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Establishment and Regeneration of Callus Cultures in Tomato (Solanum lycopersicum L.) from Various Explants

机译:不同植株番茄(Solanum lycopersicum L.)愈伤组织培养物的建立和再生

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Aims: The present investigation aimed at in vitro establishment, multiplication and regeneration of plantlets from tomato callus using leaf, internode and root explants from in vitro geminated seedlings of cv. Solan Vajr. Study Design: Completely randomized design (CRD). Place and Duration of Study: Department of Biotechnology, Dr Y S Parmar University of Horticulture and Forestry, Nauni, Solan, Himachal Pradesh, India -173230, between 2013 and July 2015. Methodology: Murashige and Skoog (MS) medium given in 1962 was used to carry out tissue culture experiments. Seeds of Tomato cv. Solan Vajr were sterilized using bavistin and sodium hypochlorite before proceeding for germination. Different concentrations of 6- Benzylaminopurine (BAP) and Naphthalene acetic acid (NAA) were tried for callus establishment, multiplication and regeneration. Results: Treatment of leaf explant with 0.1% (w/v) bavistin for ten minutes and 0.5% (v/v) sodium hypochlorite for three minutes was the most effective giving 68.05% uncontaminated cultures and 60.94% survival of seedlings. MS medium supplemented with 1.2 mg/l GA3 gave the optimum seedling germination of 32.33%. MS medium supplemented with 3.0 mg/l NAA+ 1.0 mg/l BAP gave maximum growth of callus. Leaf and root explants gave 95.21% and 81.11% callus induction than internode (100%). The medium found best for callus growth was also found most suitable for callus multiplication and regeneration. Conclusion: This study standardized protocols for callus initiation from different types of explants. Internode was found the best explant for callus induction in tomato cv. Solan Vajr. Protocol was also successfully established for multiplication, maintenance and regeneration from callus. This in vitro generated callus can further be used for cell selection studies.
机译:目的:本研究旨在利用体外培养的cv发芽幼苗的叶片,节间和根外植体,从番茄愈伤组织中建立,繁殖和再生小植株。索兰·瓦杰(Solan Vajr)。研究设计:完全随机设计(CRD)。研究的地点和持续时间:YS Parmar园艺与林业大学生物技术系,印度,喜马al尔邦索兰,Nauni,2013年至2015年7月之间。方法:采用1962年提供的Murashige和Skoog(MS)培养基进行组织培养实验。番茄的种子。在进行发芽之前,使用巴维斯汀和次氯酸钠对Solan Vajr进行灭菌。尝试了不同浓度的6-苄基氨基嘌呤(BAP)和萘乙酸(NAA)进行愈伤组织的建立,繁殖和再生。结果:用0.1%(w / v)的bavistin处理叶片外植体十分钟,用0.5%(v / v)的次氯酸钠处理叶片外植体最有效,可提供68.05%的未污染培养物和60.94%的幼苗存活率。添加1.2 mg / l GA 3 的MS培养基的最佳发芽率为32.33%。补充有3.0 mg / l NAA + 1.0 mg / l BAP的MS培养基可使愈伤组织最大程度地生长。叶片和根外植体比节间(100%)诱导出95.21%和81.11%的愈伤组织诱导。发现最适合愈伤组织生长的培养基也被发现最适合愈伤组织的繁殖和再生。结论:本研究标准化了从不同类型外植体中引发愈伤组织的方法。节点间被发现是番茄简历中愈伤组织诱导的最佳外植体。索兰·瓦杰(Solan Vajr)。还成功建立了用于从愈伤组织繁殖,维持和再生的方案。该体外产生的愈伤组织可进一步用于细胞选择研究。

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