Xanthone biosynthesis and accumulation in calli and suspended cells of Hypercium androsaemum

被引:45
作者
Dias, ACP
Seabra, RM
Andrade, PB
Ferreres, F
Fernandes-Ferreira, M
机构
[1] Univ Minho, Dept Biol, Lab Biol Vegetal, P-4710 Braga, Portugal
[2] Univ Porto, Fac Farm, CEQUP, Lab Farmacognosia, P-4050 Oporto, Portugal
[3] CSIC, CEBAS, Dept Ciencia & Tecnol Alimentos, Lab Fitoquim, Murcia 30080, Spain
关键词
Hypericum androsaemum; calli; cells suspension; xanthones; phytohormones;
D O I
10.1016/S0168-9452(99)00178-8
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
Calli and suspended cells of Hypericum androsaemum accumulated high levels of 1,3,5,6 and 1,3,6,7 oxygenated xanthones. The major compounds include simple oxygenated xanthones or derivatives with prenyl, pyran or methoxyl groups, four of them being new natural compounds. A hypothetical biosynthetic scheme is proposed based on the isolated compounds and statistical analysis. Xanthone accumulation was influenced greatly by medium factors, namely hormone supplementation. Calli grown with 4.5 mu M alpha-naphtaleneacetic acid (NAA) + 2.3 mu M kinetin (KIN) had the highest specific xanthone production (1.3% biomass dry weight (DW)), whereas suspended cells grown in similar medium accumulated a lower amount (0.87% DW). Calli displayed a negative linear relationship between total xanthone accumulation and NAA concentration, in the range of 4.5-22.5 mu M. However, in this range the xanthone 1,3,6,7/1,3,5,6 ratio and the biomass production showed a positive linear relationship with NAA concentration. Substitution of 4.5 mu M of NAA by the same molar amount of 2,4-dichlorophenoxyacetic acid (2,4-D), in the presence of 2.3 mu M of KIN, caused a decrease in xanthone accumulation in calli. The use of N(6)-benzyladenine (BA) instead of KIN reduced xanthone production, independently of the auxin used. This effect was attenuated when both hormones were present. (C) 2000 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:93 / 101
页数:9
相关论文
共 28 条
[1]   Natural product formation by plant cell biotechnology - Results and perspectives [J].
Alfermann, AW ;
Petersen, M .
PLANT CELL TISSUE AND ORGAN CULTURE, 1995, 43 (02) :199-205
[2]   XANTHONES IN CELL-SUSPENSION CULTURES OF 2 CENTAURIUM SPECIES [J].
BEERHUES, L ;
BERGER, U .
PHYTOCHEMISTRY, 1994, 35 (05) :1227-1231
[3]  
BEERHUES L, 1995, PLANTA, V197, P608, DOI 10.1007/BF00191567
[4]   THE BIOSYNTHESIS OF MANGOSTIN - THE ORIGIN OF THE XANTHONE SKELETON [J].
BENNETT, GJ ;
LEE, HH .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1988, (09) :619-620
[5]   STUDIES ON CHEMICAL CONSTITUENTS OF CENTIANACEAE .1. XANTHONES OF CANSCORA-DECUSSATA SCHULT [J].
CHAUDHURI, RK .
PHYTOCHEMISTRY, 1971, 10 (10) :2425-+
[6]   The development and evaluation of an HPLC-DAD method for the analysis of the phenolic fractions from in vivo and in vitro biomass of Hypericum species [J].
Dias, ACP ;
Seabra, RM ;
Andrade, PB ;
Fernandes-Ferreira, M .
JOURNAL OF LIQUID CHROMATOGRAPHY & RELATED TECHNOLOGIES, 1999, 22 (02) :215-227
[7]   Unusual flavonoids produced by Callus of Hypericum perforatum [J].
Dias, ACP ;
Tomás-Barberán, FA ;
Fernandes-Ferreira, M ;
Ferreres, F .
PHYTOCHEMISTRY, 1998, 48 (07) :1165-1168
[8]   Cell division versus secondary metabolite production in Morinda citrifolia cell suspensions [J].
Hagendoorn, MJM ;
Jamar, DCL ;
Meykamp, B ;
vanderPlas, LHW .
JOURNAL OF PLANT PHYSIOLOGY, 1997, 150 (03) :325-330
[9]  
HISHIGURO K, 1995, PHYTOCHEMISTRY, V38, P867
[10]  
HISHIGURO K, 1993, PHYTOCHEMISTRY, V33, P839