提出了一种测定维生素C的新方法,它是基于Folin B 试剂与抗坏血酸在pH=3的三氯乙酸酸性介质中反应生成脱氢抗坏血酸,反应产物在910nm波长处有最大吸光度进行定量分析。该方法的线性范围为(0-50.0μg/mL,相关系数r=0.99986,回收率为98.12...提出了一种测定维生素C的新方法,它是基于Folin B 试剂与抗坏血酸在pH=3的三氯乙酸酸性介质中反应生成脱氢抗坏血酸,反应产物在910nm波长处有最大吸光度进行定量分析。该方法的线性范围为(0-50.0μg/mL,相关系数r=0.99986,回收率为98.12%-102.15%。展开更多
A simple, rapid and precise method has been developed for determination of lipase activity in microbial media. The method is based on using phenyl acetate as substrate for lipase and determination of liberated phenol ...A simple, rapid and precise method has been developed for determination of lipase activity in microbial media. The method is based on using phenyl acetate as substrate for lipase and determination of liberated phenol by Folin Ciocalteu reagent. Reaction mixture containing substrate 2.4 ml of phenyl acetate 165 μM in Tris HCl buffer, 0.1 M and pH 7, with 1% (v/v) Triton X-100) and 0.1 ml lipase is incubated at 40?C during 10 minutes and the absorbance was measured at 750 nm. Linearity was observed in the concentration range 0-0.8 g/L lipase.展开更多
文摘A simple, rapid and precise method has been developed for determination of lipase activity in microbial media. The method is based on using phenyl acetate as substrate for lipase and determination of liberated phenol by Folin Ciocalteu reagent. Reaction mixture containing substrate 2.4 ml of phenyl acetate 165 μM in Tris HCl buffer, 0.1 M and pH 7, with 1% (v/v) Triton X-100) and 0.1 ml lipase is incubated at 40?C during 10 minutes and the absorbance was measured at 750 nm. Linearity was observed in the concentration range 0-0.8 g/L lipase.