Probing sesquiterpene hydroxylase activities in a coupled assay with terpene synthases

被引:16
作者
Greenhagen, BT [1 ]
Griggs, P [1 ]
Takahashi, S [1 ]
Ralston, L [1 ]
Chappell, J [1 ]
机构
[1] Univ Kentucky, Dept Agron, Plant Physiol Biochem Mol Biol Program, Lexington, KY 40546 USA
基金
美国国家科学基金会;
关键词
5-epi-aristolochene ynthase; premnaspirodiene synthase; 5-epi-aristolochene dihydroxylase hydroxylase; germacrene A; capsidiol; germacrene diol; solavetivone;
D O I
10.1016/S0003-9861(02)00613-6
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
5-epi-Aristolochene dihydroxylase (EAH) catalyzes unique stereo- and regiospecific hydroxylations of a bicyclic sesquiterpene hydrocarbon to generate capsidiol. To define functional and mechanistic features of the EAH enzyme, the utility of a coupled assay using readily available sesquiterpene synthases and microsomes from yeast overexpressing the EAH enzyme was determined. Capsidiol and deoxycapsidiol biosyntheses were readily measured in coupled assays consisting of 5-epi-aristolochene synthase and EAH as determined by the incorporation of radiolabeled farnesyl diphosphate into thin-layer chromatography-isolated products and verified by gas chromatography-mass spectrometry analysis. The assays were dependent on the amounts of synthase and hydroxylase protein added, the incubation times, and the presence of nicotinamide adenine dinucleotide phosphate. The utility of this coupled assay was extended by examining the relative efficiency of the EAH enzyme to catalyze hydroxylations of different sesquiterpene skeletons generated by other terpene synthases. (C) 2002 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:385 / 394
页数:10
相关论文
共 40 条
[1]   CLONING AND BACTERIAL EXPRESSION OF A SESQUITERPENE CYCLASE FROM HYOSCYAMUS-MUTICUS AND ITS MOLECULAR COMPARISON TO RELATED TERPENE CYCLASES [J].
BACK, K ;
CHAPPELL, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (13) :7375-7381
[2]   Identifying functional domains within terpene cyclases using a domain-swapping strategy [J].
Back, KW ;
Chappell, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (13) :6841-6845
[3]   ENZYMATIC FORMATION OF SESQUITERPENES [J].
CANE, DE .
CHEMICAL REVIEWS, 1990, 90 (07) :1089-1103
[4]   ACCUMULATION OF CAPSIDIOL IN TOBACCO CELL-CULTURES TREATED WITH FUNGAL ELICITOR [J].
CHAPPELL, J ;
NABLE, R ;
FLEMING, P ;
ANDERSEN, RA ;
BURTON, HR .
PHYTOCHEMISTRY, 1987, 26 (08) :2259-2260
[5]   GENERAL METHOD OF PREPARING FUNCTIONALIZED SPIROCYCLES - SYNTHESIS OF SPIROVETIVANE SESQUITERPENES [J].
DAUBEN, WG .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1977, 99 (22) :7307-7314
[6]   Germacrenes from fresh costus roots [J].
de Kraker, JW ;
Franssen, MCR ;
de Groot, A ;
Shibata, T ;
Bouwmeester, HJ .
PHYTOCHEMISTRY, 2001, 58 (03) :481-487
[7]   (-)-Spirolepechinene, a spirosesquiterpene from Lepechinia bullata (Lamiaceae) [J].
Eggers, MD ;
Sinnwell, V ;
Stahl-Biskup, E .
PHYTOCHEMISTRY, 1999, 51 (08) :987-990
[8]   Natural sesquiterpenoids [J].
Fraga, BN .
NATURAL PRODUCT REPORTS, 2001, 18 (06) :650-673
[9]   Analysis of a chemical plant defense mechanism in grasses [J].
Frey, M ;
Chomet, P ;
Glawischnig, E ;
Stettner, C ;
Grun, S ;
Winklmair, A ;
Eisenreich, W ;
Bacher, A ;
Meeley, RB ;
Briggs, SP ;
Simcox, K ;
Gierl, A .
SCIENCE, 1997, 277 (5326) :696-699
[10]  
GOTOH O, 1992, J BIOL CHEM, V267, P83