a Department of Food and Resource Chemistry, University of Rhode Island, Kingston, Rhode Island 02881
ABSTRACT
The biosynthesis of 4-keto and 4,4'-diketo carotenoids in Brevibacterium sp. KY-4313 was studied. Echinenone and canthaxanthin were isolated from the cultures grown on a medium containing several n-alkanes. When glutathione was added to the bacterial cultures, the formation of canthaxanthin was inhibited while ß-carotene and its hydroxy derivatives accumulated. It is suggested that these 4-hydroxy compounds, isocryptoxanthin, isozeaxanthin, and 4-hydroxy-4'-keto-ß-carotene, are intermediates in the biosynthesis of canthaxanthin. In the presence of 2-(4-chlorophenylthio)-triethylamine hydrochloride or nicotine, lycopene and neurosporene accumulated. The ß-carotene level decreased slightly but ß-zeacarotene remained unchanged. ß-carotene and its derivatives were resynthesized upon removal of the inhibitors. It was concluded that cyclization can take place at either the neurosporene or lycopene level in Brevibacterium sp. KY-4313.
2 Present address: Department of Biological Chemistry, University of Illinois Medical Center, Chicago, Ill. 60612.
1 Contribution no. 1481 of the University of Rhode Island Agricultural Experiment Station.
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