Department of Biotechnology, Maharishi Markandeshwar (Deemed to be University), Mullana, Ambala 133207, India.
Department of Biotechnology, Maharishi Markandeshwar (Deemed to be University), Mullana, Ambala 133207, India.
Ecotoxicol Environ Saf. 2021 Jan 15;208:111484. doi: 10.1016/j.ecoenv.2020.111484. Epub 2020 Oct 22.
Industrial wastes, for instance, tannery wastes are rich soups of resistant and bioremediation-potent bacteria. In the present work, Chromium (Cr) and tannic acid (TA) resistance bacterial strains were isolated from tannery effluent and identified as Bacillus subtilis (MCC 3275) and Bacillus safensis (MCC 3283) based on its 16S Ribosomal RNA homology. Hexavalent Cr is highly toxic and mutagenic due to its high mobility and reactivity. Whereas, TA is known to inhibit enzyme activity, substrate deprivation, and interaction with membranes and matrix-metal ions. The developed In vitro co-cultured microcosm of B. subtilis and B. safensis was able to remove Cr(VI) up to 95% and TA up to 23%. The bacteria cultures separately were able to degrade Cr(VI) to 88% by B. subtilis and 91% by B. safensis and TA up to 27%. Plackett Burman design (PBD) followed by Response surface methodology (RSM) was applied for the optimization of physio-chemical parameters. The optimized conditions for co-culture development were recorded as KHPO = 0.2 g/L, MgSO = 0.2 g/L, NHCl = 0.5 g/L, glucose - 0.2 g/L, TA - 5%, Cr = 200 ppm, incubation period of 96 h, agitation speed of 110 rpm, pH = 5.0, temperature= 30 °C and inoculum size = 3%. Scanning electron microscopy (SEM) and Fourier transform infrared (FTIR) revealed the thorough mechanism of cellular uptake followed by degradation of Cr(VI) and TA. The efficiency of co-culture for other heavy metals was observed as follows: Zn 65%, Pb 63%, Cd 65%, and Ni 65%. Bioremediation using bacteria is an economical and environmentally better alternative to conventional remediation methods. The isolated bacteria are useful in the effluent treatment of tannery or related industries and in metal recovery in mining processes.
工业废物,例如制革废物,是富含抗性和生物修复潜力细菌的浓汤。在本工作中,从制革废水中分离出铬(Cr)和单宁酸(TA)抗性菌株,并根据其 16S 核糖体 RNA 同源性鉴定为枯草芽孢杆菌(MCC 3275)和巴氏芽孢杆菌(MCC 3283)。六价 Cr 由于其高迁移性和反应性而具有高毒性和致突变性。而 TA 已知会抑制酶活性、底物缺乏以及与膜和基质金属离子的相互作用。开发的枯草芽孢杆菌和巴氏芽孢杆菌体外共培养微宇宙能够去除高达 95%的 Cr(VI)和高达 23%的 TA。单独培养的细菌能够将 Cr(VI)分别降解 88%由枯草芽孢杆菌和 91%由巴氏芽孢杆菌和 TA 降解至 27%。Plackett Burman 设计(PBD)随后进行响应面法(RSM)用于优化生理化学参数。共培养开发的优化条件记录为 KHPO = 0.2 g/L、MgSO = 0.2 g/L、NHCl = 0.5 g/L、葡萄糖-0.2 g/L、TA-5%、Cr=200 ppm、孵育期 96 h、搅拌速度 110 rpm、pH=5.0、温度=30°C 和接种量=3%。扫描电子显微镜(SEM)和傅里叶变换红外光谱(FTIR)揭示了细胞摄取随后 Cr(VI)和 TA 降解的彻底机制。共培养对其他重金属的效率如下:Zn 65%、Pb 63%、Cd 65%和 Ni 65%。与传统修复方法相比,细菌生物修复是一种经济且环境更好的替代方法。分离出的细菌可用于制革或相关行业的废水处理以及采矿业中的金属回收。