The aim of this study was to reach a well-defined protocol to in vitro propagate of Arganiaspinosaand overcome vitrification phenomenon. In this respect, the highest number of shoot was found at 2.0 mg/l Kin at genotype 3 for multiplication stage. MS medium supplemented with 100 mg/l calcium pantothenate was suited for to eliminate vitrification at all genotypes. For callus induction, MS medium supplemented with 1.5 mg/l NAA when incubated in the light or darkness was favorable to callus induction. MS medium supplemented with 0.5 mg/l GA3 + 1.5 mg/l BA led to increases shoot initiation.
(2024). Multiplication and Control of vitrification during culture establishment of Arganiaspinosa L.. Horticulture Research Journal, 2(1), 1-13. doi: 10.21608/hrj.2024.361887
MLA
. "Multiplication and Control of vitrification during culture establishment of Arganiaspinosa L.", Horticulture Research Journal, 2, 1, 2024, 1-13. doi: 10.21608/hrj.2024.361887
HARVARD
(2024). 'Multiplication and Control of vitrification during culture establishment of Arganiaspinosa L.', Horticulture Research Journal, 2(1), pp. 1-13. doi: 10.21608/hrj.2024.361887
VANCOUVER
Multiplication and Control of vitrification during culture establishment of Arganiaspinosa L.. Horticulture Research Journal, 2024; 2(1): 1-13. doi: 10.21608/hrj.2024.361887
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