Moore M D, Kaplan S
Department of Microbiology and Molecular Genetics, University of Texas Health Science Center, Houston 77225.
J Bacteriol. 1992 Mar;174(5):1505-14. doi: 10.1128/jb.174.5.1505-1514.1992.
We have identified intrinsic high-level resistance (HLR) to tellurite, selenite, and at least 15 other rare-earth oxides and oxyanions in the facultative photoheterotroph Rhodobacter sphaeroides grown either chemoheterotrophically or photoheterotrophically. Other members of the class Proteobacteria, including members of the alpha-2 and alpha-3 phylogenetic subgroups, were also shown to effect the reduction of many of these compounds, although genera from the alpha-1, beta-1, and gamma-3 subgroups did not express HLR to the oxyanions examined. Detailed analyses employing R. sphaeroides have shown that HLR to at least one class of these oxyanions, the tellurite class (e.g., tellurate, tellurite, selenate, selenite, and rhodium sesquioxide), occurred via intracellular oxyanion reduction and resulted in deposition of metal in the cytoplasmic membrane. The concomitant evolution of hydrogen gas from cells grown photoheterotrophically in the presence of these oxyanions was also observed. HLR to tellurite class oxyanions in R. sphaeroides was not affected by exogenous methionine or phosphate but was reduced 40-fold by the addition of cysteine to growth media. In contrast HLR to the periodate class oxyanions (e.g., periodate, siliconate, and siliconite) was inhibited by extracellular PO4(3-) but did not result in metal deposition or gas evolution. Finally, we observed that HLR to arsenate class oxyanions (e.g., arsenate, molybdate, and tungstate) occurred by a third, distinct mechanism, as evidenced by the lack of intracellular metal deposition and hydrogen gas evolution and an insensitivity to extracellular PO4(3-) or cysteine. Examination of a number of R. sphaeroides mutants has determined the obligate requirement for an intact CO2 fixation pathway and the presence of a functional photosynthetic electron transport chain to effect HLR to K2TeO3 under photosynthetic growth conditions, whereas functional cytochromes bc1 and c2 were required under aerobic growth conditions to facilitate HLR. Finally, a purification scheme to recover metals from intact bacterial cells was developed.
我们已经确定,在兼性光异养菌球形红细菌(Rhodobacter sphaeroides)以化学异养或光异养方式生长时,其对亚碲酸盐、亚硒酸盐以及至少15种其他稀土氧化物和含氧阴离子具有内在的高水平抗性(HLR)。变形菌纲的其他成员,包括α-2和α-3系统发育亚组的成员,也显示出能还原许多这类化合物,不过α-1、β-1和γ-3亚组的属对所检测的含氧阴离子未表现出HLR。利用球形红细菌进行的详细分析表明,对这些含氧阴离子中的至少一类,即亚碲酸盐类(例如碲酸盐、亚碲酸盐、硒酸盐、亚硒酸盐和三氧化二铑)的HLR,是通过细胞内含氧阴离子还原发生的,并导致金属沉积在细胞质膜中。在这些含氧阴离子存在的情况下,还观察到了光异养生长的细胞伴随产生氢气。球形红细菌对亚碲酸盐类含氧阴离子的HLR不受外源甲硫氨酸或磷酸盐的影响,但在生长培养基中添加半胱氨酸可使其降低40倍。相比之下,对高碘酸盐类含氧阴离子(例如高碘酸盐、硅酸盐和亚硅酸盐)的HLR受到细胞外PO4(3-)的抑制,但不会导致金属沉积或气体产生。最后,我们观察到对砷酸盐类含氧阴离子(例如砷酸盐、钼酸盐和钨酸盐)的HLR是通过第三种不同的机制发生的,这表现为细胞内缺乏金属沉积和氢气产生,并且对细胞外PO4(3-)或半胱氨酸不敏感。对一些球形红细菌突变体的研究确定,在光合生长条件下,完整的二氧化碳固定途径和功能性光合电子传递链是实现对K2TeO3的HLR所必需的,而在有氧生长条件下,功能性细胞色素bc1和c2是促进HLR所必需的。最后,开发了一种从完整细菌细胞中回收金属的纯化方案。