首页> 外文期刊>Online journal of biological sciences >Analysis of the Protein Profile of Cassava Plantlets ( Manihot esculenta Crantz.) Resistance to Fusarium Wilt Disease
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Analysis of the Protein Profile of Cassava Plantlets ( Manihot esculenta Crantz.) Resistance to Fusarium Wilt Disease

机译:木薯植物蛋白质谱分析(Manihot Esculenta Crantz。)对镰刀菌枯萎病的抗性

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Fusarium wilt disease is still a production constraint in Cassava ( Manihot esculenta Crantz.) cultivation. The disease is caused by the fungus Fusarium oxysporum (Fo), which to date has not been cured. It is expected that the use of varieties of cassava that are resistant to Fusarium wilt is an important alternative for disease control. Induced Resistance cassava research on Murashige and Skoog medium containing Fusaric Acid (FA) selective concentration has been done before and there were indications FA concentration tolerant to the selection of resistant plantlets in vitro . It is hoped that cassava plantlets that are resistant to FA will also be resistant to Fo . In previous studies, the inoculation of Fo fungal isolates on resistant cassava plantlets was carried out in vitro, followed by DNA pattern analysis compared to controls. The results of the DNA pattern analysis, in the form of a new (specific) DNA band that has a size of 550 bp (OPA_1) and 300 bp (OPA_10), are predicted to be candidates for RAPD markers for cassava resistance to Fo. Based on the results of these previous studies, it is necessary to study more deeply in this study to ascertain whether the new DNA strand is really a peroxidase protein that causes cassava plantlets to be resistant to Fo by protein profile analysis. The results of protein profile analysis showed that the appearance of new protein bands (around 98 kD) indicated the formation of PR-protein (peroxidase) in cassava plantlets that were resistant to Fo and missing protein bands (around 65 kD) in cassava plantlets.
机译:镰刀菌枯萎病是木薯(Manihot Esculenta Crantz)的生产约束。该疾病是由迄今为止迄今尚未治愈的真菌镰刀菌(FO)引起的。预计使用对镰刀菌枯萎的品种的多种木薯是一种重要的疾病控制替代品。在含有镰糖酸(Fa)选择性浓度的Murashige和Skoog培养基上的抗性木薯研究已经在之前进行,并且存在对体外抗性植物的选择耐受性的指示。希望对FA的耐抗性的木薯种植体也会抵抗。在先前的研究中,在体外进行抗性木薯植株的FO真菌分离株,然后与对照进行DNA图案分析。预测具有550bp(OPA_1)和300bp(OPA_10)的尺寸的新(特异性)DNA带的形式的DNA模式分析的结果预测是用于卡伐抗FO的RAPD标记的候选。基于这些前一项研究的结果,在该研究中必须更深入地研究,以确定新的DNA链是否真的是过氧化物酶蛋白,导致蛋白质谱分析抗蛋白质植物的毒性胰蛋白酶抗性。蛋白质谱分析的结果表明,新蛋白质带(约98kd)的外观表明在木薯植物中形成Pr-蛋白(过氧化物酶),所述木薯植物在木薯植物中耐蛋白(约65kd)。

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