Protocol of micropropagation of Arbutus pavarii and Haplophyllum tuberculatum was successfully achieved. In vitro plant regeneration of Arbutus pavarii was attempted using single nodal on MS medium supplemented with different concentration of three various growth regulators indole-3-butyric acid (IBA), Kinetin (K) and NIsopentenylaminopurine (2ip). Multiple shoots from single node were obtained on MS medium with the 0.5 mg/l 2ip. While, faster improving of shoots elongation was on MS contained 0.5 mg/lK. Explants obtained in micropropagation step were used for rooting step under several treatments. The best results were obtained when explants were sup-cultured on MS medium with 1 mg/l IBA. New plants were vigorous, of good quality and presented phenotypic characters similar to mother plants. Micropropagation of Haplophyllum tuberculatum was achieved from sterilized single nodal segments on MS medium supplemented with for different concentrations of 2,4-D for callus induction and other different hormones K and BA for multiplication of auxiliary branches and rooting . The highest results of the weight of callus were growing in MS medium containing 1 or 2 mg/l 2.4-D hormone with maltose. Whereas, the axillary soothing was significantly proliferated on MS medium supplemented 2 mg/ l-1 K. Acclimation of plantlet was in greenhouse
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Al-Rehaily, A. J., S. I. Alqasoumi, H. S. Yusufoglu, M. A. Al-Yahya, B. Demirci, N. Tabanca, D. E. Wedge, F. Demirci, U. R. Bernier, J. Becnel, H. E. Temel, and K. H. Baser. 2014. Chemical composition and biological activity of Haplophyllum tuberculatum Juss. essential oil. Journal of Essential Oil Bearing Plants 17 (3): 452-459.
Bertsouklis, K. F., and M. Papafotiou. 2009. In vitro propagation of Arbutus andrachne L. Acta Hort. 813: 477-479.
El-Darier, S. M., and F. M. El-Mogaspi. 2009. Ethnobotany and relative importance of some endemic plant species at El-Jabal El-Akhdar Region (Libya). World Journal of Agricultural Sciences 5 (3): 353-360.
Elmaghrabi, A. M., and S. J. Ochatt. 2006. Isoenzymes and flow cytometry for the assessment of true-to-typeness of calluses and cell suspension of barrel medic prior to regeneration. Plant Cell Tissue Org. Cult. 85: 31-43.
Elmaghrabi, A. M., E. Abughnia, and S. Hamoud. 2017. In vitro propagation of the wild medicinal plant, caper (Capparis spinosa L.). African Journal of Biotechnology. ISSN: 1684-5315. http://www. academicjournals.org/AJB. (under press).
El-Naggar, E. B., S. M. El-Darier, A. A. El-Mekanen, E. Švajdlenka, and M. Zemlièka,. 2014. Chemical Composition of Essential Oil of Haplophyllum tuberculatum (Rutaceae) Grow Wild in Different Habitats of Egypt. Global Journal of Pharmacology 8 (3): 385-393.
George, E. F., M. A. Hall, and G. J. De Klerk. 2008. Plant Propagation by Tissue Culture, 3rd Edition. Springer.
Gonçalves, J. C., G. Diogo, and S. Amâncio. 1998. In vitro propagation of chestnut (Castanea sativa × C. crenata): Effects of rooting treatments on plant survival, peroxidase activity and anatomical changes during adventitious root formation. Sci. Hort. 72 (3): 265-275.
Gholami, M., K. Javidnia, R. Miri, and M. Soltani. 2009. Micropropagated Haplophyllum patavinum HandMazz. (Rutaceae) Oil as rich source of α- Palmitolactone. Iranian Congress of Physiology and Pharmacology (19). http://en.seminars.sid.ir/View Paper.aspx?ID=1607.
Louhaichi, M., A. K. Salkini, H. E. Estita, and S. Belkhir. 2011. Initial Assessment of Medicinal Plants Across the Libyan Mediterranean Coast. Advances in Environmental Biology 5 (2): 359-370.
Murashige, T., and F. Skoog. 1962. A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiol. Plant. 15: 473-497.
Puricelli, L., G. Innocenti, G. Dellemonache, R. Caniato, R. Filippini, and E. M. Cappelletti. 2002. In vivo and in vitro production of alkaloids by Haplophyllum patavinum. Natural Product Letters 16 (2): 95-100.
Torres, J. A., F. Valle, C. Pinto, A. Gar cia-Fuentes, C. Salazar. And E. Cano. 2002. Arbutus unedo L. communities in southern Iberian Peninsula mountains. Plant Ecol. 160: 207-223.