Nutrient Consumption and Pigmentation of Deep and Surface Colonizing Sapstaining Fungi in Pinus contorta

Summary In this paper, we examined the ability of deep and surface staining fungi to utilize wood tissue nutrients. Fungal isolates were inoculated onto fresh billets and γ-sterilised sawnwood, both from Pinus contorta, and also onto defined nutrient media. The wood samples were assessed for host viability, fungal growth and nutrient status. The results indicated that the most aggressive sapstain species on fresh logs was Ceratocystis coerulescens, followed consecutively by Leptographium spp., Ophiostoma minus, O. piliferum, O. piceae, O. setosum, O. pluriannulatum and Aureobasidium pullulans. HPLC analysis of soluble sugars in fungal-infected wood indicated that mannose was the most depleted sugar, followed by glucose. Lipid analysis of infected wood indicated that Leptographium spp. and C. coerulescens greatly reduced the triglyceride fraction and that there was a wide spectrum of consumption of triglyceridederived fatty acids between the fungi. On defined media, the carbon source mannose led to the darkest pigmentation for all tested fungi. For C. coerulescens, the order of pigmentation intensity for the remaining tested carbon sources was reversed when compared to the other fungal species.

[1]  D. Fengel,et al.  Studies on the Colouring Matter of Blue-stain Fungi Part 2. Electron Microscopic Observations of the Hyphae Walls , 1989 .

[2]  S. Mansfield Enzymatic modification of Douglas-fir pulp , 1997 .

[3]  Robert A. Blanchette,et al.  Biological control of pitch in pulp and paper production by Ophiostoma piliferum , 1992 .

[4]  C. Breuil,et al.  Utilization of triglycerides, fatty acids and resin acids in lodgepole pine wood by a sapstaining fungus Ophiostoma piceae , 1993 .

[5]  M. Wingfield,et al.  The Ceratocystis species on conifers , 1998 .

[6]  Bjarne Holmbom,et al.  A convenient method for the determination of wood extractives in papermaking process waters and effluents , 1994 .

[7]  J. Webber,et al.  Comparison of bluestain fungi grown in vitro and in freshly cut pine billets , 1998 .

[8]  A. Gutiérrez,et al.  Biodegradability of Extractives in Sapwood and Heartwood from Scots Pine by Sapstain and White-Rot Fungi , 1999 .

[9]  B. Kreber,et al.  Effect of IPBC/DDAC on Spore Germination and Hyphal Growth of the Sapstaining Fungus Ophiostoma piceae , 1999 .

[10]  D. A. Knauft,et al.  Comparison of oxidative stability of high- and normal-oleic peanut oils , 1993 .

[11]  K. Seifert Sapstain of commercial lumber by species of Ophiostoma and Ceratocystis , 1993 .

[12]  H. Hill,et al.  Analysis of lipids in aging seed using capillary supercritical fluid chromatography , 1991 .

[13]  C. Breuil,et al.  Fungi that cause sapstain in Canadian softwoods , 1999 .

[14]  R. Zabel,et al.  Comparison of wood decay among diverse lignicolous fungi , 1997 .

[15]  C. Breuil,et al.  The sap-staining fungus Ophiostoma piceae synthesizes different types of melanin in different growth media , 1997 .

[16]  D. Fengel,et al.  Studies on the Colouring Matter of Blue-stain Fungi. Part 3. Spectroscopic Studies on Fungal and Synthetic Melanins , 1990 .

[17]  C. Breuil,et al.  Solid-phase extraction can rapidly separate lipid classes from acetone extracts of wood and pulp , 1994 .

[18]  A. Byrne,et al.  Production of brown stain in hemlock logs and lumber during storage , 1996 .

[19]  Roberta L. Farrell,et al.  Biodegradation of wood extractives from southern yellow pine by Ophiostoma piliferum , 1994 .

[20]  C. Breuil,et al.  Extracellular lipase production by a sapwood-staining fungus, Ophiostoma piceae , 1995, World journal of microbiology & biotechnology.