Author/Authors :
Ahmadi Hesar، A. نويسنده M.Sc. Student, Rasht Branch, Islamic Azad University, Rasht, Iran , , Kaviani، B. نويسنده , , Hashemabadi، D. نويسنده Department of Horticultural Science, Rasht Branch, Islamic Azad University, Rasht, Iran , , Bohlooli Zanjani، S. نويسنده North Biotechnology Institute, Rasht, Guilan, Iran ,
Abstract :
Tissue culture is an attractive alternative for plant propagation.
Micropropagation is a technique to ensure a constant and uniform source of
ornamental plants. Matthiola incana is an important ornamental species
mainly cultivate by seed. Matthiola incana seeds were germinated on solid
MS medium without plant growth regulators. Shoot proliferation and root
formation are possible using kinetin (Kn) and naphthalene acetic acid (NAA).
Shoot tips and leaf micro-cuttings derived from in vitro germinated seedlings
were subcultured on solid MS medium containing Kn (0, 0.5, 1 and 2 mg l-1)
and NAA (0, 0.5, 1 and 2 mg l-1) for shoot tips explants and Kn (0, 0.5 and 1
mg l-1) and NAA (0, 0.5 and 1 mg l-1) for leaf explants. Shoot tips media
supplemented with 2 mg l-1 Kn without NAA and 2 mg l-1 NAA without Kn
resulted in the best shoot length (1.20 cm) and root number (1.90), respectively.
The callus was induced from most leaf media after four weeks of culture. MS
mediums containing 0.5 mg l-1 Kn and 0.5 mg l-1. The largest number (1.94)
and the highest length (16.60 mm) of roots were obtained in MS medium
supplemented with 1 mg l-1 Kn + 0.5 mg l-1 NAA. NAA prevented root
formation originated from callus with concentration of 1 mg l-1 + 0.5 and 1 mg l-1 Kn.