This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Yaver, D. S.
Right arrow Articles by Kauppinen, S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Yaver, D. S.
Right arrow Articles by Kauppinen, S.
Agricola
Right arrow Articles by Yaver, D. S.
Right arrow Articles by Kauppinen, S.

 Previous Article  |  Next Article 

Applied and Environmental Microbiology, November 1999, p. 4943-4948, Vol. 65, No. 11
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.

Molecular Characterization of Laccase Genes from the Basidiomycete Coprinus cinereus and Heterologous Expression of the Laccase Lcc1

Debbie S. Yaver,1,* Maria Del Carmen Overjero,2 Feng Xu,1 Beth A. Nelson,1 Kim M. Brown,1 Torben Halkier,2 Sheryl Bernauer,1 Stephen H. Brown,1 and Sakari Kauppinen2

Novo Nordisk Biotech, Davis, California 95616,1 and Novo Nordisk A/S, 2880 Bagsvoerd, Denmark2

Received 26 April 1999/Accepted 10 August 1999

A laccase from Coprinus cinereus is active at alkaline pH, an essential property for some potential applications. We cloned and sequenced three laccase genes (lcc1, lcc2, and lcc3) from the ink cap basidiomycete C. cinereus. The lcc1 gene contained 7 introns, while both lcc2 and lcc3 contained 13 introns. The predicted mature proteins (Lcc1 to Lcc3) are 58 to 80% identical at the amino acid level. The predicted Lcc1 contains a 23-amino-acid C-terminal extension rich in arginine and lysine, suggesting that C-terminal processing may occur during its biosynthesis. We expressed the Lcc1 protein in Aspergillus oryzae and purified it. The Lcc1 protein as expressed in A. oryzae has an apparent molecular mass of 66 kDa on sodium dodecyl sulfate-polyacrylamide gel electrophoresis and absorption maxima at 278 and 614 nm. Based on the N-terminal protein sequence of the laccase, a 4-residue propeptide was processed during the maturation of the enzyme. The dioxygen specificity of the laccase showed an apparent Km of 21 ± 2 µM and a catalytic constant of 200 ± 10 min-1 for O2 with 2,2'-azinobis(3-ethylbenzothiazoline-6-sulfonic acid) as the reducing substrate at pH 5.5. Lcc1 from A. oryzae may be useful in industrial applications. This is the first report of a basidiomycete laccase whose biosynthesis involves both N-terminal and C-terminal processing.


* Corresponding author. Mailing address: Novo Nordisk Biotech, 1445 Drew Ave., Davis, CA 95616. Phone: (530) 757-4993. Fax: (530) 758-0317. E-mail: dyaver{at}nnbt.com.


Applied and Environmental Microbiology, November 1999, p. 4943-4948, Vol. 65, No. 11
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Alves, A. M. C. R., Record, E., Lomascolo, A., Scholtmeijer, K., Asther, M., Wessels, J. G. H., Wosten, H. A. B. (2004). Highly Efficient Production of Laccase by the Basidiomycete Pycnoporus cinnabarinus. Appl. Environ. Microbiol. 70: 6379-6384 [Abstract] [Full Text]  
  • Kiiskinen, L.-L., Kruus, K., Bailey, M., Ylosmaki, E., Siika-aho, M., Saloheimo, M. (2004). Expression of Melanocarpus albomyces laccase in Trichoderma reesei and characterization of the purified enzyme. Microbiology 150: 3065-3074 [Abstract] [Full Text]  
  • Kiiskinen, L.-L., Saloheimo, M. (2004). Molecular Cloning and Expression in Saccharomyces cerevisiae of a Laccase Gene from the Ascomycete Melanocarpus albomyces. Appl. Environ. Microbiol. 70: 137-144 [Abstract] [Full Text]  
  • Shimizu, A., Samejima, T., Hirota, S., Yamaguchi, S., Sakurai, N., Sakurai, T. (2003). Type III Cu Mutants of Myrothecium verrucaria Bilirubin Oxidase. J Biochem 133: 767-772 [Abstract] [Full Text]  
  • Larrondo, L. F., Avila, M., Salas, L., Cullen, D., Vicuna, R. (2003). Heterologous expression of laccase cDNA from Ceriporiopsis subvermispora yields copper-activated apoprotein and complex isoform patterns. Microbiology 149: 1177-1182 [Abstract] [Full Text]  
  • Soden, D. M., O'Callaghan, J., Dobson, A. D. W. (2002). Molecular cloning of a laccase isozyme gene from Pleurotus sajor-caju and expression in the heterologous Pichia pastoris host. Microbiology 148: 4003-4014 [Abstract] [Full Text]  
  • Galhaup, C., Goller, S., Peterbauer, C. K., Strauss, J., Haltrich, D. (2002). Characterization of the major laccase isoenzyme from Trametes pubescens and regulation of its synthesis by metal ions. Microbiology 148: 2159-2169 [Abstract] [Full Text]  
  • Kues, U. (2000). Life History and Developmental Processes in the Basidiomycete Coprinus cinereus. Microbiol. Mol. Biol. Rev. 64: 316-353 [Abstract] [Full Text]