John Jojy, Dineshram Ramadoss, Hemalatha Kaveripakam Raman, Dhassiah Magesh Peter, Gopal Dharani, Kumar Amit
Biological Oceanography Division, CSIR-National Institute of Oceanography, Dona Paula, India.
International Research Centre for Climate Change Studies, Sathyabama Institute of Science and Technology, Chennai, India.
Front Microbiol. 2020 Dec 21;11:594011. doi: 10.3389/fmicb.2020.594011. eCollection 2020.
Synthetic dyes, extensively used in various industries, act as pollutants in the aquatic environment, and pose a significant threat to living beings. In the present study, we assessed the potential of a halophilic bacterium HTSP isolated from a saltpan for decolorization and bioremediation of synthetic dyes. The genomic assessment of this strain revealed the presence of genes encoding the enzymes involved in decolorization mechanisms including FMN-dependent NADH azoreductase Clade III, which cleave the azo bond of the dye, and the enzymes involved in deamination and isomerization of intermediate compounds. The dye decolorization assay was performed using this bacterial strain on three water-soluble dyes in different concentrations: Coomassie brilliant blue (CBB) G-250 (500-3,000 mg/L), Safranin, and Congo red (50-800 mg/L). Within 48 h, more than 80% of decolorization was observed in all tested concentrations of CBB G-250 and Congo red dyes. The rate of decolorization was the highest for Congo red followed by CBB G-250 and then Safranin. Using UV-Visible spectrometer and Fourier Transform Infrared (FTIR) analysis, peaks were observed in the colored and decolorized solutions. The results indicated a breakdown of dyes upon decolorization, as some peaks were shifted and lost for different vibrations of aromatic rings, aliphatic groups (-CH, -CH) and functional groups (-NH, -SOH, and -SO ) in decolorized solutions. This study has shown the potential of HTSP to decolorize dyes in higher concentrations at a faster pace than previously reported bacterial strains. Thus, we propose that our isolated strain can be utilized as a potential dye decolorizer and biodegradative for wastewater treatment.
合成染料广泛应用于各个行业,在水环境中作为污染物存在,对生物构成重大威胁。在本研究中,我们评估了从盐田中分离出的嗜盐细菌HTSP对合成染料进行脱色和生物修复的潜力。对该菌株的基因组评估显示,存在编码参与脱色机制的酶的基因,包括依赖黄素单核苷酸的NADH偶氮还原酶III类,其可裂解染料的偶氮键,以及参与中间化合物脱氨和异构化的酶。使用该细菌菌株对三种不同浓度的水溶性染料进行染料脱色试验:考马斯亮蓝(CBB)G - 250(500 - 3000 mg/L)、番红和刚果红(50 - 800 mg/L)。在48小时内,所有测试浓度的CBB G - 250和刚果红染料均观察到超过80%的脱色率。脱色率最高的是刚果红,其次是CBB G - 250,然后是番红。使用紫外可见光谱仪和傅里叶变换红外(FTIR)分析,在有色和脱色溶液中观察到了峰。结果表明,脱色后染料发生了分解,因为在脱色溶液中,一些峰因芳香环、脂肪族基团(-CH、-CH)和官能团(-NH、-SOH和-SO)的不同振动而发生了位移和消失。本研究表明,HTSP有潜力以比先前报道的细菌菌株更快的速度对高浓度染料进行脱色。因此,我们建议我们分离出的菌株可作为潜在的染料脱色剂和用于废水处理的生物降解剂。