scholarly journals Applicability of Recombinant Laccases From the White-Rot Fungus Obba rivulosa for Mediator-Promoted Oxidation of Biorefinery Lignin at Low pH

Author(s):  
Jussi Kontro ◽  
Riku Maltari ◽  
Joona Mikkilä ◽  
Mika Kähkönen ◽  
Miia R. Mäkelä ◽  
...  

Utilization of lignin-rich side streams has been a focus of intensive studies recently. Combining biocatalytic methods with chemical treatments is a promising approach for sustainable modification of lignocellulosic waste streams. Laccases are catalysts in lignin biodegradation with proven applicability in industrial scale. Laccases directly oxidize lignin phenolic components, and their functional range can be expanded using low-molecular-weight compounds as mediators to include non-phenolic lignin structures. In this work, we studied in detail recombinant laccases from the selectively lignin-degrading white-rot fungus Obba rivulosa for their properties and evaluated their potential as industrial biocatalysts for the modification of wood lignin and lignin-like compounds. We screened and optimized various laccase mediator systems (LMSs) using lignin model compounds and applied the optimized reaction conditions to biorefinery-sourced technical lignin. In the presence of both N–OH-type and phenolic mediators, the O. rivulosa laccases were shown to selectively oxidize lignin in acidic reaction conditions, where a cosolvent is needed to enhance lignin solubility. In comparison to catalytic iron(III)–(2,2,6,6-tetramethylpiperidin-1-yl)oxyl (TEMPO) oxidation systems, the syringyl-type lignin units were preferred in mediated biocatalytic oxidation systems.

1992 ◽  
Vol 70 (3) ◽  
pp. 453-460 ◽  
Author(s):  
Ian D. Reid

Phlebia tremellosa dealkylates nonphenolic β-O-4-linked lignin model dimers; the phenolic products are oxidized by laccase. There is no evidence of α,β-cleavage as catalyzed by lignin peroxidase in some other white rot fungi. Methanol is the product of demethylation of 1-(3′,4′-dimethoxyphenyl)-2-(o-methoxyphenoxy)-propane-1,3-diol, and the demethylation reaction can be assayed by the release of radioactive CH3OH from the 4′-O14CH3 labelled compound. In older cultures, the methanol is metabolized to CO2. Demethylation is stimulated by oxygen and blocked by several common metabolic inhibitors. Both the mycelium and the extracellular medium are required for demethylation. Key words: lignin biodégradation, laccase, demethylation, lignin peroxidase.


Biochimie ◽  
2018 ◽  
Vol 148 ◽  
pp. 46-54 ◽  
Author(s):  
Shou-Nan Wang ◽  
Qing-Jun Chen ◽  
Meng-Juan Zhu ◽  
Fei-Yang Xue ◽  
Wei-Cong Li ◽  
...  

1998 ◽  
Vol 44 (7) ◽  
pp. 676-680 ◽  
Author(s):  
Orly Ardon ◽  
Zohar Kerem ◽  
Yitzhak Hadar

The white rot fungus Pleurotus ostreatus was grown in a chemically defined solid state fermentation system amended with cotton stalk extract (CSE).Treated cultures exhibited increased laccase activity as well as enhanced lignin mineralization. Mineralization of [14C]lignin initialized 4 days earlier in CSE-supplemented cultures than in control cultures. Total mineralization in the first 16 days was 15% in the CSE-treated cultures, compared with only 7% in the controls. Cotton stalk extract also contained compounds that serve as substrates for laccase purified from P. ostreatus as shown by oxygen consumption, as well as changes in the UV–visible spectrum.Key words: cotton, Pleurotusostreatus, white rot, laccase, lignin biodegradation.


2020 ◽  
Author(s):  
Jianqiao Wang ◽  
Tomohiro Suzuki ◽  
Hideo Dohra ◽  
Toshio Mori ◽  
Hirokazu Kawagishi ◽  
...  

Abstract Background Lignocellulosic biomass is an organic matrix composed of cellulose, hemicellulose, and lignin. In nature, lignin degradation by basidiomycetes is the key step in lignocellulose decay. The white-rot fungus Phanerochaete sordida YK-624 (YK-624) has been extensively studied due to its high lignin degradation ability. In our previous study, it was demonstrated that YK-624 can secrete lignin peroxidase and manganese peroxidase for lignin degradation. However, the underlying mechanism for lignin degradation by YK-624 remains unknown.Results Here, we analyzed YK-624 gene expression following growth under ligninolytic and nonligninolytic conditions and compared the differentially expressed genes in YK-624 to those in the model white-rot fungus P. chrysosporium by next-generation sequencing. More ligninolytic enzymes and lignin-degrading auxiliary enzymes were upregulated in YK-624. This might explain the high degradation efficiency of YK-624. In addition, the genes involved in energy metabolism pathways, such as the TCA cycle, oxidative phosphorylation, lipid metabolism, carbon metabolism and glycolysis, were upregulated under ligninolytic conditions in YK-624.Conclusions In the present study, the first differential gene expression analysis of YK-624 under ligninolytic and nonligninolytic conditions was reported. The results obtained in this study indicated that YK-624 produces more energy- and lignin-degrading enzymes for more efficient lignin biodegradation.


1991 ◽  
Vol 69 (1) ◽  
pp. 147-155 ◽  
Author(s):  
Ian D. Reid ◽  
Alain M. Deschamps

Phlebia tremellosa is a white-rot fungus which selectively degrades lignin, i.e., its ratio of lignin degradation to carbohydrate degradation during wood decay is higher than that of "simultaneous" white rots. Its need for a cosubstrate to support lignin degradation, and the effect of glucose supply on rate and extent of lignin metabolism, were examined in a synthetic, nitrogen-limited medium. Lignin metabolism by P. tremellosa, like simultaneous white rots, requires a cosubstrate. Glucose partially represses lignin degradation, but it is metabolized to extracellular intermediates, including ethanol. Subsequent utilization of ethanol as energy source supports rapid lignin degradation. Phlebia tremellosa grows well with cellulose, glucose, xylose, ethanol, or lactate as sole carbon (energy) source, and more slowly with glycerol or methanol. It appears unable to use kraft lignin, ferulate, vanillin, or acetate as sole carbon source. Cellulose, glycerol, and ethanol efficiently supported degradation of ring-labelled lignin to CO2, whereas glucose, xylose, and lactate were less efficient cosubstrates; methanol did not support lignin degradation. A relationship between tricarboxylic acid cycle operation and metabolism of lignin ring carbons to CO2, is suggested. Key words: lignin biodegradation, cosubstrate, glucose, ethanol, selectivity.


2013 ◽  
Vol 171 (6) ◽  
pp. 1525-1534 ◽  
Author(s):  
Sun-Hwa Ryu ◽  
Myung-Kil Cho ◽  
Myungkil Kim ◽  
Sang-Min Jung ◽  
Jin-Ho Seo

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