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Production of Bacillus thuringiensis biopesticide using commercial lab medium and agricultural by-products as nutrient sources.

机译:使用商业实验室培养基和农业副产品作为营养源生产苏云金芽孢杆菌生物农药。

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摘要

Bacillus thuringiensis (Bt) is a Gram-positive bacterium naturally found in soil, water and grain dust, and can be cultivated in liquid, solid and semi-solid media. The objective of this work was to test different media to grow B. thuringiensis. The seed culture (strain 344, B. thuringiensis tolworthi, belonging to Embrapa Maize and Sorghum Microorganism Bank) was produced using shake flasks and grown in LB medium plus salts during 18 hours, incubated on a rotary shaker at 200 revolutions per minute (rpm) at 30oC for 96 hours. Medium 1 was composed of: Luria Bertani (LB) plus salts (FeSO4, ZnSO4, MnSO4, MgSO4), and 0.2% glucose; medium 2 was composed of 1.5% glucose, 0.5% soybean flour plus salts; and medium 3 was composed of liquid swine manure at 4% and 0.2% glucose. All three media were sterilized and inoculated with B. thuringiensis tolwothi (seed culture) atastirrer speed of 200rpm, for 96 hours at 30oC. The pH was measured at regular intervals, viable spores were counted as c.f.u/mL, cell mass expressed in g/L- lyophilized, and spore counting per mL of medium. All three media showed pH variation during the fermentation process. Media 1 and 2 showed a tendency to shift toward a basic pH and medium 3 to an acidic pH. Media 1 and 2 showed the highest number of viable spores, 2.0 x 108 c.f.u/mL, within the 96 hours of incubation, however medium 2 showed a biomass dry weight of 1.18g/L. During the fermentation period, medium 1 showed the highest spore concentration, 1.4 x 109 spores/mL after 96h of fermentation. Efficiency against S. frugiperda first instar larvae showed that all Bt produced in all three media killed above 60% in the highest concentrations.
机译:苏云金芽孢杆菌(Bt)是天然存在于土壤,水和谷物粉尘中的革兰氏阳性细菌,可以在液体,固体和半固体培养基中培养。这项工作的目的是测试不同的培养基来生长苏云金芽孢杆菌。使用摇瓶生产种子培养物(菌株344,苏云金芽孢杆菌Tolworthi,属于Embrapa玉米和高粱微生物库),并在LB培养基和盐中生长18小时,然后在旋转摇床上以200转/分钟(rpm)的温度进行培养。在30oC下持续96小时。培养基1包括:Luria Bertani(LB)加盐(FeSO4,ZnSO4,MnSO4,MgSO4)和0.2%葡萄糖;培养基2由1.5%葡萄糖,0.5%大豆粉加盐组成;培养基3由猪粪中4%的葡萄糖和0.2%的葡萄糖组成。将所有三种培养基灭菌并接种苏云金芽孢杆菌tolwothi(种子培养),搅拌速度为200rpm,在30℃下接种96小时。以规则的间隔测量pH,将活孢子计数为c.f.u / mL,以g / L-冻干表示的细胞质量,并且每mL培养基计数孢子。所有三种培养基在发酵过程中均显示出pH值变化。介质1和2倾向于向碱性pH迁移,介质3倾向于酸性pH。在温育96小时内,培养基1和2的活孢子数量最高,为2.0 x 108 c.f.u / mL,而培养基2的生物质干重为1.18g / L。在发酵过程中,发酵96小时后,培养基1的孢子浓度最高,为1.4 x 109孢子/ mL。对S. frugiperda幼虫的初生幼虫的效率表明,在所有三种培养基中产生的所有Bt在最高浓度下均杀死了60%以上。

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