Goese M, Kammhuber K, Bacher A, Zenk M H, Eisenreich W
Lehrstuhl für Organische Chemie und Biochemie, Technische Universität München, Garching, Germany.
Eur J Biochem. 1999 Jul;263(2):447-54. doi: 10.1046/j.1432-1327.1999.00518.x.
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.
使用¹³C标记的葡萄糖或D₂O通过同位素掺入实验研究了啤酒花中一种抗菌苦味酸——葎草酮的生物合成。¹³C富集、D富集和¹³C¹³C偶合模式确定异戊酰辅酶A、丙二酰辅酶A和二甲基烯丙基焦磷酸为葎草酮的前体。作为苦味酸组成单元的二甲基烯丙基焦磷酸是通过萜类生物合成的脱氧木酮糖途径生成的。数据证实,一种对称中间体参与了葎草酮的形成。