An investigation of the storage and biosynthesis of phenylpropenes in sweet basil

被引:363
作者
Gang, DR [1 ]
Wang, JH
Dudareva, N
Nam, KH
Simon, JE
Lewinsohn, E
Pichersky, E
机构
[1] Univ Michigan, Dept Biol, Ann Arbor, MI 48109 USA
[2] Purdue Univ, Dept Hort, W Lafayette, IN 47907 USA
[3] Rutgers State Univ, Dept Plant Sci, New Brunswick, NJ 08901 USA
[4] Agr Res Org, Newe Yaar Res Ctr, Aromat Med Spice Crops Unit, IL-30095 Ramat Yishay, Israel
关键词
D O I
10.1104/pp.125.2.539
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Plants that contain high concentrations of the defense compounds of the phenylpropene class (eugenol, chavicol, and their derivatives) have been recognized since antiquity as important spices for human consumption (e.g. cloves) and have high economic value. Our understanding of the biosynthetic pathway that produces these compounds in the plant, however, has remained incomplete. Several lines of basil (Ocimum basilicum) produce volatile oils that contain essentially only one or two specific phenylpropene compounds. Like other members of the Lamiaceae, basil leaves possess on their surface two types of glandular trichomes, termed peltate and capitate glands. We demonstrate here that the volatile oil constituents eugenol and methylchavicol accumulate, respectively, in the peltate glands of basil lines SW (which produces essentially only eugenol) and EMX-1 (which produces essentially only methylchavicol). Assays for putative enzymes in the biosynthetic pathway leading to these phenylpropenes localized many of the corresponding enzyme activities almost exclusively to the peltate glands in leaves actively producing volatile oil. An analysis of an expressed sequence tag database from leaf peltate glands revealed that known genes for the phenylpropanoid pathway are expressed at very high levels in these structures, accounting for 13% of the total expressed sequence tags. An additional 14% of cDNAs encoded enzymes for the biosynthesis of S-adenosyl-methionine, an important substrate in the synthesis of many phenylpropenes. Thus, the peltate glands of basil appear to be highly specialized structures for the synthesis and storage of phenylpropenes, and serve as an excellent model system to study phenylpropene biosynthesis.
引用
收藏
页码:539 / 555
页数:17
相关论文
共 51 条
  • [11] CHATTERJEE A, 1982, J NEMATOL, V14, P118
  • [12] NEGATIVE REGULATION OF THE ARABIDOPSIS HOMEOTIC GENE AGAMOUS BY THE APETALA2 PRODUCT
    DREWS, GN
    BOWMAN, JL
    MEYEROWITZ, EM
    [J]. CELL, 1991, 65 (06) : 991 - 1002
  • [13] GAGNAIRE D, 1977, MAKROMOL CHEM, V178, P1477
  • [14] Evolution of plant defense mechanisms - Relationships of phenylcoumaran benzylic ether reductases to pinoresinol-lariciresinol and isoflavone reductases
    Gang, DR
    Kasahara, H
    Xia, ZQ
    Vander Mijnsbrugge, K
    Bauw, G
    Boerjan, W
    Van Montagu, M
    Davin, LB
    Lewis, NG
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (11) : 7516 - 7527
  • [15] ISOLATION OF SECRETORY-CELLS FROM PLANT GLANDULAR TRICHOMES AND THEIR USE IN BIOSYNTHETIC-STUDIES OF MONOTERPENES AND OTHER GLAND PRODUCTS
    GERSHENZON, J
    MCCASKILL, D
    RAJAONARIVONY, JIM
    MIHALIAK, C
    KARP, F
    CROTEAU, R
    [J]. ANALYTICAL BIOCHEMISTRY, 1992, 200 (01) : 130 - 138
  • [16] GILDEMEISTER E, 1913, ATHERISCHEN OLE
  • [17] Infraspecific taxonomy and essential oil chemotypes in sweet basil, Ocimum basilicum
    Grayer, RJ
    Kite, GC
    Goldstone, FJ
    Bryan, SE
    Paton, A
    Putievsky, E
    [J]. PHYTOCHEMISTRY, 1996, 43 (05) : 1033 - 1039
  • [18] Guenther E., 1949, The Essential Oils
  • [19] INHIBITION OF FOODBORNE PATHOGENS BY THYMOL, EUGENOL, MENTHOL AND ANETHOLE
    KARAPINAR, M
    AKTUG, SE
    [J]. INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY, 1987, 4 (02) : 161 - 166
  • [20] KLISCHIES M, 1975, CHEM COMMUN, V21, P879