Albulaihed Yazeed, Adnan Mohd, Jamal Arshad, Snoussi Mejdi, Patel Kartik, Patel Mitesh
Department of Biology, College of Science, University of Ha'il, P.O. Box 2440, Ha'il, Saudi Arabia.
Biotech Research and Development Lab, Witmans Industries Private Limited, Daman, Bhimpore, 396210, India.
Bioresour Bioprocess. 2023 Nov 13;10(1):80. doi: 10.1186/s40643-023-00703-x.
Enzymatic degradation of synthetic dyes holds an immense promise for addressing the environmental concerns associated with the textile and dye industries. This study aimed to isolate bacteria capable of producing laccase enzymes from an anthropogenic environment. Subsequently, viability of utilizing cost-effective agricultural residues as substrates for laccase production was assessed. Response Surface Methodology (RSM) and the One Variable at a Time (OVAT) approach was pursued for the optimization of laccase production, followed by pH and temperature stability, dye degradation and decolorization experiments, toxicological studies on the degraded dye metabolites. In results, laccase-producing bacterial strain was identified as Stenotrophomonas maltophilia strain E1 (S. maltophilia). Among variety of substrates, coconut husk exhibited optimal efficacy. In a statistical optimization study, it was found that S. maltophilia was capable of producing laccase 51.38 IU/mL, i.e., three times higher than the amount of laccase produced by unoptimized medium (16.7 IU/mL), and the enzyme activity was found to be steady at an acidic pH, and a mesophilic temperature range. The laccase obtained from S. maltophilia E1 demonstrated proficient dye decolorization capabilities, achieving a notable 92.1% reduction in Malachite green dye coloration at a concentration of 500 ppm. Gas chromatography-mass spectrometry (GC-MS) analysis of the decolorized derivatives of Malachite green revealed a conversion into a distinct compounds. Moreover, after undergoing laccase treatment, Malachite green exhibited decreased phytotoxic effects on Oryza sativa, pointing to enzymatic detoxification. Collectively, insights gained from the present study will contribute to the development of efficient enzymatic approaches for addressing the environmental pollution caused by synthetic dyes.
合成染料的酶促降解对于解决与纺织和染料行业相关的环境问题具有巨大潜力。本研究旨在从人为环境中分离能够产生漆酶的细菌。随后,评估了利用具有成本效益的农业残留物作为漆酶生产底物的可行性。采用响应面法(RSM)和一次一个变量(OVAT)方法优化漆酶生产,随后进行pH和温度稳定性、染料降解和脱色实验,以及对降解染料代谢物的毒理学研究。结果表明,产漆酶细菌菌株被鉴定为嗜麦芽窄食单胞菌菌株E1(嗜麦芽窄食单胞菌)。在各种底物中,椰壳表现出最佳效果。在一项统计优化研究中发现,嗜麦芽窄食单胞菌能够产生51.38 IU/mL的漆酶,即比未优化培养基产生的漆酶量(16.7 IU/mL)高出三倍,并且发现该酶活性在酸性pH和中温温度范围内稳定。从嗜麦芽窄食单胞菌E1获得的漆酶表现出出色的染料脱色能力,在500 ppm浓度下使孔雀石绿染料的着色显著降低了92.1%。气相色谱 - 质谱(GC - MS)分析孔雀石绿的脱色衍生物显示其转化为不同的化合物。此外,经过漆酶处理后,孔雀石绿对水稻的植物毒性作用降低,表明酶促解毒作用。总的来说,本研究获得的见解将有助于开发有效的酶促方法来解决合成染料造成的环境污染问题。