Articles
In vitro propagation and ex vitro acclimatization of Pittosporum angustifolium
Article number
1327_48
Pages
361 – 366
Language
English
Abstract
Pittosporum angustifolium Lodd. is an Australian native evergreen, small weeping tree, drought and frost resistant, with potential ornamental and pharmaceutical use.
In Athens, Greece the plant produces fruit, which rarely bear seeds.
The aim of the present work was to develop a protocol for clonal in vitro propagation of the species.
In vitro cultures were established by shoot tip and nodal explants excised from young vegetation of an adult tree, cultured on solid MS medium with 2.0 mg L‑1 6-benzyladenine (BA, 83-100% explant response, 1.4-1.7 shoots per responding explant). In following subcultures 1.0 or 2.0 mg L‑1 BA were necessary for shoot multiplication (77-80% explant response, 2.7-2.9 shoots explant-1), while micro-shoots had the tendency to produce axillary shoots.
Latter were mostly produced by cultures initiated by nodal explants compared to those initiated by shoot tip explants.
Shoot multiplication was further enhanced by increasing BA to 4.0 mg L‑1 but shoot length was reduced.
Axillary shoot production was significantly increased (73-81% explant response, 3.8-4.7 axillary shoots explant-1) in a medium with 2.0 or 4.0 mg L‑1 BA by increasing the culture period from 35 to 90 days.
Micro-shoots 1 cm long rooted at 95% on half-strength MS medium with 4 mg L‑1 IBA, in the dark, while 2 cm long micro-shoots rooted at 85% with 10 mg L-1 IBA. Rooting under high IBA concentrations was inhibitory for the following ex vitro acclimatization of rooted micro-shoots.
The highest acclimatization (69-79%) was achieved in peat:perlite (1:1, v/v) when micro-shoots were rooted with 2.0 mg L‑1 IBA with basal shoot darkening or in the dark.
In Athens, Greece the plant produces fruit, which rarely bear seeds.
The aim of the present work was to develop a protocol for clonal in vitro propagation of the species.
In vitro cultures were established by shoot tip and nodal explants excised from young vegetation of an adult tree, cultured on solid MS medium with 2.0 mg L‑1 6-benzyladenine (BA, 83-100% explant response, 1.4-1.7 shoots per responding explant). In following subcultures 1.0 or 2.0 mg L‑1 BA were necessary for shoot multiplication (77-80% explant response, 2.7-2.9 shoots explant-1), while micro-shoots had the tendency to produce axillary shoots.
Latter were mostly produced by cultures initiated by nodal explants compared to those initiated by shoot tip explants.
Shoot multiplication was further enhanced by increasing BA to 4.0 mg L‑1 but shoot length was reduced.
Axillary shoot production was significantly increased (73-81% explant response, 3.8-4.7 axillary shoots explant-1) in a medium with 2.0 or 4.0 mg L‑1 BA by increasing the culture period from 35 to 90 days.
Micro-shoots 1 cm long rooted at 95% on half-strength MS medium with 4 mg L‑1 IBA, in the dark, while 2 cm long micro-shoots rooted at 85% with 10 mg L-1 IBA. Rooting under high IBA concentrations was inhibitory for the following ex vitro acclimatization of rooted micro-shoots.
The highest acclimatization (69-79%) was achieved in peat:perlite (1:1, v/v) when micro-shoots were rooted with 2.0 mg L‑1 IBA with basal shoot darkening or in the dark.
Authors
M. Maniati, M. Papafotiou
Keywords
axillary shoots, 6-benzyladenine, dark, Gumby, in vitro rooting, micropropagation, multiplication
Groups involved
- Division Plant Genetic Resources, Breeding and Biotechnology
- Division Tropical and Subtropical Fruit and Nuts
- Division Temperate Tree Fruits
- Division Vine and Berry Fruits
- Division Ornamental Plants
- Division Vegetables, Roots and Tubers
- Division Plant-Environment Interactions in Field Systems
- Division Greenhouse and Indoor Production Horticulture
- Division Postharvest and Quality Assurance
- Division Precision Horticulture and Engineering
- Division Horticulture for Human Health
- Division Temperate Tree Nuts
- Division Landscape and Urban Horticulture
- Division Sustaining Horticulture in a Changing World
- Working Group Humulus and Other Cannabaceae
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