Hostname: page-component-cd9895bd7-jn8rn Total loading time: 0 Render date: 2024-12-28T00:18:21.890Z Has data issue: false hasContentIssue false

Production and isozyme pattern of extracellular laccase in the S and P intersterility groups of the root pathogen Heterobasidion annosum

Published online by Cambridge University Press:  01 March 1999

M. JOHANSSON
Affiliation:
Department of Forest Mycology and Pathology, Swedish University of Agricultural Sciences, S-750 07 Uppsala, Sweden
M. DENEKAMP
Affiliation:
Department of Forest Mycology and Pathology, Swedish University of Agricultural Sciences, S-750 07 Uppsala, Sweden
F. O. ASIEGBU
Affiliation:
Department of Forest Mycology and Pathology, Swedish University of Agricultural Sciences, S-750 07 Uppsala, Sweden
Get access

Abstract

Strains of Heterobasidion annosum belonging to the S and P intersterility groups (IGs) were compared in respect of laccase activity on various substrates. Biomass production was significantly lower in P cultures than in S cultures. By contrast, laccase activity, measured in relation to growth rate, was significantly higher for the P strains tested, compared with a similar number of S strains, particularly in substrates, rich in carbohydrates as well as in inorganic and organic nitrogen. Using the Bradford assay method, P cultures were shown to contain significantly higher amounts of protein than S. The pH optimum of laccase for both IGs was 4·5 with guaiacol as substrate and 5·3 with syringaldazine. Isozyme patterns varied greatly, depending on strain, substrate and incubation time. In P cultures 4–5 bands were obtained, whereas S strain laccase was mostly separated into 2–3 isozyme bands. Only one was significantly different in position between the IGs. The results may help to explain why P strains are more aggressive than S strains as pathogens and wood decayers.

Type
Research Article
Copyright
© The British Mycological Society 1999

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)