Biotransformation of the pentahydroxy flavone quercetin by Rhizobium loti and Bradyrhizobium strains (Lotus)

Lotus rhizobia catabolized quercetin in an arabinose-based medium via a novel form of C-ring cleavage, yielding phloroglucinol and protocatechuic acid. Conservation of the A and B rings of the flavone suggests that a chalcone could be formed as a transient intermediate

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Veröffentlicht in:Applied and Environmental Microbiology 1991-05, Vol.57 (5), p.1563-1565
Hauptverfasser: Rao, J.R. (The Queen's University of Belfast, Belfast), Sharma, N.D, Hamilton, J.T.G, Boyd, D.R, Cooper, J.E
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Sprache:eng
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Zusammenfassung:Lotus rhizobia catabolized quercetin in an arabinose-based medium via a novel form of C-ring cleavage, yielding phloroglucinol and protocatechuic acid. Conservation of the A and B rings of the flavone suggests that a chalcone could be formed as a transient intermediate
ISSN:0099-2240
1098-5336
DOI:10.1128/AEM.57.5.1563-1565.1991