Identification of an indigo precursor from leaves of Isatis tinctoria (Woad)

被引:157
作者
Maugard, T
Enaud, E
Choisy, P
Legoy, MD
机构
[1] Univ La Rochelle, Lab Genie Prote & Cellulaire, F-17042 La Rochelle 1, France
[2] CRITT Hort, F-17300 Rochefort, France
关键词
woad; Isatis tinctoria; Brassicaceae; indigo; indirubin; isoindirubin; isatan; indican;
D O I
10.1016/S0031-9422(01)00335-1
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
Indole is presumably a product of indole-3-glycerol phosphate catabolism in Isatis tinetoria. It is oxidized into indoxyl and stored in young leaves Lis indigo precursor, Further oxidation and dimerization of indoxyl produces indigoid pigments. In this work, we describe an HPLC method dedicated to the identification and quantification of indigoid pigments (indigo, indirubin, isoindigo and isoindirubin) and indigo precursors produced in I. tinetoria (Woad). This work. carried out with two cultivars of I. tinetoria. has confirmed that the quantity of indigo precursors is dependent on the species and the harvest period. In addition we have shown for the first time that young leaves of I. tinetoria, harvested in June contained a new indigo precursor in addition to isatan B (indoxyl-5-ketogluconate) and indican (indoxyl-beta -D-glucoside). We suggest the name "isatan C" for this new indigo precursor in I. tinetoria. Its chemical characteristics point to an dioxindole ester with PM of 395. We have shown that isatan C reacts with isatan B increasing the red pigment production. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:897 / 904
页数:8
相关论文
共 16 条
[1]   PLANT CYTOCHROME-P450 [J].
BOLWELL, GP ;
BOZAK, K ;
ZIMMERLIN, A .
PHYTOCHEMISTRY, 1994, 37 (06) :1491-1506
[2]  
Durst Francis, 1995, Drug Metabolism and Drug Interactions, V12, P171
[3]   EXPRESSION OF NAPHTHALENE OXIDATION GENES IN ESCHERICHIA-COLI RESULTS IN THE BIOSYNTHESIS OF INDIGO [J].
ENSLEY, BD ;
RATZKIN, BJ ;
OSSLUND, TD ;
SIMON, MJ ;
WACKETT, LP ;
GIBSON, DT .
SCIENCE, 1983, 222 (4620) :167-169
[4]   ORIGIN OF INDIGO OF WOAD [J].
EPSTEIN, E ;
NABORS, MW ;
STOWE, BB .
NATURE, 1967, 216 (5115) :547-&
[5]   PIGMENTS DERIVED FROM TRYPTOPHAN .1. UROROSEIN .2. TRYPTOCHROME [J].
FEARON, WR ;
BOGGUST, WA .
BIOCHEMICAL JOURNAL, 1950, 46 (01) :62-67
[6]   CONTRIBUTION TO THE CHEMISTRY OF LEUCAEMIC URINE [J].
FRIEDMANN, E ;
MARRIAN, DH ;
PERUTZ, MF .
BIOCHIMICA ET BIOPHYSICA ACTA, 1950, 5 (01) :45-52
[7]   Indirubin, the active constituent of a Chinese antileukaemia medicine, inhibits cyclin-dependent kinases [J].
Hoessel, R ;
Leclerc, S ;
Endicott, JA ;
Nobel, MEM ;
Lawrie, A ;
Tunnah, P ;
Leost, M ;
Damiens, E ;
Marie, D ;
Marko, D ;
Niederberger, E ;
Tang, WC ;
Eisenbrand, G ;
Meijer, L .
NATURE CELL BIOLOGY, 1999, 1 (01) :60-67
[8]   BIOSYNTHESIS OF INDOXYL DERIVATIVES IN ISATIS-TINCTORIA AND POLYGONUM-TINCTORIUM [J].
MAIER, W ;
SCHUMANN, B ;
GROGER, D .
PHYTOCHEMISTRY, 1990, 29 (03) :817-819
[9]   Indoxyl-UDPG-glucosyltransferase from Baphicacanthus cusia [J].
Marcinek, H ;
Weyler, W ;
Deus-Neumann, B ;
Zenk, MH .
PHYTOCHEMISTRY, 2000, 53 (02) :201-207
[10]   NEW ROUTE TO BACTERIAL PRODUCTION OF INDIGO [J].
MERMOD, N ;
HARAYAMA, S ;
TIMMIS, KN .
BIO-TECHNOLOGY, 1986, 4 (04) :321-324