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Modified Liquid Dual Culture Methodology for Screening Bacterial Endophytes Against Fungal Pathogens

机译:修饰液体双培养方法,用于筛选对真菌病原体的细菌内心细胞

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摘要

A modified methodology for screening bacterial endophytes against fungal pathogens was developed. This method is modified form of liquid dual culture assay which can provide rather appropriate information of antagonistic activity of the endophyte. Results indicated that the endophytes have shown significant suppression of pathogens by multiple mechanisms in the mixed culture. In this study, the modified methodology was compared with routinely followed screening methods in two soil borne pathogens Rhizoctonia solani and Sclerotium rolfsii of tomato. In modified method, lowest Rhizoctonia solani biomass (54.47mg) was observed from 6TH4b inoculation as compared to 218.52 mg in control. In Sclerotium rolfsii also, lowest biomass (18.84mg) was observed from 6TH4b inoculation as compared to 334.07 mg in control. Dual plate assay has shown maximum suppression of 70.81 per cent of Rhizoctonia solani and 78.02 per cent of Sclerotium rolfsii by endophyte 2PR9b. Host tissue extract enhanced the antagonistic potential of bacterial endophytes and the effect was pronounced in 3 A, where pathogen biomass suppressed by 26.51 mg as compared to that of 130.43 mg without host tissue extract. Isolates 3A, 6TH4b, 1TH16, 4R4 AND 4PR19 performed poorly in routine dual culture assay but found to have excellent suppression of pathogens by modified method. This modification can be effectively used for primary screening of endophyte bacteria for biological control.
机译:开发了一种改进的方法,用于筛选针对真菌病原体的细菌内心细胞。该方法是液体双培养测定的修饰形式,其可以提供相当适当的内联体的拮抗活性信息。结果表明,通过混合培养物中的多种机制表明,内心体表明了病原体的显着抑制。在这项研究中,将改性方法与常规的筛选的筛选病原体Rhizoctonia solani和Sclearium Rolfsii进行了常规的筛选方法。在改性方法中,从64B接种中观察到最低的Rhizoctonia Solani生物量(54.47mg),相比于对照组218.52mg。在Sclerotium Rolfsii中,与334.07mg的对照相比,从64b接种中观察到最低生物量(18.84mg)。双板测定显示出最大抑制70.81%的Rhizoctonia solani,Endophyte 2pr9b的78.02%的菌罗尔氏菌。宿主组织提取物增强了细菌内体细胞的拮抗潜力,并且在3A中发出了效果,其中病原体生物质抑制了26.51mg,而没有宿主组织提取物。在常规双培养测定中分离出3a,6th4b,1th16,4r4和4pr19,但发现通过改进的方法对病原体的优异抑制出来。该改性可以有效地用于生物控制的内心细菌的初级筛选。

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