Journal
JOURNAL OF ANTIBIOTICS
Volume 63, Issue 6, Pages 291-295Publisher
JAPAN ANTIBIOTICS RESEARCH ASSOC
DOI: 10.1038/ja.2010.33
Keywords
antioxidative activity; chemical mutagenesis; Halobacillus halophilus; hydroxy-3,4-dehydro-apo-8 '-lycopene; methyl hydroxy-3,4-dehydro-apo-8 '-lycopenoate
Funding
- European Commission [FP7-KBBE-2007-207948]
- German Science Foundation (DFG)
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We performed the chemical mutagenesis of Halobacillus halophilus (the producer of a C-30 carotenoid, methyl glucosyl-3,4-dehydro-apo-8'-lycopenoate) to isolate novel carotenoids that are biosynthetic intermediates of methyl glucosyl-3,4-dehydro-apo-8'-lycopenoate. As a result, we isolated two novel C-30 carotenoids, hydroxy-3,4-dehydro-apo-8'-lycopene and methyl hydroxy-3,4-dehydro-apo-8'-lycopenoate, which were biosynthesized through a novel 8'-apo C-30 pathway. These carotenoids showed antioxidative activity in the O-1(2) suppression model. The Journal of Antibiotics (2010) 63, 291-295; doi:10.1038/ja.2010.33; published online 23 April 2010
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