Somatic embryogenesis and regeneration of Cenchrus ciliaris genotypes from immature inflorescence explants
2009
Yadav, C.B.,University of Delhi (India). Dept. of Botany | Jha, P.,University of Delhi (India). Dept. of Botany | Mahalakshmi, C.,University of Delhi (India). Dept. of Botany | Anjaiah, V.,University of Delhi (India). Dept. of Botany | Bhat, V.,University of Delhi (India). Dept. of Botany
An efficient, highly reproducible system for plant regeneration via somatic embryogenesis was developed for Cenchrus ciliaris genotypes IG-3108 and IG-74. Explants such as seeds, shoot tip segments and immature inflorescences were cultured on Murashige and Skoog (MS) medium supplemented with 2.0-5.0 mg/cubic dm 2,4-dichlorophenoxyacetic acid (2,4-D) and 0.5 mg/cubic dm N6-benzyladenine (BA) for induction of callus. Callus could be successfully induced from all the three explants of both the genotypes. But the high frequency of embryogenic callus could be induced only from immature inflorescence explants. Somatic embryos were formed from nodular, hard and compact embryogenic calli when 2,4-D concentration was gradually reduced and BA concentration increased. Histological studies of somatic embryos indicated the presence of shoot apical meristem with leaf primordia. Ultrastructural details of globular and scutellar somatic embryos further validated successful induction and progression of somatic embryogenesis. Shoots were differentiated upon germination of somatic embryos on MS medium containing 2,4-D (0.25 mg/cubic dm) and BA or kinetin (1-5 mg/cubic dm). Roots were induced on half MS medium containing charcoal (0.8 %), and the regenerated plants transferred to pots and established in the soil showed normal growth and fertility.
اظهر المزيد [+] اقل [-]الكلمات المفتاحية الخاصة بالمكنز الزراعي (أجروفوك)
المعلومات البيبليوغرافية
تم تزويد هذا السجل من قبل Library of Antonin Svehla