根瘤菌提取物中的次生代谢物对镰刀菌的拮抗活性

E.O. Antwi
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摘要

背景:镰刀菌仍是重要的致病菌,可产生多种霉菌毒素,对植物和动物产生不利影响。这项工作旨在从根瘤功能细菌中鉴定生物控制剂,并利用双重培养技术评估其对镰刀菌的拮抗活性。方法:将镰刀菌的圆盘接种到马铃薯葡萄糖琼脂(PDA)平板的中心,培养 3 天。然后将细菌分离物接种到距镰刀菌菌丝顶端约 2 厘米处,培养 3 天,检查抑制区。将对真菌具有拮抗活性的分离物在营养肉汤中亚培养三天,然后用乙酸乙酯提取代谢物。使用琼脂盘扩散法测试代谢提取物对真菌的抑制作用。结果:在筛选出的 20 个对镰刀菌具有拮抗活性的根茎功能细菌分离物中,有 5 个对真菌具有活性拮抗作用,在双重培养中观察到明显的抑制区,真菌菌丝的显微镜检查显示出过多和弥散的菌丝分枝,并伴有菌丝肿胀。5 种细菌分离物均为革兰氏阳性菌株,但只有 2 种分离物(2a 和 3K)的脂肪酶呈阳性,这可能表明拮抗机制可能是由于产生了具有水解真菌细胞壁和膜脂能力的酶。结论建议对 2a 和 3K 细菌分离物进行物种水平的分子鉴定。
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Antagonistic activity of secondary metabolites from rhizofunctional bacteria extracts against Fusariumspecies
Background: Fusarium species remain important fugal pathogens that produce several mycotoxins with adverse effects on both plant  and animals. This work aimed to identify biocontrol agent from rhizofunctional bacteria and assess its antagonistic activity against  Fusarium sp. using dual culture technique. Methodology: Briefly a circular disc of the Fusarium sp. was inoculated at the center of Potato Dextrose Agar (PDA) plate and incubated  for three days. The bacterial isolates were then inoculated about 2cm from the Fusarium hyphal tips and incubated for three days, and  zone of inhibition was examined. Isolates that showed antagonistic activities against the fungi were subculture in nutrient broth for three  days and the metabolites were extracted using ethyl acetate. The metabolic extracts were tested against the fungi using the agar  disc diffusion method. Results: Of the 20 rhizofunctional bacterial isolates screened for antagonistic activities against Fusarium sp., 5 showed active antagonism  against the fungi with observed clear zone of inhibition in the dual culture, and microscopic examination of the fungal hyphae showed  excessive and diffused hyphal branching with hyphal swelling. Ethyl acetate extracts from nutrient broth cultures did not show any zone  of inhibition in dual culture against the Fusarium sp. All the 5 bacterial isolates were Gram positive strains but only 2 isolates (2a and 3K) were lipase positive, which may indicate that the mechanisms of antagonism could be due to the production of enzymes that have the  ability to hydrolyze the cell wall and membrane lipids of the fungi. Conclusion: The rhizoplane and rhizosphere of plants could be great sources of biocontrol agents and that bacterial isolates 2a and 3K  have the potential to be used as antifungal agents against Fusarium sp. Molecular identification of 2a and 3K bacterial isolates to the  species level is recommended. 
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