Isolation of a laccase-coding gene from the lignin-degrading fungus Phlebia brevispora BAFC 633 and heterologous expression in Pichia pastoris

J Appl Microbiol. 2018 Jun;124(6):1454-1468. doi: 10.1111/jam.13720. Epub 2018 Mar 23.

Abstract

Aims: Isolate and characterize a laccase-encoding gene (lac I) of Phlebia brevispora BAFC 633, as well as cloning and expressing cDNA of lac I in Pichia pastoris. And to obtain a purified and characterized recombinant laccase to analyse the biotechnological application potential.

Methods and results: Lac I was cloned and sequenced, it contains 2447 pb obtained by PCR and long-distance inverse PCR. Upstream of the structural region of the laccase gene, response elements such as metals, antioxidants, copper, nitrogen and heat shock were found. The coding region consisted of a 1563-pb ORF encoding 521 amino acids. Lac I was functionally expressed in P. pastoris and it was shown that the gene cloned using the α-factor signal peptide was more efficient than the native signal sequence, in directing the secretion of the recombinant protein. Km and highest kcat /Km values towards ABTS, followed by 2,6-dimethylphenol, were similar to other laccases. Lac I showed tolerance to NaCl and solvents, and nine synthetic dyes could be degraded to different degrees.

Conclusions: Lac I-encoding gene could be successfully sequenced having cis-acting elements located at the regulatory region. It was found that lac I cDNA expressed in P. pastoris using the α-factor signal peptide was more efficient than the native signal sequence. The purified Lac I exhibited high tolerance towards NaCl and various solvents and degraded some recalcitrant synthetic dyes.

Significance and impact of the study: The cis-acting elements may be involved in the transcriptional regulation of laccase gene expression. These results may provide a further insight into potential ways of optimizing fermentation process and also open new frontiers for engineering strong promoters for laccase production. The Lac I stability in chloride and solvents and broad decolorization of synthetic dyes are important for its use in organic synthesis work and degradation of dyes from textile effluents respectively.

Keywords: Phlebia brevispora; characterization; gene isolation; heterologous expression; laccase.

MeSH terms

  • Cloning, Molecular
  • Enzyme Stability
  • Fungal Proteins / chemistry
  • Fungal Proteins / genetics*
  • Fungal Proteins / isolation & purification
  • Fungal Proteins / metabolism
  • Gene Expression
  • Kinetics
  • Laccase / chemistry
  • Laccase / genetics*
  • Laccase / isolation & purification
  • Laccase / metabolism
  • Lignin / metabolism*
  • Pichia / genetics
  • Pichia / metabolism
  • Polymerase Chain Reaction
  • Polyporales / chemistry
  • Polyporales / enzymology*
  • Polyporales / genetics
  • Protein Sorting Signals
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism

Substances

  • Fungal Proteins
  • Protein Sorting Signals
  • Recombinant Proteins
  • Lignin
  • Laccase

Associated data

  • GENBANK/JQ728448