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Decomposition in Soil of Emodin, Chrysophanic Acid, and a Mixture of Anthraquinones Synthesized by an Aspergillus glaucus Isolate
Author(s) -
Linhares L. F.,
Martin J. P.
Publication year - 1979
Publication title -
soil science society of america journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.836
H-Index - 168
eISSN - 1435-0661
pISSN - 0361-5995
DOI - 10.2136/sssaj1979.03615995004300050025x
Subject(s) - anthraquinones , emodin , anthraquinone , incubation , chemistry , chromatography , biodegradation , orcinol , phenols , decomposition , polymer , organic chemistry , nuclear chemistry , botany , biochemistry , biology
A. glaucus synthesized 17 – 22 anthraquinones, and one to four phenolic compounds depending on cultural conditions and incubation time. The anthraquinones extracted from the culture media were equivalent to 10% or more of the total mycelium plus melanin polymers recovered. Based on two‐dimensional thin‐layer chromatography and cochromatography with reference compounds before and after separation on a silica gel column and on UV spectra, dominant anthraquinones included emodin, catenarin, physcion, erythroglaucin, endocrocin, and probably parietinic acid and questin. One of the phenols was orcinol. The anthraquinone mixtures, synthesized by A. glaucus under different cultural conditions, were only slowly degraded in soil. During a 12‐week incubation period the C losses ranged from 11 – 23%, while 69 and 47%, respectively, of emodin and chrysophanic acid C were evolved as CO 2 . Emodin when “linked” into peroxidase polymers was relatively stable to biodegradation during the earlier stages of incubation only. When in intimate physical association with a model humic acid‐type polymer, little protection was observed. The 14 C‐labeled A. glaucus anthraquinone mixture when “linked” to phenolase polymer showed a biodegradability reduction from about 25 – 11% during 12 weeks.