1Department of Plant Pathology, College of Agriculture, Jawaharlal Nehru Krishi Vishwa Vidyalaya, Jabalpur – 482 004, Madhya Pradesh (India)
Department of Agricultural Biotechnology and Molecular Biology, (FBS & H), Rajendra Agricultural University, Pusa -848 125, Bihar (India)
*E-mail: archanarani22oct@gmail.com
Online published on 29 May, 2014.
An efficient protocol for propagation of Rauvolfia serpentina through in vitro culture was standardized. Of the various combinations of phytohormones evaluated, 0.5 mg L−1 indole acetic acid (IAA) + 0.5 mg L−1 benzyl amino purine (BAP) + 1.0 mg L−1 kinetin highly favoured callus induction (32.8%). High callus-mediated shoot regeneration was seen on MS medium supplemented with 1.0mgL−1 IAA+0.5mgL−1 BAP+ 0.5 mg L−1 kinetin. Low auxin (IAA, 0.5 mg L−1) with higher concentration of cytokinin(0.5mgL−1 BAP+1.0mgL−1 kinetin) gavehighershootsculture−1 (6.6) with mean shoot length of 3.2 cm. In direct shoot regeneration, best growth of axillary shoots was achieved in MS medium supplemented with 0.2 mg L−1 IAA + 0.2 mg L−1 BAP + 0.2 mg L−1 kinetin with maximum shoots culture−1 (10.0) and shoot length (4.4 cm). The root induction was highest (84.3%) in MS medium supplemented with IBA (0.5 mg L−1). The rooted plantlets were successfully established in field.
Endangered species, in vitro propagation; medicinal plant, Rauvolfia serpentine