svetlana Gerdes; Elizabeth M Glass; Michael Kubal; Folker Meyer; Gary J Olsen; Robert Olson; Andrei L Osterman; Ross A Overbeek; Leslie K McNeil; Daniel Paarmann; Tobias Paczian; Bruce Parrello; Gordon D Pusch; Claudia Reich; Rick Stevens; Olga Vassieva; Veronika Vonstein; Andreas Wilke; Olga Zagnitko
Journal:  BMC Genomics       Date:  2008-02-08       Impact factor: 3.969

  6 in total
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  1 in total

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