Cultivated tomato (Solanum lycopersicum L.) is one of the most important horticultural crops in the world. The optimization of culture media for callus formation and tissue regeneration of different tomato genotypes presents numerous biotechnological applications. In this work, we have analyzed the effect of different concentrations of zeatin and indole-3-acetic acid on the regeneration of cotyledon explants in tomato cultivars M82 and Micro-Tom. We evaluated regeneration parameters such as the percentage of callus formation and the area of callus formed, as well as the initiation percentage and the number of adventitious shoots. The best hormone combination produced shoot-like structures after 2–3 weeks. We observed the formation of leaf primordia from these structures after about 3–4 weeks. Upon transferring the regenerating micro-stems to a defined growth medium, it was possible to obtain whole plantlets between 4 and 6 weeks. This hormone combination was applied to other genotypes of S. lycopersicum, including commercial varieties and ancestral tomato varieties. Our method is suitable for obtaining many plantlets of different tomato genotypes from cotyledon explants in a very short time, with direct applications for plant transformation, use of gene editing techniques, and vegetative propagation of elite cultivars.
The procedure for vacuum infiltration of cultivars A. caudatus L. and hybrids of A. caudatus L. x A. paniculatus L. was optimized. The functioning of gene construction pCBv19 in the Amaranthus leaves was evaluated by the transient expression after vacuum infiltration with Agrobacterium rhizogenes A4. After hypocotyl transformation of the varieties of amaranth species A. caudatus L.: Helios, Karmin, Kremovyi rannii, and hybrids A. caudatus x A. paniculatus L.cv. Sterkh, A. caudatus x Sterkh-cv. Zhaivir with the wild strain A. rhizogenes A4, the culture of "hairy roots" was obtained. Embedding and transcription of genes in the roots are confirmed by the results of the PCR analysis.
Aim. To investigate the antibacterial properties of the fl owers of melliferous plants on the cultures isolated from honeycombs affected by foulbrood. Methods. Microbiological, cultural-morphological, biochemical, electron- microscopic, statistical. Results. Antibacterial effect on the Melissococcus pluton 8.1 strain was demonstrated by the fl ower extracts of 14 plant species and that on Bacillusaspecies – by the fl ower extracts of 27 plant spe- cies blossoming in the early spring. Conclusions. To study bee colonies affected by foulbrood, it is possible to use the properties of such nectariferous plants as Lamium album, Acer campestre, Prunus tomentosa, Allium cepa, Tagetes patula, Spiraea japonica, Achillea millefolium, Calluna vulgaris, Mentha piperita, Tilia cordata, Centaurea jacea, Lysimachia nummularia. The results of the experiments on the culture of microorganisms, isolated from the honeycombs of the bee colonies affected by foulbrood, demonstrated that these plants could be effective for the
prevention and treatment of bacterial bee diseases.
Aim. To investigate the microbiota of honeycombs with affected bee brood. Methods. Visual, immunochro- matographic, cultural-morphological, biochemical, electron-microscopic methods were used to isolate and previously identify a number of microorganisms. Results. 10 samples of honeycombs with sealed brood were studied. The following agents of bee diseases were isolated and previously identifi ed: Paenibacillus larvae – American foulbrood; Вasillus paraalvei – parafoulbrood; Melissococcus pluton – European foulbrood. Con- clusions. The number of cocci, spore-forming coli and yeasts, found in the samples of honeycombs, commonly represent normal microfl ora of bees, but their number increases signifi cantly in case of viral and bacterial infections.
After “floral-dip” transformation of Amaranth plants with Agrobacterium tumefaciens strain GV3101 carrying pCBV19 gene vector that contained bar and gus genes, transgenic seeds were obtained. The functioning of the tran+sferred genes in Amaranthus tissues was confirmed with herbicide selection (PPT herbicide – phospinotricin) and gus gene activity. Positive results were obtained for cultivars “Karmin” and “Kremoviy rannii”. The percentage of GUS positive samples was 1% (for “Karmin”), 2.2% (for “Kremoviy rannii”) from the total initial quantity of plants that was prior to selection with the herbicide. The seeds of six amaranth cultivars were received after treatment with A. tumefaciens by the method “floral dip”. The lowest lethal dose of herbicide PPT was established – 40 mg/l. After spraying with herbicide, resistant plants were obtained for cultivars: “Kremoviy rannii” (21%) and “Karmin” (20%). After conduction of PCR analysis, positive results were obtained for four cultivars. The percentage of bar positive plants was 0.3% (“Helios”); 0.26% (“Sterkch”); 0.06% (“Kremoviy rannii”); 0.3% (“Rushnichok”) from total initial quantity of plants.
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