首页> 外文期刊>Annual Research & Review in Biology >Decolorization of Cibacron Blue 3G-A Dye by Agaricus bisporus CU13 Laccase - Mediator System: A Statistical Study for Optimization via Response Surface Methodology
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Decolorization of Cibacron Blue 3G-A Dye by Agaricus bisporus CU13 Laccase - Mediator System: A Statistical Study for Optimization via Response Surface Methodology

机译:双孢蘑菇CU13漆酶-介体体系对烟草蓝3G-A染料的脱色:通过响应面法优化的统计研究

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Aim : the present study aims to optimize Cibacron Blue 3G-A decolorization as a model dye through laccase ?enzymatic biocatalysis presenting the role of HBT as a redox mediator via ?RSM approach.? Study Design: RSM using Central Composite Design (CCD) was used in order to determine the most effective variables levels in Cibacron Blue 3G-A decolorization and to investigate their interactions. Place and Duration of Study: Department of Microbial Chemistry, Genetic Engineering and Biotechnology Research Division, National Research Centre (NRC), Cairo, Egypt, between August 2017 and January 2018. Methodology: The evaluation of Cibacron Blue 3G-A decolorization by A. bisporus CU13 crude laccase was conducted through different trials using a 1.5 mL reaction mixture containing different concentration of crude laccase, Cibacron Blue 3G-A, and HBT in 0.1 M sodium citrate buffer (pH 4.5) at room temperature for different incubation periods. Results: Hydroxybenzotriazole (HBT) as a mediator enhanced Cibacron Blue 3G-A decolorization levels significantly, where decolorization percentage caused by laccase enzyme alone were ?11.92 and ?23.78%, ?whereas that caused by laccase HBT mediator system under the same conditions were 43.43 and ?76.34% after 1 and 22 h of incubation, respectively. HBT concentration, dye concentration, enzyme activity, and incubation time were chosen as study variables to optimize Cibacron Blue 3G-A dye decolorization through RSM approach via central composite design (CCD). The optimum conditions for Cibacron Blue 3G-A decolorization were found to be under using 0.50 U/mL of Agaricus bisporus CU13 laccase, 92.19 ppm of Cibacron Blue 3G-A, and 1 mM of HBT in order to get decolorization percentage of 29.29% in 35 min. Conclusion: Agaricus bisporus CU13 crude laccase was used as a biocatalyst to decolorize Cibacron Blue 3G-A in presence of HBT as a mediator through utilizing the response surface methodology approach. HBT concentration, dye concentration, enzyme activity, ?and incubation time affects the decolorization levels considerably.
机译:目的:本研究旨在通过漆酶的生物催化作用优化作为模型染料的Cibacron Blue 3G-A脱色,并通过RSM方法展示HBT作为氧化还原介质的作用。研究设计:为了确定Cibacron Blue 3G-A脱色中最有效的变量水平并研究它们之间的相互作用,使用了采用中央复合设计(CCD)的RSM。研究地点和持续时间:2017年8月至2018年1月,埃及开罗国家研究中心(NRC)微生物化学系,基因工程和生物技术研究部。方法:A对烟碱蓝3G-A脱色的评估。双孔CU13粗漆酶是通过1.5 mL反应混合物进行的不同试验进行的,该混合物在室温下于0.1M柠檬酸钠缓冲液(pH 4.5)中含有不同浓度的粗漆酶,Cibacron Blue 3G-A和HBT的不同孵育时间。结果:羟基苯并三唑(HBT)作为介质可显着提高Cibacron Blue 3G-A的脱色水平,其中仅由漆酶引起的脱色率分别为?11.92和?23.78%,而在相同条件下由漆酶HBT介体系统引起的脱色率为43.43。孵育1小时和22小时后分别为?76.34%。选择HBT浓度,染料浓度,酶活性和孵育时间作为研究变量,以通过中心复合设计(CCD)通过RSM方法优化Cibacron Blue 3G-A染料脱色。发现使用0.50 U / mL双孢蘑菇CU13漆酶,92.19 ppm的Cibacron Blue 3G-A和1 mM的HBT可以使Cibacron Blue 3G-A脱色的最佳条件是,在25%的条件下获得29.29%的脱色率。 35分钟结论:双孢蘑菇CU13粗漆酶被用作生物催化剂,通过利用响应面分析方法,在HBT存在下,将Cibacron Blue 3G-A脱色。 HBT浓度,染料浓度,酶活性,孵化时间会显着影响脱色水平。

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