Micropropagation and slow growth conservation of cardamom (Elettaria cardamomum Maton)

被引:22
作者
Tyagi, Rishi K. [1 ]
Goswami, Rajni [1 ]
Sanayaima, Rajkumari [3 ]
Singh, Rakesh [2 ]
Tandon, Rajesh [3 ]
Agrawal, Anuradha [1 ]
机构
[1] Natl Bur Plant Genet Resources, Tissue Culture & Cryopreservat Unit, New Delhi 110012, India
[2] Natl Bur Plant Genet Resources, NRC DNA Fingerprinting, New Delhi 110012, India
[3] Univ Delhi, Dept Bot, Delhi 110007, India
关键词
Cardamom; Gelling agent; Germplasm conservation; Nodal segments; Propagation efficiency; Shoot tips; Slow growth medium; Spice; GENETIC STABILITY ASSESSMENT; PLANTS; RAPD; DNA; REGENERATION; BANANA; MUSA; L;
D O I
10.1007/s11627-009-9234-6
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Cardamom (Elettaria cardamomum Maton) has great commercial value as a spice crop in India. A one-step protocol for direct regeneration of plants and in vitro conservation by slow growth method has been developed. A maximum of 6.5 shoots/culture were obtained in 2 mo or 15.1 shoots/culture in 4 mo on Murashige and Skoog (Physiol Plant 15:473-497, 1962) medium (MS) + 5 mu M benzylaminopurine gelled with 0.7% agar (micropropagation medium). Rooting also occurred simultaneously on the same medium. Using one shoot tip or nodal explant, about 30,375 plants can be regenerated in a year on the micropropagation medium. In vitro conservation by slow growth method was achieved on 1/2 MS (major salts) + 5 mu M BAP + 0.7% agar (conservation medium); about 70% of the cultures survived up to 18 mo at 25 +/- 2A degrees C. Successful regrowth of plants on micropropagation medium was obtained by culturing nodal explants excised from 18-mo-old conserved plants. Some 96% of the plants survived the hardening treatment and grew normally in a greenhouse. If 24 cultures are conserved on the conservation medium, it is possible to regenerate at least 750 plants by using explants derived from 70% of the surviving shoots and culturing the same in micropropagation medium for 4 mo. These plants may be used for planting or as a source of explants for the next conservation cycle. On the basis of 20 random amplified polymorphic DNA and 13 inter-simple sequence repeat primers analyses, no significant reproducible variation was detected among the in vitro-conserved plants compared with the mother plants.
引用
收藏
页码:721 / 729
页数:9
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