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In vitro shoot regeneration from olive cultivar tissues

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Abstract

Petioles, leaf discs and midribs of several olive (Olea europaea L.) cultivars, collected from potted greenhouse plants, field-grown and in vitro shoots, were used to test their morphogenic capacity. Adventitious shoots were induced only in petioles from in vitro-grown shoots of cultivars Moraiolo, Dolce Agogia and Halkidikis, grown on Olive Medium (OM) plus 18 μM zeatin within 4 to 5 weeks. Regeneration was achieved, both on Murashige and Skoog (MS) and on modified OM, only in the dark. The highest regeneration was achieved directly from the proximal part of the petioles after 2 to 3 weeks in media containing 5 to 40 μM thidiazuron, or with both 10 μM 2-isopentenyladenine +2.2 μM 6-benzyladenine with or without low auxin concentration (not more than 2.5 μM). A few adventitious shoots were also regenerated from callus when it was shifted from auxin and cytokinin media to cytokinin only medium. The regeneration potential was higher in petioles collected from apical nodes than from basal ones. The adventitious shoots were transferred to solid half-strength MS medium supplemented with 4.5 μM zeatin for further development. Several regenerated shoots were rooted and the plantlets hardened in the greenhouse. No apparent differences regarding morphological aspects were observed among the regenerated plantlets or with those obtained by stimulation of axillary buds.

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Abbreviations

BA:

6-benzyladenine

IBA:

indole-3-butyric acid

NAA:

1-naphthaleneacetic acid

TDZ:

thidiazuron (N-phenyl-N′-1,2,3-thidiazol-5-ylurea)

2iP:

2-isopentenyladenine

MS:

Murashige and Skoog medium

1/2 MS:

half strength MS

OM:

Olive Medium

BN:

Bourgin & Nitsch

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Mencuccini, M., Rugini, E. In vitro shoot regeneration from olive cultivar tissues. Plant Cell Tiss Organ Cult 32, 283–288 (1993). https://doi.org/10.1007/BF00042290

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