硅藻土(Thottea sililiquosa, Lamk.)微繁过程中培养基褐变的控制及离体母植株生化和克隆保真度评价鼎侯。是一种重要的民族药用灌木。

IF 3.6 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Journal, genetic engineering & biotechnology Pub Date : 2023-06-02 DOI:10.1186/s43141-023-00523-8
Chandran Padikkal Krishna Vrundha, Thuruthiyil Dennis Thomas
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引用次数: 0

摘要

背景:Thottea silquiosa (Lamk.)鼎侯。是一种重要的药用灌木,被广泛应用于阿育吠陀和本土医学体系中。根是最有用的部分,植物经常被连根拔起,从而给自然种群带来压力。到目前为止,还没有关于该植物的微繁研究。本研究的目的是建立一种高效的水蛭体外繁殖方案和克隆保真度评估。结果:培养基褐变在微繁殖过程中是一个严重的问题,添加40.0 mg/L抗坏血酸可以减少培养基褐变。在添加1.0 mg/L噻脲和0.25 mg/L α-萘乙酸的WPM培养基上,7日龄子叶直接再生的效果最佳,达到92%,每外植体再生20.9个子叶。将培养物转移到添加了0.4 mg/L噻脲的WPM中,以促进芽的伸长和生长。在该培养基上,100%的培养物平均产生27.6个芽。愈伤组织诱导采用MS培养基,培养基中添加1.0 mg/L 2,4-二氯苯氧乙酸和0.5 mg/L n6 -苄基氨基嘌呤。在相同的培养基上开始芽器官发生,将幼芽细小的愈伤组织转移到添加0.5 mg/L n6 -苄基氨基嘌呤和0.25 mg/L α-萘乙酸的MS培养基上,再生率最高(100%的培养,平均每个外植体再生26.5个芽)。在添加1.0 mg/L吲哚-3-丁酸的半强度MS培养基上生根频率最高,为82%,生根数最高,为20.8根。有根的植株经驯化后移栽到田间。HPTLC和SCoT分析显示离体繁殖植株与母株的植物化学和克隆相似性。结论:本研究证实了子叶是水杨花直接和间接茎器官发生的良好外植体。对于直接诱导WPM和间接器官发生,MS培养基效果更好。通过植物化学和SCoT分析证实了体外来源植物的真性。本文所述的方法可用于水蛭优良无性系的大规模繁殖。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Control of media browning during micropropagation and assessment of biochemical and clonal fidelity of in vitro-derived and mother plants in Thottea siliquosa (Lamk.) Ding Hou., an important ethnomedicinal shrub.

Background: Thottea siliquosa (Lamk.) Ding Hou., an important medicinal shrub, is widely used in both ayurvedic and indigenous systems of medicine. Root being the most useful part, the plant is constantly uprooted and thus puts pressure on the natural population. Until date, no micropropagation study is available in this plant. The objective of the study is to develop an efficient in vitro propagation protocol and assessment of clonal fidelity of T. siliquosa.

Results: Media browning was a serious issue during micropropagation, and the addition of 40.0 mg/L ascorbic acid reduced the media browning. For direct shoot regeneration, the optimum response (92% frequency with 20.9 shoots per explant) was obtained when 7-day-old cotyledons were cultured on WPM supplemented with 1.0 mg/L thidiazuron and 0.25 mg/L α-naphthalene acetic acid. The cultures were transferred to WPM augmented with 0.4 mg/L thidiazuron for shoot elongation and growth. On this medium, 100% of cultures responded with a mean number of 27.6 shoots. For callus induction, MS medium with 1.0 mg/L 2,4-dichlorophenoxyacetic acid and 0.5 mg/L N6-benzylaminopurin was used. Shoot organogenesis was initiated on the same medium, and calli with minute shoots were transferred to MS medium fortified with 0.5 mg/L N6-benzylaminopurin and 0.25 mg/L α-naphthalene acetic acid for highest shoot regeneration (100% cultures responded with a mean number of 26.5 shoots per explant). Maximum rooting frequency (82%) and number (20.8) were obtained on half-strength MS medium with 1.0 mg/L indole-3-butyric acid. The rooted plants were acclimatized and transferred to the field. The HPTLC and SCoT analysis revealed the phytochemical and clonal similarity between the in vitro propagated plants and mother plant.

Conclusions: In this study, it is confirmed that cotyledon is an excellent explant for direct and indirect shoot organogenesis in T. siliquosa. For direct shoot induction WPM and indirect organogenesis, MS medium was found to give better response. The true-to-type nature of in vitro-derived plants were confirmed by phytochemical and SCoT analysis. The protocol described here could be used for the large-scale propagation of elite clones of T. siliquosa.

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