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Microbial Iron Reduction by Enrichment Cultures Isolated from Estuarine Sediments

机译:从河口沉积物中富集培养物还原微生物铁

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摘要

Microbial Fe reduction in acetate- and succinate-containing enrichment cultures initiated with an estuarine sediment inoculum was studied. Fe reduction was unaffected when SO42− reduction was inhibited by MoO42−, indicating that both processes could occur independently. Bacterially produced sulfide precipitated as FeS but was not completely responsible for Fe reduction. The separation of oxidized Fe particles from bacteria by dialysis tubing demonstrated that direct bacterial contact was necessary for Fe reduction. Fe reduction in cultures amended with NO3 was delayed until NO3 and NO2 were removed. However, bacterial attachment to oxidized Fe particles in NO3-amended cultures occurred early during growth in a manner similar to NO3-free cultures. During late stages of growth, bacteria not attached to Fe particles became pale and swollen, while attached cells remained bright blue when examined by 4′,6-diamidine-2-phenylindole epifluo-rescence microscopy. The presence of added oxidized Mn had no effect on Fe reduction. The results suggested that enzymatic Fe reduction was responsible for reducing Fe in these cultures even in the presence of sulfide and that cells incapable of Fe reduction became unhealthy when Fe(III) was the only available electron acceptor.
机译:研究了由河口沉积物接种物引发的醋酸盐和琥珀酸盐富集培养物中微生物的铁减少。当MoO4 2-抑制SO4 2-还原时,Fe的还原不受影响,表明这两个过程可以独立发生。细菌产生的硫化物以FeS的形式沉淀,但并不完全负责Fe的还原。通过透析管从细菌中分离出氧化的Fe颗粒表明,细菌的直接接触对于Fe的还原是必需的。在用NO3 -修正的培养物中,Fe的还原被延迟,直到去除NO3 -和NO2 -。但是,细菌在生长过程的早期以细菌附着在氧化NO3改良培养物中的氧化铁颗粒上的方式与无NO3 sups相似。在生长的后期阶段,未附着于铁颗粒的细菌变得苍白和肿胀,而当通过4',6-二idine基-2-苯基吲哚流行荧光显微镜检查时,附着的细胞保持鲜蓝色。添加的氧化锰的存在对铁还原没有影响。结果表明,即使在存在硫化物的情况下,酶促还原铁仍可导致这些培养物中的还原铁;当Fe(III)是唯一可用的电子受体时,无法还原铁的细胞将变得不健康。

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