Biodecolorization of Anthraquinone and Azo Dyes by Newly Isolated Indonesian White-Rot Fungi

K. P. Ramadhan, S. Anita, M. Oktaviani, F. P. Sari, R. P. B. Laksana, O. D. Nurhayat, D. Yanto
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引用次数: 8

Abstract

Water pollution by dyes represents from dyestuff industry becomes an environmental concern. Finding new isolates capable of decolorizing these dyes is important. The study aimed to assess the new isolates of white-rot fungi (WRF) as decolorizing agent of anthraquinone and azo dyes. Decolorization assay were conducted in Agar plates and liquid medium. During the decolorization, laccase activities produced by the fungal strains were analyzed. Identification of the fungal strains were investigated using molecular DNA analysis. The results showed that isolates M3, H18, and GP1 were able to decolorize anthraquinone and azo dyes in Agar and liquid medium. Based on DNA analysis, isolates M3, H18, and GP1 have the similarity to Trametes sanguinea, Trametes polyzona, and Neofomitella guangxiensis, respectively. Among the fungi, T. polyzona H18 exhibited high decolorization ability (70–90%) to the dyes (100 mg/L) after 96-hours incubation. Laccase activity was fluctuated during the reactions with tendency to increase at the beginning until its peak, then decreased at the end of incubation. This study demonstrated the potential of the new isolates from Indonesia to decolorize anthraquinone and azo dyes. The results of the study can provide an alteranative for bioremediation agents of contaminated water by synthetic dyes.
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新分离的印尼白腐菌对蒽醌和偶氮染料的生物脱色作用
以染料工业为代表的染料对水体的污染已成为一个令人关注的环境问题。寻找能够使这些染料脱色的新分离物是很重要的。研究了新分离的白腐菌(WRF)对蒽醌和偶氮染料的脱色作用。在琼脂平板和液体培养基中进行脱色试验。在脱色过程中,分析了真菌菌株产生的漆酶活性。采用分子DNA分析方法对真菌菌株进行鉴定。结果表明,分离菌株M3、H18和GP1在琼脂和液体培养基中均能脱色蒽醌和偶氮染料。通过DNA分析,分离株M3、H18和GP1分别与血Trametes sanguinea、多带Trametes polyzona和guangxiensis Neofomitella具有相似性。其中,多带T. polyzona H18对100 mg/L的染料培养96 h后,脱色能力达到70% ~ 90%。漆酶活性在反应过程中呈波动趋势,开始时呈上升趋势,直至达到峰值,然后在孵育结束时呈下降趋势。本研究证明了印尼新分离菌株对蒽醌和偶氮染料脱色的潜力。研究结果可为合成染料生物修复水体提供一种替代方案。
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来源期刊
CiteScore
1.20
自引率
0.00%
发文量
13
审稿时长
16 weeks
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