{"title":"担子菌对纺织废水中蒽醌染料脱色的研究。","authors":"Pragnya Paramita Sahoo, Vikas Kumar, Preeti Pallavi, Adyasha Anapurba Sahoo, Sudip Kumar Sen, Sangeeta Raut","doi":"10.1002/bab.2763","DOIUrl":null,"url":null,"abstract":"<p><p>Anthraquinone (AQ) dyes are utilized extensively in the textile industry due to their ability to fasten fabrics. The intricate and rigid structures of AQ dyes, however, prevent them from biodegradation. They also create nitrate residues, which persist as effluents in textile wastewater and harm aquatic vegetation by obstructing light from entering the water, which affects both flora and fauna. The use of bioremediation technique is most popular because it is environmentally beneficial and economical. The aim of this study was to isolate white rot fungi (WRF) for their ability to decolorize AQ dyes and their mixtures. The current study shows the decolorization of mixture of AQ dyes (MAQD), namely, Acid blue 129 (AB129), Alizarin cyanin green (ACG), and Remazol brilliant blue R (RBBR) (200 ppm) under optimized parameters: pH 7, temperature 30°C, and shaking speed 80 rpm in 24 h by using suspended fungal isolates, VS12 (93.71%) and WF2 (92.76%) isolated from decaying wood. The highest manganese peroxidase (MnP) activity (2391.77 U/mL) was found in VS12 followed by WF2 (2318.28 U/mL) in 24 h. Moreover, the study revealed that MnP is one of the causes for decolorization of MAQD, as decolorization is directly proportional to MnP activity. On the basis of morphological features and a complete sequence analysis of 18S rRNA gene and internal transcribed spacer (ITS) region, the isolates were identified as Trametes cubensis WF2 and Polyporus umbellatus VS12. 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引用次数: 0
摘要
蒽醌(AQ)染料因其具有固定织物的能力而在纺织工业中得到广泛应用。然而,AQ染料复杂而坚硬的结构阻碍了它们的生物降解。它们还会产生硝酸盐残留物,这些残留物作为纺织品废水的流出物持续存在,并通过阻挡光线进入水中而损害水生植物,从而影响动植物。生物修复技术因其环境效益和经济效益而广受欢迎。本研究的目的是分离白腐真菌(WRF),以了解其对AQ染料及其混合物的脱色能力。本研究利用从腐木中分离的悬浮菌VS12(93.71%)和WF2(92.76%)对酸性蓝129 (AB129)、Alizarin cyanin green (ACG)和Remazol brilliant blue R (RBBR) (200 ppm)的AQ染料(MAQD)混合物进行脱色,优化参数为pH 7、温度30℃、摇速80 rpm,时间为24 h。锰过氧化物酶(MnP)活性在24 h内以VS12最高(2391.77 U/mL),其次为WF2 (2318.28 U/mL)。研究表明MnP是MAQD脱色的原因之一,脱色与MnP活性成正比。根据形态特征和18S rRNA基因及内部转录间隔区(ITS)全序列分析,鉴定分离株为Trametes cubensis WF2和Polyporus umbellatus VS12。这是首次报道将白腐真菌分离株T. cubensis WF2和P. umbellatus VS12用于MAQD (AB129, ACG, RBBR)的高效脱色。
Exploration of Basidiomycetes for Anthraquinone Dyes Decolorization in Textile Wastewater.
Anthraquinone (AQ) dyes are utilized extensively in the textile industry due to their ability to fasten fabrics. The intricate and rigid structures of AQ dyes, however, prevent them from biodegradation. They also create nitrate residues, which persist as effluents in textile wastewater and harm aquatic vegetation by obstructing light from entering the water, which affects both flora and fauna. The use of bioremediation technique is most popular because it is environmentally beneficial and economical. The aim of this study was to isolate white rot fungi (WRF) for their ability to decolorize AQ dyes and their mixtures. The current study shows the decolorization of mixture of AQ dyes (MAQD), namely, Acid blue 129 (AB129), Alizarin cyanin green (ACG), and Remazol brilliant blue R (RBBR) (200 ppm) under optimized parameters: pH 7, temperature 30°C, and shaking speed 80 rpm in 24 h by using suspended fungal isolates, VS12 (93.71%) and WF2 (92.76%) isolated from decaying wood. The highest manganese peroxidase (MnP) activity (2391.77 U/mL) was found in VS12 followed by WF2 (2318.28 U/mL) in 24 h. Moreover, the study revealed that MnP is one of the causes for decolorization of MAQD, as decolorization is directly proportional to MnP activity. On the basis of morphological features and a complete sequence analysis of 18S rRNA gene and internal transcribed spacer (ITS) region, the isolates were identified as Trametes cubensis WF2 and Polyporus umbellatus VS12. This is the first report of white rot fungal isolates T. cubensis WF2 and P. umbellatus VS12 used in efficient decolorization of MAQD (AB129, ACG, RBBR).
期刊介绍:
Published since 1979, Biotechnology and Applied Biochemistry is dedicated to the rapid publication of high quality, significant research at the interface between life sciences and their technological exploitation.
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