| Literature DB >> 10406953 |
M Goese1, K Kammhuber, A Bacher, M H Zenk, W Eisenreich.
Abstract
The biosynthesis of humulone, an antibacterial bitter acid from hops, was studied by isotope-incorporation experiments using (13)C-labelled glucose or (2)H(2)O. (13)C enrichments, (2)H enrichments and (13)C(13)C coupling patterns identify isovaleryl-CoA, malonyl-CoA and dimethylallyl pyrophosphate as precursors for humulone. Dimethylallyl pyrophosphate, which serves as a building block for the bitter acid, is generated via the deoxyxylulose pathway of terpenoid biosynthesis. The data confirm that a symmetrical intermediate is involved in humulone formation.Entities:
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Year: 1999 PMID: 10406953 DOI: 10.1046/j.1432-1327.1999.00518.x
Source DB: PubMed Journal: Eur J Biochem ISSN: 0014-2956