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首页> 外文期刊>International Biodeterioration & Biodegradation >Enzymatic degradation of textile dye Reactive Orange 13 by newly isolated bacterial strain Alcaligenes faecalis PMS-1.
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Enzymatic degradation of textile dye Reactive Orange 13 by newly isolated bacterial strain Alcaligenes faecalis PMS-1.

机译:新分离出的细菌粪便产碱杆菌 PMS-1对纺织染料活性橙13的酶降解。

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The aim of the present work is to evaluate degradation of textile dye Reactive Orange 13 (RO 13) by newly isolated bacterial strain. The bacterial isolate was identified as Alcaligenes faecalis PMS-1 based on 16S rDNA analysis. The isolate was able to decolorize cyanuric chloride based RO 13 under the static anoxic condition with an average decolorization rate of 24.75 mg l-1 h-1; which is approximately 38.13 times higher than the literature reported value. Kinetic study of decolorization experiments approximates the first-order reaction. The activation energy (Ea) and frequency factor (Ao) were calculated for decolorization reaction using Arrhenius equation. The maximum rate (Vmax) and Michaelis constant (Km) were found to be 27.1 mg l-1 h-1 and 105 mg l-1, respectively by using Michaelis-Menten kinetics. Noteworthy induction of Veratryl Alcohol Oxidase, Tyrosinase and NADH-DCIP reductase enzymes were observed during decolorization of RO 13, which suggested the enzymatic decolorization and degradation of reactive dye. UV-Vis spectroscopy, FTIR and HPLC analysis confirmed decolorization of RO 13. Dye degradation pathway was determined through enzyme assay study and GC-MS analysis. The final products, naphthalene and 6-[(4-chloro-1,3,5-triazin-2-yl) amino]-2-iminonaphthalen-1(2H)-one were characterized by GC-MS analysis. The phytotoxicity study revealed the degradation of RO 13 into non-toxic product by PMS-1.
机译:本工作的目的是评估新分离的细菌菌株对纺织染料活性橙13(RO 13)的降解。基于16S rDNA分析,该细菌分离物被鉴定为粪便产碱杆菌(Alcaligenes faecalis)PMS-1。该分离物能够在静态缺氧条件下对基于氰尿酰氯的RO 13进行脱色,平均脱色率为24.75 mg l -1 h -1 。大约是文献报道值的38.13倍。脱色实验的动力学研究近似于一级反应。活化能( E a )和频率因子( A o ),使用Arrhenius方程计算脱色反应。最大速率( V max )和米氏常数( K m )为通过Michaelis-Menten动力学,结果分别为27.1 mg l -1 h -1 和105 mg l -1 。在RO 13脱色过程中观察到值得注意的Veratryl醇氧化酶,酪氨酸酶和NADH-DCIP还原酶的诱导,这提示了活性染料的酶促脱色和降解。 UV-Vis光谱,FTIR和HPLC分析证实了RO 13的脱色。通过酶测定研究和GC-MS分析确定了染料降解途径。通过GC-MS分析表征最终产物萘和6-[((4-氯-1,3,5-三嗪-2-基)氨基] -2-亚氨基萘-1(2H)-one。植物毒性研究表明,PMS-1可将RO 13降解为无毒产品。

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