ON BIOGENESIS OF FLAVONE O-GLYCOSIDES AND C-GLYCOSIDES IN LEMNACEAE

被引:49
作者
WALLACE, JW
MABRY, TJ
ALSTON, RE
机构
[1] The Cell Research Institute, Department of Botany, The University of Texas at Austin
关键词
D O I
10.1016/S0031-9422(00)85800-8
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
14C-Labeled apigenin, luteolin, orientin, isoorientin, and isovitexin were obtained either directly or by hydrolyzing the glycosides obtained from Spirodela and Lemna species which had been cultured on media containing phenylalanine-1-14C. The 14C-labeled flavones were introduced into the growth media for S. polyrhiza, S. oligorhiza and L. minor plants. When the extracts from these plants were chromatographed and the two-dimensional chromatograms examined autoradiographically, radioactivity was detected in O-glycosylated and O-methylated flavones. However, radioactivity was not detected in flavones containing new C-glycosyl linkages. The data suggest that plants in the Lemnaceae O-substitute flavones but do not C-glycosylate them. Moreover, evidence was obtained that flavones containing a 4′-monohydroxy B-ring can be oxidized to flavones with a 3′,4′-dihydroxy B-ring. None of the 14C-flavones was incorporated into any of the anthocyanins known to occur in the Lemnaceae. Isoorientin 3′-methyl ether and an O-β-d-glucoside of chrysoeriol were detected for the first time as constituents of L. minor. © 1970.
引用
收藏
页码:93 / &
相关论文
共 20 条
[11]  
MABRY TJ, 1968, RECENT ADVANCES P ED, P305
[12]  
Mabry TJ, 1969, SYSTEMATIC IDENTIFIC
[13]  
MARKHAM KR, IN PRESS
[14]   A CHEMOTAXONOMIC STUDY OF LEMNACEAE [J].
MCCLURE, JW ;
ALSTON, RE .
AMERICAN JOURNAL OF BOTANY, 1966, 53 (09) :849-&
[15]  
MCCLURE JW, 1964, THESIS U TEXAS
[16]  
OLLIS WD, 1961, CHEMISTRY NATURAL ED, P20
[17]  
VANDYKE G, 1965, THESIS U TEXAS
[18]  
WALLACE JW, 1967, THESIS U TEXAS
[19]  
WALLACE JW, 1966, PLANT CELL PHYSIOL, V1, P699
[20]  
WHALLEY WB, 1961, CHEMISTRY NATURAL PH, P20