Content area

Abstract

Extraction of medium after incubation of the fungus, Cunninghamella elegans, with 0.03% (w/v) 1-methylnaphthalene produced mainly 1-hydroxymethylnaphthalene together with some 1-naphthoic acid and hydroxynaphthoic acid. Higher concentrations of substrate were inhibitory to biotransformation. Similar incubations with 1-naphtoic acid as substrate resulted in reduction of the carboxyl group to give 1-hydroxymethylnaphthalene. When 6-methylquinoline was used, the main product was 6-hydroxymethylquinoline but also some quinoline-6-carboxylic acid and some 6-methylquinoline-N-oxide were identified. In a 2-l fermenter 2.5g substrate was transformed in 324h. The 6-hydroxymethylquinoline was also produced by reduction of quinoline-6-carboxylic acid by the organism.[PUBLICATION ABSTRACT]

Details

Title
The formation of 1-hydroxymethylnaphthalene and 6-hydroxymethylquinoline by both oxidative and reductive routes in Cunninghamella elegans
Author
Mountfield, R J; Hopper, D J
Pages
379-83
Publication year
1998
Publication date
Sep 1998
Publisher
Springer Nature B.V.
ISSN
01757598
e-ISSN
14320614
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
884662865
Copyright
Springer-Verlag Berlin Heidelberg 1998