PHENOLOGIC AND TISSUE DISTRIBUTION OF SESQUITERPENE LACTONES IN CULTIVATED SUNFLOWER (HELIANTHUS-ANNUUS L)

被引:10
作者
CHOU, JC [1 ]
MULLIN, CA [1 ]
机构
[1] PENN STATE UNIV, INTERDEPT PROGRAM PLANT PHYSIOL, University Pk, PA 16802 USA
关键词
ASTERACEAE; HELIANTHUS-ANNUUS L; DENSITOMETRY; HPTLC; ONTOGENIC VARIATION; PHENOLOGY; SESQUITERPENE LACTONE DISTRIBUTION;
D O I
10.1016/S0176-1617(11)80898-9
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Phenolic and tissue distribution of seven sesquiterpene lactones (STLs), 4,5-dihydroniveusin A, argophyllin B, argophyllin A, 15-hydroxy-3-dehydrodesoxytifruticin, niveusin B, 1,2-anhydridoniveusin A and an unidentified epoxide, in cultivated sunflower (Helianthus annuus L.), have been determined by a high-performance thin-layer chromatography and UV-reflectance scanning densitometry analysis. Leaves and flower heads were the major tissues in sunflower accumulating STLs, while the roots, stems, cotyledons, pollen, and achenes did not contain detectable STLs. The total STL amount per leaf increased from bottom to top leaves, while STL concentration (per gram fresh mass basis) was highest in top followed by bottom and then middle leaves. The total STL amounts in floral tissues were less than those in leaves but were highly concentrated on the top surface of disk florets forming a chemical defense to protect achene development from insect herbivores. Non-polar STLs (15-hydroxy-3-dehydrodesoxytifruticin, niveusin B, and 1,2-anhydridoniveusin A) were more abundant in early growth stages but were then dominated by polar STLs (4,5-dihydroniveusin A, argophyllins A and B, and an unidentified epoxide), especially argophyllin A, after four weeks of growth. Age-related expression of STL content in sunflower reveals an interesting phenomenon of secondary metabolism where 15-hydroxy-3-dehydrodesoxytifruticin may be the first stable STL and argophyllin A a final metabolite of STL biosynthesis.
引用
收藏
页码:657 / 663
页数:7
相关论文
共 19 条
[1]  
Chou J.-C., Phenologic and tissue distribution in cultivated sunflower of antifeedant sesquiterpene lactones for western corn rootworm, (1992)
[2]  
Chou J.-C,, Mullin C.A., Distribution and antifeedant associations of sesquiterpene lactones in cultivated sunflower (Helian-thus annuus L.) on western corn rootworm (Diabrotica virgifera virgifera LeConte), J. Chern. Ecol., 19, pp. 1439-1452, (1993)
[3]  
Hendry G., Why do plants have cytochrome P-450? Detoxification versus defence, New Phytologist, 102, pp. 239-247, (1986)
[4]  
Jamieson G.R., Reid E.H., Turner B.P., Jamieson A.T., Bakkenolide-A: Its distribution in Petasites species and cytotoxic properties, Phytochemistry, 15, pp. 1713-1715, (1976)
[5]  
Kelsey R.G., Morris M.S., Bhadane N.R., Shafizadeh F., Sesquiterpene lactones of Artemisia: TLC analysis and taxonomic significance, Phytochemistry, 12, pp. 1345-1350, (1973)
[6]  
Locken L.J., Kelsey R.G., Cnicin concentrations in Centaurea maculosa, spotted knapweed, Biochem. Syst. Ecol, 15, pp. 313-320, (1987)
[7]  
Melek F.R., Gage D.A., Gershenzon J., Mabry T.J., Sesquiterpene lactone and diterpene constituents of Helianthus annuus, Phytochemistry, 24, pp. 1537-1539, (1985)
[8]  
Mullin C.A., Alfatafta A.A., Harman J.L., Everett S.L., Serino A.A., Feeding and toxic effects of floral sesquiterpene lactones, diterpenes, and phenolics from sunflower (Helianthus annuus L.) on western corn rootworm, J. Agric. Food Chem., 39, pp. 2293-2299, (1991)
[9]  
Mullin C.A., Mason C.H., Chou J.-C., Linderman J.R., Phytochemical antagonism of γ-aminobutyric acid-based resistances in Diabrotica, Molecular Mechanisms of Insecticide Resistance: Diversity Among Insects, Symposium Series No. 505, pp. 288-308, (1992)
[10]  
Picman A.K., Ranieri R.L., Towers G.H.N., Lam J., Visualization reagents for sesquiterpene lactones and polyacetylenes on thin-layer chromatograms, J. Chromatog., 189, pp. 187-198, (1980)