{"title":"High-Frequency Direct Organogenesis from Cotyledonary Node Explants and Plantlet Regeneration of Peanut (Arachis hypogaea) Cultivars","authors":"Abraham Lamboro","doi":"10.17957/ijab/15.1906","DOIUrl":null,"url":null,"abstract":"The efficient plantlets regeneration of peanut is the most important and a primary step to successfully transform gene and apply recently developed genome editing techniques for crop yield improvement. The purpose of this research is to develop protocol for peanut cultivars applying different concentration of hormones for selected peanut cultivars and develop plantlets regeneration protocol. There is no previously reported protocol for the Chinese peanut cultivar N3 and Yu-hua-14. We optimized shoot and root regeneration protocol for two peanut cultivars. Both cultivars showed positive response for the cytokinin plant growth hormone 6-benzylaminopurine (BAP) and thidiazuron (TDZ). The highest shooting rate (97%) was found in a medium supplemented with 4 mg/L BAP and (94.33%) for 1 mg/L TDZ. Hence, more shoot initiation was observed at higher concentration of BAP as compared to TDZ. However, the maximum root regeneration (81%) was found on medium containing 0.3 mg/L 2, 4-dichlorophenoxyacetic acid (2,4-D) and the highest rooting rate (96.33%) was found in a medium containing 1 mg/L α-naphthalene acetic acid (NAA), indicating lower concentration of NAA induce more rooting rate than 2,4-D treatment. In this study, cotyledonary node was used, and this method was found to be efficient and rapid for in vitro peanut regeneration. © 2022 Friends Science Publishers","PeriodicalId":13769,"journal":{"name":"International Journal of Agriculture and Biology","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2022-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Agriculture and Biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.17957/ijab/15.1906","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Agricultural and Biological Sciences","Score":null,"Total":0}
引用次数: 0
花生子叶节外植体高频直接器官发生及植株再生
花生植株的高效再生是成功转化基因和应用最新开发的基因组编辑技术提高作物产量的最重要和第一步。本研究的目的是为选定的花生品种制定不同浓度的激素处理方案,并制定植株再生方案。中国花生品种N3和育花14的配种方案以前没有报道。对2个花生品种的茎、根再生方案进行了优化。两个品种对细胞分裂素、植物生长激素6-苄基氨基嘌呤(BAP)和硫代氮脲(TDZ)均呈阳性反应。在添加4 mg/L BAP和1 mg/L TDZ的培养基中,成活率最高,分别为97%和94.33%。因此,与TDZ相比,BAP浓度越高,嫩枝萌发率越高。而在含有0.3 mg/L 2,4-二氯苯氧乙酸(2,4- d)的培养基上生根率最高(81%),在含有1 mg/L α-萘乙酸(NAA)的培养基上生根率最高(96.33%),说明较低浓度NAA处理的生根率高于2,4- d处理。本研究采用子叶结法对花生进行体外再生,结果表明该方法高效、快速。©2022朋友科学出版社
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