Si Youbin, Zou Yan, Liu Xiaohong, Si Xiongyuan, Mao Jingdong
School of Resources and Environment, Anhui Agricultural University, Hefei 230036, China.
School of Resources and Environment, Anhui Agricultural University, Hefei 230036, China.
Chemosphere. 2015 Mar;122:206-212. doi: 10.1016/j.chemosphere.2014.11.054. Epub 2014 Dec 12.
Iron reduction and mercury methylation by dissimilatory iron-reducing bacteria (DIRB), Geobacter sulfurreducens and Shewanella oneidensis, were studied, and the relationship of mercury methylation coupled to iron reduction was determined. The ability of both bacteria for reducing iron was tested, and Fe(III) reduction occurred with the highest rate when ferric oxyhydroxide was used as a terminal electron acceptor. G. sulfurreducens had proven to mediate the production of methylmercury (MeHg), and a notable increase of MeHg following the addition of inorganic Hg was observed. When the initial concentration of HgCl2 was 500nM, about 177.03nM of MeHg was determined at 8d after G. sulfurreducens inoculation. S. oneidensis was tested negligible for Hg methylation and only 12.06nM of MeHg was determined. Iron reduction could potentially influence Hg methylation rates. The increase in MeHg was consistent with high rate of iron reduction, indicating that Fe(III) reduction stimulated the formation of MeHg. Furthermore, the net MeHg concentration increased at low Fe(III) additions from 1.78 to 3.57mM, and then decreased when the added Fe(III) was high from 7.14 to 17.85mM. The mercury methylation rate was suppressed with high Fe(III) additions, which might have been attributable to mercury complexation and low availability.
研究了异化铁还原菌(DIRB)嗜硫地杆菌和希瓦氏菌对铁的还原作用以及汞的甲基化作用,并确定了汞甲基化与铁还原之间的关系。测试了这两种细菌还原铁的能力,当使用氢氧化铁作为末端电子受体时,铁(III)的还原速率最高。嗜硫地杆菌已被证明能介导甲基汞(MeHg)的产生,在添加无机汞后观察到MeHg显著增加。当HgCl2的初始浓度为500nM时,嗜硫地杆菌接种8天后测定的MeHg约为177.03nM。希瓦氏菌的汞甲基化作用可忽略不计,仅测定到12.06nM的MeHg。铁还原可能会影响汞的甲基化速率。MeHg的增加与高铁还原率一致,表明铁(III)的还原刺激了MeHg的形成。此外,当低浓度的铁(III)添加量从1.78mM增加到3.57mM时,净MeHg浓度增加,而当高浓度的铁(III)添加量从7.14mM增加到17.85mM时,净MeHg浓度下降。高添加量的铁(III)抑制了汞的甲基化速率,这可能是由于汞的络合作用和低可用性所致。