4.7 Article

Development of a Highly Efficient Shoot Organogenesis System for an Ornamental Aeschynanthus pulcher (Blume) G. Don Using Leaves as Explants

Journal

PLANTS-BASEL
Volume 11, Issue 19, Pages -

Publisher

MDPI
DOI: 10.3390/plants11192456

Keywords

Aeschynanthus pulcher (Blume) G. Don; leaf explant; embryogenic callus; propagation; shoot regeneration

Categories

Funding

  1. National Natural Science Foundation of China [31972258, 32272560]

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Here, a novel in vitro regeneration method using leaf explants and optimized combination of plant growth regulators is introduced for A. pulcher. The method achieves efficient shoot regeneration, embryogenic callus induction, and shoot rooting by optimizing the composition of different culture media.
Aeschynanthus pulcher (Blume) G. Don, the lipstick plant is a prized ornamental plant with distinctive flowers. Here, we introduce a novel in vitro regeneration method for A. pulcher using leaf explants and an optimized combination of phytohormone plant growth regulators (PGRs). The optimal conditions for shoot regeneration included 1 mg L-1 polyvinyl pyrrolidone (PVP) plus 3 mg L-1 thidiazuron (TDZ), inducing a response rate of 82.4% and a shoot/explant ratio of 38.6. When the Murashige and Skoog (MS) medium contained indole-3-butyric acid (IBA) alone, leaves first differentiated into adventitious roots and then adventitious shoots. Leaves cultured on MS medium containing 1 g L-1 PVP, 3 mg L-1 TDZ, 5 mg L-1 casein, and 0.1 mg L-1 alpha-naphthaleneacetic acid (NAA) for 30 d exhibited the highest embryogenic callus (EC) induction rate (95.6%). The optimal shoot proliferation coefficient (21.5) was obtained when shoots derived from EC were cultured on the same medium as that used for EC induction for 5 weeks. The most effective medium for rooting of elongated shoots was MS medium containing 1 g L-1 PVP, 5 mg L-1 casein, 3 mg L-1 6-benzyladenine (BA), and 0.1 mg L-1 NAA, and the number of roots reached 18.8. The regenerated plants grown in a greenhouse had 100% survival following one week of hardening. Overall, our effective and efficient propagation method should result in shortened culture periods and reduced production costs, allowing for the future selective breeding and genetic improvement of A. pulcher.

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