4-hydroxy-2-pyrone formation by chalcone and stilbene synthase with nonphysiological substrates

被引:54
作者
Zuurbier, KWM
Leser, J
Berger, T
Hofte, AJP
Schröder, G
Verpoorte, R
Schröder, J
机构
[1] Univ Freiburg, Inst Biol 2, D-79104 Freiburg, Germany
[2] Leiden Univ, Gorlaeus Labs, Div Pharmacognosy, Leiden Amsterdam Ctr Drug Res, NL-2300 RA Leiden, Netherlands
[3] Leiden Univ, Gorlaeus Labs, Div Analyt Chem, Leiden Amsterdam Ctr Drug Res, NL-2300 RA Leiden, Netherlands
关键词
Pinus sylvestris; Scots pine; Humulus lupulus; hop; biosynthesis; chalcone; stilbene; phlorisovalerophenone; phlorisobutyrophenone; 4-hydroxy-2-pyrone;
D O I
10.1016/S0031-9422(98)00346-X
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Valerophenone synthase (VPS) is a polyketide synthase that catalyzes the formation of the phloroglucinol derivatives in the synthesis of the bitter acids in hop (Humulus lupulus). The reaction uses isovaleryl-CoA or isobutyryl-CoA, but otherwise it is identical to that of the chalcone synthase in flavonoid biosynthesis. Our study showed that chalcone synthase can perform the function of VPS, but not perfectly, because the majority of the reactions terminated after two condensation reactions (products: 4-hydroxy-2-pyrone derivatives). The same experiments with stilbene synthase yielded exclusively the 4-hydroxy-2-pyrone derivatives, not the products expected from three condensation reactions. The results are discussed in the context of the functional diversity and evolution in the family of CHS-related polyketide synthases. (C) 1998 Published by Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1945 / 1951
页数:7
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