Hairy root cultures of Centranthus ruber DC. were established by infec
tion of sterile plantlets with Agrobacterium rhizogenes, strain R1601.
The transformed roots were grown in 12 different, hormone-free liquid
media, and valtrate, isovaltrate, 7-desisovaleroyl-7-acetylvaltrate,
7-homovaltrate, didrovaltrate and isovaleroxyhydroxydidrovaltrate were
quantified by high performance liquid chromatography. The highest ove
rall valepotriate content (3.0% dry wt) was observed in half-strength
Gamborg B5 medium supplemented with 3% sucrose. This concentration is
very similar to that found in the roots of parent plants grown in the
field. The use of N,N-dimethylmorpholinium iodide, a plant bioregulato
r, was very detrimental to the hairy root growth and to the valepotria
te production. The hairy roots cultured in half strength Gamborg B5 li
quid medium supplemented with 3% sucrose for 45 days produced over 31
mg/g dry wt valepotriates.