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1.
Sci Rep ; 10(1): 4558, 2020 03 12.
Article in English | MEDLINE | ID: mdl-32165694

ABSTRACT

In this works, a simple, efficient and repeatable protocol was developed for in vitro regeneration via callus-mediated organogenesis of Neolamarkia Cadamba using cotyledonary petioles and hypocotyls. Effects of basal medium, plant growth regulators, the types and age of explant on the formation of adventitious buds/shoots were studied. Meanwhile, histological analysis for early ontogenic stages and genetic stability assessment by flow cytometry were investigated. Our investigation demonstrated that, compared with 6-benzyladenine (BA), N6-(2-isopentenyl) adenine (2-ip), Thidiazuron (TDZ) was the optimal cytokinin for buds/shoots induction on cotyledon and hypocotyl explants. Douglas-fir and sugar pine medium (DCR) supplemented with 22.7 µM TDZ and 0.27 µM α-naphthalene acetic acid (NAA) was most effective on bud induction, with the highest bud-induction rate and numbers of buds on cotyledon and hypocotyl explants. The available shoot per explant hit 35.2 when the induced callus sub-cultured to a medium without TDZ. It was found that TDZ could promote induction of the callus and the buds, however, continuous exposure beyond 4 weeks of supplemented high concentration (exceed 11.35 µM), TDZ was harmful to the proliferation and growth of buds/shoots. DCR appeared more efficiency than Murashige and Skoog medium (MS), Woody Plant medium (WPM), anther culture of cereal crops medium (N6) on bud induction. Age of cotyledon and hypocotyl explants in 20-day to 25-day was most beneficial to adventitious buds/shoots formation. Histological investigation confirmed that the buds originated from the wounded incisions of cotyledonary petiole and hypocotyl fragments, with callus formation. The regeneration plantlets were successfully acclimatized in greenhouse, yielded above 95% survival rate in field, exhibited normal morphology and growth characteristics. The analysis of flow cytometry on N. cadamba indicated no variation in the ploidy levels between the regenerated plantlets and the donor trees. The developed procedure can be used for mass production, germplasm exchange and transgenic studies to improve the resistance of the species via Agrobacterium-mediated.


Subject(s)
Cell Culture Techniques/methods , Cinchona/growth & development , Cotyledon/cytology , Culture Media/chemistry , Hypocotyl/cytology , Benzyl Compounds/pharmacology , Cinchona/cytology , Cinchona/genetics , Cotyledon/drug effects , Cotyledon/genetics , Cytokinins/pharmacology , Flow Cytometry , Hypocotyl/drug effects , Hypocotyl/genetics , Naphthaleneacetic Acids/chemistry , Organogenesis, Plant , Phenylurea Compounds/pharmacology , Plant Growth Regulators/pharmacology , Ploidies , Purines/pharmacology , Thiadiazoles/pharmacology , Tropical Climate
2.
Environ Toxicol Chem ; 20(12): 2670-5, 2001 Dec.
Article in English | MEDLINE | ID: mdl-11764147

ABSTRACT

This manuscript evaluates the phytotoxicity and biotransformation of n-hexadecane as well as peroxidase activity and cytochrome P450 concentration in microsomes for cell suspension cultures of Cinchona robusta and Dioscorea composita. Phytotoxicity was evaluated based on viability and growth. Cell cultures were exposed to a 2 and 4% (v/v) dose of n-hexadecane. The biotransformation of n-hexadecane was determined based on labeled recovery in polar, nonpolar, and cell residue fractions after cell culture extraction during exponential cell growth phase and stationary phase. Differences were observed in accumulation of label during cell growth phase and stationary phase for the cells of the two plants. Differences also were observed between phases for label in polar and nonpolar fractions. Thin-layer chromatography determined labeled intermediates and some were identified. The activity of peroxidase and concentration of cytochrome P450 was lower in C. robusta than in controls and greater in D. composita than in controls. In vitro biotransformation was not successful.


Subject(s)
Alkanes/metabolism , Cinchona/physiology , Dioscorea/physiology , Water Pollutants, Chemical/metabolism , Alkanes/toxicity , Biotransformation , Cell Culture Techniques , Chromatography, Thin Layer , Cinchona/growth & development , Cytochrome P-450 Enzyme System/metabolism , Dioscorea/growth & development , Dose-Response Relationship, Drug , Microsomes , Peroxidase/metabolism , Water Pollutants, Chemical/toxicity
4.
Parassitologia ; 29(2-3): 207-20, 1987.
Article in English | MEDLINE | ID: mdl-3334083

ABSTRACT

Following a short historical review of the facts which lead to the discovery of the specific action of the cinchona bark, an analysis is made of the obstacles encountered for more than two centuries by scientific expeditions to the identification, among the maze of natural hybrids, of the varieties of cinchona producing large amounts of quinine, and to obtain the best seed to establish plantations in other continents. Charles Ledger, a British general tradesman, was able to achieve that thanks to his alert spirit of observation, his (and that of his Bolivian servant Manuel) long experience of the Andes, and the chance that brought them to fall upon a group of exceptional cinchonas which had grown on an impervious slope of the Andes. Eventually the seeds were collected and Ledger offered them to the British and Dutch governments. Whereas the British failed to recognise their importance, the Dutch did not. They created extensive plantations in Java from which the world's demand for quinine was met, and the Dutch detained the practical monopoly of its production.


Subject(s)
Cinchona Alkaloids/history , Cinchona/growth & development , Plants, Medicinal , Seeds/growth & development , Geography , History, 17th Century , History, 18th Century , History, 19th Century , Malaria/drug therapy , Quinine/history , Quinine/therapeutic use
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