Modification of wood lignin by the fungus Panus tigrinus

The treatment of sawdust with the fungus Panus tigrinus VKM F-3616 D changed the contents of functional groups in lignin from wood raw material. These changes are accompanied by the release of carboxyl and phenyl hydroxyl groups involved in chemical bond formation between wood particles in pressed materials manufactured from wood wastes.     

Wood Lignin Modification by the Fungus Panus tigrinus

The treatment of sawdust with the fungus Panus tigrinus VKM F-3616 D changed the contents of functional groups in lignin from wood raw material. These changes are accompanied by the release of carboxyl and phenyl hydroxyl groups involved in chemical bond formation between wood particles in pressed materials manufactured from wood wastes.     

A new bacterial alcohol dehydrogenase active on degraded lignin and several low molecular weight aromatic compounds

A new intracellular bacterial dehydrogenase has been purified. It was active in the reversible reduction by NADH of conjugated carbonyl groups in partially degraded lignin. It was also active on various aromatic aldehydes such as vanillin, syringaldehyde and cinnamaldehyde, but had no effect on acetovanillone and lignin models carrying a conjugated ketone. It is proposed that this enzyme functions as a broadly specific lignin dehydrogenase at the level of aldehydic groups that are present in the lignin preparations.     

Ratio of erythro and threo forms of beta-O-4 structures in tension wood lignin

The ratio of erythro and threo forms of beta-O-4 structures in tension wood lignin was investigated by ozonation analysis of wood meal taken from various positions in the stem of yellow poplar (Liriodendron tulipifera). The proportion of the erythro form was higher in tension wood than in opposite wood, and the methoxyl group content showed a similar trend. The proportion of the erythro form and the methoxyl group content in the 7 positions in the stem lignin was correlated (correlation coefficient R=0.98), suggesting that the type of aromatic ring, syringyl or guaiacyl, is one of the factors which stereochemically controls the ratio of erythro and threo forms of beta-O-4 structures during lignin formation.     

Effects of decay classes and diameter classes on physico-chemical properties of Pinus koraiensis log in a typical mixed broadleaved-Korean pine forest

AimsLog is an important component for most of forest ecosystems. It plays crucial roles in maintaining soil fertility, sustaining biodiversity and cycling of carbon (C) and nutrient. However, physico-chemical properties of logs vary with decay classes and diameter classes. Our objective was to study effects of decay classes and diameter classes on physico-chemical properties of logs in a typical mixed broadleaved-Korean pine forest in northern China.MethodsIn this study, logs of Pinus koraiensis were chosen as it was the constructive species in the typical mixed broadleaved-Korean pine forest. Logs of P. koraiensis at each decay classes (I-V) were divided into four diameter classes, including diameter class i ≤ 10.0 cm, diameter class ii: 10.1-30.0 cm, diameter class iii: 30.1-50.0 cm, and diameter class iv > 50.0 cm. Then, we explored effects of different decay classes, diameter classes and their interactions on the physico-chemical properties of logs for both the heartwood and sapwood.Important findings The results showed that the physico-chemical properties of heartwood and sapwood generally exhibited similar variations. Their moisture content both increased with an increasing decay class, whereas wood density both decreased with an increased decay class and diameter class. The carbon concentrations of the sapwood showed a trend of gradual increasing during decomposition, and there was an accumulation in nitrogen (N) and phosphorus (P) concentrations of the heartwood and sapwood with an increased decay class, simultaneously. Only N and P concentrations of the heartwood increased and then decreased with an increasing diameter class. The cellulose content decreased with an increasing decay class. In contrast to the cellulose, the lignin content increased with an increased decay class. However, cellulose and lignin contents exhibited no distinct trend among diameter classes. The moisture content of logs had a significant positive correlation with C, N, P concentrations and lignin content (except P concentrations of the heartwood), but had a significant negative correlation with the cellulose content (p< 0.05). The wood density was negatively correlated with C, N, P concentrations and the lignin content, but it was positively correlated with the cellulose content (p< 0.05). Therefore, physico-chemical properties of logs had unique patterns along both decay classes and diameter classes, and the physical properties of logs (the moisture content and wood density) were important factor affecting the variations of their chemical contents.     

腐烂等级、径级对典型阔叶红松林红松倒木物理化学性质的影响

倒木是森林生态系统的重要组成部分, 在地力维护、生物多样性保持以及碳(C)和养分循环等方面具有重要意义, 但倒木物理化学性质随其腐烂等级和径级而变化。为了深入理解腐烂等级和径级对倒木物理化学性质的影响, 该研究以典型阔叶红松林的建群种——红松(Pinus koraiensis)的倒木为研究对象, 将其每个腐烂等级(I-V)下的倒木分为4个径级(径级i ≤ 10.0 cm、径级ii 10.1-30.0 cm、径级iii 30.1-50.0 cm、径级iv >50.0 cm), 研究了不同腐烂等级、径级及两者交互作用对倒木心材和边材物理化学性质的影响。结果表明: 心材和边材具有相似的变化规律。倒木心材和边材含水率随着腐烂等级增加而增加, 而木材密度随腐烂等级和径级的增加均呈下降趋势; 边材C含量以及心材和边材的氮(N)、磷(P)含量随腐烂等级增加呈上升趋势, 心材N、P含量随径级增加呈先增加后减少的趋势; 纤维素含量随腐烂等级增加呈下降趋势, 而木质素含量呈上升趋势, 纤维素和木质素含量随径级增加没有明显变化规律。倒木含水率与C、N、P、木质素含量(除心材P含量)显著正相关, 与纤维素含量显著负相关; 木材密度与C、N、P、木质素含量显著负相关, 与纤维素含量显著正相关。由此可见, 倒木物理化学性质受不同腐烂等级和径级的影响有各自的变化规律, 且倒木的物理性质(含水率和木材密度)是影响化学含量变化的重要因素。     

Monitoring of hydroxyl groups in wood during heat treatment using NIR spectroscopy

This paper deals with the evaluation of thermally treated wood by near-infrared (NIR) spectroscopy. In the NIR second derivative spectrum, the absorption band at 6913 cm(-1) appeared with the procession of heat treatment, which conclusively assigned to the phenolic hydroxyl groups due to the lignin in comparison with the spectrum of acetylated spruce wood. As a result of the changes in the ratio of the areal integral calculated from spectral separation in the region of hydroxyl groups (7200-6100 cm(-1)) by the Gauss-Newton method, it was clear that the degradation of hydroxyl group in the cellulose started predominantly from the amorphous region and followed to semicrystalline and crystalline region. There was an obvious correlation between the weight decrement of wood and the decrement of hydroxyl groups in the cellulose by heat treatment.     

Degradation of C-Labeled Lignins and C-Labeled Aromatic Acids by Fusarium solani

Abilities of isolate AF-W1 of Fusarium solani to degrade the side chain and the ring structure of synthetic dehydrogenative polymerizates, aromatic acids, or lignin in sound wood were investigated under several conditions of growth substrate or basal medium and pH. Significant transformations of lignins occurred in 50 days in both unextracted and extracted sound wood substrates with 3% malt as the growth substrate and the pH buffered initially at 4.0 with 2,2-dimethylsuccinate. Degradation of lignin in such woods also occurred under unbuffered pH conditions when a basal medium of either 3% malt or powdered cellulose in deionized water was present. Decomposition of the lignin in these woods did not occur in cultures where d-glucose was present as a growth substrate. F. solani significantly transformed, as measured as evolved CO(2), both synthetic side chain (beta, gamma)-C- and U-ring-C-labeled lignins in 30 days under liquid culture conditions of only distilled deionized water and no pH adjustment. Degradation of dehydrogenative polymerizates by F. solani was reduced drastically when D(2) was the liquid medium. AF-W1 also cleaved the alpha-C from p-hydroxybenzoic acid and evolved CO(2) from the substrate, [3-C]cinnamic acid. Thus, the fungus cleaved side chain carbon from substrate that originally lacked hydroxyl substitution on the aromatic nucleus. Surprisingly, small amounts of C cleaved from aromatic acids by F. solani were incorporated into cell mass. Initial buffering of the culture medium to pH 4.0 or 5.0 with 0.1 M 2,2-dimethylsuccinate significantly increased F. solani degradation of all lignins or aromatic acids. Results indicated that AF-W1 used lignin as a sole carbon source.     

Evidence for cleavage of lignin by a brown rot basidiomycete

Biodegradation by brown-rot fungi is quantitatively one of the most important fates of lignocellulose in nature. It has long been thought that these basidiomycetes do not degrade lignin significantly, and that their activities on this abundant aromatic biopolymer are limited to minor oxidative modifications. Here we have applied a new technique for the complete solubilization of lignocellulose to show, by one-bond ¹H-¹³C correlation nuclear magnetic resonance spectroscopy, that brown rot of spruce wood by Gloeophyllum trabeum resulted in a marked, non-selective depletion of all intermonomer side-chain linkages in the lignin. The resulting polymer retained most of its original aromatic residues and was probably interconnected by new linkages that lack hydrogens and are consequently invisible in one-bond ¹H-¹³C correlation spectra. Additional work is needed to characterize these linkages, but it is already clear that the aromatic polymer remaining after extensive brown rot is no longer recognizable as lignin.     

Decay of fossil wood from kimberlite pipes of Lac de Gras in the Canadian sub-Arctic area

Some fossil wooden samples of the Tertiary period, extracted from the crater of the kimberlite BHP-Panda pipe from the Lac de Gras region (in the Canadian sub-Arctic area), and previously identified as Sequioxylon canadense Blokhina, were chemically examined to both assess their state of preservation and discuss about the possible causes of their decay. The chemical composition of fossils (in terms of holocellulose, lignin and ash amounts) was evaluated by means of wet analyses, together with the chromatographic analysis of dichloromethane extracts, and additionally measurements of the cation exchange capacity (CEC) of fossils were also carried out. The analyses revealed the complete loss of holocellulose (except for 2 out of 9 samples), whereas lignin became the predominant component, together with ash (whose amount in one case was as high as 47.5%). Moreover, CEC data showed that all acid carboxyls were transformed into carboxylates. They represented the most important form of residual carboxyl groups in the fossils, and were even more abundant than in the reference (fresh) wood. All these occurrences evidenced a generally high level of decay for the fossils, as a consequence of water leaching during burial, which determined both the hydrolysis of esters groups and the partial depolymerisation of lignin.     

Covalent linkages between cellulose and lignin in cell walls of coniferous and nonconiferous woods

Covalent linkages between wall polysaccharides and lignin, especially linkage between cellulose and lignin were discussed by carboxymethylation technique of whole cell walls of coniferous and nonconiferous woods. Hydroxyl groups of plant cell walls polysaccharides were highly substituted, but not those of lignin by carboxymethyl groups under the used conditions, and separated into water-soluble and insoluble fractions by water extraction. Carboxymethylated wall polysaccharides linked covalently with lignin were distributed into the water-insoluble fractions. Composition of carboxymethylated sugar residues in the both fractions was analyzed quantitatively by 1H NMR spectroscopy after hydrolyzation with D2SO4 in D2O. More than half of cellulose linked covalently with lignin in coniferous wood, but only one-sixth of cellulose was involved in the linkage in nonconiferous wood. The major noncellulosic wall polysaccharides of coniferous wood also linked significantly with lignin. On the other hand, noncellulosic wall polysaccharides of nonconiferous wood were involved slightly in the covalent linkage with lignin. The situation of linkage between wall polysaccharides containing cellulose and lignin was visualized by scanning electron micrographs.     

Characterization of lignin in situ by photoacoustic spectroscopy

Photoacoustic spectroscopy is a recently developed nondestructive analytical technique that provides ultraviolet, visible, and infrared absorption spectra from intensely light scattering, solid, and/or optically opaque materials not suitable for conventional spectrophotometric analysis. In wood and other lignocellulosics, the principal ultraviolet absorption bands, in the absence of photosynthetic pigments, arise from the aromatic lignin component of the cell walls. Photoacoustic spectra of extracted lignin fragments (milled wood lignin) and synthetic lignin-like polymers contain a single major absorption band at 280 nanometers with an absorption tail extending beyond 400 nanometers. Photoacoustic spectra of pine, maple, and oak lignin in situ contain a broad primary absorption band at 300 nanometers and a longer wavelength shoulder around 370 nanometers. Wheat lignin in situ, on the other hand, exhibits two principle absorption peaks, at 280 nanometers and 320 nanometers. The presence of absorption bands at wavelengths greater than 300 nanometers in intact lignin could result from (a) interacting, nonconjugated chromophores, or (b) the presence of more highly conjugated structural components formed as the result of oxidation of the polymer. Evidence for the latter comes from the observation that, on the outer surface of senescent, field-dried wheat culms (stems), new absorption bands in the 350 to 400 nanometer region predominate. These new bands are less apparent on the outer surface of presenescent wheat culms and are virtually absent on the inner surface of either senescent or presenescent culms, suggesting that the appearance of longer wavelength absorption bands in senescent wheat is the result of accumulated photochemical modifications of the ligin polymer. These studies also demonstrate photoacoustic spectroscopy to be an important new tool for the investigation of insoluble plant components.     

Expression of an aromatic-dependent decarboxylase which provides growth-essential CO2 equivalents for the acetogenic (Wood) pathway of Clostridium thermoaceticum.

The acetogen Clostridium thermoaceticum generates growth-essential CO2 equivalents from carboxylated aromatic compounds (e.g., 4-hydroxybenzoate), and these CO2 equivalents are likely integrated into the acetogenic pathway (T. Hsu, S. L. Daniel, M. F. Lux, and H. L. Drake, J. Bacteriol. 172:212-217, 1990). By using 4-hydroxybenzoate as a model substrate, an assay was developed to study the expression and activity of the decarboxylase involved in the activation of aromatic carboxyl groups. The aromatic-dependent decarboxylase was induced by carboxylated aromatic compounds in the early stages of growth and was not repressed by glucose or other acetogenic substrates; nonutilizable carboxylated aromatic compounds did not induce the decarboxylase. The decarboxylase activity displayed saturation kinetics at both whole-cell and cell extract levels, was sensitive to oxidation, and was not affected by exogenous energy sources. However, at the whole-cell level, metabolic inhibitors decreased the decarboxylase activity. Supplemental biotin or avidin did not significantly affect decarboxylation. The aromatic-dependent decarboxylase was specific for benzoates with a hydroxyl group in the para position of the aromatic ring; the meta position could be occupied by various substituent groups (-H, -OH, -OCH3, -Cl, or -F). The carboxyl carbon from [carboxyl-14C] vanillate went primarily to 14CO2 in short-term decarboxylase assays. During growth, the aromatic carboxyl group went primarily to CO2 under CO2-enriched conditions. However, under CO2-limited conditions, the aromatic carboxyl carbon went nearly totally to acetate, with equal distribution between the carboxyl and methyl carbons, thus demonstrating that acetate could be totally synthesized from aromatic carboxyl groups. In contrast, when cocultivated (i.e., supplemented) with CO under CO2-limited conditions, the aromatic carboxyl group went primarily to the methyl carbon of acetate.     

Rapid biodegradation of calcium lignosulfonate by means of a mixed culture of microorganisms

In this paper we discuss the aerobic biodegradation of calcium libnosulfonate (CLS) in a beechwood sulfite waste liquor by means of a mixed culture of microorganisms consisting of two Trichosporn Years and bacteria in the Arthrobacter (two species), Psedomonas, and Chromobacterium genera. Under the established parameters 50% CLS was biodegraded in 24 hr accompanied by the demethylation of methoxyl groups, the splitting of sulpher–carbon bonds, and the appearance of carbonyl and carboxyl groups. The achieved results by determination of phenolic OH groups, as well as established changes of the absorption bands of IR spectra of the CLS molecule and the results of the shortening of the analyses of the C, H, O, and S, show that the degradation of the aromatic nuclei-culture biodegradation, which confirms the increase in the concentration of conjugated carbonyl groups and carboxyl groups.     

Aromatic compound degradation by the wood-feeding termite Coptotermes formosanus (Shiraki)

Wood-feeding termites (WFT) have proven to be highly efficient for wood digestion. There is evidence to support the hypothesis that there are ligninolytic enzymes existing in the gut of WFT responsible for wood pretreatment toward cellulose utilization. Elucidating the mechanism of biomass pretreatment through lignin modification in termites will help to develop more efficient lignocellulosic biofuel production processes. The in-vivo degradation of aromatic compounds with different substructures, including dyes, lignin model monomers and dimers, and lignin sulfonate, by Coptotermes formosanus (Shiraki) was investigated. The degradation of aromatic compounds was determined using pyrolysis-gas chromatography/mass spectrometry. The results revealed that WFT were able to metabolize the conjugated aromatic structures and that the degradation efficiency is higher in the foregut and midgut regions than in the hindgut. This is the first time that evidence has been provided to show different aromatic compound degradation in the separate gut segments of a termite. This study provides information on the C. formosanus (Shiraki) lignin modification phenomenon, and it demonstrates that phenomenon’s potential in the breakdown of the plant cell wall. Understanding this lignin modification could contribute to technology that will supplant current harsh pretreatment protocols for plant cell walls and thereby better facilitate the conversion of cellulose and hemicellulose.     

Patterns of lignin degradation and oxidative enzyme secretion by different wood- and litter-colonizing basidiomycetes and ascomycetes grown on beech-wood

The degradation of lignocellulose and the secretion of extracellular oxidoreductases were investigated in beech-wood (Fagus sylvatica) microcosms using 11 representative fungi of four different ecophysiological and taxonomic groups causing: (1) classic white rot of wood (e.g. Phlebia radiata), (2) 'nonspecific' wood rot (e.g. Agrocybe aegerita), (3) white rot of leaf litter (Stropharia rugosoannulata) or (4) soft rot of wood (e.g. Xylaria polymorpha). All strong white rotters produced manganese-oxidizing peroxidases as the key enzymes of ligninolysis (75-2200 mU g(-1)), whereas lignin peroxidase activity was not detectable in the wood extracts. Interestingly, activities of two recently discovered peroxidases - aromatic peroxygenase and a manganese-independent peroxidase of the DyP-type - were detected in the culture extracts of A. aegerita (up to 125 mU g(-1)) and Auricularia auricula-judae (up to 400 mU g(-1)), respectively. The activity of classic peroxidases correlated to some extent with the removal of wood components (e.g. Klason lignin) and the release of small water-soluble fragments (0.5-1.0 kDa) characterized by aromatic constituents. In contrast, laccase activity correlated with the formation of high-molecular mass fragments (30-200 kDa). The differences observed in the degradation patterns allow to distinguish the rot types caused by basidiomycetes and ascomycetes and may be suitable for following the effects of oxidative key enzymes (ligninolytic peroxidases vs. laccases, role of novel peroxidases) during wood decay.     

古田山国家级自然保护区木腐真菌物种多样性及分布

木腐真菌是微生物的一个重要类群, 主要以倒木为生长基质, 通过产生各种水解酶将倒木的纤维素、木质素和半纤维素分解为小分子物质, 对促进森林生态系统中的营养物质循环发挥着重要的生态功能。于2016年8月在浙江古田山国家级自然保护区开展的木腐真菌野外调查, 利用形态学和DNA序列分析对采集的标本进行了物种鉴定, 并分析了木腐真菌的物种组成和地理成分。在采集的158份标本中鉴定木腐真菌45属92种, 其中白腐真菌78种, 褐腐真菌14种。古田山的木腐真菌物种区系组成中, 热带-亚热带成分比例最高。在158份木腐真菌标本中, 97份标本采自直径大于10 cm的倒木或树桩上, 分属于76个种, 是木腐真菌生长的主要基质大小类型; 48份标本采自直径为2-10 cm的枝干上, 分属38个种; 13份标本采自直径小于2 cm的枝干上, 分属12种。不同腐烂等级倒木上生长的真菌数量和种类差异明显, 其中一级腐烂倒木上采集到9份标本(7种), 二级腐烂倒木上采集到86份标本(45种), 三级腐烂倒木上49份标本(29种), 四级腐烂倒木上14份标本(14种)。结果表明, 林分中倒木直径大小和腐烂程度是影响木腐真菌生长与分布的重要因子。     

Effect of steam treatment on the properties of wood cell walls

Steam treatment is a hygrothermal method of potential industrial significance for improving the dimensional stability and durability of wood materials. The steaming results in different chemical and micromechanical changes in the nanostructured biocomposite that comprise a wood cell wall. In this study, spruce wood ( Picea abies Karst.) that had been subjected to high-temperature steaming up to 180 °C was examined, using imaging Fourier Transform Infrared (FT-IR) microscopy and nanoindentation to track changes in the chemical structure and the micromechanical properties of the secondary cell wall. Similar changes in the chemical components, due to the steam treatment, were found in earlywood and latewood. A progressive degradation of the carbonyl groups in the glucuronic acid unit of xylan and a loss of mannose units in the glucomannan backbone, that is, a degradation of glucomannan, together with a loss of the C═O group linked to the aromatic skeleton in lignin, was found. The development of the hygroscopic and micromechanical properties that occurred with an elevation in the steam temperature correlated well with this pattern of degradation in the constituents in the biocomposite matrix in the cell wall (hemicellulose and lignin).     

Characterization of the NiFeCO complex of carbon monoxide dehydrogenase as a catalytically competent intermediate in the pathway of acetyl-coenzyme A synthesis.

Many anaerobic bacteria fix CO2 via the acetyl-CoA pathway. Carbon monoxide dehydrogenase (CODH), a key enzyme in the pathway, condenses a methyl group, a carbonyl group from CO, CO2, or the carboxyl group of pyruvate, and CoA to form acetyl-CoA. When treated with CO, CODH exhibits an EPR signal which results from an organometallic complex containing nickel, at least 3 iron, and CO and has been referred to as the NiFeC signal. Although this EPR signal has been presumed to be the spectroscopic signature of the enzyme-bound C-1 precursor of the carbonyl group of acetyl-CoA, its catalytic relevance had not been rigorously studied. We have demonstrated the catalytic competence of this NiFeC species by showing that the rate of formation of the NiFeC EPR signal is faster than the rate of an isotope exchange reaction between CO and acetyl-CoA, a partial reaction in the overall synthesis. Generation of the NiFeC signal in the absence of CO by acetyl-CoA has been demonstrated and requires a one-electron reduction at a midpoint potential of -541 mV versus the standard hydrogen electrode. In addition, we have observed and characterized an isotope exchange reaction between the carbonyl group of acetyl-CoA and the carbonyl group of the NiFeC complex, indicating that the C in the NiFeC complex is in the form of CO. These combined results demonstrate that the NiFeCO complex exhibits the characteristics expected of the precursor of the carbonyl group of acetyl-CoA.