T. P. Krishna, N. M. Krishnakumar, T. Maharajan, S. A. Ceasar
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The nodal explant was regenerated in three different steps: (1) initial shoot induction, (2) shoot multiplication and elongation, and (3) rooting.\n \n \n \n The results revealed that all individual concentrations (10, 20, 30, or 40 mg/L) of BAP or KIN responded to induce shoot initiation. The highest shoot multiplication and elongation were achieved in the MS medium with 20 mg/L BAP and 20 mg/L KIN. The regenerated plantlets produced better roots on MS medium containing 1.0 mg/L of each IAA or IBA. The well-established rooted plantlets were maintained in the culture room and greenhouse for better acclimatization and achieved a 100% survival rate. We analyzed the genetic fidelity of in vitro regenerated plants using random amplified polymorphic DNA (RAPD) markers. No genetic polymorphisms were observed in vitro plants compared to the mother plants.\n \n \n \n This efficient protocol could benefit future biotechnological applications like mass multiplication, genetic transformation and gene editing for improving the bioactive molecules in A. triplinervis.\n","PeriodicalId":296126,"journal":{"name":"The Open Biotechnology Journal","volume":"28 3","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-01-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Rapid In Vitro Regeneration and Genetic Fidelity Assessment of Regenerated Plants in Ayapana Triplinervis (Vahl) R.M. King & H. Robinson: An Ethnomedicinal and Ornamental Herb\",\"authors\":\"T. P. Krishna, N. M. Krishnakumar, T. Maharajan, S. A. 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引用次数: 0
摘要
Ayapana triplinervis 是一种广受欢迎的民族药用和观赏植物。由于其药用价值极高,A. triplinervis 最近被收录到《法国药典》中。 快速高效的组织培养方案开发对于该植物的高产和生物技术应用至关重要。 在这项研究中,我们利用三叶金线莲的节状外植体开发了一种高效的植物再生组织培养方案。在添加了不同浓度细胞分裂素(BAP 和 KIN)和辅酶(IAA 和 IBA)的 Murashige 和 Skoog(MS)培养基中处理节的外植体。节的外植体分三个不同步骤再生:(1)初始芽诱导,(2)芽增殖和伸长,(3)生根。 结果表明,所有浓度(10、20、30 或 40 毫克/升)的 BAP 或 KIN 都能诱导芽的萌发。在含有 20 毫克/升 BAP 和 20 毫克/升 KIN 的 MS 培养基中,芽的繁殖和伸长率最高。在含有 1.0 毫克/升 IAA 或 IBA 的 MS 培养基上,再生小植株生出的根更好。为了更好地适应环境,这些生根良好的小植株被放在培养室和温室中养护,成活率达到了 100%。我们利用随机扩增多态性 DNA(RAPD)标记分析了离体再生植株的遗传保真度。与母株相比,离体植株未发现基因多态性。 这种高效的方案将有利于未来的生物技术应用,如大规模繁殖、基因转化和基因编辑,以改进三疣梭子蟹的生物活性分子。
Rapid In Vitro Regeneration and Genetic Fidelity Assessment of Regenerated Plants in Ayapana Triplinervis (Vahl) R.M. King & H. Robinson: An Ethnomedicinal and Ornamental Herb
Ayapana triplinervis is a popular ethnomedicinal and ornamental plant species. Due to its high medicinal importance, A. triplinervis was recently documented in the French Pharmacopeia.
Rapid and efficient tissue culture protocol development is crucial for the high production and biotechnological applications of this plant.
In this study, an efficient tissue culture protocol was developed for plant regeneration using nodal explants of A. triplinervis. The nodal explants were treated in Murashige and Skoog’s (MS) medium supplemented with various individual concentrations of cytokinins (BAP and KIN) and auxins (IAA and IBA). The nodal explant was regenerated in three different steps: (1) initial shoot induction, (2) shoot multiplication and elongation, and (3) rooting.
The results revealed that all individual concentrations (10, 20, 30, or 40 mg/L) of BAP or KIN responded to induce shoot initiation. The highest shoot multiplication and elongation were achieved in the MS medium with 20 mg/L BAP and 20 mg/L KIN. The regenerated plantlets produced better roots on MS medium containing 1.0 mg/L of each IAA or IBA. The well-established rooted plantlets were maintained in the culture room and greenhouse for better acclimatization and achieved a 100% survival rate. We analyzed the genetic fidelity of in vitro regenerated plants using random amplified polymorphic DNA (RAPD) markers. No genetic polymorphisms were observed in vitro plants compared to the mother plants.
This efficient protocol could benefit future biotechnological applications like mass multiplication, genetic transformation and gene editing for improving the bioactive molecules in A. triplinervis.