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Ethylene‐associated phase change from juvenile to mature phenotype of daylily ( Hemerocallis ) in vitro
Author(s) -
Smith David L.,
Kelly Kevin,
Krikorian A. D.
Publication year - 1989
Publication title -
physiologia plantarum
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.351
H-Index - 146
eISSN - 1399-3054
pISSN - 0031-9317
DOI - 10.1111/j.1399-3054.1989.tb05464.x
Subject(s) - ethylene , chemistry , shoot , botany , in vitro , horticulture , biophysics , biology , biochemistry , catalysis
Hemerocallis plantlets maintained in vitro for extended periods of time in tightly closed culture vessels frequently show a phenotype, albeit on a miniaturized scale, typical of more mature, field‐grown plants. The positive relationship of elevated ethylene in the headspace of such vessels to the phase shift from juvenile to mature form is established. Rigorous restriction in air exchange with the external environment by means of silicone grease seals hastens the phase change and improves uniformity of response. Although some plantlets may take longer to accumulate enough ethylene in sealed jars to undergo change, added ethylene and ethylene‐releasing agents promote it. Ethylene adsorbants (e.g. mercuric perchlorate) block the shift of juvenile to mature form. Critical ambient ethylene level for the shift is ca 1 μl l −1 . Levels up to 1000 μl l −1 do not hasten the response but are not toxic. The phase change is fully reversible when air exchange permits ethylene to drop below 1 μl l −1 . At least 1 μl l −1 ethylene is required to sustain the mature phenotype. The ethylene synthesis inhibitor aminoethoxyvinylglycine (AVG) prevents the phase change, while the ethylene biosynthesis intermediate 1‐aminocyclopropanecarboxylic acid (ACC) improves it. KOH, as a CO 2 absorbant, does not prevent the phase change. Histology sections demonstrate subtle changes in the form of shoot tips of plantlets undergoing phase change.