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Screening, identification, optimization of fermentation conditions, and extraction of secondary metabolites for the biocontrol of Rhizoctonia Solani AG-3

机译:筛选,鉴定,优化发酵条件和提取次生代谢物以用于生防菌Solani AG-3

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ABSTRACT In this study a strain of Streptomyces sp. was isolated from soil and identified by 16S rRNA gene sequencing technology. The strain was screened for antibiotics production effective against biocontrol of Rhizoctonia solani AG-3 to cure the target spot disease in tobacco. For enhance production of secondary metabolites, central composite design of response surface methodology (RSM) was applied in submerged fermentation. The maximum metabolite production was using medium volume of 55????mL in 250????mL flask, agitation speed of 165????rpm, incubation temperature 30 ???°C, initial medium pH of 6.8 and inoculum size of 7%. Solvent extraction method was used to extract the secondary metabolites and active compounds were purified by silica gel column chromatography. The purified fractions were further investigated by gas chromatography-mass spectrophotometer (GC-MS). GC-MS analysis showed 48 compounds, among them 12 were active against pathogen. These findings indicated that the strain Streptomyces TA 1123 was a potential antagonist against R. solani AG-3.
机译:摘要在这项研究中,链霉菌属的一种菌株。从土壤中分离并通过16S rRNA基因测序技术进行鉴定。筛选菌株以生产有效抗生根瘤菌AG-3的抗生素,以治疗烟草中的目标斑病。为了提高次生代谢产物的产生,将响应面方法(RSM)的中央复合设计应用于深层发酵。在250毫升的烧瓶中使用55毫升/ mL的培养基体积,165毫升/分钟的搅拌速度,孵育温度30摄氏度,初始培养基pH值为6.8和接种物可产生最大的代谢产物大小为7%。用溶剂萃取法提取次生代谢产物,并通过硅胶柱色谱法纯化活性化合物。通过气相色谱-质谱仪(GC-MS)进一步研究纯化的级分。 GC-MS分析显示48种化合物,其中12种对病原体具有活性。这些发现表明,链霉菌TA 1123菌株是抗R.solani AG-3的潜在拮抗剂。

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