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1.
Aluminium is the most abundant metal in the Earth's crust and yet, paradoxically, it has no known biological function. Aluminium is biochemically reactive, it is simply that it is not required for any essential process in extant biota. There is evidence neither of element-specific nor evolutionarily conserved aluminium biochemistry. This means that there are no ligands or chaperones which are specific to its transport, there are no transporters or channels to selectively facilitate its passage across membranes, there are no intracellular storage proteins to aid its cellular homeostasis and there are no pathways which evolved to enable the metabolism and excretion of aluminium. Of course, aluminium is found in every compartment of every cell of every organism, from virus through to Man. Herein we have investigated each of the ‘silent’ pathways and metabolic events which together constitute a form of aluminium homeostasis in biota, identifying and evaluating as far as is possible what is known and, equally importantly, what is unknown about its uptake, transport, storage and excretion. 相似文献
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Robert P. Hausinger 《Journal of biological inorganic chemistry》1997,2(3):279-286
The five known nickel-dependent enzymes include urease, hydrogenase, carbon monoxide dehydrogenase (and CO dehydrogenase/acetyl-coenzyme
A synthase), methyl-S–coenzyme M reductase, and one class of superoxide dismutase. Consistent with their disparate functions, these Ni enzymes
have distinct metallocenter structures that vary in Ni coordination geometry, number and types of metals, and the presence
of additional components. Sophisticated cellular Ni processing systems have been devised to allow for specific and functional
incorporation of Ni into these proteins. This review highlights several themes that are common to the enzyme activation processes
and summarizes current concepts related to the enzyme-specific Ni assembly pathways.
Received, accepted: 3 April 1997 相似文献
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The antipredator behavior diel vertical migration (DVM), common in aquatic keystone species Daphnia, involves daily migration from warmer surface waters before dawn to cooler deeper waters after dusk. Plasticity in Daphnia DVM behavior optimizes fitness via trade-offs between growth, reproduction, and predator avoidance. Migration behavior is affected by co-varying biotic and abiotic factors, including light, predator cues, and anthropogenic stressors making it difficult to determine each factor's individual contribution to the variation in this behavior. This study aims to better understand this ecologically significant behavior in Daphnia by: (1) determining how Daphnia pulicaria thermal preferences vary within and among natural populations; (2) distinguishing the role of temperature verses depth in Daphnia vertical migration; and (3) defining how two anthropogenic stressors (copper and nickel) impact Daphnia migratory behavior.Simulated natural lake stratification were constructed in 8 L (0.5 m tall, 14.5 cm wide) water columns to monitor under controlled laboratory conditions the individual effects of temperature gradients, depth, and metal stressors on Daphnia vertical migration. Three major findings are reported. First, while no difference in thermal preference was found among the four populations studied, within lake populations variability among isolates was high. Second, decoupling temperature and depth revealed that depth was a better predictor of Daphnia migratory patterns over temperature. Third, exposure to environmentally relevant concentrations of copper or nickel inhibited classic DVM behavior. These findings revealed the high variability in thermal preference found within Daphnia populations, elucidated the individual roles that depth and temperature have on migratory behavior, and showed how copper and nickel can interfere with the natural response of Daphnia to fish predator cues. Thus contributing to the body of knowledge necessary to predict how natural populations of Daphnia will be affected by climate related changes in lake temperatures and increased presence of anthropogenic stressors. 相似文献
6.
Copper is an essential yet toxic metal ion. To satisfy cellular requirements, while, at the same time, minimizing toxicity,
complex systems of copper trafficking have evolved in all cell types. The best conserved and most widely distributed of these
involve Atx1-like chaperones and P1B-type ATPase transporters. Here, we discuss current understanding of how these chaperones bind Cu(I) and transfer it to the
Atx1-like N-terminal domains of their cognate transporter. 相似文献
7.
Sebastian Polarz Author Vitae Carlos Lizandara Pueyo Author VitaeAuthor Vitae 《Inorganica chimica acta》2010,363(15):4148-4157
In the current article, we present a concept for the synthesis of complex nanoscaled materials. The synthetic strategy involves a stepwise assembly of materials starting from special molecular precursors possessing multiple information. Therefore, the article focuses on a strong pervasion of inorganic materials chemistry, solid-state chemistry and molecular chemistry. The concept introduced is finally highlighted by examples from our current research in the field of zinc oxide materials. 相似文献
8.
Ranganathan Santhanam 《Inorganica chimica acta》2008,361(2):473-478
A novel method of preparation of hexahydroaluminate complexes M3AlH6 (M = Li, Na or K) from the corresponding alkali metal hydride and tetrahydroaluminate has been explored, using dimethyl ether (Me2O) as a solvent at near-ambient temperatures. The results are compared with those obtained using a recently established mechanochemical approach. Characterization of the products by powder X-ray diffraction revealed M3AlH6 to be formed in high yield for M = Li and Na, but not for M = K. The attempted preparation of Li2NaAlH6 and Li2KAlH6 was unsuccessful. 相似文献
9.
The preferred mechanisms of racemization for three tris chelate complexes, Co(acac)3, Fe(phen)3 3+ and Fe[S2CN(CH2)4]3, were investigated by molecular modeling. The transition states for both a Bailar twist and a Rây-Dutt twist were considered; semi-empirical calculations (PM3) yielded activation energies. The preferred mechanism was the Bailar twist for Co(acac)3 and Fe[S2CN(CH2)4]3 with activation energies of 83.2 and 7.3 kcal mol−1, respectively, and the Rây-Dutt twist for Fe(phen)3 3+ with an activation energy of 114.4 kcal mol−1. These results are compared with those of geometrical models. 相似文献
10.
《Developmental cell》2020,52(4):461-476.e4