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Our research goal has been to find the optimal nutrient media for initiation of the primary callus in the species of the Cactaceae family. Common methods of plant biotechnology were used. Primary explants of the cacti were cultivated on Murashige and Skoog medium (MS medium). The content of macro- and microelements has been diluted twice (½ MS) and the vitamins (B1 and B6 – 0.5 mg/l, PP – 1 mg/l) were added, as well as 100 mg/l meso-isonitol and 20 g/l of sucrose. It was determined that callus formation formed efficiently when cultivated on half MS media with 20 g/l sucrose, 3 mg/l 6- benzylaminopurine, 0,2 mg/l indole-3-acetic acid,0,1 mg/l α-napthaleneacetic acid and 5 mg/l ascorbic acid. It was discovered, that for initiation of tissue differentiation and cacti callus formation, high concentrations of cytokinine-active growth regulators are required.

The study revealed the results of the comparative analysis of the deoxyribonucleoproteid complex (chromatin) lipid composition in the callus and explant nuclei of plants, belonging to different systematic groups (winter rye, potatoes, peas). It provided the data on the phospho- and neutral lipid composition of the investigated plants and showed that the phospholipid content in the explants from dormant winter rye seed embryos and potato stems, having low metabolic activity, is significantly higher than in the calluses in the stage of active proliferation. Both winter rye and potato calluses tend to have a lower share of neutral lipids, including sterols, in their composition. The revealed factors can be used as markers of metabolic activity of the plant cell biology objects (callus and cell cultures).

The availability of high-quality seeds is now a necessity. This is due to a government program to replace oil palm trees in smallholder plantations with high quality seeds. An efficient protocol to produce a large number of embryos is needed. To increase the number of embryogenic callus production, the callus proliferation experiment was carried out through suspension culture. This study aimed to examine the proliferation ability of embryogenic callus from three different oil palm clones, in several repeated subcultures. Liquid MS media added with 1 ppm 2.4-D and 0.1 ppm NAA were used. Embryogenic callus was weighed by 0.1 - 0.2 g, transferred into the liquid media, shaking at 60-80 rpm and 27 ºC for 8 weeks without light. Continues subcultures were repeated up to 7 times. The results showed that the growth rate of embryogenic callus increased in the third and fourth subcultures and then decreased in subsequent subcultures. It also revealed that the entire embryogenic callus from the first subculture up to seventh subculture still has the ability to regenerate into new plants. These results indicate that oil palm embryogenic callus can be proliferated by suspension culture with a limit up to the fourth subculture. Ketersediaan benih kelapa sawit berkualitas saat ini merupakan kebutuhan karena adanya program pemerintah untuk menggantikan tanaman sawit di kebun-kebun petani. Salah satu cara vegetatif yang dapat dilakukan adalah meningkatkan jumlah kalus embriogenik yang dihasilkan melalui pengembangan kultur suspensi. Penelitian ini bertujuan mengkaji kemampuan proliferasi kalus embriogenik dari tiga klon kelapa sawit, pada beberapa kali subkultur yang berulang. Media cair MS dengan penambahan 1 ppm 2,4-D dan 0,1 ppm NAA digunakan untuk memperbanyak 0,1–0,2 g kalus embriogenik, dikocok pada 60-80 rpm dan suhu 27 ºC tanpa cahaya selama 8 minggu. Subkultur berulang dilakukan hingga 7 kali. Hasil percobaan menunjukkan bahwa kemampuan proliferasi kalus dipengaruhi oleh genotip tanaman induk. Rata-rata kalus embriogenik dapat meningkat pada subkultur ke-3 dan ke-4 dan semakin menurun pada subkultur selanjutnya. Kalus embriogenik hasil proliferasi subkultur pertama hingga ke-7 dapat tumbuh menjadi calon tanaman baru. Hasil ini menunjukkan bahwa kalus embriogenik kelapa sawit dapat diperbanyak dengan kultur suspensi pada batas sampai subkultur ke-4.

The availability of high-quality seeds is now a necessity. This is due to a government program to replace oil palm trees in smallholder plantations with high quality seeds. An efficient protocol to produce a large number of embryos is needed. To increase the number of embryogenic callus production, the callus proliferation experiment was carried out through suspension culture. This study aimed to examine the proliferation ability of embryogenic callus from three different oil palm clones, in several repeated subcultures. Liquid MS media added with 1 ppm 2.4-D and 0.1 ppm NAA were used. Embryogenic callus was weighed by 0.1 - 0.2 g, transferred into the liquid media, shaking at 60-80 rpm and 27 ºC for 8 weeks without light. Continues subcultures were repeated up to 7 times. The results showed that the growth rate of embryogenic callus increased in the third and fourth subcultures and then decreased in subsequent subcultures. It also revealed that the entire embryogenic callus from the first subculture up to seventh subculture still has the ability to regenerate into new plants. These results indicate that oil palm embryogenic callus can be proliferated by suspension culture with a limit up to the fourth subculture. Ketersediaan benih kelapa sawit berkualitas saat ini merupakan kebutuhan karena adanya program pemerintah untuk menggantikan tanaman sawit di kebun-kebun petani. Salah satu cara vegetatif yang dapat dilakukan adalah meningkatkan jumlah kalus embriogenik yang dihasilkan melalui pengembangan kultur suspensi. Penelitian ini bertujuan mengkaji kemampuan proliferasi kalus embriogenik dari tiga klon kelapa sawit, pada beberapa kali subkultur yang berulang. Media cair MS dengan penambahan 1 ppm 2,4-D dan 0,1 ppm NAA digunakan untuk memperbanyak 0,1–0,2 g kalus embriogenik, dikocok pada 60-80 rpm dan suhu 27 ºC tanpa cahaya selama 8 minggu. Subkultur berulang dilakukan hingga 7 kali. Hasil percobaan menunjukkan bahwa kemampuan proliferasi kalus dipengaruhi oleh genotip tanaman induk. Rata-rata kalus embriogenik dapat meningkat pada subkultur ke-3 dan ke-4 dan semakin menurun pada subkultur selanjutnya. Kalus embriogenik hasil proliferasi subkultur pertama hingga ke-7 dapat tumbuh menjadi calon tanaman baru. Hasil ini menunjukkan bahwa kalus embriogenik kelapa sawit dapat diperbanyak dengan kultur suspensi pada batas sampai subkultur ke-4.

The current study aimed to adopt a method for inducing callus cells and regenerating the important common red bean using different types of growth regulators such as N6-benzylaminopurine (BAP), Naphthalene acetic acid (NAA), and Thidiazuron (TDZ). Different types of common bean pinto cultivar explants, such as internodes, cotyledons and roots, were inoculated on Murashige and Skoog medium (MS) provided with different combinations of plant growth regulators, including 1- BAP (5 mg/l) 2-BAP (4.5 mg/l) NAA (0.5 mg/l), 3- BAP (4.5 mg/l), and TDZ (0.1mg/l). Callus was initiated on MS culture medium supplied with 5 mg/l BAP for all explants (internodes, cotyledons, and roots) at 50, 20, and 10% respectively, while adding NAA with 0.5mg/l showed a low percentage of callus (30%) only in the internode explants. Optimum results were obtained by growing the internodes on MS medium with 4.5 mg/l BA and either 0.5 mg/l NAA or 0.1 mg/l TDZ, transplanting the derived shoots into internodes and cotyledons with 70 and 10% respectively. This study concludes that the internodes as explants have the best growth results.

Mass propagation of cassava on several hectares of arable land due to increasing demand for its starch is not feasible due to land availability, pests and disease invasion, and long cultivation period. Plant cell culture technology is a promising solution despite the scarcity of cassava callus culture for starch production applications. Therefore, a systematic mapping study (SMS) was performed to identify the applications of cassava tissue culture and its prospects in starch production and investigate the important parameters for cassava callus culture initiation. The SMS began with formulating research questions (RQs), conducting searches on various databases, collecting and screening related articles, and extracting and mapping the selected articles. A total of 56 of 589 articles in the initial searching phase were chosen to be used as references to answer each RQ. The extracted data indicates that cassava tissue culture was mostly used for micropropagation, while starch production from its tissue culture is still limited. Basal medium and plant growth regulators influence cassava callus culture initiation most. The findings of the SMS offer a better understanding of cassava tissue culture and the prospects of producing cassava starch.

Title: Effect of 6, Benzyl amino purine (BAP) on callus production and shoot regeneration in Bunium persicum B.Fedtsch Authors & Afffiliation: Iram Bashir1, Zahoor A. Kaloo2, Nahida Tun Nisa Chishti3, Sabreena Rashid4, Nusrath Sayeed5 1, 2, 4 Plant Tissue Culture Research Laboratory, Department of Botany, University of Kashmir, Hazratbal Srinagar-190006 Jammu & Kashmir, INDIA 3, 5 Government College for Women, M.A Road Srinagar-190001 Jammu & Kashmir, INDIA mir.irambashir@gmail.com, zakallu@yahoo.com, nahidtn@gmail.com, sababhat80@gmail.com, gochi8@gmail.com ABSTRACT Various concentrations of BAP were used in order to find out the optimum concentration of this growth substance for callus production as well as for shoot regeneration in Bunium persicum. The optimum concentration of BAP for callus production was BAP 1mg/l, in terms of average number of days taken for callus production (6 days), amount of callus produced and percent culture response (100%). However, BAP at a concentrationof 4 mg/l was found optimum for shoot regeneration. URL: http://www.ijbst.org/Home/papers-published/ijbst-2018-volume-11-issue-5

Moringa oleifera Lam. tree has often been considered a medicinal and economical plant for its nutritional and medicinal properties. This study is intended to use plant tissue culture and elicitation technologies to increase secondary metabolites in the callus cultures of the M. oleifera. Young nodal segments were cultured on Murashige and Skoog (MS) medium supplemented with different concentrations of plant growth regulators (PGRs). A combination of 1.5 mg/l NAA plus 0.5 mg/l TDZ resulted in a high callusing rate (70%) with the largest size. Various concentrations of Salicylic acid (SA) and Methyl jasmonate (MeJa) were individually added to the growth medium to evaluate their impact on the biomass of callus cultures, DPPH antioxidant activity, and accumulation of some flavonoids. Results indicated that all elicitors doses reduced weights and growth index of callus. While DPPH assay recorded high significant values at high concentrations of SA and MeJa compared to other treatments. HPLC analysis revealed that every concentration of SA and MeJa used led to rising flavonoids content, including Baicalin, Rutin, Hesperidin, Rosmarinic acid, Quercitrin, Quercetin, and Kaempferol. It should be noted that 20 mg/l MeJa gave the highest flavonoid content compared to the control and other treatments. In conclusion, the in vitro elicitation by SA or MeJa can improve beneficial biological substances like flavonoids and other antioxidant compounds in Moringa callus cultures.