The oxygenation of cyclohexane under Gif conditions - The catalytic behaviour of iron complexes

The catalytic oxygenation of cyclohexane to cyclohexanol (-ol) and cyclohexanone (-one) using a series of di- and trivalent iron-picolinate complexes under Gif^IV conditions (10:1 v/v pyridine-acetic acid, zinc powder at room temperature under aerobic atmosphere) proceeds with turnover numbers [defined as (moles of oxygenated products)/(moles of catalyst)] of 161-184 and -one:-ol ratios of 4.2-4.7. The corresponding values for the binuclear picolinate complex [Fe₂(μ-OMe)₂(pic)₄] (237 turnovers, -one:-ol ratio 7.2) are significantly higher. Iron complexes bearing functionalised pyridyl ligands exhibit turnover numbers and ketone selectivities of similar magnitude to, and in some cases higher than, the picolinate complexes.     

Rapid mobilization of ferritin iron by ascorbate in the presence of oxygen

L-(—)-ascorbate mobilizes iron from horse-spleen ferritin in the presence of oxygen at pH 8.0. The reaction is strongly stimulated by Cu²⁺. Dehydroascorbate and other stable oxidation products of ascorbate are ineffective. We present evidence that monodehydroascorbate mobilizes ferritin iron by reduction.     

Effects of hypolimnetic oxygenation on water quality: results from five Danish lakes

Stratified eutrophic lakes often suffer from hypolimnetic oxygen depletion during summer. This may lead to low redox conditions and accumulation of phosphate and ammonia in the hypolimnion. Hypolimnetic oxygenation has been used as a lake management strategy to improve the water quality in five eutrophic dimictic Danish lakes where oxygenation was conducted for 4–20 years. In one lake, the hypolimnetic oxygen concentration clearly improved by oxygenation, whereas the other four lakes still exhibited low mean summer levels (<2.2 mg O₂ l⁻¹). Oxygenation generally increased the hypolimnetic water temperature by 0.5–2°C, but in one lake it increased by 4–6°C. In all lakes, oxygenation significantly reduced the hypolimnetic concentrations of phosphorus and ammonia during stratification. The accumulation of phosphorus and ammonia typically decreased by 40–88%. In two lakes oxygenation was stopped for 1–2 years and here hypolimnion concentrations of both phosphorus and ammonia increased again. Surface water quality only improved in one lake, but was likely also influenced by simultaneously occurring changes in external nutrient loading. Overall, it is concluded that hypolimnetic oxygenation reduces the hypolimnetic accumulation of phosphorus and ammonia and may prevent anoxia in the deeper parts of the lake. However, long-term oxygenation is required and it is uncertain whether the overall lake water quality can be improved by oxygenation. Reduction of the external nutrient loading is still essential to improve lake water quality. Handling editor: Luigi Naselli-Flores     

Ischemia-induced brain iron delocalization: Effect of iron chelators

Tissue damage in cerebral ischemia may be produced by acidosis-induced delocalization of intracellular iron which acts as a catalyst in oxidative reactions. Acidosis was induced either by homogenization and incubation of rat cortical homogenates in acidified buffers or by submitting hyperglycemic rats to complete ischemia, a procedure that leads to intracellular lactic acidosis. The level of low molecular weight species (LMWS) iron was measured after filtration of tissue homogenates through a 10,000 Mr ultrafiltration membrane. When cortical tissue was homogenized in buffer pH 7, the level of LMWS iron was equal to 0.21 μg/g. It was significantly enhanced by acidification of the homogenization medium, reaching 0.34 μg/g at pH 6 and 0.75 μg/g at pH 5. When the tissue was homogenized in water, the LMWS iron level reached 0.17 μg/g in normoglycemic rats and 0.38 μg/g (p < 0.5) in hyperglycemic rats. Both aerobic incubation of homogenates for 1 h at 37°C and inclusion of EDTA in the homogenization medium led to further increases in the iron level. In order to demonstrate the deleterious role of iron in brain ischemia, the effect of treatment with bipyridyl, an iron-chelating agent, was assessed by measuring regional brain edema by the specific gravity method, 24 h following induction of thrombotic brain infarction. The treatment significantly attenuated the development of brain edema, reducing the water content of the infarcted area by about 2.5%. Taken together, these results support the hypothesis that a significant component of brain ischemic injury involves an iron-dependent mechanism.     

Toward model complexes of Co-containing nitrile hydratases: synthesis, complete characterization and reactivity toward ligands such as CN- and NO of the first square planar CoIII complex with two different carboxamido nitrogens and two thiolato sulfur donors

A [Co^III(N₂S₂)]NEt₄ complex, with two carboxamido nitrogens and two alkylthiolato sulfurs, was prepared from N,N′-(2-thioacetyl-isobutyryl)-2-aminobenzylamine, and characterized. It crystallizes with a distorted square planar structure including two short Co–N bonds (≈1.882 Å) and two short Co–S bonds (≈2.134 Å). The ligand defines an 11-atom chelate, which may be Co ligands in the mean plane of Co-containing nitrile hydratase. The Co^III oxidation state, reversibly reduced at −1.13 V (vs. SCE) and irreversibly oxidized at +1.29 V (vs. SCE) in DMF, is stable over a 2 V potential range. From the temperature dependence of its magnetic susceptibility, cobalt(III) was found to be in an S=1 triplet ground state, in agreement with the broad resonances observed in its ¹H-NMR spectrum. Preliminary spectral studies showed that this complex does not interact with imidazole, H₂O or HO⁻, but binds two CN⁻ anions or two NO molecules. The IR spectrum of the dinitrosyl complex exhibits two NO stretches at 1765 and 1820 cm⁻¹, in the range previously observed for dinitrosylated complexes derived from cobalt(I). This result suggests that, similarly to Fe NHases, Co NHases might readily bind NO.     

Trace metals in mangrove seedlings: role of iron plaque formation

Metal-rich mineral deposits on the roots of aquatic plants, denominated iron plaques, may moderate the uptake of essential, but potentially toxic metals by roots. We investigated the iron plaque formation on the fine, nutritive roots of mangrove seedlings growing in contrasting environments (oxidizing sand flat sediments and reducing mangrove forest sediments) in southeast Brazil. The results indicate that Avicennia schaueriana, Laguncularia racemosa, and Rhizophora mangle seedlings developed an efficient exclusion of Fe, Mn, and Zn through iron plaque formation. This process seems to be influenced substantially by species-specific responses to environmental conditions. While Fe and Zn translocation to leaves appear to be suppressed by accumulation within root tissues, this did not appear to occur for Mn, suggesting that Mn trapping in rhizosphere sediments and iron plaque formation are the main mechanisms responsible for the Mn exclusion from the organism level. In addition to factors well recognized as affecting mangrove seedling development (e.g., salinity stress and nutrient availability), the mediation of trace metal uptake by iron plaque formation possibly contribute to determine the seedling adaptability to waterlogged conditions.     

Entamoeba histolytica and Entamoeba invadens: Effects of temperature and oxygen tension on growth and survival

The temperature ranges for axenic growth of Entamoeba histolytica strain HM-1 and Entamoeba invadens strain 165 clone II in TYI-S-33 medium were: 32 to 40 C for E. histolytica with an optimum of 35.5 to 37 C; whereas the range for E. invadens 165 II was 20 to 30 C, optimum 24 to 27 C. Growth of strain HM-1 at 40 C was dependent upon the cell density of the culture used as a source of the inoculum. Clonal growth in agar was used to assay survival of Entamoeba spp. trophozoites after exposure to deleterious physical conditions. The lowest temperature for thermal killing of E. histolytica HM-1 was 41.5 C and for E. invadens 165, 35.5 C. Both were killed rapidly at 42 C, but slowly at 0 C. Killing of E. histolytica HM-1 trophozoites by exposure to increased oxygen tensions was a function of temperature and time. At 24 C and 35.5 C, there was little loss of viability during the first 7 hr exposure, then killing was quite rapid. The cells were killed sooner if the medium was preexposed to air. In contrast, at 0 C there was less killing by oxygen. E. invadens 165 II appeared to be more oxygen sensitive at 24 than at 0 C. Other E. histolytica strains tested were similar to HM-1 in their responses to temperature and air.     

Synthesis, characterization, X-ray molecular structure and catalase-like activity of a non-heme iron complex: Dichloro[N-propanoate-N,N-bis-(2-pyridylmethyl)amine]iron(III)

In this work we present the synthesis and characterization of the complex dichloro[N-propanoate-N,N-bis-(2-pyridylmethyl)amine]iron(III) [Fe^III(PBMPA)Cl₂]. The ligand LiPBMPA was synthesized through the Michael reaction of BMPA with methylacrylate, followed by alkaline hydrolysis. The complex [Fe^III(PBMPA)Cl₂] has been synthesized by the reaction of the ligand with FeCl₃ · H₂O and was mainly characterized by cyclic voltammetry, conductivimetry, and electronic, infrared and Mössbauer spectroscopies, and by X-ray structural analysis, which showed an iron center coordinated by one carboxylate oxygen in a monodentate way, one tertiary amine, two pyridine groups and two chloride ions. It has been proposed that in water the chloride ligands are shifted by the solvent molecules and the species [Fe^III(PBMPA)(H₂O)₂]Cl₂ is predominant. The catalase-like activity of the complex was tested in water, and it proved to be active in the hydrogen peroxide dismutation. Kinetics studies were conducted following the initial rates method. The reaction is first order in relation to both the complex and the hydrogen peroxide. Based on the presence of a lag phase that depends on the initial complex concentration, we propose that the active species that shows in situ catalase-like activity, is a binuclear complex.     

The influence of metal cations and pH on the heat sensitivity of photosynthetic oxygen evolution and chlorophyll fluorescence in spinach chloroplasts

The heat-sensitivity of photosynthetic oxygen evolution of thylakoids isolated from spinach increases by increasing the pH above neutral value. The temperature for inactivation (transition temperature) is lowered from about 45° C (pH 6.0–7.4) to 33°C (pH 8.5). Similar results are obtained with intact chloroplasts. At pH 7.0 the transition temperature of washed thylakoids decreases by lowering the salt concentration below 20 mM with monovalent cations (Li⁺, Na⁺, K⁺) and below 3–4 mM with divalent cations (Mg²⁺, Ca²⁺, Sr²⁺). Illumination decreases the heat-sensitivity of oxygen evolution in intact chloroplasts, but even increases the heat-sensitivity in uncoupled chloroplasts. In intact chloroplasts the transition temperature of the heat-induced rise in chlorophyll fluorescence yield (F_o; see Schreiber and Armond 1978) decreases from 44° C to 38° C when the pH of the suspending medium is increased from 6.5 to 8.5. At 20° C, F_o is almost insensitive to pH (6.0–8.5). At 40° C, however, F_o is constant between 6.0 and 7.0, but strongly increases by increasing the pH above neutral value. The results are discussed in terms of a close relation between electrostatic forces at the thylakoid membrane and thermal sensitivity of photosynthetic apparatus. It is suggested that the heat-sensitivity of the photosystem II complex partially depends on the ionization state of fixed groups having alkaline pK. The packed volume of thylakoids suspended in a low salt medium increases when the temperature is increased above 30° C (pH 7.0) and above 20° C (pH 8.0), respectively. This result suggests a heat-induced increase in surface charge density of the thylakoid membrane.Abbreviations HEPES N-2-hydroxyethylpiperazine-N-2-ethane sulfonic acid - MES morpholinoethane sulfonic acid - MOPS 2-N-morpholinopropane sulfonic acid - TRICIN N-[tris(hydroxymethyl)-methyl] glycine     

Virulence of Vibrio vulnificus: association with utilization of transferrin-bound iron, and lack of correlation with levels of cytotoxin or protease production

16 Vibrio vulnificus strains isolated from clinical and environmental sources were studied. 6 strains (4 clinical and 2 environmental) were virulent in both an infant mouse intragastric inoculation model and an iron-loaded adult mouse model; there was a close correlation between results in the two models. Virulence was not associated with increased in vitro production of extracellular cytotoxin-hemolysin or protease. There was some correlation between virulence and the ability of a strain to grow in an iron-limited medium, with a significant association observed between virulence and utilization of transferrin as an iron source. Our results suggest that the ability to make use of available host iron is an important determinant for pathogenicity of V. vulnificus.     

N-terminal iron-mediated self-cleavage of human frataxin: regulation of iron binding and complex formation with target proteins

Frataxin is an iron-binding mitochondrial matrix protein that has been shown to mediate iron delivery during iron–sulfur cluster and heme biosynthesis. Mitochondrial processing peptidase (MPP) yields a form of human frataxin corresponding to residues 56–210. However, structural and functional studies have focused on a core structure that results from an ill-defined cleavage event at the N-terminus. Herein we show that the N-terminus of MPP-processed frataxin shows a unique high-affinity iron site and that this iron center appears to mediate a self-cleavage reaction. Moreover, the N-terminus appears to block previously defined iron-binding sites located on the carboxylate-rich surface defined by the helix (α1) and the β-sheet (β1), most likely through electrostatic contact with the carboxylate-rich surface on the core protein, as well as inhibiting iron-promoted binding of the iron–sulfur cluster assembly scaffold partner protein, ISU. The physiological significance of iron-mediated release of the N-terminal residues from this anionic surface is discussed.     

Co(II) complexes with tripodal N-donor ligands: Thermodynamics of formation in anaerobic conditions and oxygen binding

The complex formation of Co(II) with N-donor ligands in dimethylsulfoxide (DMSO) is investigated by means of calorimetric and spectroscopic methods. The ligands considered in this work are tripodal polyamines and polypyridines: 2,2′,2′′-triaminotriethylamine (TREN), tris(2-(methylamino)ethyl)amine (Me₃TREN), tris(2-(dimethylamino)ethyl)amine (Me₆TREN), tris[(2-pyridyl)methyl]amine (TPA) and 6,6′-bis-[bis-(2-pyridylmethyl)aminomethyl]-2,2′-bipyridine (BTPA).These ligands are characterized by a systematic modification of the donor groups in order to study how their structure is related to the stability of the complexes formed and to their ability to bind oxygen. A comparison with thermodynamic data for similar Cd(II) systems as well as with data referred to linear tetra-amines in DMSO is also made. The solvent effect on the nature and stability of the species formed is discussed. DFT calculations are carried out to explain the trend in thermodynamic parameters for Me₆TREN. Only Co(TREN)²⁺ is able to bind oxygen and two successive species (μ-superoxo and μ-peroxo) are formed. The kinetics of oxygen uptake by Co(TREN)²⁺ is found to be less solvent-dependent than other Co(II)-polyamine complexes when the formation of the mononuclear μ-superoxo complex is considered.     

Structural and computational characterization of Fe-M bonds (M = Ru or Os): From heterobinuclear compounds to oligonuclear iron clusters

Structural survey of the compounds in Cambridge Structural Database was carried out to investigate the Fe-M bonds (where M is either Ru or Os). Compounds ranging from heterobinuclear complexes to heterohexanuclear compounds were included in the survey. The osmium atom has clearly less tendency to participate than ruthenium in the clusters. No compound was found, where all of the three metals were included in the structure. In general, the Fe-M distance seems to get longer, when the number of the participating atoms increases. A computational study carried out at the b3lyp/cep-121 level of theory indicated that metal-metal bonding is dependent on the metal species involved.     

土壤呼吸的温度敏感性——全球变暖正负反馈的不确定因素

基于模型模拟结果表明,全球变暖与大气CO2浓度增加将形成正反馈关系,这种正反馈效应将明显加速21世纪的气候变暖。然而,这些模拟模型都基于一个重要假设,即不同平均驻留时间的土壤有机质分解具有相同的温度敏感性(Q10)。这一假设与酶动力学理论相悖,而且不同学者对不同质量土壤有机质分解温度敏感性的差异的认识存在严重分歧,所以,全球变暖与大气CO2浓度增加的正反馈关系的显著性仍值得商榷。围绕土壤呼吸的温度敏感性问题进行了讨论和评述,涉及1)土壤有机质分解温度敏感性争论的焦点问题;2)通过经验模型曲线拟合估计Q10值存在的分歧及Q10变异的机理解释;3)实验室土壤培养实验估计Q10值存在的问题;4)土壤培养实验中Q10值计算方法的改进。进一步深化有关土壤有机质分解温度敏感性不确定性的认识,将为今后土壤呼吸及其对气候变化响应的相关研究提供参考。     

The iron complex of Dp44mT is redox-active and induces hydroxyl radical formation: An EPR study

Iron chelation therapy was initially designed to alleviate the toxic effects of excess iron evident in iron-overload diseases. However, some iron chelator-metal complexes have also gained interest due to their high redox activity and toxicological properties that have potential for cancer chemotherapy. This communication addresses the conflicting results published recently on the ability of the iron chelator, Dp44mT, to induce hydroxyl radical formation upon complexation with iron (B.B. Hasinoff and D. Patel, J Inorg. Biochem.103 (2009), 1093-1101). This previous study used EPR spin-trapping to show that Dp44mT-iron complexes were not able to generate hydroxyl radicals. Here, we demonstrate the opposite by using the same technique under very similar conditions to show the Dp44mT-iron complex is indeed redox-active and induces hydroxyl radical formation. This was studied directly in an iron(II)/H₂O₂ reaction system or using a reducing iron(III)/ascorbate system implementing several different buffers at pH 7.4. The demonstration by EPR that the Dp44mT-iron complex is redox-active confirms our previous studies using cyclic voltammetry, ascorbate oxidation, benzoate hydroxylation and a plasmid DNA strand-break assay. We discuss the relevance of the redox activity to the biological effects of Dp44mT.     

Inhibition by silver ions of gas space (aerenchyma) formation in adventitious roots of Zea mays L. subjected to exogenous ethylene or to oxygen deficiency

We have studied the role of ethylene in accelerating the lytic formation of gas spaces (aerenchyma) in the cortex of adventitious roots of maize (Zea mays L.) growing in poorly aerated conditions. Such roots had previously been shown to contain increased concentrations of ethylene. Ten day-old maize plants bearing seminal roots and one whorl of emerging adventitious roots were grown in nutrient solution bubbled with air, ethylene in air (0.1 to 5.0 l l^–1), or allowed to become oxygen-deficient in nonaerated (but not completely anaerobic) solution. Additions of 0.1 l l^–1 ethylene or more promoted the formation of aerenchyma, with lysis of up to 47% of the cortical cells. The effects of non-aeration were similar to those of exogenous ethylene. When silver ions, an ethylene antagonist, were present at low, non-toxic concentrations (circa 0.6 M), aerenchyma formation was prevented in ethylene treated roots and in those exposed to oxygen deficiency. Silver ions also blocked the inhibiting effect of exogenous ethylene on root extension. By contrast, the suppression of aerenchyma formation by silver ions under oxygendeficient conditions was associated with a retardation of root extension, indicating the importance of aerenchyma for root growth in poorly aerated media. Rates of production of ethylene by excised roots were stimulated by a previous non-aeration treatment. The effectiveness of Ag⁺ in inhibiting equally the action on cortical cells of exogenous ethylene and of non-aeration, supports the view that gas space (aerenchyma) formation in adventitious roots adpted to oxygendeficient environments is mediated by increased concentrations of endogenous ethylene. The possibility that extra ethylene could arise from increased biosynthesis of a precursor in root tissues with a restricted oxygen supply is discussed.     

Entamoeba histolytica and Giardia lamblia: effects of cysteine and oxygen tension on trophozoite attachment to glass and survival in culture media

Attachment of Entamoeba histolytica and of Giardia lamblia trophozoites to glass was monitored during the culture cycle. Attachment of each parasite was greatest during the exponential phase of axenic growth. The effects of l-cysteine upon the kinetics of attachment of trophozoites to glass were determined quantitatively. Attachment in complex growth media required cysteine, even under N₂, atmosphere. With cysteine, the rates of attachment were greatest for the first 2 hr, then continued more slowly. The numbers of attached trophozoites decreased immediately upon exposure to medium without cysteine. The role of cysteine in protecting trophozoites of both species from the lethal effects of oxygen was assessed using clonal growth in agar or agarose medium to determine viability following exposure to varying oxygen tensions in liquid medium. Cysteine was required for viability of trophozoites. Without cysteine, decreasing the oxygen tension prolonged survival. Under increased oxygen tension, cysteine delayed the onset of exponential killing. Although it has no thiol reducing group, l-cystine similarly protected E. histolytica.     

Synthesis and structure of iron (III) and iron (II) complexes in S4P2 environment created by diethyldithiocarbamate and 1,2-bis(diphenylphosphino)ethane chelation: Investigation of the electronic structure of the complexes by Mössbauer and magnetic studies

Iron (II) and iron (III) complexes, [Fe^II(DEDTC)₂(dppe)] · CH₂Cl₂ (1), [Fe^II(ETXANT)₂(dppe)] (2) (DEDTC = diethyldithiocarbamate, ETXANT = ethyl xanthate, dppe = 1,2-bis (diphenylphosphino) ethane), and [Fe^III(DEDTC)₂(dppe)] [Fe^IIICl₄] (3) have been synthesized and characterized. Since 3 contains two magnetic centers, an anion metathesis reaction has been conducted to replace the tetrahedral FeCl₄⁻ by a non-magnetic BPh₄⁻ ion producing [Fe^III(DEDTC)₂(dppe)]BPh₄ (4) for the sake of unequivocal understanding of the magnetic behavior of the cation of 3. With the similar end in view, the well-known FeCl₄⁻ ion, the counter anion of 3, is trapped as PPh₄[Fe^IIICl₄] (5) and its magnetic property from 298 to 2 K has been studied. Besides the spectroscopic (IR, UV-Vis, NMR, EPR, Mass and XPS) characterization of the appropriate compounds, especially 2, others viz. 1, 3 and 4 have been structurally characterized by X-ray crystallography. While Fe^II complexes, 1 and 2, are diamagnetic, the Fe^III systems, namely the cations of 3, and 4 behave as low-spin (S = 1/2) paramagnetic species from 298 to 50 K. Below 50 K 3 shows gradual increase of χ_MT up to 2 K suggesting ferromagnetic behavior while 4 exhibits gradual decrease of magnetic moment from 60 to 2 K, indicating the occurrence of weak antiferromagnetic interaction. These conclusions are supported by the Mössbauer studies of 3 and 4. The Mössbauer pattern of 1 exhibits a doublet site for diamagnetic (2-400 K) Fe^II. The compounds 1, 2 and 4 encompass interesting cyclic voltammetric responses involving Fe^II, Fe^III and Fe^IV.