Author/Authors :
Shirdel، M. نويسنده Department of Horticultural Sciences, Faculty of Agriculture, Tabriz University, Tabriz, Iran. , , Motallebi-Azar، A. نويسنده Department of Horticultural Sciences, Faculty of Agriculture, Tabriz University, Tabriz, Iran. , , Matloobi، M. نويسنده Department of Horticultural Sciences, Faculty of Agriculture, Tabriz University, Tabriz, Iran. , , Zaare-Nahandi، F. نويسنده Department of Horticultural Sciences, Faculty of Agriculture, Tabriz University, Tabriz, Iran. ,
Abstract :
Dog rose (Rosa canina) has been using as a rootstock for ornamental
roses also it is one of the medicinal plants. It can be propagated under in vitro
conditions. After removing chilling requirement of buds, axillary wood buds
of dog rose were cut in three nodal positions (lower, middle and terminal) on
the stem and then explants after decontamination, cultured on Murashige and
Skoog medium (MS medium) supplemented with 1 mg l-1 GA3 and 1 mg l-1
BAP. For shoot proliferation, MS medium supplemented with 1 mg l-1 GA3
and different concentration of PGRs. The results showed that maximum bud
break percentage and highest shoot length were observed in lower nodal
position. Minimum bud break percentage and shoot length were observed in
middle nodal position. In the media with different concentrations of PGRs the
highest shoot length was observed in combinations of BAP 1 mg l-1 and Ads 2
mg l-1. The large number of node and maximum axillary shoot percentage
were observed in BAP 6 mg -1. The growth of dog rose was affected by
different explants nodal position and growth regulators on in vitro. Assessment
of BAP and Ads on axillary shoot percentage and node number was more
effective than kinetin + TDZ and BAP + TDZ combination. In media with low
concentration of BAP, TDZ and NAA and so kinetin, TDZ and NAA did not
produce any axillary shoots or elongated shoots.