Juniperus drupacea Labill. (Cupressaceae) is a species with ecological and medicinal value. In Europe, it is native only in southern Greece, and is listed as endangered. Due to its uniqueness, this study attempted, for the first time, an in vitro propagation effort of Syrian juniper. Explants of the lateral shoot tips were surface-sterilized and cultured on Murashige and Skoog (MS) medium. The cultures were subcultured on MS, woody plant medium (WPM), and Driver and Kuniyaki Walnut (DKW) supplemented with different concentrations of 6-benzylaminopurine (BA), thidiazuron (TDZ), or meta-topolin [6-(3-hy-droxybenzylamino)purine] for shoot induction. Explants derived from female trees exhibited 54.17% bud proliferation on DKW medium with 4 μM meta-topolin or 4 μM TDZ and on WPM with 4 μM meta-topolin or 4 μM BA. A total of 62.50% of the male tree derived explants produced multiple shoots on DKW with 4 μM BA. The maximum average number of shoots per explant were 1.17 per explant in both cases. The length of the shoot derived from explants of female origin was 2.94 mm compared to 2.69 mm of the in vitro shoots from the explants of male trees. Overall, the best medium and plant growth regulator combination for the explants derived from both female and male trees, for the traits under study, was proven to be DKW + 4 µM TDZ. Our experiments show that Juniperus drupacea, under in vitro conditions, shows recalcitrance in rooting, as the applications of IBA, NAA, and IAA concentrations were proven to be ineffective treatments. Although the results show low values, this avant-garde study provides a foundation for further research on the in vitro regeneration of Juniperus drupacea.
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