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首页> 外文期刊>International Journal of Pharmacy and Pharmaceutical Sciences >BIOCONTROL OF FUSARIUM OXYSPORUM IN UNSTERILIZED SOIL BY NOVEL STREPTOMYCES CACAOI SUBSP CACAOI [M20]
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BIOCONTROL OF FUSARIUM OXYSPORUM IN UNSTERILIZED SOIL BY NOVEL STREPTOMYCES CACAOI SUBSP CACAOI [M20]

机译:新型链球菌可可亚可可亚对非灭菌土壤中的钾氧化钾的生物防治[M20]

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摘要

Objective: To find bio fungicide from mangrove actinomycetes for controlling seed and soil borne pathogen- Fusarium oxysporum. Methods: A total of 25 actinomycetes were isolated by pour plate method. These were screened for fungicidal activity by agar plug method. The isolate M20 was characterised further for identification. The phytotoxicity study was done; biocontrol of Fusarium oxysporum with 10% culture filtrate was done using food poisoning technique. Volatile toxicity of isolate M20 was studied by inverted plate technique. The methanolic crude extract was subjected for UV–Vis spectral analysis for identifying the group of compound present. Results: The isolated M20 found to be better in antifungal activity. 10% culture filtrate actively inhibited the growth of Fusarium oxysporum (77.7%), 10% culture filtrate was taken as a standard concentration for biocontrol of Fusarium oxysporum using green gram as the test plants. The 15 th -day green gram plants under treatment with the antagonist (A), antagonist+pathogen (A+P), antagonist+pathogen+rhizobium (A+P+R) yielded high biomass and better growth. The disease development by the pathogen in green gram was controlled by the antagonist. The compounds (pyrimidine nucleosides-neutral and acidic polyoxins (230 nm), (270-290 nm) and heptaene antifungal antibiotics (406-417 nm)) are preliminarily confirmed from the methanolic crude extract of the isolate M20- Streptomyces cacaoi subsp cacaoi. Conclusion: Since the isolate M20 controlled the growth and disease causing potentiality of Fusarium oxysporum , it can be effectively used to control seed and soil borne diseases that are caused by Fusarium oxysporum .
机译:目的:从红树林放线菌中寻找生物杀真菌剂,以控制种子和土壤传播的病原体-尖孢镰刀菌。方法:通过倾板法分离出25种放线菌。通过琼脂塞法筛选这些菌株的杀真菌活性。分离株M20进一步表征用于鉴定。进行了植物毒性研究;采用食物中毒技术,以10%的培养滤液对尖孢镰刀菌进行了生物防治。用倒板技术研究了分离物M20的挥发性毒性。对甲醇粗提物进行UV-Vis光谱分析,以鉴定存在的化合物组。结果:发现分离出的M20具有更好的抗真菌活性。 10%的培养滤液能有效地抑制尖孢镰刀菌的生长(77.7%),以绿克作为试验植物,以10%的培养滤液作为生物防治尖孢镰刀菌的标准浓度。用拮抗剂(A),拮抗剂+病原体(A + P),拮抗剂+病原体+根瘤菌(A + P + R)处理的第15天绿色革兰植物产生高生物量和更好的生长。绿菌中由病原体引起的疾病发展由拮抗剂控制。从分离物M20-可可链霉菌亚种可可树的甲醇粗提物中初步确认了化合物(嘧啶核苷-中性和酸性多氧化合物(230 nm),(270-290 nm)和庚烯抗真菌抗生素(406-417 nm))。结论:由于分离株M20控制了尖孢镰刀菌的生长和致病潜力,因此可以有效地控制由尖孢镰刀菌引起的种子和土壤传播的疾病。

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