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micropropagation studies in dracaena and cordyline - ETD ...

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MICROPROPAGATION STUDIES IN DRACAENA AND<br />

CORDYLINE<br />

CHINNU JOSEPH KATTOOR 2010 Dr. A. N. MOKASHI<br />

Major Advisor<br />

ABSTRACT<br />

An <strong>in</strong>vestigation on <strong>micropropagation</strong> <strong>in</strong> Dracaena <strong>and</strong> Cordyl<strong>in</strong>e was conducted<br />

dur<strong>in</strong>g 2009-2010 <strong>in</strong> the tissue culture lab of the Department of Horticulture, College of<br />

Agriculture, University of Agricultural Sciences, Dharwad. The study on surface sterilization of<br />

explants pretreated with a fungicide (bavist<strong>in</strong>) <strong>and</strong> a bactericide (streptomyc<strong>in</strong>) revealed that<br />

0.1% HgCl2 for 5 m<strong>in</strong>utes showed m<strong>in</strong>imum contam<strong>in</strong>ation without any toxicity to both the<br />

plants.<br />

As regards suitability of explants, shoot tip <strong>and</strong> nodal cutt<strong>in</strong>gs were the best for<br />

culture establishment <strong>in</strong> case of Cordyl<strong>in</strong>e. Shoot tips gave the quickest response for <strong>in</strong>itial<br />

growth <strong>and</strong> nodal cutt<strong>in</strong>gs took more time for growth. In case of multiple shoot production,<br />

there was no significant difference between nodal cutt<strong>in</strong>gs <strong>and</strong> shoot tips. The explants of<br />

<strong>dracaena</strong> did not show any response.<br />

In vitro proliferated explants were sub cultured on MS medium with BAP at different<br />

concentrations. Increase <strong>in</strong> the concentration of BAP <strong>in</strong> the media led to an <strong>in</strong>crease <strong>in</strong> the<br />

multiplication rate. However there was a decrease <strong>in</strong> shoot length which resulted <strong>in</strong> formation<br />

of clumps. Media with 4 mg/l BAP showed better response <strong>in</strong> terms of shoot production. The<br />

comb<strong>in</strong>ation of BAP <strong>and</strong> NAA improved shoot multiplication as aga<strong>in</strong>st BAP alone result<strong>in</strong>g <strong>in</strong><br />

more number of multiple shoots (4 mg/l BAP + 0.5 mg/l NAA). As the shoots formed were<br />

relatively shorter, GA3 was added to improve shoot length. Media fortified with 4 mg/l BAP +<br />

0.5 mg/l NAA +5 mg/l GA 3 produced more number of shoots of more length.<br />

Shoots obta<strong>in</strong>ed <strong>in</strong> the present study were transferred to root<strong>in</strong>g media but the<br />

multiplied shoots did not respond to <strong>in</strong> vitro root<strong>in</strong>g rather callus tissues were formed <strong>in</strong>stead<br />

of roots, so ex vitro root<strong>in</strong>g was undertaken. Treat<strong>in</strong>g the microshoots with 25 ppm IBA <strong>and</strong><br />

harden<strong>in</strong>g the shoots <strong>in</strong> peat media found to be effective with respect to percent root<strong>in</strong>g,<br />

number of roots <strong>and</strong> root length.

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