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Isolation and characterization of a Rhodococcus species strain able to grow on ortho- and para-xylene

  • Yeon Jang Jung
  • , Dockyu Kim
  • , Won Bae Hyun
  • , Young Choi Ki
  • , Jong Chan Chae
  • , Gerben J. Zylstra
  • , Min Kim Young
  • , Eungbin Kim*
  • *Corresponding author for this work
  • Yonsei University
  • University of Ulsan
  • Korea Research Institute of Bioscience and Biotechnology
  • Rutgers - The State University of New Jersey, New Brunswick

Research output: Contribution to journalJournal articlepeer-review

Abstract

Rhodococcus sp. strain YU6 was isolated from soil for the ability to grow on o-xylene as the sole carbon and energy source. Unlike most other o-xylene-degrading bacteria, YU6 is able to grow on p-xylene. Numerous growth substrate range experiments, in addition to the ring-cleavage enzyme assay data, suggest that YU6 initially metabolizes o- and p-xylene by direct aromatic ring oxidation. This leads to the formation of dimethylcatechols, which was further degraded largely through meta-cleavage pathway. The gene encoding meta-cleavage dioxygenase enzyme was PCR cloned from genomic YU6 DNA using previously known gene sequence data from the o-xylene-degrading Rhodococcus sp. strain DK17. Subsequent sequencing of the 918-bp PCR product revealed a 98% identity to the gene, encoding methylcatechol 2,3-dioxygenase from DK17. PFGE analysis followed by Southern hybridization with the catechol 2,3-dioxygenase gene demonstrated that the gene is located on an approximately 560-kb megaplasmid, designated pJYJ1.

Original languageEnglish
Pages (from-to)325-330
Number of pages6
JournalJournal of Microbiology
Volume43
Issue number4
StatePublished - 2005.08

Keywords

  • Catechol 2,3-dioxygenase
  • Megaplasmid
  • Rhodococcus
  • Xylene isomers

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