Brown Rot-Type Fungal Decomposition of Sorghum Bagasse: Variable Success and Mechanistic Implications

Presley, Gerald N.; Ndimba, Bongani K.; Schilling, Jonathan S.

doi:https://doi.org/10.1155/2018/4961726

International Journal of Microbiology

On this page

Abstract Introduction Methods Results Discussion Conclusion Disclosure Conflicts of Interest Acknowledgments References Copyright Related Articles

Research Article | Open Access

Volume 2018 | Article ID 4961726 | https://doi.org/10.1155/2018/4961726

Brown Rot-Type Fungal Decomposition of Sorghum Bagasse: Variable Success and Mechanistic Implications

Gerald N. Presley,¹Bongani K. Ndimba,^2,3and Jonathan S. Schilling^1,4

Academic Editor: Giuseppe Comi

Received17 Oct 2017

Accepted27 Feb 2018

Published03 Apr 2018

Abstract

Sweet sorghum is a promising crop for a warming, drying African climate, and basic information is lacking on conversion pathways for its lignocellulosic residues (bagasse). Brown rot wood-decomposer fungi use carbohydrate-selective pathways that, when assessed on sorghum, a grass substrate, can yield information relevant to both plant biomass conversion and fungal biology. In testing sorghum decomposition by brown rot fungi (Gloeophyllum trabeum, Serpula lacrymans), we found that G. trabeum readily degraded sorghum, removing xylan prior to removing glucan. Serpula lacrymans, conversely, caused little decomposition. Ergosterol (fungal biomarker) and protein levels were similar for both fungi, but S. lacrymans produced nearly 4x lower polysaccharide-degrading enzyme specific activity on sorghum than G. trabeum, perhaps a symptom of starvation. Linking this information to genome comparisons including other brown rot fungi known to have a similar issue regarding decomposing grasses (Postia placenta, Fomitopsis pinicola) suggested that a lack of CE 1 feruloyl esterases as well as low xylanase activity in S. lacrymans (3x lower than in G. trabeum) may hinder S. lacrymans, P. placenta, and F. pinicola when degrading grass substrates. These results indicate variability in brown rot mechanisms, which may stem from a differing ability to degrade certain lignin-carbohydrate complexes.

1. Introduction

Renewable biofuel and bio-based products are an avenue towards energy independence and rural economic growth in southern Africa [1]. In the case of bioethanol in southern Africa, the predominant plant feedstock is water-intensive sugar cane [2], but changes in Sub-Saharan climates are predicted to result in dryer conditions and demand more diverse crop options in order for agriculture to adapt [3]. Sweet stem sorghum (Sorghum bicolor) is a native African plant grown for sugar that is more tolerant of arid climates and saline soils [4, 5], making it an attractive alternative bioenergy crop for southern Africa, and its residues after sugar extraction (bagasse) are an attractive biomass crop for many different bio-based product options. The lignocellulose in extracted sorghum bagasse could be utilized for silage or as a feedstock for biofuels and bioproducts, given efficient deconstruction [6]. The sugars locked in sorghum bagasse, however, are more difficult to liberate than those extractable in hot water, requiring harsher pretreatments to liberate fermentable sugars [7].

To better understand how sorghum bagasse could be deconstructed using milder, bio-based techniques, it is logical to study how sorghum is deconstructed by lignocellulose-degrading fungi. For this study, we chose to assess the mechanisms of lignocellulose-degrading “brown rot” fungi, a current research focus due to their carbohydrate-selective extraction pathways and their consolidation of oxidative pretreatments with enzymatic saccharification, two steps that remain separate in industrial processing [8]. In addition to a relevant bioprocessing system, investigating brown rot of sorghum is logical due to the varying abilities to degrade lignin and monocot grasses [9], something that is rarely tested among decomposer fungi associated with wood substrates. Brown rot fungi are polyphyletic [10], and while some characteristics such as early hemicellulose removal are common among brown rot fungi [11, 12], their genomes harbor significant variability [13, 14] and brown rot fungi can be found in a wide variety of niches in nature [15]. This implies variability in decay mechanisms among brown rot fungal clades, a useful model system for probing decay pathways for an understudied feedstock such as sweet stem sorghum bagasse as well as offering a useful context for probing fungal biochemical variability.

For our study, we chose to focus specifically on Gloeophyllum trabeum and Serpula lacrymans from two distinct clades (Gloeophyllales and Boletales, resp.). S. lacrymans has several key genomic distinctions from G. trabeum. These include the retention of exoacting cellobiohydrolase (CBH) cellulase genes, but, similar to Postia placenta, the absence of carbohydrate esterase family 1 (CE 1), a family containing feruloyl esterases (EC 3.1.1.73) that might be involved in decoupling xylan from lignin, particularly in the decay of grasses [16]. We have also seen on wood substrates (spruce, [17]) that S. lacrymans preferentially produced mannanase activity and G. trabeum produced higher xylanase activity, despite causing a similar type of decay. Sorghum, like other Poaceae substrates [18], is a xylan-rich substrate that would require S. lacrymans to alter its mannanase-dominant glycoside hydrolase profile in order to survive, as well as decoupling xylan from lignin by the hydrolysis of ferulic acid esters. Xylan is a barrier to the majority of the utilizable carbon in plant biomass [19], and failure by fungi to remove it could result in starvation and associated cell autolysis [20].

In this study, G. trabeum and S. lacrymans were compared for their ability to grow on water-extracted sweet stem sorghum biomass, the bagasse substrate (after extraction) most relevant to sorghum bioconversion. The fungi were grown for 7, 14, and 21 days and the loss of major structural carbohydrates, relative to undegraded sorghum, was measured along with polysaccharide-degrading enzyme activity and ergosterol contents. Decay strategies were compared to previous patterns generated on wood, as well as to other works showing variable decay patterns on other grass substrates.

2. Methods

2.1. Sorghum Collection and Preparation

Sweet stem sorghum (Sorghum bicolor) stalks were grown outside of East London, South Africa, maintained on Agricultural Research Council of South Africa research plots, and were harvested in May 2016. Four stalks were cut into ~2 cm long sections near the top of the stalks (<2 cm diameter). The stalk sections were dried at 70°C and then extracted in water at 90°C with 5 exchanges of fresh water. This approach removes some hemicellulose, along with other more soluble sugars and is a more biotechnologically relevant substrate, as compared to postextracted bagasse. After extraction, the stems were dried at 70°C and stored until further use.

2.2. Fungal Cultivation and Decay Microcosms

Serpula lacrymans S7.3 and Gloeophyllum trabeum ATCC 11539 cultures were maintained on potato dextrose agar. Agar plugs (1 cm dia) from plates colonized by either fungus were used to inoculate modified soil block jars, as previously described [17]. Extracted sorghum sections were vacuum-impregnated with water, sterilized (121°C, 16 psi, 1 hour), and cooled. Four sections were added to each soil block microcosm after allowing the fungus to colonize for 2 weeks, and then the microcosms were incubated at room temperature in the dark for 7, 14, and 21 days. Sorghum sections prepared in parallel but not inoculated were used as control material for characterization.

2.3. Protein Extraction, Purification, and Activity Assays

At each timepoint, degraded and nondegraded sorghum discs were chopped into smaller pieces by hand, suspended in 80 ml of extraction buffer (50 mM acetate, 0.5 M NaCl, 0.05% Tween 80, pH 5.0), and then extracted at 4°C with gentle shaking for 24 hours. Two replicate extracts of four pooled sorghum discs at each timepoint were used to generate protein extracts for each fungus. Coarse material was filtered using a polyester mesh, dried at 70°C, and reserved for chemical analysis. The filtrate was centrifuged (4000, 30 min) to remove particulates, filtered through 0.2 μm polyethersulfone (PES) filters, and exchanged into 50 mM citrate buffer pH 5.0 through 10 kDa PES membranes. Protein concentration was determined using a Bio-Rad protein assay kit (Hercules, CA, USA).

Cellulase and hemicellulase specific activities were measured by the dinitrosalicylic acid (DNS) method using solutions of 1.5% carboxymethyl cellulose (endoglucanase), 2% birchwood xylan (xylanase), and 0.5% locust bean gum (mannanase) [21]. Protein extracts were incubated with substrate at 50°C in 50 mM citrate pH 5.0 in triplicate. The absorbance at 540 nm was measured after color development, and reducing sugars were determined as glucose, xylose, and mannose reducing equivalents for endoglucanase, xylanase, and mannanase activities, respectively. Activities for β-glucosidase and β-xylosidase were determined by measuring the release of 4-nitrophenol (4NP) from 4-nitrophenol-β-glucoside (4NPG) and 4-nitrophenol-β-xylopyranoside (4NPX), respectively. Reactions were carried out in 10 mM 4NP-substrate in 50 mM citrate, pH 5.0 at 50°C, and were quenched with 2 volumes of 0.2 M Na₂CO₃. Absorbance at 400 nm was measured to determine free 4NP.

2.4. Ergosterol Extraction and Assay

Total ergosterol was measured to be used as a biomarker for fungal biomass and was extracted from three separate sorghum sections for each fungus at 7, 14, and 21 days of decay and from nondegraded sorghum using established methods [22]. Ergosterol was measured by HPLC using a Phenomenex™ (Torrance, CA, USA) 4 μ Hydro-RP 80a column by detection at 282 nm using previously described methods [23].

2.5. Sorghum Mass Loss, Density, and Compositional Analyses

Mass loss was determined for sorghum degraded for 7, 14, and 21 days and density of degraded and nondegraded sorghum sections were determined in triplicate by measuring the mass of water displaced by submerging fully hydrated sorghum sections in excess water (g cm⁻³). Degraded and nondegraded sorghum biomass previously extracted for protein were milled to 40 mesh in a Wiley mill. Sorghum powder was hydrolyzed in dilute acid and the concentration of glucan, xylan, and arabinan were measured by HPLC using an Aminex HPX87-P column (Bio-Rad, Hercules, CA) according to standard procedures [24]. The percent loss of each component was calculated from original component mass calculated using average mass losses at each timepoint.

3. Results

3.1. Decay Rates and Fungal Biomass on Sorghum

Gloeophyllum trabeum degraded sorghum more completely than Serpula lacrymans, causing nearly 5x greater mass loss (37.8% versus 7.9%, respectively) after 21 days of decay (Table 1). As typical of brown rot, early-stage strength loss was evident and residues were easily crumbled in the hand, more so for sorghum incubated with G. trabeum. Despite differences in degradative ability, ergosterol levels, a proxy for fungal biomass, did not differ at equivalent timepoints between the fungi and indicated ample colonization but minimal substrate degradation for S. lacrymans (Table 1). The mass of total protein extracted from sorghum biomass was also similar between the two fungi at most timepoints, ranging from 71 to 107 μg cm⁻³ of biomass (Table 1).

3.2. Sorghum Carbohydrate Losses

Xylan was removed more rapidly from sorghum than glucan by both species, with 24.5% and 29% xylan loss after 7 days of decay compared to 3.2% and 5% glucan loss over the same period by G. trabeum and S. lacrymans, respectively (Figure 1). Arabinan loss at 7 days for both species tended to be higher than glucan, but not significantly at 95% confidence (Tukey’s HSD, ). Glucan removal proceeded rapidly in the later stages of decay by G. trabeum, but this was not the case for S. lacrymans, reaching 38.4% loss by 21 days of decay in the former, and only 5.3% loss in the latter.

In relative terms (% of calculated original polymer mass), xylan was the most labile polysaccharide for G. trabeum, and 62.2% of the original xylan was lost after 21 days of decay (Figure 1). In absolute terms (mg of polymer), the mass of glucan and xylan removed by G. trabeum did not differ significantly until after 21 days of decay, where the total mass of glucan and xylan lost was 81 mg and 54.7 mg, respectively. S. lacrymans removed relatively more xylan and arabinan than glucan by 21 days of decay and did not remove either of the major hemicelluloses preferentially. The mass of polysaccharide components removed over time did not differ significantly from one another for sorghum degraded by S. lacrymans indicating no sugar preference. S. lacrymans also degraded lower percentages of all components than G. trabeum, collectively explaining low mass loss values.

3.3. Enzyme Activities

In G. trabeum extracts, most enzyme specific activities increased from early to late stages of decay except for endoglucanase activity, which remained flat throughout decay stages (Figure 2) (, Tukey’s HSD). In S. lacrymans, enzyme activities tended to be much lower, despite similar levels of total protein to G. trabeum. All measured activities in S. lacrymans, except for xylanase at 21 days, were not significantly above nondegraded controls (, Tukey’s HSD). In line with patchy growth patterns observed in S. lacrymans, xylanase activity at 7 days was highly variable between the two replicate extractions, with activity from one extract matching that of nondegraded controls. For both fungi, xylanase was the highest polysaccharide-degrading enzyme activity. Despite this, β-xylosidase (BXL) activity was lower than β-glucosidase (BGL) activity in G. trabeum extracts.

4. Discussion

In this study, the brown rot fungus Gloeophyllum trabeum (Gloeophyllales) effectively degraded sorghum while the fungus Serpula lacrymans (Boletales) struggled to release carbohydrates from the substrate. This variability in apparent recalcitrance of the sorghum substrate is an important result, but the variability between the fungi is also informative. Brown rot fungi are often assumed to have a preference for conifer substrates (gymnosperms) rather than angiosperm substrates in nature, and it is notable that G. trabeum is commonly found on the wood of both conifers and angiosperms [15]. This lack of substrate specificity for G. trabeum might partially explain its superiority to S. lacrymans on sorghum, although these substrate associations are poorly understood and often do not persist outside of a natural setting. Wood-degrading fungi that are host-specific in the field are often capable of growing and deconstructing a wider range of substrates when grown in culture [25, 26]. These results also support a broader variability in fungal deconstruction pathways among the brown rot types.

Successful growth on xylan-rich sorghum by G. trabeum may be due in part to high xylanase activity, a trait that would also enable decay of angiosperm wood whose hemicellulose is dominated by xylan. Both of our test fungi initiated the decomposition process by removing xylan, reflecting the protective role of xylan in shielding glucan from enzymatic hydrolysis [19]. Similar to the distinction between these fungi previously on spruce wood [17], xylanase specific activities were approximately 3x higher on average for G. trabeum than for S. lacrymans. It is plausible that G. trabeum has more responsive xylanase induction than S. lacrymans, stimulated by endoxylanase-produced xylo-, di-, and oligosaccharides as in other fungal species [27, 28]. In G. trabeum, BXL activity after 7 days was considerably lower than xylanase activity, implying that the majority of xylanase activity at the early decay stages is due to endo-acting xylanases required to liberate β-xylosidase substrates [29].

Differences in the degradative capacity of brown rot fungi may also be explained by the number and types of lignocellulose-degrading genes in their genomes that would be effective on a grass substrate. Along with S. lacrymans, Postia placenta and Fomitopsis pinicola have been shown to be ineffective in degrading a wide range of Poaceae substrates [9]. Grasses such as corn stover contain hemicelluloses that are similar to sorghum, primarily consisting of glucuronoarabinoxylan with ferulic acid ester linkages between xylan and lignin [30]. Among the types of genes involved in the degradation of grass polysaccharides, CE 1 feruloyl esterases (FAE) (EC 3.1.1.73) are absent in the genomes of P. placenta, F. pinicola, and S. lacrymans (Table 2) [14]. Absence of FAE activity has also been demonstrated in cultures of Postia placenta, indicating a minimal capacity to hydrolyze ferulic acid esters in lignocellulose [31]. In contrast, G. trabeum is known to effectively degrade Poaceae substrates [9] and possesses a CE 1 that is actively secreted on wood [17], suggesting CE 1 proteins could be the basis of the difference in degradative abilities observed in this study.

Despite differences in degradative ability, both fungi produced similar amounts of ergosterol, a proxy for total fugal biomass [22], as well as similar amounts of secreted protein on sorghum when compared at equivalent timepoints. Ergosterol/protein ratios (E/P) for the two fungi did not differ significantly at any decay stage, unlike previous observations on spruce where G. trabeum produced relatively more protein and less ergosterol (lower E/P) than S. lacrymans [17]. These patterns in E/P are likely explained by increased protein investments on sorghum, particularly for S. lacrymans; however, polysaccharide-degrading enzyme specific activity was on average 13x lower on sorghum biomass compared to spruce, whereas the same discrepancy was less than 4x lower for G. trabeum. The differences in specific activity may be linked to the relative inability of S. lacrymans to metabolize sorghum, causing C-starvation, cell autolysis, and the dilution of secreted protein with cellular protein as seen in C-starved cultures of Paxillus involutus and Aspergillus niger [20, 32]. This indicates that quantifying protein investments as a “trait,” including nitrogen-use efficiencies, might yield very different trait values for the same wood-degrading fungi, depending on the substrates used to calculate these values.

5. Conclusion

This study highlights differences in the biodegradative ability and decay mechanisms among phylogenetically disparate brown rot fungi. S. lacrymans, like some other brown rot fungi, may have general difficulty degrading grass substrates. The more generalist substrate associations of G. trabeum, however, may impart an ability to degrade grasses. The discrepancies in sorghum-degrading ability may be linked to the presence of fungal genes coding for enzymes that target xylan-lignin bonds and xylan, itself. This would be useful to explore in other brown rot clades, as well, and may help explain substrate-specificities among wood-degrading fungi.

Disclosure

Any opinions, findings, and conclusions or recommendations expressed in this material are those of the authors and do not necessarily reflect the views of the DOE, NSF, or USAID.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

Acknowledgments

This work was funded in part by the US Department of Energy (DOE) Office of Science (Early Career Grant DE-SC0004012 to Jonathan S. Schilling, from the Office of Biological and Ecological Research (BER), and BER Grant DE-SC0012742 to Jonathan S. Schilling). This work was also funded by the National Science Foundation Graduate Research Fellowship Programs under Grant no. 00039202 to Gerald N. Presley, an international travel allowance through the Graduate Research Opportunities Worldwide (GROW), and a United States Agency for International Development Research and Innovations Fellowship through the US Global Development Lab (Grant no. AID-LAB-T-15-00002) to Gerald N. Presley.

References

A. Gasparatos, G. P. Von Maltitz, F. X. Johnson et al., “Biofuels in sub-Sahara Africa: drivers, impacts and priority policy areas,” Renewable & Sustainable Energy Reviews, vol. 45, pp. 879–901, 2015.
View at: Publisher Site | Google Scholar
R. Diaz-Chavez and C. Jamieson, “Biofuels possibilities in the Southern Africa context,” Journal of Biobased Materials and Bioenergy, vol. 4, no. 3, pp. 256–266, 2010.
View at: Publisher Site | Google Scholar
O. Serdeczny, S. Adams, F. Baarsch et al., “Climate change impacts in Sub-Saharan Africa: from physical changes to their social repercussions,” Regional Environmental Change, vol. 17, no. 6, pp. 1585–1600, 2017.
View at: Publisher Site | Google Scholar
W. Zegada-Lizarazu and A. Monti, “Are we ready to cultivate sweet sorghum as a bioenergy feedstock? A review on field management practices,” Biomass & Bioenergy, vol. 40, pp. 1–12, 2012.
View at: Publisher Site | Google Scholar
T. H. Regassa and C. S. Wortmann, “Sweet sorghum as a bioenergy crop: literature review,” Biomass & Bioenergy, vol. 64, pp. 348–355, 2014.
View at: Publisher Site | Google Scholar
H. Cai, J. B. Dunn, Z. Wang, J. Han, and M. Q. Wang, “Life-cycle energy use and greenhouse gas emissions of production of bioethanol from sorghum in the United States,” Biotechnology for Biofuels, vol. 6, article 141, 2013.
View at: Publisher Site | Google Scholar
H. Rabemanolontsoa and S. Saka, “Various pretreatments of lignocellulosics,” Bioresource Technology, vol. 199, pp. 83–91, 2016.
View at: Publisher Site | Google Scholar
J. Zhang, G. N. Presley, K. E. Hammel et al., “Localizing gene regulation reveals a staggered wood decay mechanism for the brown rot fungus Postia placenta,” Proceedings of the National Acadamy of Sciences of the United States of America, vol. 113, no. 39, pp. 10968–10973, 2016.
View at: Publisher Site | Google Scholar
J. T. Kaffenberger and J. S. Schilling, “Using a grass substrate to compare decay among two clades of brown rot fungi,” Applied Microbiology and Biotechnology, vol. 97, no. 19, pp. 8831–8840, 2013.
View at: Publisher Site | Google Scholar
D. S. Hibbett and M. J. Donoghue, “Analysis of character correlations among wood decay mechanisms, mating systems, and substrate ranges in homobasidiomycetes,” Systematic Biology, vol. 50, no. 2, pp. 215–242, 2001.
View at: Publisher Site | Google Scholar
T. L. Highley, “Changes in chemical-components of hardwood and softwood by brown-rot fungi,” Material und Organismen, vol. 22, no. 1, pp. 39–45, 1987.
View at: Google Scholar
J. S. Schilling, J. Ai, R. A. Blanchette, S. M. Duncan, T. R. Filley, and U. W. Tschirner, “Lignocellulose modifications by brown rot fungi and their effects, as pretreatments, on cellulolysis,” Bioresource Technology, vol. 116, pp. 147–154, 2012.
View at: Publisher Site | Google Scholar
D. Floudas, M. Binder, R. Riley et al., “The paleozoic origin of enzymatic lignin decomposition reconstructed from 31 fungal genomes,” Science, vol. 336, no. 6089, pp. 1715–1719, 2012.
View at: Publisher Site | Google Scholar
R. Riley, A. A. Salamov, D. W. Brown et al., “Extensive sampling of basidiomycete genomes demonstrates inadequacy of the white-rot/brown-rot paradigm for wood decay fungi,” Proceedings of the National Acadamy of Sciences of the United States of America, vol. 111, no. 27, pp. 9923–9928, 2014.
View at: Google Scholar
R. L. Gilbertson and L. Ryvarden, North American Polypores, vol. 1, Fungiflora, Oslo, Norway, 1986.
V. F. Crepin, C. B. Faulds, and I. F. Connerton, “A non-modular type B feruloyl esterase from Neurospora crassa exhibits concentration-dependent substrate inhibition,” Biochemical Journal, vol. 370, no. 2, pp. 417–427, 2003.
View at: Publisher Site | Google Scholar
G. N. Presley and J. S. Schilling, “Distinct growth and secretome strategies for two taxonomically divergent brown rot fungi,” Applied and Environmental Microbiology, vol. 83, no. 7, Article ID e02987-16, 2017.
View at: Publisher Site | Google Scholar
J. Vogel, “Unique aspects of the grass cell wall,” Current Opinion in Plant Biology, vol. 11, no. 3, pp. 301–307, 2008.
View at: Publisher Site | Google Scholar
X. Zhao, L. Zhang, and D. Liu, “Biomass recalcitrance. Part I: The chemical compositions and physical structures affecting the enzymatic hydrolysis of lignocellulose,” Biofuels, Bioproducts and Biorefining, vol. 6, no. 4, pp. 465–482, 2012.
View at: Publisher Site | Google Scholar
B. M. Nitsche, T. R. Jørgensen, M. Akeroyd, V. Meyer, and A. F. J. Ram, “The carbon starvation response of Aspergillus niger during submerged cultivation: insights from the transcriptome and secretome,” BMC Genomics, vol. 13, article 380, 2012.
View at: Publisher Site | Google Scholar
T. K. Ghose, “Measurement of cellulase activities,” Pure and Applied Chemistry, vol. 59, no. 2, pp. 257–268, 1987.
View at: Publisher Site | Google Scholar
S. Y. Newell, T. L. Arsuffi, and R. D. Fallon, “Fundamental procedures for determining ergosterol content of decaying plant-material by liquid-chromatography,” Applied and Environmental Microbiology, vol. 54, no. 7, pp. 1876–1879, 1988.
View at: Google Scholar
J. S. Schilling and J. Jellison, “Oxalate regulation by two brown rot fungi decaying oxalate-amended and non-amended wood,” Holzforschung, vol. 59, no. 6, pp. 681–688, 2005.
View at: Publisher Site | Google Scholar
A. Sluiter, B. Hames, R. Ruiz et al., “Determination of structural carbohydrates and lignin in biomass,” Tech. Rep., NREL Laboratory and Analytical Procedures, 2008, https://www.nrel.gov/bioenergy/biomass-compositional-analysis.html.
View at: Google Scholar
T. L. Highley, “Influence of carbon source on cellulase activity of white-rot and brown-rot fungi,” Wood Fiber, vol. 5, pp. 50–58, 1973.
View at: Google Scholar
V. Valášková and P. Baldrian, “Degradation of cellulose and hemicelluloses by the brown rot fungus Piptoporus betulinus - production of extracellular enzymes and characterization of the major cellulases,” Microbiology, vol. 152, no. 12, pp. 3613–3622, 2006.
View at: Publisher Site | Google Scholar
D. Haltrich, B. Nidetzky, K. D. Kulbe, W. Steiner, and S. Župančič, “Production of fungal xylanases,” Bioresource Technology, vol. 58, no. 2, pp. 137–161, 1996.
View at: Publisher Site | Google Scholar
J. Zhang and J. S. Schilling, “Role of carbon source in the shift from oxidative to hydrolytic wood decomposition by Postia placenta,” Fungal Genetics and Biology, vol. 106, pp. 1–8, 2017.
View at: Publisher Site | Google Scholar
P. Biely, S. Singh, and V. Puchart, “Towards enzymatic breakdown of complex plant xylan structures: State of the art,” Biotechnology Advances, vol. 34, no. 7, pp. 1260–1274, 2016.
View at: Publisher Site | Google Scholar
R. Kumar, G. Mago, V. Balan, and C. E. Wyman, “Physical and chemical characterizations of corn stover and poplar solids resulting from leading pretreatment technologies,” Bioresource Technology, vol. 100, no. 17, pp. 3948–3962, 2009.
View at: Publisher Site | Google Scholar
P. Haase-Aschoff, D. Linke, and R. G. Berger, “Detection of feruloyl- and cinnamoyl esterases from basidiomycetes in the presence of interfering laccase,” Bioresource Technology, vol. 130, pp. 231–238, 2013.
View at: Publisher Site | Google Scholar
M. Ellström, F. Shah, T. Johansson, D. Ahrén, P. Persson, and A. Tunlid, “The carbon starvation response of the ectomycorrhizal fungus Paxillus involutus,” FEMS Microbiology Ecology, vol. 91, no. 4, Article ID fiv027, 2015.
View at: Publisher Site | Google Scholar

Copyright

Copyright © 2018 Gerald N. Presley et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

PDF Download Citation

Download other formats

Order printed copies

Views

1406

Downloads

872

Citations