Yang Honglin, Yuan Honglin, Du Cunmei, Liang Liyun, Chen Meiling, Zou Lijuan
Ecological Security and Protection Key Laboratory of Sichuan Province, Mianyang Normal University, Mianyang 621000, China.
State Key Laboratory of Crop Gene Exploration and Utilization in Southwest China, Sichuan Agricultural University at Wenjiang, Chengdu 611130, China.
Plants (Basel). 2022 Sep 21;11(19):2456. doi: 10.3390/plants11192456.
(Blume) G. Don, the "lipstick plant" is a prized ornamental plant with distinctive flowers. Here, we introduce a novel in vitro regeneration method for using leaf explants and an optimized combination of phytohormone plant growth regulators (PGRs). The optimal conditions for shoot regeneration included 1 mg L polyvinyl pyrrolidone (PVP) plus 3 mg L 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 PVP, 3 mg L TDZ, 5 mg L casein, and 0.1 mg L α-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 PVP, 5 mg L casein, 3 mg L 6-benzyladenine (BA), and 0.1 mg L 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 .
(布卢姆)G. 唐,“口红吊兰”是一种珍贵的观赏植物,花朵独特。在此,我们介绍一种利用叶片外植体和植物激素植物生长调节剂(PGRs)优化组合的新型离体再生方法。芽再生的最佳条件包括1毫克/升聚乙烯吡咯烷酮(PVP)加3毫克/升噻苯隆(TDZ),诱导响应率为82.4%,芽/外植体比率为38.6。当Murashige和Skoog(MS)培养基仅含有吲哚 - 3 - 丁酸(IBA)时,叶片先分化为不定根,然后分化为不定芽。在含有1克/升PVP、3毫克/升TDZ、5毫克/升酪蛋白和0.1毫克/升α - 萘乙酸(NAA)的MS培养基上培养30天的叶片,胚性愈伤组织(EC)诱导率最高(95.6%)。当将源自EC的芽在用于EC诱导的相同培养基上培养5周时,获得了最佳的芽增殖系数(21.5)。对于伸长芽生根最有效的培养基是含有1克/升PVP、5毫克/升酪蛋白、3毫克/升6 - 苄基腺嘌呤(BA)和0.1毫克/升NAA的MS培养基,根的数量达到18.8。在温室中生长的再生植株经过一周的炼苗后存活率为100%。总体而言,我们有效且高效的繁殖方法应能缩短培养周期并降低生产成本,为未来的选择性育种和遗传改良提供可能。