Australian Journal of Chemistry Australian Journal of Chemistry Society
An international journal for chemical science
RESEARCH ARTICLE

Products of 1,8-Cineole Oxidation by a Pseudomonad

IC Macrae, V Alberts, RM Carman and IM Shaw

Australian Journal of Chemistry 32(4) 917 - 922
Published: 1979

Abstract

A bacterium having close affinity with Pseudomonas flava was isolated from eucalypt leaves for its ability to utilize 1,8-cineole (1) as a carbon source. The bacterium is also capable of utilizing α-terpineol, camphor, isoborneol and geraniol but failed to grow on borneol, limonene and piperitone. Growth of the organism in mineral salts medium containing 1,8-cineole resulted in the formation of four oxidation products. Keto lactone (2), alcohols (3) and (4) and ketone (5) arereported as natural products arising from the oxidation of 1,8-cineole by the bacterium.

http://dx.doi.org/10.1071/CH9790917

© CSIRO 1979


Export Citation Cited By (27)