Isolation and characterization of two cryptic plasmids in the ammonia-oxidizing bacterium Nitrosomonas sp. strain ENI-11

J Bacteriol. 1999 Jun;181(11):3375-81. doi: 10.1128/JB.181.11.3375-3381.1999.

Abstract

Two plasmids were discovered in the ammonia-oxidizing bacterium Nitrosomonas sp. strain ENI-11, which was isolated from activated sludge. The plasmids, designated pAYS and pAYL, were relatively small, being approximately 1.9 kb long. They were cryptic plasmids, having no detectable plasmid-linked antibiotic resistance or heavy metal resistance markers. The complete nucleotide sequences of pAYS and pAYL were determined, and their physical maps were constructed. There existed two major open reading frames, ORF1 in pAYS and ORF2 in pAYL, each of which was more than 500 bp long. The predicted product of ORF2 was 28% identical to part of the replication protein of a Bacillus plasmid, pBAA1. However, no significant similarity to any known protein sequences was detected with the predicted product of ORF1. pAYS and pAYL had a highly homologous region, designated HHR, of 262 bp. The overall identity was 98% between the two nucleotide sequences. Interestingly, HHR-homologous sequences were also detected in the genomes of ENI-11 and the plasmidless strain Nitrosomonas europaea IFO14298. Deletion analysis of pAYS and pAYL indicated that HHR, together with either ORF1 or ORF2, was essential for plasmid maintenance in ENI-11. To our knowledge, pAYS and pAYL are the first plasmids found in the ammonia-oxidizing autotrophic bacteria.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Ammonia / metabolism*
  • Bacterial Proteins / genetics
  • Base Sequence
  • DNA Replication
  • DNA, Recombinant / genetics
  • Gene Dosage
  • Genes, Bacterial / genetics
  • Genetic Markers / genetics
  • Kanamycin Resistance / genetics
  • Molecular Sequence Data
  • Nitrosomonas / genetics*
  • Nitrosomonas / metabolism
  • Open Reading Frames / genetics
  • Oxidation-Reduction
  • Plasmids / genetics*
  • Sequence Analysis, DNA
  • Sequence Deletion
  • Sequence Homology
  • Transformation, Bacterial

Substances

  • Bacterial Proteins
  • DNA, Recombinant
  • Genetic Markers
  • Ammonia

Associated data

  • GENBANK/AB018480
  • GENBANK/AB018481
  • GENBANK/AB018482
  • GENBANK/AB018483