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Bioremediation of Disposed X-Ray Film For Enzymes Production

机译:用于酶生产的X射线胶片的生物修复

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摘要

Annually, the production of X-ray films sheets can utilize up to 1000 tons of total silver chemically produced worldwide and being wasted when these films are used. To avoid waste, the biological methods are used to study the effect of disposed X-ray on production of two different types of enzyme by using microbial power. Firstly, production of CMCase enzyme by using disposed X-ray as a carbon source. Secondly, production of nitrate reductase enzyme responsible to catalyse the reduction of silver nitrate inside X-ray film. Both bring the disposed X-ray as a substrate. Different bacterial isolates were used for production of both enzymes and being optimized by using several parameters. The protein and enzyme assay were analysed using optical density measurement. CMCase production found to be optimal in 140 rpm incubator with lactose as carbon source by 1.365±0.026 (U/ml), malt extract as nitrogen source by 0.485±0.028 (U/ml), pH 9.0 by 0.129±0.007 (U/ml), 1.5 g substrate concentration by 0.217±0.007 (U/ml), 2ml inoculum size by 0.143±0.029 (U/ml), and thiamine for vitamin by 0.208±0.041 (U/ml). While nitrate reductase production, the most potent isolates achieved optimum condition in static incubation condition by 1.182±0.000μg/ml, 0.5g substrate concentration by 1.500±0.020μg/ml with 15 days incubation periods in darkness, NaNO3 as nitrogen source by 166.773±0.054μg/ml and pH 3.0 by 0.773±0.001μg/ml. This study proved that the power of most potent isolates successfully used the disposed X-ray as substrate to produce valuable by-products using green technology to reduce environmental pollution.
机译:每年,X射线胶片的生产可以利用全世界化学生产的多达1000吨的总银,并且在使用这些胶片时会浪费掉。为了避免浪费,使用了生物学方法来研究利用微生物产生的X射线对两种不同类型酶产生的影响。首先,通过使用布置的X射线作为碳源来生产CMCase酶。其次,硝酸盐还原酶的产生负责催化X射线胶片内部硝酸银的还原。两者都将所放置的X射线作为基材。使用不同的细菌分离物生产两种酶,并通过使用几个参数进行优化。使用光密度测量分析蛋白质和酶测定。发现在140 rpm培养箱中以乳糖为碳源(1.365±0.026(U / ml),以麦芽提取物为氮源(0.485±0.028(U / ml)),pH 9.0(0.129±0.007(U / ml))时,CMCase的产量最佳。 ),1.5 g底物浓度为0.217±0.007(U / ml),2ml接种物大小为0.143±0.029(U / ml),硫胺素的维生素为0.208±0.041(U / ml)。在生产硝酸还原酶的过程中,最强的分离物在静态孵育条件下达到最佳条件为1.182±0.000μg/ ml,在黑暗中孵育15天时底物浓度为1.500±0.020μg/ ml达到0.5g,在黑暗中以NaNO3作为氮源为166.773± 0.054μg/ ml,pH 3.0为0.773±0.001μg/ ml。这项研究证明,大多数有效分离株的功效已成功利用处置的X射线作为底物,并利用绿色技术减少了环境污染,从而产生了有价值的副产物。

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