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Rapid regeneration of stable transformants in cultures of potato by improving factors influencing Agrobacterium-mediated transformation

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Advances in Bioscience and Biotechnology 2010年第5期1卷 409-416页

作者： Bipasha Chakravarty Gefu Wang-Pruski 不详

An efficient and rapid Agrobacterium tumefaciens-mediated transformation protocol was developed to generate activation-tagged mutant lines with the aim of large-scale functional analysis of the potato genome. The explants were inoculated with an Agrobacterium strain harboring the binary plasmid pSKI074 containing four CaMV 35S enhancers in the T-DNA region which activates the downstream genes in the host plant after its integration. Various parameters investigated to increase transformation efficiency were the type and age of explant, cultivar, hormone combinations, preculture of explants, period of co-cultivation with bacteria and concentration of bacterial cultures used for transformation. Stem explants from 5 week old plantlets of cv. Bintje which had undergone phytohormone pretreatment for 4 days, inoculation with diluted bacterial concentration of OD600 = 0.2 containing acetosyringone followed by 2 days of co-cultivation and selection in media with IAA and trans-zeatin all helped in greatly improving the transformation efficiency. The total time required from infection to rooted shoots was 6-7 weeks. Initial evidence for stable integration and expression of the transgenes by PCR analysis showed that over 93% of the regenerated lines were transgenic and this was confirmed by Southern hybridization.

关键词： Bacterial Concentration Cultivar Explant Potato Transformation preculture

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Cocoa (<i>Theobroma cacao</i>L.) Somatic Embryos Tolerate Some Ice Crystallization during Cryopreservation

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Agricultural Sciences 2020年第3期11卷 223-234页

作者： Raphael Adu-Gyamfi Andy Wetten Agronomy Department University for Development Studies Tamale Ghana Centre for Research in Biosciences University of the West of England Bristol UK

Secondary somatic embryos (SSEs) of cocoa, a recalcitrant tropical, seed-producing species, were cryopreserved using a vitrification approach and Differential Scanning Calorimetry (DSC) was employed to optimise sucrose preculture and Plant Vitrification Solution 2 (PVS2) incubation. The objective of the study was to evaluate the influence of sucrose preculture and PVS2 dehydration on water content of SSE that will enable it to survive cryostorage. SSEs were precultured for 3 or 5 days on media containing 0.5 M or 0.75 M sucrose and cryoprotected in loading solution (2 M glycerol and 0.4 M sucrose in medium) for 20 min before they were dehydrated with cold PVS2 for 0 - 90 min. Thermal analysis revealed the occurrence of ice crystallization in the SSEs with the extent declining with increasing PVS2 exposure. Maximal survival of SSEs was promoted by preculture on 0.5 M sucrose medium and dehydration with PVS2 for 45 - 60 min, which was characterised by small ice crystallization. Exposure of SSEs beyond 60 min leads to excessive dehydration as characterized by no change in the thermograms. Based on these findings, preculture of SSEs on 0.5 M sucrose medium and dehydration with cold PVS2 for 60 min has been adopted for the successful cryopreservation of cocoa germplasm.

关键词： Differential Scanning Calorimetry Sucrose preculture Cocoa Somatic Embryo Vitrification PVS2

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Cryopreservation of Cat’s Claw (<i>Uncaria tomentosa</i>)

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American Journal of Plant Sciences 2015年第18期6卷 2960-2972页

作者： J. Perez A. Guillen K. Ramos F. Engelmann A. Abdelnour-Esquivel Escuela de Biología Instituto Tecnológico de Costa Rica Cartago Costa Rica IRD UMR DIADE Montpellier France Centro de Investigación en Biotecnología Instituto Tecnológico de Costa Rica (ITCR) Cartago Costa Rica

Uncaria tomentosa presents tomentum that resembles cat’s claws, hence its common name, is a plant that produces various secondary metabolites that are traditionally used in alternative medicine. The natural distribution of this species has been affected by indiscriminate harvesting from its habitat. In the present research, cryopreservation (liquid nitrogen, LN, -196°C) was evaluated as an option for ex situ conservation of this species. The following techniques were evaluated: vitrification and encapsulation-dehydration of apices, vitrification of cell suspensions, and seed desiccation and vitrification. preculture conditions and exposure times to LS and PVS2 were evaluated. Apex survival was the highest (82%) with preculture in 0.25 M sucrose followed by incubation for 20 and 30 min in LS and PVS2, respectively, prior to cooling in LN. The encapsulation-dehydration technique was evaluated by using sucrose preculture and different capsule moisture contents. Survival of apices cooled in LN was not significantly different between treatments and varied from 31.8% to 52.9% for capsule moisture contents between 22.7% and 20.3%. For cell suspensions precultured in 0.5 M sucrose, cell multiplication and formation of calli with very good appearance were observed in 61.1% of the cultures following vitrification. For cryopreservation of seeds, germination was 89.5% using the desiccation technique and 67.6% to78.1% using vitrification.

关键词： Uncaria tomentosa Vitrification Encapsulation-Dehydration Conservation of Plant Genetic Resources PVS2 preculture Regeneration Media

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