ABSTRACT
Background: This research is intended to determine suitable types and concentrations of plant growth regulators (PGRs) to induce callus on stem and leaf sections of 4 species of the genus Garcinia, namely, Garcinia mangostana, Garcinia schomburgkiana, Garcinia cowa, and Garcinia celebica. The base medium was MS medium containing 30 g l -1 sucrose, 0.5 g l-1 polyvinylpyrrolidone (PVP), and 7 g l-1 agar, and for the different treatments, PGRs were added to the medium as follows: thidiazuron (TDZ) at concentrations of 0, 0.1, 0.5, 1, and 2 mg l-1; 6-(3- hydroxybenzylamino) purine (meta-topolin) at concentrations of 0, 0.5, 2.5, and 5 mg l-1; 4-amino-3,5,6- trichloro-2-pyridinecarboxylic acid (picloram) at concentrations of 0, 0.5, 2.5, and 5 mg l-1; and 2,4- dichlorophenoxyacetic acid (2,4-D) at concentrations of 0, 0.5, 1, 2, and 4 mg l-1. The occurrence of callus was observed after 4 weeks. Results: A maximum of 100% and 93% of G. mangostana leaf explants formed callus in the 0.5 mg l-1 and 1 mg l-1 TDZ treatments, respectively, while 100% of G. schomburgkiana stem explants formed callus in the 1 mg l-1 TDZ treatment and 89% of G. schomburgkiana leaf explants formed callus in the 0.5 mg l-1 picloram treatment. The highest callus induction rate for G. cowa was 62% in the 1 mg l-1 TDZ treatment and for G. celebica was 56% in the 0.5 mg l-1â¢mT-1 treatment. Conclusions: For all 4 species, the greatest amount of large nodular callus was observed in the TDZ treatments. White, friable callus was observed on most of the 2,4-D and picloram treatment groups. Most meta-topolin treatments resulted in minimal callus formation.
Subject(s)
Plant Growth Regulators/metabolism , Garcinia/growth & development , Phytochemicals/metabolism , Phenylurea Compounds , Thiadiazoles , Time Factors , Transformation, Genetic , Clusiaceae/growth & development , Garcinia/physiology , Tissue Culture TechniquesABSTRACT
Roots of plantlets of Garcinia indica when cultured for long time on half strength MS medium supplemented with BAP (0.44-2.22 microM) showed production of de novo shoots. Roots attached to mother plant showed more number of shoots, while excised root segments produced lesser shoots. Shoots (0.5-0.8 cm) were transferred to elongation medium consisting of Woody Plant Medium (WPM) supplemented with BAP (4.44-22.69 microM), IAA (5.71 microM) and kinetin (4.65 microM). It was observed that shoot length increased to 1-2 cm. WPM medium supplemented with NAA (2.69-10.74 microM) and IBA (4.90 microM) induced rooting within 20-25 days. Using the present protocol, 20-25 plantlets could be regenerated from single root explant within 3 to 4 months. The protocol has potential for large scale production of elite plants.
Subject(s)
Culture Techniques , Garcinia/growth & development , Plant Roots , Plant Shoots/physiology , RegenerationABSTRACT
Germination tests on Garcinia intermedia (Clusiaceae) seeds showed the growth of two types of roots: additionally to the primary root, a secondary root crosses the seed lengthwise. To determine its possible role on the survival and growth of this species, 90 seedlings at least six months old (collected in Central Costa Rica) were planted in plastic bags with organic soil, and placed in a greenhouse. The seedlings were treated as follows: treatments in which the primary or secondary root was cut off, and a control group with both roots intact (30 replicates each). After three months 10 seedlings/month/treatment were extracted to measure their height, basal diameter, root length (main and secondary root), and biomass of the stem, roots and seed (without its coat). Control seedlings had the highest growth, followed by those without secondary roots. Nonetheless, more than 90% of the seedlings whose primary roots were cut off, survived after five months of the excision treatment, in part due to the capacity of this species to regenerate its radical system through the seed reserves, sprouting of a primary-like root, and/or the growth stimulus of the secondary root (60% of the total: 20% with sprouts from the primary root stump, 13.3% with a growth stimulus of the secondary root, and 26.7% with both conditions). The length of the sprouted roots was significantly different only on those plants that were extracted during the first two monthly measurements, when compared with the control (F6 = 18.6, F7 = 16.0, p < 0.01).