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Research objective. Investigation of consistent patterns of the induction of flax morphogenesis process, assessment of genetic and physiological aspects of this process and optimization methodologies. Proposition: 1. MOrphogenesis capacity of flax isolated explants depends on a genotype only, but on a composition of a medium and the cultivar type (fibre flax or linseed)also. 2. Cells of different organs of the same genotype have different morphogenic capacity. 3. Combining hormonal ratio with the affect on explats by exogenic factors enables targeted control of the morphogenesis process in vitro. / Darbo tikslas - ištirti linų morfogenezės proceso indukcijos dėsningumus, įvertinti šio proceso genetinius ir fiziologinius aspektus bei optimizuoti regeneravimo metodikas. Ginamieji disertacijos teiginiai: 1. Linų izoliuotų eksplantų morfogeninė galia priklauso ne tik nuo genotipo, maitinamosios terpės sudėties, bet ir nuo veislės tipo (pluoštiniai ar sėmeniniai). 2.To paties genotipo skirtingų organų ląstelės turi skirtingą morfogeninę galią. 3.Derinant hormoninį balansą su eksplantų paveikimu egzogeniniais veiksniais galima kryptingai valdyti morfogenezės procesą in vitro.

The effects of cytokinin-like Thidiazuron growth regulator on the regeneration responses of callus cultures of Turkish bread Triticum aestivum L. cv. (BaSak 95, Gerek 79, and Bezostaja 1) and durum Triticum durum Desf. cv. (Kunduru, &Ccedil / akmak 79, and Kirmizi 5132) wheat varieties have been investigated in this study. High callus induction frequencies are found to be independent of bread and durum wheat varieties ( &rsaquo / 96%) whereas the callus weight is found to be variety-dependent. For bread wheat, BaSak 95 and for the durum wheat Kunduru is found to be the best performers. TDZ treatments are found to be negatively affecting the regeneration capacity of all the tested bread wheat varieties whereas for the durum wheat variety of Kunduru positive effect is observed. Since the culture efficiency is a derivation from the regeneration capacity, this parameter yielded very similar results as in the case of regeneration capacity for both bread and durum wheat varieties. In bread wheat varieties, the TDZ treatments increased the number of regenerated plants more than 2-fold when compared with the control and likewise very similar results were obtained from durum wheat varieties. Unfortunately, following their transfer to soil, plants that were treated with various concentrations of TDZ displayed reduced vigor probably due to underdeveloped roots. In addition, majority of these plants did not sufficiently develop above the ground parts when compared with the control plants. The simplicity and rapid development of shoots using mature embryos could potentially be used for regenerating superior plants following gene transfer studies in the future.

ABSTRACT Three different genotypes of sugar beet (diploid, triploid and tetraploid) / 4 varieties from diploid and triploid genotypes Soraya (KWS8123) and Leila (diploid), Visa (H68121) and Kassandra (triploid) and 2 lines from tetraploid genotype &Ccedil / BM315 and EA2075 (tetraploid) were used for investigating the effects of ploidy level on plant regeneration. Within three sugar beet genotypes, with respect to the treatments, triploids or tetraploids were found to respond to treatments significantly different when compared with diploids. The responses of polyploids were superior over the responses of diploids. Moreover, varieties from same genotype responded differently to treatments. Two types of calli were obtained / one white and friable with regenerative capacity and the other green and compact with no regenerative capacity. Concentration of sucrose on callus development was observed to be important. High concentration of sucrose (30 g/L) was found to cause discoloration and irresponsiveness of formed calli at callus enlargement and subsequent shoot regeneration stages. Therefore, low concentration (10 g/L) is advised to be used at these stages / although this caused less callus induction. Although initially used for the prevention of tissue discoloration, L-ascorbic acid inclusion into the medium was found to be positively affecting the regeneration capacity. When used at 20 mg/100 mL concentration, the only two spontaneous shoots from the tetraploid EA2075 line were obtained. Subsequently, these shoots were successfully rooted and whole plants were obtained. The effect of silver nitrate, in combination with L-ascorbic acid, on the prevention of sugar beet tissue discoloration was investigated. Unfortunately, the symptoms of discoloration did not diminish. Moreover, callus formation was reduced and the subsequent shoot recovery could not be achieved. Since a total of 3456 explants were used during this study, and only 2 whole plants were regenerated, the efficiency of plant recovery was calculated as a rather low value of 0.058 %.

The objective of the study was to investigate the optimum conditions for in vitro regeneration of common juniper (Juniperus communis L.) by using indirect organogenesis approach. Throughout the study / callus induction, organogenesis, improved organogenesis and root induction experiments were performed sequentially. It was found that explant position, genotype, gender, treatments and sampling time had significant effects on callus induction rate in common juniper. The results of treatments indicated that IBA (indole-3-butyric acid) at concentration range 0.5-4.0 mg/l combined with MS medium supplemented with 0.1 mg/l BAP (benzylaminopurine), 3 % sucrose and 0.7% agar was the best one among the treatments to induce callus formation from common juniper explants collected as Spring buds. Also, a two-month culture was adequate period for the callus induction of common juniper regardless of position, before transferring the explants into organogenesis media. After a two-month culture in callus induction media, explants were transferred to organogenesis treatments in order to investigate adventitious bud development from callus tissues. There were significant differences among genotypes, treatments and explant-sampling times in initiation of organ development in common juniper. Additionally, it was found that excluding the auxin components while maintaining 1.0-2.0 mg/l BAP concentration in culture media, as refreshing after a month, stimulated the formation and development of adventitious buds and shoots. Among the treatments tested, it was found that 1.0 mg/l BAP plus 0.5 mg/l 2,4-D was the optimum culture media with adventitious bud formation capacity of 37.5% was though ageing of callus significantly affected the frequency of adventitious bud formation. Finally, rooting experiments were performed to investigate rooting efficiency of adventitious shoots. In the adventitious rooting experiments, no rooting was observed in any of the treatments used with common juniper explants. Although whole plantlet development from callus tissues could not be achieved as indirect organogenesis, the results of the study could aid to future studies dealing in vitro regeneration and production of secondary chemicals from common juniper.