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Screening of lincomycin-degrading bacteria by silica gel plate and visible spectrophotometry

机译:硅胶板和可见光分光光度法筛选林可霉素降解菌

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Due to the existence of antibiotic residues, waste mycelium of lincomycin was difficult to be treated and used as resources, which had become a major problem in the production enterprise. So it is very necessary to isolate and screen lincomycin -degrading bacteria to biodegrade the waste mycelium. In this paper, Box-Behnken Experimental Scheme was performed to optimize the experimental conditions for the treatment of silica gel plates, and the visible spectrophotometry was used to determine the concentration of lincomycin in the silica gel plates to indicate the degradation capacity. The results showed that the optimal conditions were to add 4 ml of water to a silica gel plate, and immerse for 40min, and repeat this process for four times. Under these conditions, the linear correlation between the lincomycin concentration and absorbance was satisfactory in the calibration standards at the range of 0-5mg/ml (r=0.99976). The method precision values (RSD=0.1126%), accuracy values (RSD=0.2358%), reproducibility values (RSD=0.2358%), stability values (RSD=0.1129%) and recovery values (98.1318%) of lincomycin in silica gel aqueous solution were adequate. Application of this method to 1311 strain showed the lincomycin -degradation rate was of 35.81 ±2%. Taken together, we have established a simple, convenient, rapid and valid visible spectrophotometry method to detect lincomycin in silica gel plates for screening lincomycin -degrading bacteria.
机译:由于存在抗生素残留物,林可霉素的废菌丝体难以处理和用作资源,这已成为生产企业的主要问题。因此,分离和筛选降解林可霉素的细菌以生物降解废菌丝体是非常必要的。本文采用Box-Behnken实验方案优化了硅胶板处理的实验条件,并采用可见分光光度法测定了硅胶板中林可霉素的浓度,以表明其降解能力。结果表明,最佳条件是在硅胶板上加入4 ml水,浸泡40分钟,然后重复此过程四次。在这些条件下,林可霉素浓度与吸光度之间的线性关系在0-5mg / ml的校准标准范围内令人满意(r = 0.99976)。林可霉素在硅胶水溶液中的方法精密度值(RSD = 0.1126%),准确度值(RSD = 0.2358%),重现性值(RSD = 0.2358%),稳定性值(RSD = 0.1129%)和回收率(98.1318%)解决方案是足够的。用该方法对1311菌株进行降解,林可霉素的降解率为35.81±2%。综上所述,我们建立了一种简单,方便,快速且有效的可见光分光光度法,用于检测硅胶板上的林可霉素,以筛选可降解林可霉素的细菌。

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