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Microplate diffusion assay for screening of beta-glucanase-producing microorganisms

机译:微孔板扩散测定法筛选产生β-葡聚糖酶的微生物

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摘要

A method is described to screen fungal strains rapidly for overexpression of extracellular beta-1,4-endoglucanase in the presence of high levels of sugar compounds. The semi-quantitative assay utilizes microplates in a 96-well format and an azurine dye covalently cross-linked (AZCL) chromogenic substrate. The digestion of AZCL-hydroxyethyl-beta-1,4-endoglucanase results in the release of a blue dye directly proportional to the amount of enzyme activity present in the sample. Sample absorbance was read at 590 nm, and the enzyme activity was determined by reference to a standard curve. The results from the microplate diffusion assay were similar to the results derived from the Ostazin Brilliant Red-hydroxyethyl cellulose assay. The technique described allowed the rapid comparison and screening beta-1,4-glucanase activity directly in spent fungal supernatant, from cultures grown in potato dextrose broth. The method could also be easily adapted for the screening of the presence of other activities such as beta-1,3-glucanase activity by using either AZCL-beta-glucan or AZCL-pachyman in place of the AZCL-hydroxyethyl-cellulose. This assay could be used to measure supernatant within an activity range of 0.1-2 U/mL.
机译:描述了一种在高水平糖类化合物存在下快速筛选真菌菌株以过度表达细胞外β-1,4-内切葡聚糖酶的方法。半定量分析利用96孔格式的微孔板和一种天青染料共价交联(AZCL)生色底物。 AZCL-羟乙基-β-1,4-Endoglucananase的消化导致蓝色染料的释放与样品中存在的酶活性成正比。在590nm处读取样品吸光度,并通过参考标准曲线确定酶活性。微孔板扩散测定的结果与Ostazin亮红色羟乙基纤维素测定的结果相似。所描述的技术可以快速比较和直接从马铃薯右旋糖肉汤中生长的培养物中的用过的真菌上清液中筛选β-1,4-葡聚糖酶活性。通过使用AZCL-β-葡聚糖或AZCL-pachyman代替AZCL-羟乙基纤维素,该方法还可轻松适用于筛选其他活性,例如β-1,3-葡聚糖酶活性。该测定法可用于测量0.1-2 U / mL活性范围内的上清液。

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