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Developmental and hormonal regulation of direct shoot organogenesis and somatic embryogenesis in sugarcane (Saccharum spp. interspecific hybrids) leaf culture
Authors:Prakash Lakshmanan  R Jason Geijskes  Lifang Wang  Adrian Elliott  Christopher P L Grof  Nils Berding  Grant R Smith
Institution:(1) David North Plant Research Centre, BSES Limited, 50 Meiers Road, Indooroopilly, Brisbane, Queensland, 4068, Australia;(2) CSIRO-Plant Industry, Queensland Bioscience Precinct, 306 Carmody Road, St Lucia, Queensland, 4067, Australia;(3) Meringa Sugar Experiment Station, BSES Limited, Bruce Highway, Gordonvale, Queensland, 4865, Australia;(4) Present address: Queensland University of Technology, School of Life Sciences, 2 George Street, Brisbane, Queensland, 4001, Australia;(5) New Zealand Institute for Crop & Food Research Limited, Private Bag 4704, Christchurch, New Zealand
Abstract:Rapid and efficient in vitro regeneration methods that minimise somaclonal variation are critical for the genetic transformation and mass propagation of commercial varieties. Using a transverse thin cell layer culture system, we have identified some of the developmental and physiological constraints that limit high-frequency regeneration in sugarcane leaf tissue. Tissue polarity and consequently the orientation of the explant in culture, size and developmental phase of explant, and auxin concentration play a significant role in determining the organogenic potential of leaf tissue in culture. Both adventitious shoot production and somatic embryogenesis occurred on the proximal cut surface of the explant, and a regeneration gradient, decreasing gradually from the basal to the distal end, exists in the leaf roll. Importantly, auxin, when added to the culture medium, reduced this spatial developmental constraint, as well as the effect of genotype on plant regeneration. Transverse sections (1-2 mm thick) obtained from young leaf spindle rolls and orienting explants with its distal end facing the medium (directly in contact with medium) are critical for maximum regeneration. Shoot regeneration was observed as early as 3 weeks on MS medium supplemented with alpha-naphthalenencetic acid (NAA) and 6-benzyladenine, while somatic embryogenesis or both adventitious shoot organogenesis and somatic embryogenesis occurred on medium with NAA and chlorophenoxyacetic acid. Twenty shoots or more could be generated from a single transverse section explant. These shoots regenerated roots and successfully established after transplanted to pots. Large numbers of plantlets can be regenerated directly and rapidly using this system. SmartSett, the registered name for this process and the plants produced, will have significant practical applications for the mass propagation of new cultivars and in genetic modification programs. The SmartSett system has already been used commercially to produce substantial numbers of plants of orange rust-resistant and new cultivars in Australia.
Keywords:Direct regeneration                  Saccharum                SmartSett?                Somaclonal variation  Somatic embryogenesis  Sugarcane  Thin cell layer culture
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