评价细菌分离物生物表面活性剂对小麦和花生根核孢子菌和菌核菌感染的保护作用

Janki Fulwala, S. Prabhu
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摘要

这项工作是两位作者合作完成的。作者SP构思并设计了本研究。作者JF进行实验,作者SP进行数据分析。作者JF撰写了稿件的初稿,并负责文献检索。作者SP编辑和校对最后的手稿。摘要目的:从自然生境中分离生物表面活性剂,并检测其对植物真菌病原菌的抑菌活性。活动。有效的生物表面活性剂生产分离物的生物化学特征和鉴定达到属水平使用伯杰的手册。采用氯仿-甲醇法提取生物表面活性剂。采用蓝色琼脂平板法和orcinol法对提取的生物表面活性剂进行表征。采用琼脂孔扩散法测定生物表面活性剂的抑菌活性。在小麦和花生幼苗的体内实验中证实了生物表面活性剂对植物真菌病原体的保护作用。结果:筛选出3株生物表面活性剂活性较好的分离株BMW1、BMW2和BPS1用于生物表面活性剂的制备。它们分别属于假单胞菌属、芽孢杆菌属和微球菌属。提取培养上清得到白色残渣,作为生物表面活性剂用于进一步研究。分离物BMW1和BPS1产的生物表面活性剂为糖脂阴离子型生物表面活性剂,而CTAB培养基显示BMW2产的生物表面活性剂为非离子型生物表面活性剂。从三个分离株中提取的生物表面活性剂均具有良好的抗菌活性。BMW1和BPS1所产生的生物表面活性剂分别对花生菌核菌和小麦根丝核菌的感染具有最有效的保护作用。结论:本研究提出了一种利用微生物表面活性剂清除植物病原真菌的方法。
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Evaluating Efficacy of Biosurfactants from Bacterial Isolates in Conferring Protection against Rhizoctonia and Sclerotium Infection in Wheat and Peanut Plants
This work out in collaboration between both the authors. Author SP conceived and designed the study. Author JF carried out the experiments and author SP performed the analysis of data. Author JF wrote the first draft of the manuscript and managed the literature searches. Author SP edited and proofread the final manuscript. Both authors read approved the final ABSTRACT Aims: To isolate biosurfactant producers from natural habitat and to test the antimicrobial activity of the extracted biosurfactant against fungal plant pathogens. activity. Potent biosurfactant producing isolates were biochemically characterized and identified up to genus level using Bergey’s manual. Biosurfactant was extracted by chloroform: Methanol method. Characterization of extracted biosurfactant was done using blue agar plate and orcinol assay. Agar well diffusion method was used to test antimicrobial activity of biosurfactants. Ability of the biosurfactants to provide protection against fungal plant pathogens was demonstrated in vivo using wheat and peanut plant seedlings. Results: Three isolates BMW1, BMW2 and BPS1 showing good biosurfactant activity were selected for biosurfactant production. They belonged to genus Pseudomonas, Bacillus and Micrococcus . Extraction of culture supernatant gave white residue which was used in further studies as biosurfactant. The biosurfactant produced by isolates BMW1 and BPS1 was glycolipid anionic biosurfactant while CTAB medium indicated non-ionic nature of biosurfactant from BMW2. Biosurfactant extracted from all three isolates showed good antimicrobial activity. Biosurfactant produced by BMW1 and BPS1 most effectively protected peanut plantlets from Sclerotium rolfsii infection and wheat plantlets from Rhizoctonia solani infection respectively. Conclusion: Our study suggested a strategy for eliminating plant pathogenic fungi by using microbial biosurfactants.
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