Organogenesis and Propagation "In Vitro" of Simmondsia Chinensis (Link) Schn. (Jojoba) From Vegetative Fragments.

Effect of different growth regulators and genotype onin vitropropagation of jojoba

“…In our work only 20% of explants initiated were lost. Proliferation rates reported here were similar to those reported by Radice & Caso (1989), but in contrast to these authors, we observed basal tissue proliferation when using BA, as was also reported by Lee (1988), Scaramuzzi & D'Ambrosio (1988), and Chaturvedi & Sharma (1989). Stem cuttings of these plants have been reported to be difficult to root in vitro as well as in soil (Aragao & Hogan 1976;Chaturvedi & Sharma 1989;Garcia Berenguer 1992).…”

“…There are reports on jojoba somatic embryogenesis (Lee & Thomas 1985;Wang & Janick 1986a,b) and both axillary and apical buds in vitro culture (Aragao & Hogan 1976;Birnbaum 1976;Scaramuzzi & D'Ambrosio 1988). A number of workers have described culture of single node explants (Zunino 1988;Radice & Caso 1989;Llorente et al 1992), as reported here.…”

In vitro Shootlets Multiplication and Callus Proliferation of Jojoba (Simmondsia chinensis) Plant

“…While, BA with IAA enhanced shootlet number. The results are supported the findings of Scaramuzzi and D'Ambrosio (1988), Sardana and Batra (1998), Kumar et al (2009), who mentioned that BAP with NAA or IAA was very effective for the in vitro establishment and multiplication of jojoba. Mousa and Bakhashwain (2014) stated that higher concentrations of BAP + IAA were better for shoot formation and multiplication than BAP + NAA.…”

Crop Physiology of Sweetpotato

“…Within 3 to 4 weeks, somatic embryos and plantlets with roots and shoots could be successfully regenerated from embryogenic callus derived from the shoot apical meristem (Elliot 1969;Over de Linden and Elliot 1972;Alconero et al 1975;Scaramuzzi and DeGaetano 1983;Jarret et al 1984;Liu and Cantliffe 1984;Chee and Cantliffe 1988;Komaki et al 1989;Chee et al 1990;MandaI and Chandal 1991;AVRDC 1991;Acedo 1991;Schultheis and Cantliffe 1992;Mukherjee et al 1993), stern and root explants (Liu and Cantliffe 1984;Mukherjee et al 1993), leaf explants (Sehgal 1975;Belarmino et al 1992), anther (Kobayashi and Shikata 1975;Sehgal 1978;Tsay and Tseng 1979;Tsay et al 1982;Mukherjee et al 1991), nodal explants MandaI and Chandal1990;Paul et al 1991), petiole explants (Prakash et al 1996), petiole protoplasts (Murata et al 1987), stem and petiole protoplasts (Murata et al 1987;Sihachakr and Ducreux 1987;Belarmino et al 1994), and mesophyll cell suspension (Murata et al 1994). Within 3 to 4 weeks, somatic embryos and plantlets with roots and shoots could be successfully regenerated from embryogenic callus derived from the shoot apical meristem (Elliot 1969;Over de Linden and Elliot 1972;Alconero et al 1975;Scaramuzzi and DeGaetano 1983;Jarret et al 1984;…”