J. Berlin et al., ARE TISSUE-CULTURES OF PEGANUM-HARMALA A USEFUL MODEL SYSTEM FOR STUDYING HOW TO MANIPULATE THE FORMATION OF SECONDARY METABOLITES, Plant cell, tissue and organ culture, 38(2-3), 1994, pp. 289-297
This article reviews our present knowledge on the formation of tryptop
han derived secondary metabolites in tissue cultures of Peganum harmal
a. With the presence of beta-carboline alkaloids and serotonin, P. har
mala contains two rather simple, interrelated biosynthetic pathways. T
he long term disadvantage of low and unstable productivity of P. harma
la suspension culture has recently been overcome by establishing highl
y productive hairy root cultures. The first beta-carboline alkaloid bi
osynthetic enzymes, specific for the O-methylation of harmalol and har
mol as well as for the oxidation of harmaline to harmine, have been de
tected in these cultures, and they should thus provide a suitable sour
ce for studying the yet unknown initial two enzymatic steps of beta-ca
rboline alkaloid biosynthesis. Seedlings of P harmala have also been s
uccessfully transformed with constructed strains of Agrobacterium, as
demonstrated by the overexpression of a tryptophan decarboxylase gene
from Catharanthus roseus in cultures of P. harmala. In such transgenic
cultures a large overproduction of serotonin was observed. The relati
ve simplicity of these pathways and the rather easy handling of the cu
ltures could make P. harmala a useful and attractive model system for
studying the interaction, regulation and manipulation of secondary pat
hways in cultured cells.