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Identifying somaclonal variants of the apple rootstock Mailing 7TI Identifying somaclonal variants of the apple rootstock Mailing 7 resistant to white root rot

机译:识别苹果砧木邮寄7TI的体细胞克隆变异体识别苹果砧木邮寄7的体细胞克隆变异体对白根腐烂有抵抗力

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A study was conducted with the objective to develop a technique for in vitro screening of cells/shoots of apple rootstock Mailing 7 (M7) against Dematophora necatrix culture filtrate. Large amounts of profuse, creamish white and friable calli was obtained from leaf explants when cultured on MS medium supplemented with 5 mg/l naphthalene acetic acid (NAA) and 1 mg/l Benzyladenine (BA). Adventitious shoots were regenerated from leaves cultured on MS medium containing BA (4.0, 4.5 mg/l) or thidiazuran (TDZ, 0.2-1.0 mg/l) and indole-3-acetic acid (IAA), indole butyric acid (IBA) or NAA (0.5-1.5 mg/l) for 6 weeks. Friable callus as well as regenerants were exposed separately to selection medium fortified with different levels (10-90%) of fungal culture filtrate (FCF) of D. necatrix to isolate tolerant cells/regenerants. 5.18% callus lines and 40% shoots survived on 70% FCF which were further subjected to three cycles of treatment using continuous in vitro selection approach. The surviving calli were subcultured on shoot regeneration medium to obtain plantlets but were unable to regenerate. This study also examined total sugars, phenol, protein content and activity of enzyme polyphenol oxidase (PPO) in FCF tolerant calli, and found higher levels of all except sugars. FCF tolerant and unselected regenerants were rooted and hardened. These plants were then screened for disease tolerance by planting in pathogen infested soil in pots. The data revealed that all five regenerants survived over control after 60 days of inoculation, thus showing resistance to white root rot disease
机译:进行了一项研究,目的是开发一种技术来体外筛选苹果根茎寄主7(M7)对抗Dematophora necatrix培养滤液的细胞/芽。当在补充了5 mg / l萘乙酸(NAA)和1 mg / l苯并拉丁腺嘌呤(BA)的MS培养基上培养时,从叶外植体中获得了大量的丰富,乳白色和脆性的愈伤组织。从在含有BA(4.0,4.5 mg / l)或噻二唑啉(TDZ,0.2-1.0 mg / l)和吲哚-3-乙酸(IAA),吲哚丁酸(IBA)或吲哚丁酸的MS培养基上培养的叶片再生不定芽。 NAA(0.5-1.5 mg / l),持续6周。将易碎的愈伤组织和再生剂分别暴露于选择培养基中,该选择培养基用不同水平(10-90%)的中生梭状芽孢杆菌真菌培养滤液(FCF)强化,以分离耐受性细胞/再生剂。 5.18%的愈伤组织和40%的芽在70%FCF上存活,然后使用连续体外选择方法对其进行三个处理周期。将存活的愈伤组织在枝条再生培养基上继代培养以获得小植株,但不能再生。这项研究还检查了耐FCF的愈伤组织中的总糖,苯酚,蛋白质含量和酶多酚氧化酶(PPO)的活性,发现除糖以外的所有糖的含量都较高。耐受FCF的和未选择的再生剂生根并硬化。然后通过种植在盆中病原体侵染的土壤中筛选这些植物的抗病性。数据显示,接种后60天,所有五个再生体均在控制之下存活,因此显示出对白根腐病的抵抗力

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