Dash Hirak R, Das Surajit
Laboratory of Environmental Microbiology and Ecology (LEnME), Department of Life Science, National Institute of Technology, Rourkela, 769 008, Odisha, India.
Environ Sci Pollut Res Int. 2016 Apr;23(7):6960-71. doi: 10.1007/s11356-015-5991-4. Epub 2015 Dec 19.
Both point and non-point sources increase the pollution status of mercury and increase the population of mercury-resistant marine bacteria (MRMB). They can be targeted as the indicator organism to access marine mercury pollution, besides utilization in bioremediation. Thus, sediment and water samples were collected for 2 years (2010-2012) along Odisha coast of Bay of Bengal, India. Mercury content of the study sites varied from 0.47 to 0.99 ppb irrespective of the seasons of sampling. A strong positive correlation was observed between mercury content and MRMB population (P < 0.05) suggesting the utilization of these bacteria to assess the level of mercury pollution in the marine environment. Seventy-eight percent of the MRMB isolates were under the phylum Firmicutes, and 36 and 31% of them could resist mercury by mer operon-mediated volatilization and mercury biosorption, respectively. In addition, most of the isolates could resist a number of antibiotics and toxic metals. All the MRMB isolates possess the potential of growth and survival at cardinal pH (4-8), temperature (25-37 °C), and salinity (5-35 psu). Enterobacteria repetitive intergenic consensus (ERIC) and repetitive element palindromic PCR (REP-PCR) produced fingerprints corroborating the results of 16S rRNA gene sequencing. Fourier transform infrared (FTIR) spectral analysis also revealed strain-level speciation and phylogenetic relationships.
点源和非点源都加剧了汞的污染状况,并增加了耐汞海洋细菌(MRMB)的数量。除了用于生物修复外,它们还可作为指示生物来评估海洋汞污染。因此,在2010年至2012年的两年间,沿着印度孟加拉湾的奥里萨邦海岸采集了沉积物和水样。无论采样季节如何,研究地点的汞含量在0.47至0.99 ppb之间变化。汞含量与MRMB数量之间观察到强烈的正相关(P < 0.05),这表明利用这些细菌来评估海洋环境中的汞污染水平。78%的MRMB分离株属于厚壁菌门,其中36%和31%的分离株分别可以通过mer操纵子介导的挥发和汞生物吸附来抵抗汞。此外,大多数分离株可以抵抗多种抗生素和有毒金属。所有MRMB分离株都具有在基本pH值(4 - 8)、温度(25 - 37°C)和盐度(5 - 35 psu)下生长和存活的潜力。肠杆菌重复基因间共有序列(ERIC)和重复元件回文PCR(REP-PCR)产生的指纹图谱证实了16S rRNA基因测序的结果。傅里叶变换红外(FTIR)光谱分析也揭示了菌株水平的物种形成和系统发育关系。