BIOSYNTHESIS OF INDIGO PRECURSORS IN HIGHER-PLANTS

被引：48
作者：
XIA, ZQ
ZENK, MH
机构：
[1] D-8000 München 2
来源：
PHYTOCHEMISTRY | 1992年 / 31卷 / 08期
关键词：
BAPHICACANTHUS-CUSIA; ACANTHACEAE; CALANTHE-VERATRIFOLIA; ORCHIDACEA; ISATIS-TINCTORIA; BRASSICACEAE; POLYGONUM-TINCTORIUM; POLYGONACEAE; BIOSYNTHESIS; INDOXYL DERIVATIVES;
D O I：
10.1016/0031-9422(92)83613-4
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：
Contradictory results in the literature concerning the role of L-tryptophan in the biosynthesis of the indigo precursors, indican and isatan B, in four higher plants belonging to four plant families have been resolved. [3-C-13]-Indole and L-[3-C-13]-tryptophan were synthesized by standard techniques. Feeding experiments with the labelled precursors unequivocally showed by C-13 NMR and mass spectroscopy, that indole and not L-tryptophan is the biosynthetic precursor for the indoxyl derivatives found in plants.
引用
收藏
页码：2695 / 2697
页数：3
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