Abstract
Callus cultures were established from the plant Ipomoea cairica (L.) Sweet, to verify whether they produce the same lignans, arctigenin and trachelogenin, as the intact plant. Medium components (auxin, pH, carbohydrates) were changed to influence the production level of the two compounds. Optimal conditions for culture growth and lignan production were determined, and the implications for in vitro lignan production are discussed.
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