Abstract

Abstract An efficient protocol for in vitro plant regeneration from cotyledonary nodal segment explants of Prosopis cineraria (L.) Druce., a multipurpose leguminous tree, was established. Nodal explants were excised from 5-day-old seedlings and cultured on Murashige and Skoog (MS) medium fortified with different concentrations of BAP (0.44–2.22 µmol/l) alone for shoot bud regeneration. Highest percent of shoot bud regeneration (87.66%) was noticed on MS medium supplemented with 2.22 µmol/l BAP. The nodal segments derived from seedlings were placed on MS medium with different concentrations of BAP (0.44–2.22 µmol/l) in combination with 0.46 µmol/l for shoot bud multiplication. The highest percent of shoot bud multiplication (93.50%) with 3.5 shoots/explant was recorded on MS medium containing 2.22 µmol/l BAP and 0.46 µmol/l KIN combination. The number of multiple shoots was further increased to 12.0 shoots/culture when the combination of 2.22 µmol/l BAP, 0.46 µmol/l KIN and 0.59 µmol/l AgNO3 was used. For rooting, the elongated shoots (>2 cm) were cultured on MS medium augmented with various concentrations of NAA (0.53–2.68 µmol/l) along with 0.46 µmol/l KIN and 0.59 µmol/l AgNO3. Among the combinations tested, the highest percent of root formation (87.66%) with 4 roots/shoot was observed in the medium containing 0.53 µmol/l NAA, 0.46 µmol/l KIN and 0.59 µmol/l AgNO3 combination. Rooted plantlets were successfully transferred into plastic cups and acclimatized under greenhouse conditions. Subsequently, they were established in the field and grew normally.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call