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Study of lignin biotransformation by Aspergillus fumigatus and white‐rot fungi using 14 C‐labeled and unlabeled kraft lignins
Author(s) -
Kadam Kiran L.,
Drew Stephen W.
Publication year - 1986
Publication title -
biotechnology and bioengineering
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.136
H-Index - 189
eISSN - 1097-0290
pISSN - 0006-3592
DOI - 10.1002/bit.260280313
Subject(s) - lignin , chemistry , aspergillus fumigatus , fermentation , cellulose , biodegradation , kraft paper , organic chemistry , biotransformation , depolymerization , biochemistry , botany , biology , materials science , enzyme , composite material
The biodegradation of lignin by fungi was studied in shake flasks using 14 C‐labeled kraft lignin and in a deep‐tank fermentor using unlabeled kraft lignin. Among the fungi screened, A. fumigatus —isolated in our laboratories—was most potent in lignin biotransformation. Dialysis‐type fermentation, designed to study possible accumulation of low MW lignin‐derived products, showed no such accumulation. Recalcitrant carbohydrates like mi‐crocrystalline cellulose supported higher lignolytic activity than easily metabolized carbohydrates like cellobiose. An assay developed to distinguish between CO 2 evolved from lignin and carbohydrate substrates demonstrated no stoichiometric correlation between the metabolism of the two cosubstrates. The submerged fermentations with unlabeled lignin are difficult to monitor since chemical assays do not give accurate and true results. Lignolytic efficiencies that allowed monitoring of such fermentations were defined. Degraded lignins were analyzed for structural modifications. A. fumigatus was clearly superior to C. versicolor in all aspects of lignin degradation; A. fumigatus brought about substantial demethoxylation and dehydroxylation, whereas C. versicolor degraded lignins closely resembled undegraded kraft lignin. There was a good agreement among the different indices of lignin degradation, namely, 14 CO evolution, OCH 3 loss, OH loss, and monomer and dimer yield after permanganate oxidation.