Regeneration of Chlorophytum amaniense ‘Fire Flash’ Through Indirect Shoot Organogenesis

Abstract

<jats:p><jats:italic>Chlorophytum amaniense</jats:italic> Engl. ‘Fire Flash’ is a popular exotic ornamental foliage plant as a result of its unique coral-colored midribs and petioles and tolerance to interior low light levels. Currently, demand for propagative materials exceeds the availability of seeds. This study was intended to develop an in vitro culture method for rapid propagation of this cultivar. Leaf and sprouted seed explants were cultured on a Murashige and Skoog basal medium supplemented with different cytokinins with 1.1 μM α-naphthalene acetic acid (NAA) or 2.3 μM 2,4-dichlorophenoxyacetic acid (2,4-D). Leaf explants showed poor responses in callus production and no adventitious shoots were obtained. Callus formation frequencies from sprouted seeds were 71% and 85% when induced by 9.8 μM N<jats:sub>6</jats:sub>-(2-isopentyl) adenine (2iP) with 1.1 μM NAA and 9.1 μM N-phenyl-N′-1,2,3-thiadiazol-5-ylurea (TDZ) with 1.1 μM NAA, respectively. Adventitious shoots occurred after the induced calluses were subcultured on the same concentrations of TDZ or 2iP with NAA. Shoot formation frequencies from calluses cultured on TDZ with NAA and 2iP with NAA were 92% and 85%, and the corresponding mean shoot numbers were 37 and 31 per piece of callus (1 cm<jats:sup>3</jats:sup>), respectively. Adventitious shoots rooted at 100% after transferring to the basal medium containing 4.4 μM 6-benzylaminopurine (BA) with 2.7 μM NAA. Plantlets, after transplanting to a soilless substrate were easily acclimatized in a shaded greenhouse under a photosynthetic photon flux (<jats:italic>PPF</jats:italic>) density of 200 μmol·m<jats:sup>−2</jats:sup>·s<jats:sup>−1</jats:sup>. Regenerated plants grew vigorously without undesirable basal branching or distorted leaves. This newly established regeneration method can provide the foliage plant industry with a means for rapidly propagating ‘Fire Flash’ liners in a year-round fashion.</jats:p>

Regeneration and Genetic Fidelity Analysis of &lt;i&gt;Chlorophytum borivilianum&lt;/i&gt; Using Flower Stalk as Explant Source

“…Due to these is limitations, in vitro culture based methods are in demand and have been successfully used for micropropagation of different species of Chlorophytum [7] [8]. Tissue culture which includes callus induction, micro-propagation and in vitro tuberization has been reported in different species of Chlorophytum such as C. comosum [9], C. borivilianum [10], C. amanienese [11] and C. arundianceum [8]. In vitro micropropagation depends on the type of explants and growth regulators used in the medium.…”