Hostname: page-component-8448b6f56d-wq2xx Total loading time: 0 Render date: 2024-04-23T23:11:25.614Z Has data issue: false hasContentIssue false

Molecular and biochemical evidence for manganese-dependent peroxidase activity in Tylospora fibrillosa

Published online by Cambridge University Press:  01 September 1999

S. M. CHAMBERS
Affiliation:
Mycorrhiza Research Group, School of Science, University of Western Sydney (Nepean), PO Box 10, Kingswood, NSW 2747, Australia
R. M. BURKE
Affiliation:
Department of Biomolecular Science, UMIST, PO Box 88, Manchester, M60 1QD, U.K.
P. R. BROOKS
Affiliation:
Moredun Research Institute, 408 Gilmerton Rd, Edinburgh, EH17 7JH, U.K.
J. W. G. CAIRNEY
Affiliation:
Mycorrhiza Research Group, School of Science, University of Western Sydney (Nepean), PO Box 10, Kingswood, NSW 2747, Australia
Get access

Abstract

Gel-based and spectrophotometric assays were used to demonstrate expression of a manganese-dependent peroxidase (MnP) activity in culture filtrates of the ectomycorrhizal basidiomycete Tylospora fibrillosa. PCR amplification using a primer pair specific for a 260 bp fragment from the 5′-end of a gene encoding an H3-like MnP isozyme in Phanerochaete chrysosporium, produced single amplification products of 260 bp from DNA extracted from two isolates of T. fibrillosa. The amplified fragment from T. fibrillosa had a 93·7% nucleotide overlap (over 201 bases) with a published sequence for a 260 base amplification product from the P. chrysosporium H3 MnP isozyme gene, strongly suggesting the presence of a homologous gene in the ectomycorrhizal fungus. The results are discussed in the context of lignin degradation by ectomycorrhizal fungi.

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.)