Molecular cloning and characterization of a newly isolated pyrethroid-degrading esterase gene from a genomic library of Ochrobactrum anthropi YZ-1

PLoS One. 2013 Oct 14;8(10):e77329. doi: 10.1371/journal.pone.0077329. eCollection 2013.

Abstract

A novel pyrethroid-degrading esterase gene pytY was isolated from the genomic library of Ochrobactrum anthropi YZ-1. It possesses an open reading frame (ORF) of 897 bp. Blast search showed that its deduced amino acid sequence shares moderate identities (30% to 46%) with most homologous esterases. Phylogenetic analysis revealed that PytY is a member of the esterase VI family. pytY showed very low sequence similarity compared with reported pyrethroid-degrading genes. PytY was expressed, purified, and characterized. Enzyme assay revealed that PytY is a broad-spectrum degrading enzyme that can degrade various pyrethroids. It is a new pyrethroid-degrading gene and enriches genetic resource. Kinetic constants of Km and Vmax were 2.34 mmol·L(-1) and 56.33 nmol min(-1), respectively, with lambda-cyhalothrin as substrate. PytY displayed good degrading ability and stability over a broad range of temperature and pH. The optimal temperature and pH were of 35°C and 7.5. No cofactors were required for enzyme activity. The results highlighted the potential use of PytY in the elimination of pyrethroid residuals from contaminated environments.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Cloning, Molecular
  • Esterases / chemistry
  • Esterases / genetics*
  • Esterases / isolation & purification*
  • Gene Expression Regulation, Bacterial / drug effects
  • Genes, Bacterial / genetics
  • Genomic Library*
  • Hydrogen-Ion Concentration / drug effects
  • Ions
  • Kinetics
  • Metals / pharmacology
  • Molecular Sequence Data
  • Ochrobactrum anthropi / drug effects
  • Ochrobactrum anthropi / enzymology*
  • Ochrobactrum anthropi / genetics*
  • Phylogeny
  • Pyrethrins / metabolism*
  • Sequence Alignment
  • Sequence Analysis, DNA
  • Substrate Specificity / drug effects
  • Temperature
  • Transformation, Genetic / drug effects

Substances

  • Ions
  • Metals
  • Pyrethrins
  • Esterases

Grants and funding

This work was supported by the Hi-Tech Research and Development Program of China (2008AA10Z402), the National Natural Science Foundation of China (31170119), and the Basic Research Fund of CAAS (Nos. 0042012003 and 0042011006). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.