Effect of Vitamins (pyridoxine and nicotinic acid), Thiamine-Hcl and Myo-Inositol at Different Concentrations on Free Amino Acids and Indoles Content of Embryogeinic Callus of in vitro Date Oalm (Sakkoty and Bartamuda Cultivar)

The potential of using tissue culture technique for the production of some bioactive compounds since it allows the manipulation of the biosynthetic routes to increase the production and accumulation of specific compounds. This study was conducted to investigate the effect of vitamins (pyridoxine and nicotinic acid), thiamine-Hcl at different cocentrations (0.5, 1.0 & 2.0 mg/l) and myo-inositol at different concentrations (25, 50, and 100mg/l) at different cocentrations supplemented in MS basal nutrient medium of embryogenic callus of date palm on the production of secondary metabolites of amino acids and indoles. Tow egyption cultivars (Sakkoty and Bartamuda cultivars) of date palm were used. Pyridoxine concentration at 0.5mg/l was the most effective concentration in the production of amino acids and indoles from embryonic callus of the tow studied cultivars of date palm. Nicotinic acid at 0.5mg/l showed also the best results of production of amino acids and indoles from embryogenic callus of two cultivars. Acording to thiamine at 2mg/l concentration was the most effective in inducing the highest significant value of amino acids and indoles from embryonic callus of two cultivars of date palm. Myo-inositol concentration at 25mg/l produced the highest significant value of amino acids and indoles. Introduction Many higher plants are major sources of natural product used as pharmaceuticals, agrochemicals, flavor and fragrance ingredients, food additives, and pesticides [1]. The search for new plant derived. In the search for alternatives to production of desirable medicinal compounds from plants, biotechnological approaches, specifically, plant tissue cultures, are found to have potential as a supplement to traditional agriculture in the industrial production of bioactive plant metabolites [2]. Date palm tree Phoenix dactylifera L. is a multipurpose tree from whole tree, the cultivation of this crop was distributed in North Africa and Middle East specially in Arabian Peninsula. Date palm tree can accumulate many chemicals in their tissues, as primary metabolites containing carbohydrates and proteins, and secondary metabolites which are produced from primary ones [3,4]. The yield of secondary compounds in plants cells can be enhanced by precursor feeding in culture medium it has been a normal and a popular approach to increase this bioactive compounds [5]. secondary metabolite formation has shown that the media components have an influence on metabolism [6]. Vitamins, myoinositol and thiamineHCl are considered important copmonents which induce plant cell growth also thier role in stimulated the bioactve metabolites as precursors has been reported [6-9]. The aim of this work is By-Products of Palm Trees and Their Applications Materials Research Forum LLC Materials Research Proceedings 11 (2019) 244-252 doi: https://doi.org/10.21741/9781644900178-20 245 to study the effect of some vitamins (Pyridoxine hydrochloride, Nicotinic acid, Thiamine hydrochloride, Myoinositol ) on (free amino acids content, total indols content) in embryogeinic callus stage of in vitro date palm (Sakkoty and Bartamuda cultivars). Materials and Methods Callus explants of two cultivars Bartamuda and Sakkoty were produced from indirect protocol of date palm micropropagation discribed by [10,11]. In this study received embryonic callus explants for both cultivars were cultured on basic nutrient medium for callus formation which composed of MS basal medium [12], supplemented 30 g/l sucrose and 3.0 g/l activated charcoal with 40 mg/l adenine – sulfate, 200 mg/l glutamine, 100 mg/l myo-inositol, 0.1 mg/l biotin, 170 mg/l NaH2PO4,0.1 mg/l thiamine HCl 0.5 mg/l pyridoxine, 0.5 mg/l nicotinic acid, 3.0 mg/l 2isopentenyl adenine (2iP) + 10.0 mg/l 2,4 –D dichlorophenoxy acetic acid (2,4 – D). Callus explants of tow cultivars Bartamuda and Sakkoty were produced from indirect protocol of date palm micropropagation discribed by [10,11]. In this study recived embryonic callus explants for both cultivars were cultured on basic nutrient medium for callus formation which composed of MS basal medium [12], supplemented 30 g/l sucrose and 3.0 g/l activated charcoal with 40 mg/L adenine – sulfate, 200 mg/l glutamine, 100 mg/l myo-inositol, 0.1 mg/l biotin, 170 mg/L NaH2PO4,0.1 mg/l thiamine HCL 0.5 mg/l pyridoxine,0.5 mg/l nicotinic acid, 3.0 mg/L 2isopentenyl adenine (2iP) + 10.0 mg/l 2,4 –D dichlorophenoxy acetic acid (2,4 – D). The studied treatments were added as followed:1. Effect of vitamins Effect of Pyridoxine hydrochloride concentration on secondary metabolites in embryogenic callus. Pyridoxine hydrochloride concentration: a) 0.5 mg/l b) 1.0 mg/l c) 2.0 mg/l. Effect of Nicotinic acid concentration on secondary metabolites in embryogenic callus. Nicotinic acid concentration: a) 0.5 mg/l b) 1.0 mg/l c) 2.0 mg/l. Effect of thiamine hydrochloride concentrations on secondary metabolites in embryogenic callus. 2. Effect ofThiamine-Hcl concentrations: a) 0.5 mg/ b) 1.0 mg/l c) 2.0 mg/l. Effect of Myoinositol concentrations a) 25 mg/l b) 50 mg/l c) 100 mg/l. 6.0 g/l agar were used to solidified culture medium which were distributed in culture jars (250 ml); each jar contained 25 ml of culture nutrient medium. Culture jars were immediately capped with polypropylene closure autoclaved at 121°C at 1.05 kg/cm for 20 min. The cultured jars were incubated under total darkness at 27±1°C and data were recorded every (6 weeks) for three subcultures on total steroids (mg/g dry weight). Callus sampels were collected from all studied treatments of the micro elements compounds, manganese sulfate (), zinc sulfate ( MnSO4.4H2O) heptahydrate (ZnSO4.7H2O) and copper sulfate (CuSO4.5H2O) for both Bartamuda and Sakkoty cv. for the following assay. 1. Determination of free amino acids Total amino nitrogen or free amino acids were determined according to Rosein [13]. For assay, one ml of sample was pipetted out into a series of test tubes, and then total volume made up to 4 ml with distilled water. One ml of ninhydrin reagent (4 %, 4 g ninhydrin was dissolved in 50 ml By-Products of Palm Trees and Their Applications Materials Research Forum LLC Materials Research Proceedings 11 (2019) 244-252 doi: https://doi.org/10.21741/9781644900178-20 246 acetone and 50 ml acetate buffer) was added to each tube, mixed well, and the tubes were kept in a boiling water bath for 15 min. Then, the tubes were cooled and the volume was made up to 10 ml in measuring flask with ethanol 50 %. The pink color developed was measured using a spectrophotometer at 570 nm DL-alanine. The concentration of total amino nitrogen as DLalanine were calculated from the standard curve. 2. Extraction of Indoles and Phenols One gram of fresh samples in three replicates were sectioned into minute pieces and extracted with 5 ml cold methanol 80 % and stored in cold condition for 24h. The combined extracts were collected and filtered. Then, the volume of sample was raised up to known volume with cold methanol. A-Determination of Total Indoles The total indoles were determined in the methanolic extract using p-dimethyl amino benzaldehyde (PDAB) reagent, 1 g was dissolved in 50 ml HCl conc. and 50 ml ethanol 95 %) test according to Larsen et al. [14]. One ml of aliquot methanolic extract was pipetted into a test tube, then 4 ml of PDAB reagent was added and incubated at 30 – 40 °C for 1 h. The intensity of the resultant color was spectrophotometerically measured at 530 nm. A standard curve was established which refer to the relationship between different concentrations of IAA and their corresponding absorbance values. B-Determination of Total Phenols Phenols determination was carried out according to Danial and George [15]. For estimation of total phenols, 1 ml of the methanol tissue extract was added to 0.5 ml of Folin-Ciocalteu’s Phenol Reagent and shaken 3 min. Then, 1 ml saturated Na2CO3 (25 % w/v) plus 17.5 ml distilled water added. The mixtures were left for one hour at 3040 °C. Optical density of these samples was measured by a colorimeter using wavelength 730 nm. Concentrations of total phenols in different samples were calculated as mg phenol/100g FW. Amount of total phenolic compounds was calculated according to standard curve of pyrogalol (99.5 %). Statistical analysis The obtained data were subjected to analysis of variance. The mean values were compared using LSD test at the 5% level of probability. The data were tabulated and statistically factorial analysed according to the randomized complete block design with three replicates Snedecor & Cochran [16]. Results and Discussion 1. Effect of PyridoxineHCl on total amino acids content (mg/g fresh weight). Data in Table 1 clearly showed that no significant differences were found between the two cultivars under investigation (0.99, 0.94 mg/g fresh weight respectively),the pyridoxine concentration (0.5mg/l) was the most effective as it induced the highest significant value (1.65 mg/g fresh weight), concerning the interaction between cultivars and pyridoxine concentrations, these results illustrated that the highest significant value (1.65 mg/g fresh weight) was for Sakkoty and Bartamuda cultivars embryogenic callus grown on medium contained( 0.5 mg/l) pyridoxine. The lowest value (0.47 mg/g fresh weight) was for Bartamuda cultivar embryogenic callus grown on medium contained (1.0 mg/l) pyridoxine. By-Products of Palm Trees and Their Applications Materials Research Forum LLC Materials Research Proceedings 11 (2019) 244-252 doi: https://doi.org/10.21741/9781644900178-20 247 Table 1: Effect of Pyridoxine -HCl on total amino acids content (mg/g fresh weight). 2. Effect of PyridoxineHCl on total indoles content (mg/g fresh weight). Table 2: Effect of Pyridoxine HCl on total indoles content (mg/g fresh weight). Data in Table 2 clearly showed that, significant differences were found between the two cultivars under investigation (0.30, 0.35 mg/g fresh weight respectively), the p