[Enantiomeric monoterpenes in ether oil from Achillea millefolium s. I.--a taxonomically useful marker?]. / Enantiomere Monoterpene im ätherischen Ol von Achillea millefolium s. l.--eine zusätzliche taxonomische Bestimmungshilfe?

The Achillea millefolium complex is a group of taxonomically hardly separable species. Yarrow has the tendency to hybridize and to vary in phenotype. An obvious characterization of the species or hybrids is not just important for the taxonomical distinction but also for a reliable assessment of herbal drug quality. Most of the Achillea plants are still gathered from natural populations. According to the variation in phenotype, mixtures with Achillea species, which contain allergy setting compounds, often cannot be determined. Morphometric investigations exclusively do not replace a further chemical characterization. Therefore we tried to assess the composition of the chiral monoterpenes alpha-pinene, beta-pinene and sabinene. They were selected because of their frequency in the essential oil of Achillea species. By method of M.C.S.S. (Moving Capillary Stream Switching) the differentiation of stereoisomeres succeeded directly from the essential oil, which was distilled or extracted by headspace trapping at room temperature. The enantiomeric distribution neither depends on the method of extraction, nor on the habitat or the developmental stage of Yarrow. Since the compositions of enantiomeres from several Achillea species and their hybrides are of different pattern, it seemed to represent an additional marker. Though investigations of all species within the Achillea millefolium group and possibly of further chiral compounds are necessary to ensure these results.

Identification of benzodiazepines in Artemisia dracunculus and Solanum tuberosum rationalizing their endogenous formation in plant tissue.

Sterile cultivated plant cell tissues and cell regenerates of several species were tested for their binding affinity to the central human benzodiazepine receptor. Binding activity was found in extracts of Artemisia dracunculus cell tissue (IC(50) = 7 microg/ml) and, to a lesser extent, in plant regenerates of potato herb (Solanum tuberosum). Preparative HPLC led to the isolation of fractions with a significant displacing potency in the benzodiazepine receptor binding assay. Using on-line HPLC-electrospray-tandem mass spectrometry (HPLC-ESI-MS/MS) in the "selected reaction monitoring" (SRM) mode, delorazepam and temazepam were found in amounts of about 100 to 200 ng/g cell tissue of Artemisia dracunculus, whereas sterile potato herb contained temazepam and diazepam ranging approximately from 70 to 450 ng/g cell tissue. It is the first report on the endogenous formation of benzodiazepines by plant cells, as any interaction of microorganisms and environmental factors was excluded.

Identification of Melissa officinalis Subspecies by DNA Fingerprinting.

The random amplified polymorphic DNA analysis (RAPD) is a method to study genetic variability within and between populations and species on the basis of the amplification of anonymous fragments from genomic DNA templates by means of polymerase chain reaction (PCR). We applied RAPD analysis in order to distinguish medicinal plant subspecies at the level of their genomes. In this study we investigated various samples of two MELISSA subspecies and showed that RAPD analysis is a fast and reliable method to distinguish subspecies on the pharmaceutical market that have been previously classified according to the distribution pattern of compounds present in the lemon balm oil.

Fructan Synthesis in Tissue Cultures of Symphytum officinale; L. Initiation, Differentiation, and Metabolic Activity.

Tissue cultures originating from different organs i.e. leaves, leaf-stalks, ovaries, anthers, and roots of SYMPHYTUM OFFICINALE were initiated under various growth conditions and subcultured several times to give the first callus generation. From all these calli, whole plants could be regenerated which again were used for the preparation of tissue cultures resulting in the formation of the second callus generation. The different calli and the regenerated plants were analyzed with respect to the fructan-synthesizing capacity. Only calli derived from the leaves of the original plant synthesized fructan whereas calli derived from ovaries, anthers, and roots, which are known to contain large amounts of fructan, were not capable of synthesizing fructan. The regenerated plants obtained from the first callus generation showed ability for fructan synthesis only if the originating callus synthesized fructan. The calli of the second generation, which were prepared from fructan-containing leaves and roots of regenerated plants, showed the capacity for fructan formation. The calli of the second generation obtained from leaves and roots of regenerated, fructan-free plants were not able to synthesize this specific reserve polysaccharide. From these data it can be concluded that the calli of the first generation prepared from roots, ovaries, and anthers have lost their ability for fructan synthesis. Calli initiated from leaves and leaf-stalks preserved the capacity for fructan formation even after many calli generations and regeneration to entire plants. Different phytohormones used in the tissue cultures had only a slight effect upon the fructan formation. An influence of light on fructan synthesis could not be detected.

[Investigations on harpagophytum.]. / Untersuchungen der Gattung Harpagophytum.

Comparing the analytical results of the constituants of naturally growing roots and callus of Harpagophytum procumbens, it could be demonstrated that both, the products of the primary and the secondary metabolism, showed important differences. Harpagosid which is present in significant amounts in the roots and tubers of the fresh plants, was shown to be completely absent in the callus. Stachyose the main reserve carbohydrate again was only produced in minor amounts. Fructose was the predominant sugar in the callus cells.