Formation of new PHE plasmids in pseudomonads in a phenol-polluted environment

Plasmid. 2020 Jul:110:102504. doi: 10.1016/j.plasmid.2020.102504. Epub 2020 Apr 11.

Abstract

Several years ago, a laboratory-constructed plasmid with a single-component phenol monooxygenase gene (pheBA operon) flanked by two IS elements was released to a phenol-polluted area. During the following years, we found in the test area widely distributed pheBA operon-containing bacteria. The new pheBA+ strains belong predominantly to the Pseudomonas fluorescens group, and they did not arise via selection of the released PHE plasmid. On the contrary, the formation of several different types of PHE plasmids occurred, namely pPHE101 (60,958 bp) from the IncP-9 group, non-transferable plasmid pPHE69 (44,717 bp), mobilizable plasmid pPHE20 (39,609 bp) and the IncP-7 type plasmid pPHE24ΔpheBA (120,754 bp), in which the pheBA operon was translocated from the plasmid to the chromosome. In two cases, PHE plasmid-bearing strains exist in a multi-plasmid state, also containing the non-catabolic plasmids pG20 (133,709 bp) and pG69 (144,433 bp) with backbones sharing 97% DNA identity and with redundant genes for the initiation of replication, repA1and repA2, of which only one was active. Seemingly, several other plasmids and bacterial features besides the pheBA operon were involved in selective distribution of catabolic operons in the natural environment. The comparison of the genetic structure of plasmids and IS elements' functions, as well as resistance to heavy metals of seven completely sequenced plasmids, are discussed.

Keywords: Conjugative transfer; Mobile genetic elements; Phenol degradation; Plasmids.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Proteins / genetics*
  • Biodegradation, Environmental
  • DNA, Bacterial / genetics
  • Gene Expression Regulation, Bacterial / drug effects*
  • Mixed Function Oxygenases / genetics*
  • Operon
  • Phenol / toxicity*
  • Plasmids / genetics*
  • Promoter Regions, Genetic
  • Pseudomonas / drug effects
  • Pseudomonas / enzymology
  • Pseudomonas / genetics*

Substances

  • Bacterial Proteins
  • DNA, Bacterial
  • Phenol
  • Mixed Function Oxygenases
  • phenol 2-monooxygenase