INDUCTION CALLUS OF MORINGA PLANT (MORINGA OLEIFERA) IN VITRO

Zahraa Abbas trad Abdul-Sadah (Al- Qasim Green University College of Biotechnology)
Rahma Abd Al gabar Ahmed (University of Fallujah College of applied Sciences Department of Biotechnology)
Sarah Salam Talib Fadhel (University of Fallujah College of applied Sciences Department of Biotechnology)
Mohammed Allawi Abed Ibrahim (University of Fallujah/College of Applied 4 Sciences/Department of Biotechnology)
Nawras Saadoun Majbas Jiyad (University of Fallujah/College of Applied Sciences/Department of Biotechnology)

JMGCB
Vol. 1 No. 8 (2024): Journal of Medical Genetics and Clinical Biology

This study aims to find an easy and efficient way to induce callus tissue of (Moringa oleifera) in vitro. The seeds were used as explant for cultivation in vitro, these parts were sterilized with sodium hypochlorite (Naocl) at concentrations (0.0, 0.5, 1.0, 2.0%) for a period of time (5,10 ,15, 20 minutes) and mercury chloride solution 0.06,0.07,0.08 0.1 mg/L) and for a period of time (2,3,4,5 minutes). Explant were planted in the medium (Murashige and Skoog (MS) in addition to different concentrations of plant growth regulators (BA, NAA), either individually or in combination. The results showed that the use of sodium hypochlorite solution (NaocL) with a concentration of 2% and a sterilization period of 20 minutes gave the highest sterilization rate of 100% without causing damage to the plant part. Also, the seeds produced callus after 48 days of culture on Ms medium containing the best combination of plant growth regulators (BA 4.0, NAA 0.5 mg/L)