IN VITRO TISSUE CULTURE OF SACCHARUM OFFICINARUM L. (SUGARCANE)
Ranjeeta Kumari, Dr. Dilip Gena, Rawoof Ahmad Bhat, Rajveer Singh Rawat, Dr. Bhanwar Lal Jat*
Abstract
Sugarcane assumes the important position in the economy of India by
contributing nearly 1.9% of National GDP. Sugarcane is cultivated in
over 4 million hectares spreading over a wide range of agro-ecological
situations. Sugarcane farmers are facing serious problems such as pest
and disease infestation especially red rot, non-availability of good seed
material, support from industry etc. It is need for the hour to find out
and implement technological interventions for the same. Plant Tissue
culture is a tool for obtaining rapid, mass multiplication of disease free,
true to type planting material. Mass propagation protocol once
standardize, can be utilized for rapid multiplication of disease free
stock material, which further be, multiplied in strict management
conditions for bulking up. Plant Tissue culture can also be used for rapid dissemination of
newly released varieties with important agronomic characters. In the present investigation,
we have tried to optimize the culture conditions of CoJ 85, which is an important variety in
Punjab. Through our work, we have found that MS Basal + 0.5mg/liter BAP + 0.5mg/liter
KN + 30gm/liter Sugar + 8.0gm/liter agar are the best among the different combinations for
the initiation of this variety. For the multiplication stage, best multiplication rate is observed
in MS Basal + 1.0mg/liter BAP + 1.5mg/liter KN + 30gm/liter. We have also found that MS
+ 5mg/liter NAA + 70gm/liter sugar responded significantly for the rooting and for callus
formation, MS + 2,4-D (4mg/liter) was found to be the best for the callus induction.
Keywords: .
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