In this study, the regeneration of the Colchicum soboliferum species, one of the medicinal aromatic plants growing naturally in Türkiye, was examined by the somatic embryogenesis method. Within the scope of experiments on somatic embryogenesis, corms of the Colchicum soboliferum species were used as explant source. 16 media containing 2,4-Dichlorophenoxyacetic acid (2,4-D) (0, 0.5, 1, 2 mg.L⁻¹), Benzyl adenine (BA) (0, 0.1, 0.5 mg.L⁻¹), and 2-Isopentenyladenine (2IP) (0, 0.1, 0.5 mg.L⁻¹) as plant growth regulators were used in this regeneration research. Different ratios and combinations of Murashige ve Skoog (MS) media were tested. In the applications, the highest embryogenic callus formation was observed with a rate of 60% in Murashige ve Skoog (MS) media containing 0.5 mg.L⁻¹ 2,4-Dichlorophenoxyacetic acid (2,4-D) + 0.1 mg.L⁻¹ 2-Isopentenyladenine (2IP). The highest embryo formation, with a rate of 48.33%, was obtained in MS media containing 2 mg.L⁻¹ 2,4-Dichlorophenoxyacetic acid (2,4-D) + 0.5 mg.L⁻¹ Benzyl adenine (BA) and 2 mg.L⁻¹ 2,4-Dichlorophenoxyacetic acid (2,4-D) + 0.1 mg.L⁻¹ 2-Isopentenyladenine (2IP). No growth was observed in the control application that did not contain plant growth regulators.

In this study, the regeneration of the Colchicum soboliferum species, one of the medicinal aromatic plants growing naturally in Türkiye, was examined by the somatic embryogenesis method. Within the scope of experiments on somatic embryogenesis, corms of the Colchicum soboliferum species were used as explant source. 16 media containing 2,4-Dichlorophenoxyacetic acid (2,4-D) (0, 0.5, 1, 2 mg.L⁻¹), Benzyl adenine (BA) (0, 0.1, 0.5 mg.L⁻¹), and 2-Isopentenyladenine (2IP) (0, 0.1, 0.5 mg.L⁻¹) as plant growth regulators were used in this regeneration research. Different ratios and combinations of Murashige ve Skoog (MS) media were tested. In the applications, the highest embryogenic callus formation was observed with a rate of 60% in Murashige ve Skoog (MS) media containing 0.5 mg.L⁻¹ 2,4-Dichlorophenoxyacetic acid (2,4-D) + 0.1 mg.L⁻¹ 2-Isopentenyladenine (2IP). The highest embryo formation, with a rate of 48.33%, was obtained in MS media containing 2 mg.L⁻¹ 2,4-Dichlorophenoxyacetic acid (2,4-D) + 0.5 mg.L⁻¹ Benzyl adenine (BA) and 2 mg.L⁻¹ 2,4-Dichlorophenoxyacetic acid (2,4-D) + 0.1 mg.L⁻¹ 2-Isopentenyladenine (2IP). No growth was observed in the control application that did not contain plant growth regulators.

Tea (Camellia sinensis) is the world's most popular beverage plant, as well as an important plantation crop with high commercial value. It has been maintained for centuries through conventional vegetative propagation. Tea clonal propagation in vitro has the advantage of producing a large number of elite plants. If an efficient in vitro regeneration technology is available, this technique could be exploited for selection of tea plants for desired trait. The selected plants could be later on multiplied through in vitro or ex vitro techniques. The study aimed to induced somatic embryogenesis from immature embryo explants to genetic variaton. Different concentrations of phenylboronic acid with benzyladenine and phenylboronic acid with kinetin were tested in MS medium with 30 g/L sucrose and 8 g/L agar. MS medium without any plant growth regulators was used as control group. Considering the embryo survival rate, 1.5 mg/ L-1 phenylboronic acid + 1 mg/ L-1 kinetin produced highest result as 87.3% while lowest was in control group as 36.7%. The highest plant regeneration rate was found in 1,5 mg/ L-1 phenylboronic acid + 1 mg/ L-1 kinetin and 1.5 mg/ L-1 phenylboronic acid + 1 mg/ L-1 benzyladenine medium respectively as 58.3% and 55.6%. Kinetin treatment with increasing phenylboronic acid concentrations gave the best results in terms of somatic embryo survival rate. Also, kinetin treatment produced better results when compared to benzyladenine concentrations.

Tea (Camellia sinensis) is the world's most popular beverage plant, as well as an important plantation crop with high commercial value. It has been maintained for centuries through conventional vegetative propagation. Tea clonal propagation in vitro has the advantage of producing a large number of elite plants. If an efficient in vitro regeneration technology is available, this technique could be exploited for selection of tea plants for desired trait. The selected plants could be later on multiplied through in vitro or ex vitro techniques. The study aimed to induced somatic embryogenesis from immature embryo explants to genetic variaton. Different concentrations of phenylboronic acid with benzyladenine and phenylboronic acid with kinetin were tested in MS medium with 30 g/L sucrose and 8 g/L agar. MS medium without any plant growth regulators was used as control group. Considering the embryo survival rate, 1.5 mg/ L-1 phenylboronic acid + 1 mg/ L-1 kinetin produced highest result as 87.3% while lowest was in control group as 36.7%. The highest plant regeneration rate was found in 1,5 mg/ L-1 phenylboronic acid + 1 mg/ L-1 kinetin and 1.5 mg/ L-1 phenylboronic acid + 1 mg/ L-1 benzyladenine medium respectively as 58.3% and 55.6%. Kinetin treatment with increasing phenylboronic acid concentrations gave the best results in terms of somatic embryo survival rate. Also, kinetin treatment produced better results when compared to benzyladenine concentrations.

The present study was conducted to find out an in vitro efficient method for multiple shoot regeneration of two local chickpea varieties. The mature embryos were excised of two chickpea varieties i.e. Bittle-98 and Dasht-2000 (with cotyledon and without cotyledon) used as explants. The explants were cultured on Murashige and Skoog (MS) medium supplemented with three concentrations of (2, 3, 4 mg/l) 6-benzylaminopurine (BAP) using explant with and without cotyledon. Further, 0.5 mg/l α-naphthaleneacetic acid (NAA) along with varied concentrations of BAP (2, 3, 4 mg/ l) was also tested using explant with cotyledon. 3 mg/l BAP alone and 3 mg/l BAP with 0.5 mg/l NAA were found the most effective cytokinin in multiple shoot induction in both tested varieties. Bittle-98 and Dasht-2000 showed 82% and 76% elongation in shoots induction with 0.2 mg/l Indole-3-acetic acid (IAA). Root formation was recorded 80% and 60% in Bittle-98 and Dasht-2000 with 1.0 mg/l Indole-3-butyric acid (IBA). Whereas, recorded root formation was 40 and 20% in Bittle-98 and Dasht-2000 with 1.0 mg/l NAA. The best response for rooting observed in Bittle-98 as its roots were thick, long and strong. Plantlets of Bittle-98 were acclimatized in solid medium for 7-14 days. The successful invitro regeneration of Bittle-98 was observed, when excised embryo with cotyledon were used as explant, made it valuable for genetic transformation.