Our research group mainly studies the metabolism and physiological functions of growth regulators, polyamines, and phenolic compounds in plants. We investigate the role of these biologically active compounds in plant development and in the response of plants to abiotic stresses.
In our experiments, we use diverse plant systems from whole plants to cell cultures. Our research is primarily focused on the somatic embryogenesis of conifers. Within this topic, we study the regulation of somatic embryo development, the role of phytohormones in somatic embryogenesis, and the effects of abiotic stresses on somatic embryos. We also deal with the in vitro propagation of medicinal cannabis. In particular, we investigate the effect of phytohormones (auxins and cytokinins) added to the culture medium on the process of organogenesis from segments of cannabis plants grown from seeds in vitro.
We use a wide array of approaches:
Microscopy – light, confocal, and electron microscopy, enhanced by advanced computer image analysis
Biochemical methods – studies of activities of enzymes involved in the metabolism of biologically active compounds (e.g. radiometry)
Molecular biology methods – specific gene expressions, and transformation of tissue cultures
Analytical methods – qualitative and quantitative determination of biologically active compounds by gas- and liquid chromatography in tandem with mass spectroscopic detection (cooperation with the IEB Laboratory of Growth Regulators and Laboratory of Hormonal Regulations in Plants).
The FLOWERING LOCUS T like 2–1 gene of Chenopodium ficifolium and Chenopodium quinoa acts as a strong activator of flowering in Arabidopsis, triggering flowering at cotyledon stage and causing lethality when overexpressed.
Our expertise cover methods of anatomy, histochemical detections, and indirect immunofluorescence, determination of the content of plant hormones, and analysis of gene expression. Newly we are also implementing methods of in-vitro virus detection. To control the developmental processes of in-vitro cultures, we use a broad spectrum of newly synthesized bioactive molecules as well as modulators of plant hormone metabolism and perception (e.g. anti-auxins, anti-gibberellins, cytokinin derivatives).
In Norway spruce, as in many other conifers, the germination capacity of somatic embryos is strongly influenced by the desiccation phase inserted after maturation. The intensity of drying during desiccation eminently affected the formation of emblings (i.e., seedlings developed from somatic embryos). Compared to non-desiccated embryos, the germination capacity of embryos desiccated at 100% relative humidity was about three times higher, but the reduction of relative humidity to 95% and 90% had a negative effect on the subsequent embryo development.
The transition from vegetative growth to reproduction is an essential commitment in plant life. It is triggered by environmental cues (day length, temperature, nutrients) and regulated by the very complex signaling gene network and by phytohormones. The control of flowering is well understood in Arabidopsis thaliana and in some crops, much less is known about the other angiosperms.
The survival and adaptation of angiosperms depend on the proper timing of flowering. The weedy species Chenopodium ficifolium serves as a useful diploid model for comparing the transition to flowering with the important tetraploid crop Chenopodium quinoa due to the close phylogenetic relationship. The detailed transcriptomic and hormonomic study of the floral induction was performed in the short-day accession C. ficifolium 459. The plants grew more rapidly under long days but flowered later than under short days.
