Publications
NIBIOs employees contribute to several hundred scientific articles and research reports every year. You can browse or search in our collection which contains references and links to these publications as well as other research and dissemination activities. The collection is continously updated with new and historical material.
2011
Abstract
Coated wooden claddings in building facades are widely used in the Scandinavian countries, and are often preferred to other materials. Wood is facing increasing competition from other materials that are less labor intensive at the construction site and materials with less demand for maintenance thru service life, and makes further development of wooden claddings essential. Growth of discoloring moulds on exposed coated wooden claddings is mainly of aesthetic concern, and is especially disfiguring for light-colored surfaces. Growth of surface fungi often initiates repeated cleaning and shorter maintenance intervals, which in turn increase the total cost of ownership for wooden claddings. Cost and effort of ownership are often important factors considered when choosing a product, and the traditionally good market situation for wooden claddings is therefore threatened. The development of real-time PCR (polymerase chain reaction) and taxon-specific primers has provided new possibilities for specific detection and quantification of fungi in their natural substrates. In qPCR (quantitative real-time PCR), the accumulation of the PCR product is detected for each amplification cycle. An efficient and reproducible sampling and extraction of DNA is required for a high-throughput qPCR based quantification of discoloring fungi. The authors have now adjusted DNA isolation protocols and optimized real-time PCR assays for species specific detection of fungi frequently found on painted surfaces (Aureobasidium pullulans, Alternaria alternata, Cladosporium cladosporides, Ulocladium atrum).
Authors
Igor A. Yakovlev Ari M. Hietala Pierre-Emmanuel Courty Taina Lundell Jan Stenlid Halvor Solheim Carl Gunnar FossdalAbstract
In forest soils, saprotrophic, necrotrophic and ectomycorrhizal fungi are involved in carbon cycling. Heterobasidion annosum, white rot necrotrophic fungi, is known to decompose wood lignocellulose by secreting a broad range of oxidative enzymes. The genome H. annosum s.l. was sequenced by JGI to a 8.23X coverage and assembled into 39 scaffolds with a total size of 33.7 Mb covering more than 98% of the whole genome. Based on the genome sequence we have characterized gene families coding for enzymes known to participate in conversion of wood lignin: multicopper oxidases (MCOs, 18 genes) as laccases (Lcc), class II peroxidases (8 genes) as manganese peroxidases (MnP), glyoxal oxidases (5 genes, GLOX), quinone-reducing oxidoreductases (19 genes, QOR) and GMC oxidoreductases (12 genes) as aryl alcohol oxidases (AAO). We studied the genomic organisation and phylogeny of these genes as well as their expression using qRT-PCR. Comparative and phylogenetic analyses of genes coding for enzymes involved in wood lignin conversion and decomposition (i.e. lignin-modifying class II peroxidases) reveal differences between white- and brown-rot, necrotrophic and saprotrophic wood-decaying basidiomycetes. Transcript profiling using qRT-PCR revealed that some transcripts were very abundant in lignin-rich media, in cellulose-rich media, in wood or in the free-living mycelium grown liquid culture, suggesting specific functions of these genes, which need to be studied further.
2010
Abstract
Traditional wood preservatives based on biocides are effective against wood-deteriorating organisms because of their toxicity. By contrast, modified woods are non-toxic by definition. To investigate the efficiency of various wood modifications, quantitative real-time polymerase chain reaction (qPCR) was used to profile the DNA amounts of the white-rot fungus Trametes versicolor (L.) [Lloyd strain CTB 863 A] during an 8-week-long growth period in treated Pinus sylvestris (L.) sapwood. The studied wood was modified by acetylation, furfurylation, and thermal treatment. The traditional wood preservatives bis-(N-cyclohexyldiazeniumdioxy)-copper (Cu-HDO) and chromated copper arsenate (CCA) were used as references, whereas untreated P. sylvestris (L.) sapwood served as a control. The maximum levels of fungal DNA in native wood occurred at the end of the experiment. For all wood treatments, the maximum fungal DNA level was recorded after an incubation period of 2 weeks, followed by a decline until the end of the trial. For the preservative-treated woods, Cu-HDO showed the lowest level of fungal DNA throughout the experiment, indicating that exploratory hyphal growth is limited owing to the phytotoxicity of the treatment. The other treatments did not inhibit the exploratory hyphal growth phase. We conclude that qPCR studies of hyphal growth patterns within wood should provide a powerful tool for evaluating and further optimizing new wood protection systems.
Authors
Igor A. Yakovlev Ari M. Hietala Pierre-Emmanuel Courty Francis Martin Jan Stenlid Halvor Solheim Carl Gunnar FossdalAbstract
The genome H. annosum s.l. was sequenced by JGI to a 8.23X coverage and assembled into 39 scaffolds with a total size of 33.7 Mb covering more than 98% of the whole genome. Based of genome sequence we annotated a number of genes for fungal enzymes that are believed to participate in lignin degradation, including: laccases (Lcc18 genes), manganese peroxidases (MnP8 genes) and hydrogen peroxide forming enzymes such as glyoxal oxidases (GLOX5 genes), quinone oxidoreductases (QOR17 genes) and aryl alcohol oxidases (AAO16 genes), which is in concordance with these gene family sizes observed in other sequenced white-rot fungi. We studied the genomic organisation and phylogeny of these genes as well as their expression using NimbleGen arrays and qRT-PCR. Transcript profiling using whole-genome oligo arrays and qRT-PCR revealed that some transcripts were very abundant in lignin-rich media (Lcc5 15, MnP2, GLOX4, QOR2 10, AAO9), in cellulose-rich media (lcc2, 7 16, MnP3 4, GLOX3, QOR4 6, AAO2, 7 10), in wood (Lcc3, MnP4, QOR2, GLOX1, AAO10) or in the free-living mycelium grown liquid culture (Lcc1, 3, 10 13), suggesting specific functions of these genes, which need to be studied further.
Abstract
Coated wooden claddings in building facades are widely used in the Scandinavian countries, and are often preferred to other materials. Wood experience an increasing competition from other materials that are less labor intensive at the construction site and materials with less demand for maintenance thru service life, and makes further development of wooden claddings essential. Growth of discoloring moulds on exposed coated wooden claddings is mainly of aesthetic concern, and is especially disfiguring for light-colored surfaces. Growth of surface fungi often initiates repeated cleaning and shorter maintenance intervals, which in turn increase the total cost of ownership for wooden claddings. Cost and effort of ownership is often an important factor considered when choosing a product, and the traditionally good market situation for wooden claddings is therefore threatened. The development of real-time PCR (polymerase chain reaction) and taxon-specific primers has provided new possibilities for specific detection and quantification of fungi in their natural substrates. In qPCR (quantitative real-time PCR), the accumulation of the PCR product is detected for each amplification cycle. An efficient and reproducible sampling and extraction of DNA is required for a high-throughput qPCR based quantification of discoloring fungi. The authors have now adjusted DNA isolation protocols and optimized real-time PCR assays for species specific detection of fungi frequently found on painted surfaces (Aureobasidium pullulans, Alternaria alternata, Cladosporium cladosporides, Ulocladium atrum).
2009
Abstract
No abstract has been registered
Abstract
No abstract has been registered
Authors
Ari Hietala Nina Elisabeth Nagy Arne Steffenrem Harald Kvaalen Carl Gunnar Fossdal Halvor SolheimAbstract
No abstract has been registered
Abstract
Two mature clones of Norway spruce (Picea abies (L.) Karst.) shown to have different level of resistance towards inoculation of Heterobasidion parviporum were compared with respect to spatiotemporal expression of transcripts related to biosynthesis of lignin, stilbenes and other phenolic compounds in response to fungal inoculation and physical wounding. Both clones responded to H. parviporum and physical wounding at transcriptional and chemical levels. Taxifolin, detected in the resistant clone only, increased in concentration following both wounding and inoculation. Concentrations of stilbenoid glucosides were highest in the susceptible clone. Following wounding or inoculation, concentrations of these glucosides increased in the susceptible clone, and quantities of their corresponding aglycones increased dramatically in both clones close to the treatment point. Significant changes in transcription were detected over the entire lesion length for all transcripts, and only the changes in a few transcripts indicated a response to inoculation with H. parviporum differing from that caused by wounding alone. The resistant clone had higher basal concentrations of lignin (LTGA) compared to the susceptible clone; concentrations increased in both clones after wounding and wounding plus inoculation treatments, but remained consistently higher in the resistant clone, suggesting higher lignin levels in the cell walls compared to the susceptible clone. In addition, the transcript level in the same clones was also measured the following year and we saw indications of primed defences for a number of gene products likely resulting from the inoculations performed 12 months prior.
Abstract
To identify differentially expressed genes of the white-rot fungus Heterobasidion parviporum subtractive cDNA libraries were constructed using suppressive subtraction hybridization (SSH) technique with RNA extracted from an advanced stage of decay area and from colonization front next to the reaction zone of the stem of a mature Norway spruce trees. Besides cytochrome P450s and proteins with unknown function, the SSH libraries constructed contained genes involved in basic cellular processes, andcell wall degradation. To examine the role of selected candidate genes three trees, showing a variable degree of wood decay, were used for real-time RT-PCR profiling of candidate genes. In the decay transition areas the study revealed activity centers that showed remarkable similarity in the transcript profiles of monitored genes.