Improvement of regeneration ability in Phleum pratense L. in vitro culture by dicamba |
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Authors: | Agnieszka P?a?ek Maria Filek Maria W?dzony |
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Institution: | (1) Department of Plant Physiology, the Agricultural University of Kraków, Podłużna 3, PL-30239 Kraków, Poland;(2) Department of Plant Physiology, Polish Academy of Sciences, Podłużna 3, PL-30239 Kraków, Poland |
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Abstract: | Calli were induced from mature caryopses of timothy grass (Phleum pratense L.) on MS medium (Murashige and Skoog 1962) supplemented with 500 mg·dm−3 casein hydrolysate and 5 mg·dm−3 2,4-D (2,4-dicholorophenoxyacetic acid) or 2 mg·dm−3 dicamba (3,6-dichloro-o-anisic acid). Twelve-week-old calli were passaged on media with reduced levels of auxins (2 mg·dm−3 2,4-D or 1 mg·dm−3 dicamba). Tissues induced on medium with 2,4-D were transferred on medium with 2,4-D and on medium with dicamba; parallely
calli initiated on medium with dicamba were passaged on medium with 2,4-D or dicamba. Calli from various media sequences were
used to establish cell suspension cultures in media containing 2 mg·dm−3 2,4-D or 1 mg·dm−3 dicamba. An assessment of regeneration ability of calli was made on MS medium containing 0.2 mg·dm−3 kinetin. Callus tissue induced and/or subcultured on any of the media with 2,4-D did not regenerate plants while dicamba
added to the media was the effective stimulator of regenerability. In the presence of 2,4-D calli and suspensions produced
a jelly-like extracellular matrix. In cell suspension this phenomenon was observed 4–5 days after each passage. The measurements
of electric potential of calli, growing on MS medium with kinetin were performed. Non-regenerating callus areas had an electric
potential close to 0 mV while parts of tissue with meristematic centres were characterized by lower values of electric potential. |
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Keywords: | callus cell suspension dicamba 2 4-D electric potential Phleum pratense regeneration timothy grass |
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