Isolation of cDNA and genomic fragments encoding the major manganese peroxidase isozyme from the white rot basidiomycetePleurotus ostreatus

We have isolated the cDNA and genomic sequences encoding the major isozyme of manganese peroxidase, MnP3, from the white rot basidiomycetePleurotus ostreatus strain IS1. The genemnp3 is interrupted by 10 introns and encodes a mature protein of 357 amino acid residues with a 26-amino-acid signal peptide. The amino acid residues known to be involved in peroxidase function and those that form the Mn-binding site in thePanerochaete chrysosporium MnP isozyme are conserved in MnP3. Comparison of the deduced primary structure of MnP3 with those of other peroxidases from various white rot fungi suggested that MnPs fromP. ostreatus andTrametes versicolor belong to a subgroup that is more similar to the lignin peroxidases than MnPs fromP. chrysosporium orCeriporiopsis subvermispora.     

Lignin-degrading activity of edible mushroom <Emphasis Type="Italic">Strobilurus ohshimae</Emphasis> that forms fruiting bodies on buried sugi (<Emphasis Type="Italic">Cryptomeria japonica</Emphasis>) twigs

Strobilurus ohshimae is an edible mushroom, and it specifically forms its fruiting bodies on buried sugi (Cryptomeria japonica) twigs. In this research, we studied lignindegrading activity of S. ohshimae. We isolated 18 strains of S. ohshimae from various regions of Japan, and determined their lignin degradation rates on sugi wood meal medium. All the strains of S. ohshimae degraded approximately 6%–12% of sugi lignin in 30 days, and these lignin degradation rates were 1.5–3 times higher than those of Trametes versicolor, which is a typical lignin-degrading fungus. Among the three main lignin-degrading enzymes, activity of lignin peroxidase and manganese peroxidase was not observed, while 4340U/g of laccase was produced in 30 days. To investigate the effect of wood species on lignin degradation by S. ohshimae, the lignin degradation rate and laccase productivity on sugi wood meal medium were compared with those on beech (Fagus crenata). In T. versicolor, both lignin degradation rate and laccase productivity were higher on beech than on sugi. Conversely, in S. ohshimae, lignin degradation rate and laccase productivity were higher on sugi than on beech. Therefore, it was suggested that coniferous lignin is not always difficult to degrade for the fungi that inhabit softwood. Part of this article presented at the 54th Annual Meeting of the Japan Wood Research Society, Sapporo, August 2004     

Reduction of ferric chelate caused by various wood-rot fungi

The reduction of ferric chelate caused by various wood-rot fungi was analyzed. Ferric chelate reductive activity was detected in cell-free extracts of seven wood-rot fungi:Phanerochaete chrysosporium, P. sordida YK-624,Ganoderma sp. YK-505,Coriolus versicolor, Bjerkandera adusta, Tyromyces palustris, andGloeophyllum trabeum. These fungi produced NADPH- or NADH-dependent ferric chelate reductive enzymes (or both) of different molecular weight. In the liquid culture ofP. sordida YK-624 andC. versicolor, a positive correlation was observed between extracellular MnP activity and intracellular NADPH-dependent ferric chelate reductive activity.     

Polyethylene degradation by manganese peroxidase in the absence of hydrogen peroxide

A possible role of Tween 80 in the polyethylene degradation by manganese peroxidase (MnP) and the basis of the MnP action in the absence of hydrogen peroxide were investigated. The MnP activity in the system was retained its maximum level for 6 days in the presence of Tween 80. Tween 20 and CHAPSO stabilized MnP in the system similarly to Tween 80, and these surfactants also promote the polyethylene degradation. The system containing malonate buffer, Mn(II), and MnP produced Mn(III) in the absence of hydrogen peroxide, but the effect of Tween 80 addition on Mn(III) production in the absence of hydrogen peroxide was small. The results show that Mn(III) is generated by the MnP action initiated and amplified by the decomposition of malonate by Mn(III) and that a surfactant such as Tween 80 is required to stabilize MnP in the system.This study was presented in part at the 42nd lignin symposium, Sapporo, October 1997 and the 43rd lignin symposium, Fuchu, Tokyo, October 1998     

Biological characteristics of five wood-rotting fungi and wood-decaying ability to Betula platyphylla

In this paper, the growth rate of five wood-rotting fungi, i.e., Coriolus versicolor, Irpex lacteus, Fomes fomentarius, Piptoporus betulinus and Pholiota adiposa, in solid medium and their biomass in liquid culture medium were compared by measuring mycelium length and dry mass. The activity of three main ligninolytic enzymes in those fungi, namely LiP, MnP and Lac, were also tested by colorimetry. At the same time, these fungi were used to decay the wood samples from 300 natural trees of white birch, to study their wood-decaying ability by measuring wood mass loss. The result showed that the growth rate, biomass, ligninolytic enzyme activity, and wood-decaying ability of the fungi were incompletely correlated. The growth rates of C. versicolor and I. lacteus were faster than those of P. betulinus and F. fomentarius; P. adiposa was the slowest in growth. The biomass of P. betulinus was the highest; C. versicolor, I. lacteus and F. fomentarius were in the middle, and P. adiposa was the lowest. There existed LiP, MnP and Lac activities in all fungi except P. betulinus, and the enzyme activities induced by wood powder were all higher than those of the control. The Lac of I. lacteus and the LiP of F. fomentarius and P. adiposa were only expressed in wood powder medium; the longer the fungi were cultured, the higher activity the enzyme had. The decomposition ability of C. versicolor to wood samples was the highest, followed by F. fomentarius and P. betulinus; I. lacteus and P. adiposa were the lowest.     

Screening of wood-rotting fungi for kraft pulp bleaching by the Poly R decolorization test and biobleaching of hardwood kraft pulp byPhanerochaete crassa WD1694

From among 419 wood-rotting fungi 10 were selected by the Poly R decolorization test, and their ability to bleach hardwood kraft pulp was assayed. Of the 10 selected, 6 fungi (i.e.,Phanerochaete crassa WD1694 and F150;Pleurotus pulmonarius PSC-H, PSC-M, and PSC-T;and Pleurotus species A119) showed much higher bleaching ability thanPhanerochaete chrysosponum BKMF1767 orTrametes versicolor WD1670, both of which are well-known high ligninolytic fungi.P. crassa WD1694 had the highest bleaching ability among the selected strains, and it increased the pulp brightness from 28 to 54, with a corresponding decrease in kappa number from 16 to 6 after 10 days of cultivation and alkali extraction. MnP was a predominant ligninolytic enzyme ofP. crassa WD1694 during the biobleaching.This research was presented in part at the 46th Annual Meeting of the Japan Wood Research Society, Kumamoto, April 1996     

In vitro decay of Aextoxicon punctatum and Fagus sylvatica woods by white and brown-rot fungi

Summary The in vitro decay of Aextoxicon punctatum and Fagus sylvatica wood by the fungi Trametes versicolor, Ganoderma australe, Phlebia chrysocrea and Lentinus cyathiformis was studied by the agar-block method, and then the decayed woods were analyzed by chemical and spectroscopic techniques. The results demonstrated the strong resistance of the A. punctatum wood to the brown-rot fungus L. cyathiformis; the resistance might be related to the low S/G lignin ratio in this Austral hardwood. Wood decay by the Austral white-rot fungi G. australe and P. chrysocrea was rather limited, and preferential degradation of lignin was not produced although all the fungi studied increased wood digestibility. The most characteristic white and brown-rot decay patterns were observed during the in vitro decay with T. versicolor and L. cyathiformis, respectively. Trametes versicolor caused high weight losses and reduced the lignin content of the wood, whereas L. cyathiformis produced a preferential removal of xylan. No important changes in the solid-state ¹³C NMR spectra were observed after wood degradation by T. versicolor, but this technique evidenced an increase in aromatic carbon by L. cyathiformis. This increase was higher than that found in the Klason lignin content, suggesting the presence of altered lignin fractions in the brown-rotted wood.The authors are indebted to Prof. H. D. Lüdemann for the facilities at the Institut für Biophysik und physikalische Biochemie (Regensburg), to A. Navarrete (INIA, Madrid) for her collaboration, and to C. F. Warren (ICE, Alcalá de Henares) for her linguistic assistance. The computer program for spectra treatment was developed by G. Almendros (Centro de Ciencias Medioambientales, CSIC, Madrid). This investigation has been funded by the Spanish Biotechnology Program (Grant BIO88-0185)     

杏鲍菇和乳白耙齿菌锰过氧化物酶活性规律的研究

采用LNAS培养基在4种不同培养液中,对白腐菌杏鲍菇和乳白耙齿菌在28℃下进行静止培养,得到了不同时间内的培养液,用紫外-可见分光光度计检测了在470 nm处对于2,6-DMP的氧化作用后光密度值的变化情况,作为锰过氧化物酶（MnP）产生和活性大小的依据,从而获得了杏鲍菇和乳白耙齿菌锰过氧化物酶与培养基的成分和酶作用底物的关系。结果表明,杏鲍菇和乳白耙齿菌均可产生MnP,对比4种成分不同的培养基酶活力测定结果,在培养液内添加酶的底物木屑和2,6-DMP后可提高MnP的分泌量。以前的研究认为：Mn2＋是MnP产生的必要因子。而本试验研究结果表明,Mn2＋并不是杏鲍菇和乳白耙齿菌产生MnP所必需的。论文为进一步利用这两种真菌产木质素降解酶,以及为进一步深入研究这两种真菌MnP对木质素及其它异生物质降解的作用机理提供基础的酶学研究。     

木质素降解真菌的筛选及其对森林地表可燃物的降解效果

【目的】筛选帽儿山人工林地表可燃物中的木质素降解真菌,探究木质素降解菌对不同森林地表可燃物的分解效果,以期找到能够有效降解森林可燃物的真菌菌种,为应用生物降解方法降低森林地表可燃物载量从而降低森林火灾发生概率与森林火险指数提供理论依据和基础数据。【方法】采集东北林业大学帽儿山实验林场尖砬沟森林培育实验站的落叶松、胡桃楸、水曲柳纯林与胡桃楸-落叶松、水曲柳-落叶松混交林内的凋落叶,采用添加抗生素的麦芽浸粉(MEA)培养基进行真菌的分离培养,之后采用愈创木酚平板显色法进行初筛,根据测定菌株的显色情况及菌落圈与显色圈比值筛选高活性木质素降解酶菌株,复筛利用苯胺蓝平板脱色法对菌株木质素氧化酶系进行定性测定,对2次筛选获得的菌株进行形态学及分子鉴定,然后以胡桃楸、水曲柳、落叶松3种可燃物样品作为分解基质,接入木质素降解菌单一及混合菌液,于28℃恒温培养7 d,分别测定经培养后基质中的木质素含量,分析木质素分解规律。【结果】由MEA培养基筛选出的9株真菌有5株在PDA-愈创木酚培养基上发生了显色反应,且菌株B6和Y3的R/r <1,即该2株菌能优先降解木质素;苯胺蓝平板脱色试验结果显示菌株B6和Y3均可使培养基蓝色褪去,即均具有LiP与MnP酶活性;经形态学及分子鉴定,菌株B6为白囊耙齿菌Irpex lacteus,菌株Y3为桦褶孔菌Lenzites betulinus;地表可燃物样品降解试验结果显示,经单一菌液与两者混合菌液培养后,样品中木质素含量均有下降,且经混合菌液处理后的3种可燃物基质表现出相对较好的降解效果;3种基质降解率从高到低依次为水曲柳>胡桃楸>落叶松;菌种Y3对木质素的降解效果较菌种B6好。【结论】混合菌液对可燃物中木质素的分解能力较单一菌液强;菌株B6和Y3之间无拮抗作用,混合后产生协同效应,使木质素降解酶系活力提高,从而可提高木质素降解率;菌种Y3降解能力强于B6;可燃物样品中木质素降解效果因基质不同而存在差异,阔叶可燃物比针叶可燃物易分解。经筛选出的木质素降解菌能有效降解可燃物中的木质素,可在一定程度上减少森林地表可燃物载量,从而降低森林火灾风险。     

Comparative study on the durability of heat-treated White Birch (Betula papyrifera) subjected to the attack of brown and white rot fungi

Abstract

The effect of heat treatment on decay resistance of white birch was evaluated for different incubation periods ranging from 2 to 12 weeks using three species of brown rot and one species of white rot fungus. The results of weight loss tests showed that the white rot fungus, Trametes versicolor, effectively degraded the untreated wood (73.5%). While the degradation of untreated wood by brown rot fungi species, Gloephyllum trabeum (11.6%) and Conifora puteana (6.2%), was considerably less compared to T. versicolor, the third brown rot fungi studied, Poria placenta, caused an appreciable degradation of the same species (52.4%). The results clearly showed that the heat treatment reduced the effect of fungi attack on white birch. Increasing the heat treatment temperature from 195 to 215°C resulted in reduction of weight loss, consequently, reduction in fungal attack. As an example, the weight loss reductions due to T. versicolor, P. placenta, G. trabeum and C. puteana attack was 62.2%, 71.3%, 89.6% and 100%, respectively, compared to the weight loss of untreated wood when it is heat treated at 215°C. Thus, these results confirmed that the heat treatment increased the biological resistance of white birch.     

Identification and partial characterization of an extracellular manganese-dependent peroxidase in Armillaria ostoyae and Armillaria mellea

Laccase and manganese-dependent peroxidase (Mn peroxidase) activities were detected in the culture media of Armillaria ostoyae and A. mellea. Mn peroxidase was produced in significantly higher quantity by the A. ostoyae isolates and was purified by chromatography from one isolate of this species. Some properties of the purified enzyme were examined (absorption spectrum, H₂O₂ and MnSO₄ optimal concentrations, pH optimum and lactate stimulation). Enzymes of potential importance in the lignin degradation (especially Mn peroxidase) by Armillaria sp. are compared to those of other root-rotting fungi. The possible role of Mn peroxidase in modulating the pathogenicity of Armillaria sp. is discussed.     

Micromorphological characteristics of decayed wood and laccase produced by the brown-rot fungus <Emphasis Type="Italic">Coniophora puteana</Emphasis>

Microscopic examination showed the cell wall decay pattern produced by the brown-rot fungus Coniophora puteana to be different from the degradation pattern known to be typical for brown-rot fungi. Erosion and thinning of cell walls in patterns considered to be characteristic of white-rot decay were observed. In particular, the fungal strain COP 20242 degraded secondary cell wall layers extensively, and also degraded lignin-rich middle lamellae. Some strains of C. puteana produced soft-rot type cavities in the S2 layer. All strains of C. puteana employed in the present work showed a positive reaction to tannic acid in the Bavendamm test, indicating the production of laccase. Microscopic and enzymatic studies provided evidence to suggest that the wood decay by C. puteana is unique both in terms of micromorphological and enzymatic patterns of cell wall degradation. This is because brown-rot fungi are not generally known to form cavities in the cell walls or to produce lignin-degrading enzymes. These observations suggest that lignin degradation capacity of brown-rot fungi may be greater than previously considered.     

Studies on hypersaline-tolerant white-rot fungi III: biobleaching of unbleached kraft pulp by hypersaline-tolerant manganese peroxidase from a marine white rot isolate, <Emphasis Type="Italic">Phlebia </Emphasis>sp. MG-60

 A marine white rot isolate, Phlebia sp. MG-60, secreted lignin peroxidase (LiP), manganese peroxidase (MnP), and laccase under different sea salt incubation conditions. Its MnP production was strongly enhanced by adding 3% sea salts, and the MnP showed high tolerance to sea salts and NaCl. The crude enzyme secreted at 3% sea salt concentration by Phlebia sp. MG-60, in which the main component was MnP (cMnP), was then used to bleach unbleached hardwood kraft pulp (UKP) in vitro. The pulp was brightened 11 points by 4 U of cMnP, and the kappa number was decreased 6 points when only 0.5 mM H₂O₂ was added continuously. When 0.5 mM H₂O₂ (1.22 mg H₂O₂ /g pulp) was added at the initial bleaching, the pulp brightness increased 6 points with a dosage of 4 U of cMnP. When crude MnPs were employed to bleach UKP with organic-free model white-water instead of the Milli Q water usually used, the pulp was brightened 10 and 13 points by 4 and 20 U of cMnP, respectively, and 5 and 6 points by 4 and 20 U of MnP, respectively, of Phanerochaete chrysosporium. Received: September 28, 2001 / Accepted: March 15, 2002 Correspondence to:R. Kondo     

Biobleaching of unbleached and oxygen-bleached hardwood kraft pulp by culture filtrate containing manganese peroxidase and lignin peroxidase fromPhanerochaete chrysosporium

Unbleached and oxygen-bleached hardwood kraft pulp (UKP and OKP), respectively, were bleached with a culture filtrate containing manganese peroxidase (MnP) and lignin peroxidase (LiP) fromPhanerochaete chrysosporium Burds. The brightness increases of UKP upon biobleaching with the culture filtrate with and without MnSO₄ were the same. The brightness increase of OKP with MnSO₄ decreased to about half that seen without MnSO₄. Changes in the brightness of UKP and OKP by treatment with the culture filtrate were determined. The brightness increased sharply by about eight points during the first 3h. The 3-h treatment was repeated seven times. The brightness increased linearly with the bleaching of UKP. On bleaching of OKP, the brightness increased slowly and stopped at about 78%.Part of this report was presented at the 62nd Pulp and Paper Research Conference of the Japan Tappi, Tokyo, June 1995     

Optimisation of a two-stage heat treatment process: durability aspects

Heat treatment of wood at relatively high temperatures (in the range of 150–280°C) is an effective method to improve biological durability of wood. This study was performed to investigate the effect of heat treatment process optimisation on the resistance against fungal attack, including basidiomycetes, molds and blue stain fungi. An industrially used two-stage heat treatment method under relatively mild conditions (<200°C) was used to treat the boards. Heat treatment of radiata pine sapwood revealed a clear improvement of the resistance against the brown rot fungi Coniophora puteana and Poria placenta. Increasing process temperature and/or effective process time during the first process stage, the hydro thermolysis, appeared to affect the resistance against C. puteana attack, but the effect on the resistance against P. placenta was rather limited. Heat treated radiata pine showed a limited resistance against the white rot fungus Coriolus versicolor and process variations during the hydro thermolysis stage appeared not to affect this resistance. A clear difference between the resistance of heat treated Scots pine sapwood and heartwood against fungal attack is observed. Scots pine heartwood showed a higher resistance against C. puteana and P. placenta but also against the white rot fungus C. versicolor. Similar results were obtained when heat treated birch was exposed to brown and white rot fungi. Heat treatment showed an improved resistance against C. puteana attack, especially at higher temperatures during the hydro thermolysis stage. A clear improvement of the durability was also observed after exposure to the white rot fungus C. versicolor and especially Stereum hirsutum. Increasing the process temperature or process time during the hydro thermolysis stage appeared to have a limited effect on the resistance against C. versicolor attack. Heat treated radiata pine and Norway spruce were still susceptible to mold growth on the wood surface, probably due to the formation of hemicelluloses degradation products (e.g. sugars) during heat treatment. Remarkable is the absence of blue stain fungi on heat treated wood specimen, also because the abandant blue stain fungi were observed on untreated specimen. Molecular reasons for the resistance of heat treated wood against fungal attack are discussed in detail contributing to a better understanding of heat treatment methods.     

Genomic gene encoding manganese peroxidase from a white-rot fungus Phanerochaete crassa WD1694

The gene encoding manganese peroxidase of a white-rot fungus Phanerochaete crassa WD1694 was cloned and sequenced. Four genomic clones were sequenced in which 3 clones were existed as alleles. The analysis of intron–exon structures divided the 4 clones into three subfamilies that corresponded to mnp2 and mnp3 of Phanerochaete chrysosporium, and a new subfamily possessing only five introns. The purified P. crassa WD1694 MnP consisted of 4 isozymes with same molecular weight, same N-terminal sequence, and different pI. N-terminal sequence of deduced protein of P. crassa mnpB3 gene was identical to those of 4 MnP isozymes; however, the other 3 mnp genes had different N-terminal sequence. The molecular weight of encoded mature protein of mnpB3 gene and purified MnP had a gap that could be difference between MnP proteins encoded by single gene. The results suggested that 4 MnP isozymes of P. crassa WD1694 arose from single gene.     

Degradation of lipophilic wood extractive constituents in Pinus sylvestris by the white-rot fungi Bjerkandera sp. and Trametes versicolor

The white-rot fungi Trametes versicolor and Bjerkandera spp. are among the most frequent decomposers of angiosperm wood in forest ecosystems and in wood products in service. Wood extractives have a major impact on wood properties and wood utilization. This work evaluated the ability of two white-rot fungal strains (Bjerkandera sp. strain BOS55 and T. versicolor strain LaVec94-6) to degrade the main lipophilic extractive constituents in Scots pine (Pinus sylvestris L.). The time course of wood decay and wood extractive degradation was monitored in stationary batch assays incubated for eight weeks. The strains tested eliminated high levels of total resin, 34 to 51% in two weeks. Wood triglycerides were the most readily degraded extractive components (over 93% elimination in only two weeks). Free fatty acids and resin acids, which are potential fungal inhibitors, were also rapidly decomposed by the fungal strains. Sterols were used more slowly, nonetheless, the fungal degradation of this extractive fraction ranged from 50 to 88% after four weeks. Received 19 March 1999     

Identification of wood‐decay fungi and assessment of damage in log depots of Western Black Sea Region (Turkey)

The aim of this study was to determine and quantify the wood‐decay fungi found on logs of forest tree species (beech, oak, hornbeam, Scots pine and fir) stored in log depots located in six different provinces in the Western Black Sea Region of Turkey. Additionally, it was aimed to determine the natural durability of some important wood species against the most commonly detected wood‐decay fungi. Eighteen families, 31 genera and 45 species belonging to the division Basidiomycota were detected; Antrodia crassa was identified for the first time in Turkey. The abundance of Panus neostrigosus, Polyporus meridionalis, Trametes hirsuta, T. versicolor and Stereum hirsutumincreased significantly with the holding time of the logs (r = 0.99, 0.87, 0.53, 0.57 and 0.78, respectively, p < 0.05). The majority of the fungal species were detected on logs stored in depots for 4–6 years (66%). The percentage of fungal species found on the logs with a holding time of three years or less was 29%, whereas the percentage for those detected on logs stored for seven or more years was 31%. Among the wood species, the greatest number of fungal species (29) and highest amount of fungi (2,539) occurred on beech wood. Natural durability tests showed that T. versicolor caused the greatest loss of wood mass, with an average of 23%. Field studies and natural durability tests performed in the laboratory showed that beech wood lost the most mass among the timber species studied.     

Response of maple sapwood to injury and infection

In sapwood challenge experiments in Acer rubrum, columns of discolouration initiated by wounding and inoculation with pioneer fungi (Cephalosporium sp., Phialophora sp.) were similar in size to untreated wounds. Inoculation with decay fungi (Pleurotus ostreatus, Trametes versicolor) produced larger columns of wound-initiated discolouration. The removal of bark around a bore wound caused a significantly larger column to form compared to the sum of the columns inititiated by separate wounds. Stage-I discoloured wood, not associated with obviously rotted wood, had concentrations of mobile cations and soluble phenols similar to sapwood. Stage-II discoloured wood, spatially associated with rotted wood, was frequently bounded by a chemically distinct boundary layer and the discoloured wood contained significantly greater concentrations of mobile cations and soluble phenols than stage-I discoloured wood.     

A histological investigation of Oriental beech wood decayed by Pleurotus ostreatus and Trametes versicolor

Chemical, light and electron microscopic studies were carried out on wood of Oriental beech (Fagus orientalis Lipsky) decayed by the white‐rot fungi Pleurotus ostreatus and Trametes versicolor for 30, 60 and 120 days according to the modified European standard EN 113. Mass loss as well as lignin, cellulose and carbohydrate content were determined before and after fungal attack. There were no significant differences of wood mass loss and chemical composition between both fungi at the end of incubation. After each incubation period, small specimens were stained for microscopic studies. The micromorphology of fungal cell wall degradation was rather similar for both fungi. Both decreased the cell wall thickness to the same extent. The accumulation of hyphae as well as the rupture of cell walls was also similar. The occurrence of hyphae, cavities in the pits and vessel walls followed nearly the same patterns. The parenchyma cells were completely destroyed. Altogether, both fungi produced a simultaneous white rot in Oriental beech wood.