Kultur suspensi sel tanaman gajah beranak (Goniothalamus tapis Miq) terhadap kandungan zat goniotalamin

Zat goniotalamin pada tanaman gajah beranak (Goniothalamus tapis) merupakan obat alternatif penyembuhan kanker. Penelitian bertujuan untuk mendapatkan zat goniotalamin melalui kultur kalus dan kultur suspensi sel. Metode penelitian eksperimen Rancangan Acak Lengkap (RAL) dengan kombinasi 2,4-D (1-10 mgL-1) dan BAP (0,5-2 mgL-1) menggunakan eksplan batang muda, terdiri dari 17 perlakuan dan 3 kali ulangan. Analisis data menggunakan Analysis of Variances dan uji lanjut Duncan Multiple Range Test (DMRT) taraf 5%. Hasil menunjukkan bahwa kultur kalus G. tapis pada media 5,0 mg L-1 2,4-D + 1 mg L-1 BAP adalah yang terbaik dengan waktu muncul kalus 28,33 hari dan persentase pembentukan kalus 100%. Kalus untuk kultur suspensi sel bertekstur remah dan berwarna kuning kehijauan. Kultur suspensi sel menghasilkan pertumbuhan sel yang cepat, tidak lembek berair dan mudah dipisahkan. Hasil kualitatif Kromatografi Lapis Tipis kultur suspensi sel sangat jelas, bersih dan terdapat potensi kandungan zat goniotalamin pada perlakuan 2,4-D 5 mg L-1 + BAP 0,5 mg L-1, 2,4-D 5 mg L-1 + BAP 1 mg L-1, 2,4-D 5 mg L-1 + BAP 2 mg L-1, 2,4-D 10 mg L-1 + BAP 0,5 mg L-1 dan 2,4-D 10 mg L-1 + BAP 1 mg L-1. Hasil kuantitatif zat goniotalamin dengan Kromatografi Cair Prestasi Tinggi terdapat pada perlakuan 2,4-D 5,0 mgL-1 + BAP 1 mg L-1 yaitu 9,57 mg g-1.The goniothalamine compound on Goniothalamus tapis is an alternative cancer medicine. This study aimed to obtain gonotalamin through callus culture and suspension cell culture. The experiment research method was Completely Randomized Design (CRD) with a combination of 2.4-D (1-10 mg L-1) and BAP (0.5-2 mg L-1) using young stem explants consisting of 17 treatments with 3 replications. Data analysis used ANOVA and DMRT at 5%. The results showed that G. tapis callus culture on 5.0 mg L-1 2.4-D + 1 mg L-1 BAP was the best treatment medium with callus emergence time of 28.33 days and percentage of callus formation 100%. The callus used for suspension cell culture was friable and greenish-yellow in color. Suspension cell culture resulted in rapid cell growth, was not fleshy, and easily separated. The quality test by Thin Layer Chromatography (TLC) from suspension cell culture resulted very clear, clean, and potential content of goniothalamin found in treatments 2.4-D 5.0 mg L-1 + BAP 0.5 mg L-1, 2.4-D 5.0 mg L-1 + BAP 1 mg L-1, 2.4-D 5.0 mg L-1 + BAP 2 mg L-1, 2.4-D 10 mg L-1 + BAP 0.5 mg-1 and 2.4-D 10 mg-1 + BAP 1 mg-1. The quantitative results of the best goniotalamine compounds in cell suspension cultures using High-Performance Liquid Chromatography (HPLC) on medium 2,4-D 5.0 mgL-1 + BAP 1 mg L-1 ie 9.57 g-1.

Development of an elicitation strategy on enhanced accumulation of oleanolic acid in suspension cultures of Ocimum tenuiflorum L.

Ocimum tenuiflorum Linn. is an important aromatic medicinal plant which produces several secondary metabolites responsible for diverse pharmacological activities. The present study focuses on enhanced production of biomass as well as oleanolic acid (OA), an anticancer and antioxidant compound, in suspension cell cultures of O. tenuiflorum upon elicitation with different elicitors. Leaf explants derived friable calli were inoculated intol iquid Murashige and Skoog (MS) media containing plant growth regulators [0.25 mg/L of α-naphthaleneacetic acid (NAA) and 0.5 mg/L of 6-benzyl amino purine (BAP)] for the establishment of suspension cultures. Influence of several factors such as, age of the suspension cultures, different concentrations, and exposure times of various elicitors such as yeast extract (YE), methyl jasmonate (MeJ) and salicylic acid (SA) respectively were analysed for cell biomass production and accumulation of OA during this study. Among the elicitors tested, YE at 50 mg/L was found to be the most efficient in terms of increased biomass production and accumulation of OA in the cultures. The highest increase in OA production (13.16-fold in elicited cultures compared to untreated cultures) was noted on 17-day-old suspension cultures when exposed to 50 mg/L of YE for four days. Enhancement of 2.72-fold in OA content was also recorded in 17-day-old cultures when treated with MeJ (60 mg/L) during two days of exposure. SA was not efficient in inducing accumulation of OA in 17- and 22-day-old suspension cultures at any concentration and exposure time. Furthermore, it was observed that the effect of different elicitors on biomass production and OA content depended on concentration and the duration of exposure times. Therefore, utilization of elicitation method could be a promising tool to enhance cell growth and OA accumulation in the suspension cell cultures of O. tenuiflorum.