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首页> 外文期刊>Geobiology >Chemical and structural status of copper associated with oxygenic and anoxygenic phototrophs and heterotrophs: possible evolutionary consequences.
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Chemical and structural status of copper associated with oxygenic and anoxygenic phototrophs and heterotrophs: possible evolutionary consequences.

机译:与有氧和无氧光养生物和异养生物有关的铜的化学和结构状态:可能的进化结果。

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Copper adsorption on the surface and intracellular uptake inside the cells of four representative taxons of soil and aquatic micro-organisms: aerobic rhizospheric heterotrophs (Pseudomonas aureofaciens), anoxygenic (Rhodovulum steppense) and oxygenic (cyanobacteria Gloeocapsa sp. and freshwater diatoms Navicula minima) phototrophs were studied in a wide range of pH, copper concentration, and time of exposure. Chemical status of adsorbed and assimilated Cu was investigated using in situ X-ray absorption spectroscopy. In case of adsorbed copper, XANES spectra demonstrated significant fractions of Cu(I) likely in the form of tri-coordinate complexes with O/N and/or S ligands. Upon short-term reversible adsorption at all four studied micro-organisms' cell surface, Cu(II) is coordinated by 4.0 +/- 0.5 planar oxygens at an average distance of 1.97 +/- 0.02 A, which is tentatively assigned to the carboxylate groups. The atomic environment of copper incorporated into diatoms and cyanobacteria during long-term growth is similar to that of the adsorbed metal with slightly shorter distances to the first O/N neighbor (1.95 A). In contrast to the common view of Cu status in phototrophic micro-organisms, XAFS failed to detect sulfur in the nearest atomic environment of Cu assimilated by freshwater plankton (cyanobacteria) and periphyton (diatoms). The appearance of S in Cu 1st coordination shell at 2.27-2.32 A was revealed only after long-term interaction of Cu with anoxygenic phototrophs (and Cu uptake by soil heterotrophs), suggesting Cu scavenging in the form of sulfhydryl, histidine/carboxyl or a mixture of carboxylate and sulfhydryl complexes. These new structural constraints suggest that adsorbed Cu(II) is partially reduced to Cu(I) already at the cell surface, where as intracellular Cu uptake and storage occur in the form of both Cu(I)-S linked proteins and Cu(II) carboxylates. Obtained results allow to better understand how, in the course of biological evolution, micro-organisms elaborated various mechanisms of Cu uptake and storage, from passive adsorption and uptake to active, protein-controlled surface reduction, and intracellular storage. Copyright 2011 Blackwell Publishing Ltd.
机译:铜吸附在土壤和水生微生物的四个代表性分类群的表面和细胞内的吸收:有氧根际异养菌(Pseudomonas aureofaciens),产氧性(Rhodovulum steppense)和有氧性(蓝细菌Gloeocapsa sp。和淡水硅藻Navicula minima)。在广泛的pH值,铜浓度和暴露时间中进行了研究。使用原位X射线吸收光谱法研究了吸附和吸收的Cu的化学状态。在吸附了铜的情况下,XANES光谱显示出大量的Cu(I)可能以具有O / N和/或S配体的三配位络合物的形式出现。在所有四个研究的微生物的细胞表面上进行短期可逆吸附后,Cu(II)与4.0 +/- 0.5平面氧配位,平均距离为1.97 +/- 0.02 A,并暂时分配给羧酸盐组。在长期生长过程中,掺入硅藻和蓝细菌中的铜的原子环境与被吸附金属的原子环境相似,与第一个O / N邻域(1.95 A)的距离略短。与光养微生物中的铜状态的一般观点相反,XAFS无法在淡水浮游生物(蓝细菌)和附生生物(硅藻)吸收的最近的铜原子环境中检测到硫。仅在Cu与产氧光养菌长期相互作用(以及土壤异养菌吸收Cu)后,才发现S在Cu第1配位壳在2.27-2.32 A处出现,这表明Cu以硫氢基,组氨酸/羧基或α形式清除。羧酸盐和巯基配合物的混合物。这些新的结构约束表明,已吸附的Cu(II)在细胞表面已经部分还原为Cu(I),在细胞表面,随着细胞内Cu的吸收和储存以Cu(I)-S连接蛋白和Cu(II)的形式发生)羧酸盐。所获得的结果可以更好地理解微生物在生物进化过程中如何阐明铜的吸收和储存的各种机制,从被动吸附和吸收到主动,蛋白质控制的表面还原和细胞内储存。版权所有2011 Blackwell Publishing Ltd.

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