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Direct regeneration from in vitro leaf and petiole tissues of Populus tremula ‘Erecta’

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Abstract

Dormant buds from a mature tree of Populus tremula ‘Erecta’ were incubated on a Murashige and Skoog (MS) medium supplemented with 1.0 μM thidiazuron (TDZ). Induced shoots were then proliferated on medium of MS or Woody Plant Medium (WPM), or Driver and Kuniyuki Walnut (DKW) supplemented with varying levels of benzyladenine (BA). Overall, shoots grown on MS medium supplemented with 1.25–2.5 μM BA exhibited the highest frequency of shoot proliferation (>95%) and more than 60% of responding explants produced more than five shoots per explant. Shoot organogenesis was induced from both leaf and petiole explants incubated on WPM medium containing BA, or TDZ, or zeatin. Among the different cytokinins tested, zeatin induced the highest frequency (average 72.1%) of shoot organogenesis. None of explants survived on media containing no cytokinins within 6–8 weeks following culture. Overall, a higher frequency of shoot regeneration was obtained from petioles than from leaf explants. The highest frequency of regeneration was achieved when petioles were incubated on WPM containing 10–20 μM zeatin. Addition of naphthaleneacetic acid (NAA) did not have a significant effect on shoot regeneration in all treatments. Shoot organogenesis was directly induced from petiole explants without intervening callus. Regenerated shoots were easily rooted on all tested media supplemented with 0.5 μM NAA. Rooted plants were transferred to potting mix and grown in the greenhouse.

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Acknowledgments

This research was supported in part by McIntire-Stennis Project ND06212. The authors thank Dr. T. Helms for his help on statistical analysis and Drs. H. Hatterman-Valenti and C. Lee for reviewing this manuscript.

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Correspondence to Wenhao Dai.

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Huang, D., Dai, W. Direct regeneration from in vitro leaf and petiole tissues of Populus tremula ‘Erecta’. Plant Cell Tiss Organ Cult 107, 169–174 (2011). https://doi.org/10.1007/s11240-011-9955-1

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