Nelson YM, Lion LW, Ghiorse WC, Shuler ML
School of Civil and Environmental Engineering, Cornell University, Ithaca, New York 14853, USA.
Appl Environ Microbiol. 1999 Jan;65(1):175-80. doi: 10.1128/AEM.65.1.175-180.1999.
Biogenic Mn oxides were produced by the bacterium Leptothrix discophora SS-1 (= ATCC 3182) in a chemically defined mineral salts medium, and the Pb binding and specific surface area of these oxides were characterized. Growth of SS-1 in the defined medium with pyruvate as a carbon and energy source required the addition of vitamin B12. Complete oxidation of Mn(II) within 60 h required the addition of >/=0.1 &mgr;M FeSO4. Pb adsorption isotherms were determined for the biogenic Mn oxides (and associated cells with their extracellular polymer) and compared to the Pb adsorption isotherms of cells and exopolymer alone, as well as to abiotic Mn oxides. The Pb adsorption to cells and exopolymer with biogenic Mn oxides (0.8 mmol of Mn per g) at pH 6.0 and 25 degreesC was 2 orders of magnitude greater than the Pb adsorption to cells and exopolymer alone (on a dry weight basis). The Pb adsorption to the biogenic Mn oxide was two to five times greater than the Pb adsorption to a chemically precipitated abiotic Mn oxide and several orders of magnitude greater than the Pb adsorption to two commercially available crystalline MnO2 minerals. The N2 Brunauer-Emmet-Teller specific surface areas of the biogenic Mn oxide and fresh Mn oxide precipitate (224 and 58 m2/g, respectively) were significantly greater than those of the commercial Mn oxide minerals (0.048 and 4. 7 m2/g). The Pb adsorption capacity of the biogenic Mn oxide also exceeded that of a chemically precipitated colloidal hydrous Fe oxide under similar solution conditions. These results show that amorphous biogenic Mn oxides similar to those produced by SS-1 may play a significant role in the control of trace metal phase distribution in aquatic systems.
生物源锰氧化物由盘长形纤发菌SS-1(=美国典型培养物保藏中心3182)在化学成分明确的矿物盐培养基中产生,并对这些氧化物的铅结合能力和比表面积进行了表征。以丙酮酸作为碳源和能源时,SS-1在限定培养基中的生长需要添加维生素B12。在60小时内将Mn(II)完全氧化需要添加≥0.1 μM的硫酸亚铁。测定了生物源锰氧化物(以及带有细胞外聚合物的相关细胞)的铅吸附等温线,并与单独的细胞和胞外聚合物的铅吸附等温线以及非生物锰氧化物的铅吸附等温线进行了比较。在pH 6.0和25℃条件下,生物源锰氧化物(每克含0.8 mmol锰)存在时,细胞和胞外聚合物对铅的吸附(以干重计)比单独的细胞和胞外聚合物对铅的吸附大2个数量级。生物源锰氧化物对铅的吸附比化学沉淀的非生物锰氧化物对铅的吸附大2至5倍,比两种市售结晶二氧化锰矿物对铅的吸附大几个数量级。生物源锰氧化物和新鲜锰氧化物沉淀的N2布鲁诺尔-埃米特-特勒比表面积(分别为224和5 m2/g)显著大于市售锰氧化物矿物的比表面积(0.048和4.7 m2/g)。在相似的溶液条件下,生物源锰氧化物对铅的吸附能力也超过了化学沉淀的胶体水合氧化铁。这些结果表明,类似于SS-1产生的无定形生物源锰氧化物可能在水生系统中痕量金属相分布的控制中发挥重要作用。