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Transgenic rice as a novel production system for Melanocarpus and Pycnoporus laccases

  • Chris De Wilde
  • , Eva Uzan
  • , Zhongyi Zhou
  • , Kristiina Kruus
  • , Martina Andberg
  • , Johanna Buchert
  • , Eric Record
  • , Marcel Asther
  • , Anne Lomascolo*
  • *Corresponding author for this work

Research output: Contribution to journalArticleScientificpeer-review

24 Citations (Scopus)

Abstract

Laccases have numerous biotechnological applications, among them food processing. The widespread use of laccases has increased the demand for an inexpensive and safe source of recombinant enzyme. We explored the use of a rice-based system for the production of two fungal laccases derived from the ascomycete Melanocarpus albomyces and the basidiomycete Pycnoporus cinnabarinus. High-expression levels of active recombinant laccases were achieved by targeting expression to the endosperm of rice seeds. The laccase cDNAs were fused to a plant-derived signal sequence for targeting to the secretory pathway, and placed under the control of a constitutive seed-specific promoter fused to an intron for enhanced expression. This construct enabled the recovery of on average 0.1-1% of soluble laccase in total soluble proteins (TSP). The highest yields of recombinant laccases obtained in rice seeds were 13 and 39 ppm for riceMaL and ricePycL, respectively. The rice-produced laccases were purified and characterized. The wild-type and the recombinant proteins showed similar biochemical features in terms of molecular mass, pI, temperature and optimal pH and the N-terminus was correctly processed. Although presenting lower kinetic parameters, the rice-produced laccases were also suitable for the oxidative cross-linking of a food model substrate [maize-bran feruloylated arabinoxylans (AX)].

Original languageEnglish
Pages (from-to)515-527
Number of pages13
JournalTRANSGENIC RESEARCH
Volume17
Issue number4
DOIs
Publication statusPublished - 1 Aug 2008
MoE publication typeA1 Journal article-refereed

Funding

Acknowledgements We are deeply grateful to David Navarro (UMR 1163 INRA, Marseille, France), Outi Liehunen and Birgit Hillebrandt (VTT, Finland) for technical assistance, Christophe Flaudrops (AFMB, CNRS, Marseille, France) for mass spectrometry analysis and Willem Broekaert and Yves Hatzfeld (CropDesign NV) for their valuable contribution in construct design. This work has been carried out with financial support from the Commission of the European Communities, specifically the RTD programme ‘‘Quality of Life and Management of Living Resources’’, proposal number QLK1-2002-02208 ‘‘Novel cross-linking enzymes and their consumer acceptance for structure engineering of foods’’, acronym CROSSENZ. It does not reflect its views and in no way anticipates the Commission’s future policy in this area.

Keywords

  • Heterologous protein production
  • Laccase
  • Melanocarpus albomyces
  • Oryza sativa
  • Pycnoporus cinnabarinus
  • Recombinant fungal enzyme
  • Rice

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