The effect of red (RL, 660 nm) and blue (BL, 450 nm) light on phy mutant tomato plants was studied. The rates of photosynthesis (Pn) and transpiration, the efficiency of the primary photochemical processes of photosynthesis, the contents of flavonoids and phenolic compounds, the low-molecular-weight antioxidant capacity (Trolox equivalent antioxidant capacity (TEAC)) of leaf extracts, and the expression of light-dependent genes were evaluated. Under RL, BL, and white fluorescent light (WFL), the Pn values decreased in the order: WT > phyb2 > phyaphyb2 > phyaphyb1phyb2, except for the Pn in phyb2 on BL. Phyb2 also had a larger number of stomata under BL and, as a result, it reached maximum transpiration. The noticeable accumulation of flavonoids and phenolic compounds was observed only in the phyb2 and phyaphyb2 mutants upon irradiation with BL, which agrees with the increased TEAC in the leaf extracts. We suggest that the increased antioxidant activity under PHYB2 deficiency and the maintenance of high photosynthesis under BL are based on an increase in the expression of the early signaling transcription factors genes BBX, HY5. The largest decrease in the content of flavonoids and TEAC was manifested with a deficiency in PHYB1, which is probably the key to maintaining the antioxidant status in BL plants.
8 April 2021 in Proceedings of the National Academy of Sciences, India Section B: Biological Sciences
A new Dienia type of the embryogenesis of orchid plants differing from the Liparis type, earlier observed for the tribe Malaxideae, has been described in Dienia ophrydis (J. Köenig) Seidenf. (Orchidaceae). The Dienia-type embryogenesis is characterized by the following features: (1) development of a single-celled suspensor formed by a cb-derivative, (2) linear arrangement of embryo cells at the tetrad stage, (3) atypical origin of some tiers, and (4) no divisions of the ci and cb cells. A hypothesis about the convergent similarity between the Dienia and Caryophyllaceae types of embryogenesis has been proposed. A number of embryo sac and embryo structures typical for D. ophrydis, including “petassum,” “fitting,” and “suspensor mantle,” have been first described. A “petassum” represents the remains of cell walls of the pollen tube and probably the filamentous apparatus of synergids sealing the micropyle side of a fertilized embryo sac. The sole suspensor cell has a special appendix (“fitting”), which connects it to the embryo. The suspensor and the fitting are surrounded by a special envelope (“suspensor mantle”), which does not cover the basal cell of the embryo (ci).
1 May 2019 in Russian Journal of Developmental Biology
Embryogenesis of the plant Liparis parviflora, a representative of the tribe Malaxideae (Orchidaceae), was studied. The multivariance of the first cell divisions in embryos belonging to...
The infectious structures for the development and differentiation of Erysiphe graminis DC. f. sp. tritici March., the pathogen of wheat powdery mildew, under the effects of exogenous zeatin was studied by methods of light and electron scanning microscopy. It was shown for the first time that physiologically active substances, specifically phytohormones of the cytokinin type, can affect dimensions of the halo revealed in the pathogen penetration site at cytochemical staining. Treatment with zeatin affected conidia germination and pathogen growth in the ectophytic stage. The concentration curve of the action of zeatin for the number of mature pathogen colonies (6 days after infection) was represented by a multiphase curve with two maxima (1 and 3 μM) and one minimum (1.5 μM). Similar curves have been obtained for the number of normal appressoria and for large halo diameters, which possibly indicates the existence of the factors affecting these both parameters, as well as the final number of pathogen colonies. The obtained data indicate that the origin of the multiphase dose response curve for effect of cytokinins on the development of powdery mildew pathogen is connected with factors that are active at the early stages of pathogenesis.