<i>In vitro</i>propagation of<i>Pistacia vera</i>L. and the commercial cultivars Ohadi and Kalleghochi

Barghchi, M.; Alderson, P. G.

doi:10.1080/14620316.1985.11515647

Cited by 41 publications

(20 citation statements)

References 4 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…Regeneration from P. vera L. with seed or seedling tissues has been the most successful to date (Barghchi and Alderson 1983a, b;1985;Yang and Ludders 1993;Parfitt and Almehdi 1994;Dolcet Sanjuan and Claveria 1995;Onay et al 1995Onay et al , 2000Onay 2000a). The initiation of cultures from mature trees has been reported by a few researchers (Barghchi and Martinelli 1984;Gonzales and Frutos 1990;Onay 2000b, Tilkat 2006Tilkat et al 2008).…”

Section: Introductionmentioning

confidence: 91%

Direct shoot organogenesis from in vitro-derived mature leaf explants of pistachio

Tilkat

Onay

2008

In Vitro Cell.Dev.Biol.-Plant

View full text Add to dashboard Cite

An efficient system was developed for direct plant regeneration from in vitro-derived leaf explants of Pistacia vera L. cv. Siirt. The in vitro procedure involved four steps that included (1) induction of shoot initials from the regenerated mature leaf tissue, (2) regeneration and elongation of shoots from the shoot initials, (3) rooting of the shoots, and (4) acclimatization of the plantlets. The induction of shoot initials was achieved on an agarified Murashige and Skoog (MS) medium with Gamborg vitamins supplemented in different concentrations of benzylaminopurine (BA) and indole-3-acetic acid (IAA). The best medium for shoot induction was a MS medium with 1 mgl −1 IAA and 2 mgl −1 BA. Numerous shoot primordia developed within 2-3 wk on the leaf margin and the midrib region, without any callus phase. In the second step, the shoot clumps were separated from the leaf explants and transferred to a MS medium supplemented with 1 mgl −1 BA, resulting in a differentiation of the shoot initials into well-developed shoots. The elongated shoots (>3 cm long) were rooted on a full-strength MS basal medium supplemented with 2 mgl −1 of indole-3-butyric acid in the third stage. Finally, the rooted plants were transferred to soil with an 80% success rate. This protocol was utilized for the in vitro clonal propagation of this important recalcitrant plant species.

show abstract

Section: Introductionmentioning

confidence: 91%

Direct shoot organogenesis from in vitro-derived mature leaf explants of pistachio

Tilkat

Onay

2008

In Vitro Cell.Dev.Biol.-Plant

View full text Add to dashboard Cite

show abstract

“…Brand & Lineberger (1986) found WPM better than MS medium for the proliferation of Halesia carolina. Barghchi & Alderson (1985) encountered shoot tip necrosis during culture of Pistacia vera on MS medium. Because symptoms were absent on shoots that had developed roots, they thought that there may be insufficient uptake of calcium due to callusing and the low transpiration rate caused by the high humidity conditions in the vessel.…”

Section: Shoot Tip Necrosismentioning

confidence: 99%

In vitro propagation of Dipterocarpus alatus and Dipterocarpus intricatus

Linington

1991

Plant Cell Tiss Organ Cult

View full text Add to dashboard Cite

show abstract

“…Generally, it occurs at the initial stage of culture but can be overcome by adding substances such as ascorbic acid, citric acid, polyvinyl pyrrolidone (PVP) and activated charcoal to the growth medium. This phenomenon is widely reported in literature, not only for Pecan, but also for other nut crops such as Chestnut (Osterc et al, 2005), Walnut (Payghamzadeh and Kazemitabar, 2011) and Pistachio (Barghchi and Alderson, 1985). For in vitro germination of Pecan for instance, testa is generally removed, since it produces phenols that can inhibit the growth of callus (Haroon, 2011).…”

Section: Sterilization Procedures Referencementioning

confidence: 98%

Propagation of Pecan (Carya illinoensis): A review

Casales¹,

Watt²,

Coetzer³

2018

Afr. J. Biotechnol.

View full text Add to dashboard Cite

The Pecan (Carya illinoensis) is the most important species that belongs to the Carya genus. It is cultivated mainly for its nut, which is rich in oils and proteins, and for its good quality wood. Pecan is conventionally propagated by budding or grafting onto rootstocks obtained by open pollination. However, these techniques are not very efficient due to low propagation rates, poor survival and difficult establishment. Therefore, in vitro propagation of pecan can play a very important role in rapid multiplication of cultivars with desirable traits and production of healthy and disease-free plants in a short time. In the present review, the improvements over the years in the propagation of pecans, the refinements of protocols for obtaining high shoot multiplication and regeneration through organogenesis and/or somatic embryogenesis is discussed. Some basics of genetic transformation and its possible benefits are also discussed.

show abstract

In vitropropagation ofPistacia veraL. and the commercial cultivars Ohadi and Kalleghochi

Cited by 41 publications

References 4 publications

Direct shoot organogenesis from in vitro-derived mature leaf explants of pistachio

Direct shoot organogenesis from in vitro-derived mature leaf explants of pistachio

In vitro propagation of Dipterocarpus alatus and Dipterocarpus intricatus

Propagation of Pecan (Carya illinoensis): A review

Contact Info

Product

Resources

About