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Rapid micropropagation of
three elite Sugarcane (Saccharum officinarum L.)
varieties by shoot tip culture
Sabaz Ali Khan1, 3*,
Hamid Rashid2, M. Fayyaz Chaudhary1,
Zubeda Chaudhry2 and Amber Afroz2
1Quaid-i-Azam
University, Islamabad, Pakistan.
2Agricultural
Biotechnology Programme (ABP), Institute of Agricultural
Biotechnology and Genetic Resources (IABGR), NARC,
Islamabad, Pakistan.
3Plant
Research International (PRI) Building 107
Droevendaalsesteeg-1 6708 PB, Wageningen, The Netherlands.
*Corresponding author. E-mail:
sabzktk@yahoo.com.
Tel:
+31-317486081. Fax +31-317418094.
Abbreviations: BAP, 6-Benzyl amino purine; GA3,
gibberellic acid; IBA, indole-3-butyric acid; Kin, Kinetin;
MS, Murashige and Skoog; NAA, naphthalene acetic acid;
P-value, probability value.
Accepted
6 June, 2008 |
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Studies were carried out for rapid micropropagation of three
sugarcane varieties i.e., HSF-240, CP-77-400 and CPF-237.
Shoot tip was used as explant source. Shoot initiation from
explant of all three varieties was achieved at 1 mg/l Kin
and 0.1 mg/l GA3. For rapid multiplication the
regenerated shoots were transferred on liquid Murashige and
Skoog medium containing 2% sucrose, supplemented with BAP in
combinations with GA3. Optimum multiplication was
observed at 1 mg/l BAP in combination with 0.1 mg/l GA3
for variety HSF-240. Best response of multiplication for
variety CP-77-400 was observed at 0.5 mg/l BAP with 0.1 mg/l
GA3. Variety CPF-237 was multiplied at 1.0 mg/l
BAP with 0.5 mg/l GA3. Rooting response was
observed on half strength liquid MS medium with 6% sucrose
containing different concentrations of IBA and NAA. The
sugarcane plantlets were acclimatized in greenhouse.
Key
words:
Micropropagation, Sugarcane, Shoot tip, Hormone and Meristem
culture.
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