Milana Trifunovic

Morpho-histological study of direct somatic embryogenesis in endangered species Frittilaria meleagris

Direct somatic embryogenesis of Frittilaria meleagris L. was induced using leaf base explants excised from in vitro grown shoots. Somatic embryos occurred at the basal part of leaf explants 4 weeks after culture on a Murashige and Skoog (MS) medium supplemented with various concentrations of 2,4-dichlorophenoxyacetic acid (2,4-D) or kinetin (KIN). The highest number of somatic embryos (SEs) were formed (9.74) from leaf explant on MS medium supplemented with 0.1 mg dm−3 2,4-D after 4 weeks of culture initiation. An initial exposure to a low concentration of KIN in the medium also enhanced SEs induction. Our observations by light and scanning electron microscopy revealed that SEs originate directly from the epidermal and subepidermal layers of leaf explant. The developmental stages of somatic embryogenesis from the first unequal cell division through the meristematic clusters, multi-cellular globular somatic embryos to the fully formed cotyledonary embryos were determined. After 4 weeks on MS medium without plant growth regulators, SEs developed into bulblets.

Plant regeneration in leaf culture of Centaurium erythraea Rafn. Part 1: The role of antioxidant enzymes

Centaurium erythraea Rafn. is a medicinal plant rich in secoiridoids and xanthones and used for gastrointestinal disorders, fever, anemia and many other conditions. C. erythraea is characterized with extraordinary developmental plasticity and manageability in vitro; thus we propose it as an excellent experimental model system for studies in developmental biology. Hereby we describe regeneration of centaury from leaf explants that can proceed via somatic embryogenesis or organogenesis on inductive media containing 2,4-D and CPPU. In the absence of growth regulators, shoots and roots appeared without callusing, on light or in darkness, respectively. Indirect somatic embryogenesis was induced in the presence of growth regulators occurring both on light and in darkness. Light was obligatory for indirect shoot development, where adventitious buds formed simultaneously with somatic embryos. Dynamic changes of antioxidative activities of superoxide dismutase (SOD), catalase (CAT) and peroxidase (POX) in response to morphogenetic changes were followed during developmental pathways in vitro. Wounding of centaury leaves immediately induced all SOD and CAT isoforms but caused a decrease in POX activity. In control leaves and leaf explants, three Cu/Zn-SOD activities were detected, which gradually decreased on inductive treatments on light, but remained unchanged during growth in darkness. Morphogenetic paths on all hormonal and light treatments where characterized with dynamic changes of CAT activity (comprised of three major CAT isoforms), but generally CAT was reduced during morphogenesis induction. POX activity was strongly induced during morphogenesis in all treatments.

Changes in cytokinin content and altered cytokinin homeostasis in AtCKX1 and AtCKX2-overexpressing centaury (Centaurium erythraea Rafn.) plants grown in vitro

The plant hormones cytokinins (CKs) regulate a number of physiological processes. Their homeostasis is controlled by the rate of de novo synthesis and the rate of catabolism. The aim of this work was to analyze the content of total as well as individual groups of endogenous CKs in AtCKX1 and AtCKX2-overexpressing centaury (Centaurium erythraea Rafn.) plants grown in vitro. Transgenic CKX plants represent a suitable model system for studying physiological and morphological processes controlled by CKs. In this work we clearly demonstrate a significant effect of AtCKX transgenes on CK metabolism in transgenic centaury plants. However, shoots and roots of only one AtCKX1 line and three AtCKX2 lines with a significant reduction of bioactive CKs were obtained. We also show that changes in the CKs metabolism considerably affected endogenous indole-3-acetic acid (IAA) levels in plant tissues. All analyzed transgenic AtCKX centaury lines exhibited decreased amount of endogenous IAA in shoots as well as in roots. Consequently, the IAA/bioactive CK forms ratios showed a significant variation in the shoots and roots of all analyzed AtCKX centaury transformants.

The Role of Arabinogalactan Proteins in Morphogenesis of Centaurium erythraea Rafn In Vitro

Histochemical localization using the β-Glc Yariv reagent and immunolocalization with arabinogalactan protein (AGP) reactive antibodies (LM2, JIM13, JIM15, JIM16, MAC207) were performed during morphogenic induction in root cultures of Centaurium erythraea Rafn cultured on half-strength MS medium without plant growth regulators. The observations revealed that β-Glc Yariv reagent specifically bound to AGPs in cells of the root epidermis and central cylinder. Monoclonal antibodies recognizing AGPs were localized in epidermal cells and cells of the central cylinder (LM2 , JIM16), vascular tissue (JIM15), globular somatic embryos (LM2, MAC207), and de novo-formed meristematic centers in the root cortex (JIM16). The effect of β-Glc Yariv reagent was investigated after supplementation (0–75 μM) in the culture medium. The morphogenetic potential was increased at lower concentrations (15–25 μM) of treatment with β-Glc Yariv reagent but inhibited (40 %) at the highest concentration. These results implicate that AGPs play a significant role during the development of somatic embryos and adventitious shoots in root cultures of C. erythraea.