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首页> 外文期刊>Plant Cell Reports >In vitro generation of somaclonal variant plants of sugarcane for tolerance to Fusarium sacchari.
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In vitro generation of somaclonal variant plants of sugarcane for tolerance to Fusarium sacchari.

机译:甘蔗体细胞克隆变体植物的体外产生,用于耐蔗糖镰刀菌。

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Eldana saccharina is a destructive pest of the sugarcane crop in South Africa. Fusarium sacchari PNG40 (a fungal strain harmful to E. saccharina) has the potential to be an endophytic biological control agent of the stalk borer. However, the fungus causes Fusarium stalk rot in sugarcane. In the current study, sugarcane plants tolerant and resistant to F. sacchari PNG40 were produced by exposing embryogenic calli to the chemical mutagen ethyl methanesulfonate (EMS), followed by in vitro selection during somatic embryogenesis and plantlet regeneration on media containing F. sacchari culture filtrates (CF). The incorporation of 100 ppm CF in the culture media at the embryo maturation stage, at germination, or at both, resulted in callus necrosis and consequent reduced plantlet yield. Subsequent trimming of the roots of regenerated plants and their exposure to 1,500 ppm CF served as a further selection treatment. Plants produced from EMS-treated calli displayed improved root re-growth in the presence of CF pressure compared with those from non-treated calli. The tolerance of CF-selected plants was confirmed in greenhouse tests by inoculation with F. sacchari PNG40, re-isolation of Fusarium spp. from undamaged tissue of asymptomatic plants and establishment of the identity of fungal isolates as PNG40 using molecular analysis. The restriction of PNG40 presence to the inoculation lesion in some plants suggested their resistance to the fungus. Genotypes exhibiting symptomless endophytic colonization by PNG40 were identified and will be utilised for testing biological control strategies against E. saccharina.
机译:Eldana saccharina是南非甘蔗作物的毁灭性害虫。枯萎病菌PNG40(一种对酿酒酵母有害的真菌菌株)有潜力成为茎bore的内生生物防治剂。但是,这种真菌会导致甘蔗中镰刀菌腐烂。在当前的研究中,通过将胚性愈伤组织暴露于化学诱变的甲烷磺酸乙酯(EMS)中,然后在体细胞胚发生和在含蔗糖培养物滤液的培养基上再生植株的过程中进行体外选择,生产出了耐糖蔗PNG40的甘蔗植物。 (CF)。在胚胎成熟阶段,发芽时或同时在这两个过程中,在培养基中掺入100 ppm CF会导致愈伤组织坏死,进而降低植株产量。随后修剪再生植物的根,并使其暴露于1,500 ppm CF中作为进一步的选择处理。与未处理的愈伤组织相比,在有CF压力的情况下,由EMS处理的愈伤组织产生的植物显示出更好的根再生长。在温室试验中,通过接种蔗糖镰刀菌PNG40,再分离镰孢属,证实了CF选择植物的耐受性。从无症状植物的未受损组织中分离得到的真菌,并使用分子分析确定真菌分离株的身份为PNG40。在某些植物中,PNG40的存在对接种病灶的限制表明它们对真菌具有抗性。鉴定出表现出由PNG40引起的无症状内生菌落定型的基因型,并将其用于测试针对大肠杆菌的生物防治策略。

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