Uptake of cadmium and zinc by the alga Chlorella vulgaris: part 1. Individual ion species

The ability of algae and bacteria to accumulate heavy metals from the surrounding environment is a widely recognized phenomenon that has a number of important implications. This work reports on the development of a quantitative model that addresses the basic mechanisms inherent in many uptake processes. The model postulates two mechanisms: an initial rapid metal ion uptake due to attachment onto the cell wall followed by a relatively slow uptake due to membrane transport of the metal into the cell. The mathematical model has been tested using the alga Chlorella vulgaris in the presence of cadmium and zinc in solution under various experimental conditions.     

Influence of soil waterlogging on subsequent plant growth and trace metal content

Summary The uptake of trace metals by two plant species (French bean and maize) has been measured on two soils subjected to various waterlogging regimes. Uptake of both manganese and iron was increased due to soil waterlogging, although reoxidation of the soil affected iron more than manganese. Zinc and copper uptake was influenced by a species factor; French bean (Phaseolus vulgaris) showed preferential uptake of zinc, whereas maize (Zea mays) took up copper preferentially. Uptake of cobalt by both species was increased due to waterlogging, following the pattern of manganese.The abilities of these species to take up trace metals from soil followed the pattern predicted by selective extraction of soil for manganese, iron and cobalt, but not for zinc and copper.     

Cadmium uptake in isolated adrenocortical cells of rainbow trout and yellow perch

Cadmium uptake was studied in isolated adrenocortical cells of rainbow trout (Oncorhynchus mykiss) and yellow perch (Perca flavescens) to test the hypothesis that the greater sensitivity of trout cells to Cd-induced disruption of cortisol secretion observed in previous studies is correlated to higher level of metal accumulation. There was no evidence for interspecies differences in accumulation level, and a specific transport mechanism of similar affinity has been characterized in both fish species. However, inhibition of Cd uptake by calcium was observed in rainbow trout exclusively. The free metal ion Cd(2+) and chlorocomplexes CdCl(n)(2-n) both contribute to Cd accumulation with different level of contribution between fish species. We conclude that interspecies differences in sensitivity to Cd endocrine disrupting effect are not necessarily related to different levels of metal accumulation but would rather be linked to transport pathways and metal speciation. Cadmium/calcium competition for uptake could be a determinant of the early Cd-induced impaired cortisol secretion in trout but not perch cells.     

Cadmium and copper accumulation in the common mussel Mytilus edulis in the Western Scheldt estuary: a model approach

The Western Scheldt of the Dutch Delta area is severely contaminated with trace metals. Accumulation models of trace metals in the mussel Mytilus edulis are required to predict the biological efficiency of reductions in the metal and organic matter load. Two models are constructed: a black-box model and a physiologically structured model. The black-box model predicts metal accumulation in mussels from uptake and elimination parameters. The physiological model attempts to improve predictions by taking into account the kinetics of individual uptake and elimination routes. These in turn, are taken as depending upon two more general physiological processes, the ventilation rate and the metabolic rate. Metal uptake via food and water are expressed as relative fractions. Metal input is differentiated into particulate adsorbed, and dissolved species.The reliability of the two models is evaluated by comparing predicted concentrations for mussels with measurements. Model predictions for copper deviate less than 100% from measured concentrations, but neither model appears to predict cadmium concentration with sufficient accuracy since deviations of more than 100% occured. The introduction of physiological refinements did not improve performance. Food mediated contributions for cadmium and copper to total body burden had been overestimated in the model by a factor of 100 when compared to literature values. The physiological model did predict that the ratio of food mediated contribution to total body burden is probably different for cadmium and copper and decreases with increasing salinity for both. As yet there are no measurements available to confirm such predictions.We conclude that additional laboratory experiments should be done for a better understanding of why there is poor agreement between the few field observations and the simulations. In these experiments mussels grown under different environmental condition can be tested for their accumulation capacity of trace metals. More field observations are needed.     

Competition alters plant species response to nickel and zinc

Phytoextraction can be a cost-efficient method for the remediation of contaminated soils. Using species mixtures instead of monocultures might improve this procedure. In a species mixture, an effect of heavy metals on the species' performance can be modified by the presence of a co-occuring species. We hypothesised that (a) a co-occuring species can change the effect of heavy metals on a target species, and (b) heavy metal application may modifiy the competitive behaviour between the plants. We investigated these mechanisms in a greenhouse experiment using three species to serve as a model system (Carex flava, Centaurea angustifolia and Salix caprea). The species were established in pots of monocultures and mixtures, which were exposed to increasing concentrations of Ni and Zn, ranging from 0 to 2,500 mg/kg. Increased heavy metal application reduced the species' relative growth rate (RGR); the RGR reduction being generally correlated with Ni and Zn concentrations in plant tissue. S. caprea was an exception in that it showed considerable Zn uptake but only moderate growth reduction. In two out of six cases, competitors significantly modified the influence of heavy metals on a target species. The interaction can be explained by an increased uptake of Zn by one species (in this case S. caprea) that reduced the negative heavy metal effect on a target species (C. flava). In two further cases, increasing heavy metal application also altered competitive effects between the species. The mechanisms demonstrated in this experiment could be of relevance for the phytoextraction of heavy metals. The total uptake of metals might be maximised in specific mixtures, making phytoextraction more efficient.     

Plant and rhizosphere processes involved in phytoremediation of metal-contaminated soils

This paper reviews the recent advances in understanding of metal removal from contaminated soils, using either hyperaccumulator plants, or high biomass crop species after soil treatment with chelating compounds. Progress has been made at the physiology and molecular level regarding Zn and Ni uptake and translocation in some hyperaccumulators. It is also known that natural hyperaccumulators do not use rhizosphere acidification to enhance their metal uptake. Recently, it has been found that some natural hyperaccumulators proliferate their roots positively in patches of high metal availability. In contrast, non-accumulators actively avoid these areas, and this is one of the mechanisms by which hyperaccumulators absorb more metals when grown in the same soil. However, there are few studies on the exudation and persistence of natural chelating compounds by these plants. It is thought that rhizosphere microorganisms are not important for the hyperaccumulation of metals from soil. Applications of chelates have been shown to induce large accumulations of metals like Pb, U and Au in the shoots of non-hyperaccumulators, by increasing metal solubility and root to shoot translocation. The efficiency of metal uptake does vary with soil properties, and a full understanding of the relative importance of mass flow and diffusion in the presence and absence of artificial chelates is not available. To successfully manipulate and optimise future phytoextraction technologies, it is argued that a fully combined understanding of soil supply and plant uptake is needed.     

Root-zone modeling of heavy metal uptake and leaching in the presence of organic ligands

We present a mechanistic model which describes root uptake and leaching of heavy metals in the plant root zone, accounting for solution- and surface-complexation, (kinetic) mineral dissolution, heavy metal diffusion towards the root, root uptake, root exudation, ligand degradation and convective-dispersive transport of the soluble species. The model was used to simulate the influence of EDTA addition on Cu transport and plant uptake and the effect of oxalate exudation by roots on Cu transport and bioavailability using parameter values from the literature. In the simulations we assumed that free Cu²⁺ is the bioavailable form. Under slightly acidic conditions (pH 6) the model predicted that EDTA stabilizes Cu while at a slightly alkaline pH (pH 7.5), EDTA mobilizes Cu. The addition of EDTA approximately halved the cumulative Cu uptake after 360 days at pH 4.5, and reduced the uptake by a factor of 100 and 1000 at pH 6 and 7.5, respectively. Although the total dissolved concentration was increased, plant uptake was reduced by the formation of bio-inavailable complexes. The exudation of oxalate resulted in a decrease of the Cu concentration breaking through below the root zone, due to sorption of Cu-oxalate. In the presence of dissolved organic carbon (DOC), the exudation of oxalate increased Cu leaching considerably at pH 6 and 7.5. In the absence of DOC, the exudation of oxalate reduced Cu uptake due to the formation and adsorption of Cu-oxalate on goethite surface sites. Exudation of oxalate in the presence of DOC resulted in a further decrease of Cu uptake. Oxalate gradually takes over from DOC in binding Cu due to simultaneous production of oxalate and leaching of DOC. The simulations show that addition or exudation of ligands does not necessarily increase the solubility, transport and bioavailability of metals. Depending on the conditions (mainly the pH), also reduced transport and uptake can be observed, either by formation of ternary surface complexes or reduction of free metal concentration. The model can be easily extended to include further processes.     

Biosorption of heavy metals by Saccharomyces cerevisiae: a review

Heavy metal pollution has become one of the most serious environmental problems today. Biosorption, using biomaterials such as bacteria, fungi, yeast and algae, is regarded as a cost-effective biotechnology for the treatment of high volume and low concentration complex wastewaters containing heavy metal(s) in the order of 1 to 100 mg/L. Among the promising biosorbents for heavy metal removal which have been researched during the past decades, Saccharomyces cerevisiae has received increasing attention due to the unique nature in spite of its mediocre capacity for metal uptake compared with other fungi. S. cerevisiae is widely used in food and beverage production, is easily cultivated using cheap media, is also a by-product in large quantity as a waste of the fermentation industry, and is easily manipulated at molecular level. The state of the art in the field of biosorption of heavy metals by S. cerevisiae not only in China, but also worldwide, is reviewed in this paper, based on a substantial number of relevant references published recently on the background of biosorption achievements and development. Characteristics of S. cerevisiae in heavy metal biosorption are extensively discussed. The yeast can be studied in various forms for different purposes. Metal-binding capacity for various heavy metals by S. cerevisiae under different conditions is compared. Lead and uranium, for instances, could be removed from dilute solutions more effectively in comparison with other metals. The yeast biosorption largely depends on parameters such as pH, the ratio of the initial metal ion and initial biomass concentration, culture conditions, presence of various ligands and competitive metal ions in solution and to a limited extent on temperature. An assessment of the isotherm equilibrium model, as well as kinetics was performed. The mechanisms of biosorption are understood only to a limited extent. Elucidation of the mechanism of metal uptake is a real challenge in the field of biosorption. Various mechanism assumptions of metal uptake by S. cerevisiae are summarized.     

New insights into fish ion regulation and mitochondrion-rich cells

Compared to terrestrial animals, fish have to cope with more-challenging osmotic and ionic gradients from aquatic environments with diverse salinities, ion compositions, and pH values. Gills, a unique and highly studied organ in research on fish osmoregulation and ionoregulation, provide an excellent model to study the regulatory mechanisms of ion transport. The present review introduces and discusses some recent advances in relevant issues of teleost gill ion transport and functions of gill ionocytes. Based on accumulating evidence, a conclusive model of NaCl secretion in gills of euryhaline teleosts has been established. Interpretations of results of studies on freshwater fish gill Na+/Cl- uptake mechanisms are still being debated compared with those for NaCl secretion. Current models for Na+/Cl- uptake are proposed based on studies in traditionally used model species. Many reported inconsistencies are claimed to be due to differences among species, various experimental designs, or acclimation conditions. Having the benefit of advanced techniques in molecular/cellular biology, functional genomics, and model animals, several new notions have recently been raised concerning relevant issues of Na+/Cl- uptake pathways. Several new windows have been opened particularly in terms of molecular mechanisms of ionocyte differentiation and energy metabolite transport between gill cells during environmental challenge.     

Bioavailability of trace metals to aquatic microorganisms: importance of chemical, biological and physical processes on biouptake

An important challenge in environmental biogeochemistry is the determination of the bioavailability of toxic and essential trace compounds in natural media. For trace metals, it is now clear that chemical speciation must be taken into account when predicting bioavailability. Over the past 20 years, equilibrium models (free ion activity model (FIAM), biotic ligand model (BLM)) have been increasingly developed to describe metal bioavailability in environmental systems, despite the fact that environmental systems are always dynamic and rarely at equilibrium. In these simple (relatively successful) models, any reduction in the available, reactive species of the metal due to competition, complexation or other reactions will reduce metal bioaccumulation and thus biological effects. Recently, it has become clear that biological, physical and chemical reactions occurring in the immediate proximity of the biological surface also play an important role in controlling trace metal bioavailability through shifts in the limiting biouptake fluxes. Indeed, for microorganisms, examples of biological (transport across membrane), chemical (dissociation kinetics of metal complexes) and physical (diffusion) limitation can be demonstrated. Furthermore, the organism can employ a number of biological internalization strategies to get around limitations that are imposed on it by the physicochemistry of the medium. The use of a single transport site by several metals or the use of several transport sites by a single metal further complicates the prediction of uptake or effects using the simple chemical models. Finally, once inside the microorganism the cell is able to employ a large number of strategies including complexation, compartmentalization, efflux or the production of extracellular ligands to minimize or optimize the reactivity of the metal. The prediction of trace metal bioavailability will thus require multidisciplinary advances in our understanding of the reactions occurring at and near the biological interface. By taking into account medium constraints and biological adaptability, future bioavailability modeling will certainly become more robust.     

Accumulation of heavy-metal ions by Zoogloea ramigera

Biomass has been produced from glucose using the organism Zoogloea ramigera 115. This biomass has been used to remove copper, cadmium, and uranyl ions from water solutions. The metal uptake was studied with two different methods: either by spectrophotometric measurements on the solutions after flocculation or by potentiometric measurements with amalgam electrodes in order to follow the entire complex formation. The metal-biopolymer interaction in 0.1M NaClO(4) is practically the same as when no neutral salt is added. The metal uptake is dependent on pH and is selective. A reversible process suitable for metal complexation is described.     

Phytoextraction of zinc, copper, nickel and lead from a contaminated soil by different species of Brassica

In a pot culture experiment, five different species of Brassica (Brassica juncea, Brassica campestris, Brassica carinata, Brassica napus, and Brassica nigra) were grown for screening possible accumulators of heavy metals, viz. Zn, Cu, Ni, and Pb. The plants were grown to maturity in a soil irrigated with sewage effluents for more than two decades in West Delhi, India. The soil analysis showed enhanced accumulation of Zn, Cu, Ni, and Pb in this sewage-irrigated soil. Among all species, B. carinata showed the highest concentration (mg kg(-1)) as well as uptake (microg pot(-1)) of Ni and Pb at maturity. Although B. campestris showed a higher concentration of Zn in its shoots (stem plus leaf), B. carinata extracted the largest amount of this metal due to greater biomass production. However, B. juncea phytoextracted the largest amount of Cu from the soil. In general, the highest concentration and uptake of metal was observed in shoots compared to roots or seeds of the different species. Among the Brassica spp., B. carinata cv. DLSC1 emerged as the most promising, showing greater uptake of Zn, Ni, and Pb, while B. juncea cv. Pusa Bold showed the highest uptake of Cu. The B. napus also showed promise, as it ranked second with respect to total uptake of Pb, Zn, and Ni, and third for Cu. Total uptake of metals by Brassica spp. correlated negatively with available as well as the total soil metal concentrations. Among the root parameters, root length emerged as the powerful parameter to dictate the uptake of metals by Brassica spp. Probably for the first time, B. carinata was reported as a promising phytoextractor for Zn, Ni, and Pb, which performed better than B. juncea.     

Transport and utilization of ferrioxamine-E-bound iron inErwinia herbicola (Pantoea agglomerans)

Summary We have analyzed ferrioxamine-E-mediated iron uptake and metabolization inErwinia herbicola K4 (Pantoea agglomerans) by means of in vivo Mössbauer spectroscopy and radioactive labeling techniques. A comparison of cell spectra with the spectrum of ferrioxamine clearly demonstrates that ferrioxamine E is not accumulated in the cell, indicating a fast metal transfer. Only two major components of iron metabolism can be detected, a ferric and a ferrous species. At 30 min after uptake, 86% of the internalized metal corresponded to a ferrous ion compound and 14% to a ferric iron species. Metal transfer apparently involves a reductive process. With progressing growth, the oxidized species of the two major proteins becomes dominant. The two iron metabolites closely resemble species previously isolated fromEscherichia coli. These components of iron metabolism differ from bacterio-ferritin, cytochromes and most iron-sulfur proteins. All other iron-containing cellular components are at least one order of magnitude lower in concentration. We suggest that the ferrous and ferric iron species correspond to two different oxidation states of a low-molecular mass protein.     

Heavy metal uptake by plankton and other seston particles

Abstract

The distribution of heavy metals Cd, Cu and Pb between the dissolved phase and the suspended matter has been studied in a stagnant fresh-water lake Zoommeer with the aim of finding a link between heavy metals and seston particles. Phytoplankton and Zooplankton were identified to species level and their density was determined. The average surface area and average volume, respectively, of each plankton species was calculated from the measured dimensions of 20–200 specimens of each species. Heavy metal concentrations in the dissolved phase and the particulate matter were determined by differential pulse anodic stripping voltammetry.

The seston particles were divided into 10 subdivisions and the total surface area and volume, respectively, of each subdivision was taken as an independent variable for the subsequent multiple regression analysis to find the possible correlations with the heavy metal concentrations. The obtained models can explain a very large part (up to 98% for Pb, 99% for Cd and 87% for Cu) of the variation in heavy metal concentration. An adsorption process appears to govern Cd and Pb uptake by Chlorophyceae and Dinophyceae. In addition, both Cd and Pb can penetrate into Chlorophyceae. In the case of Cu, a specific interaction with the Cyanophyceae has been found. In general, the uptake of heavy metals is highly specific for both the respective metal and the organism.     

酿酒酵母吸附重金属离子的研究进展

重金属污染成为当今最重要的环境问题之一。生物吸附法是处理大体积低浓度重金属废水的一种理想方法,近年来有关的研究报道不断增多,但尚未实现工业化应用。酿酒酵母(Saccharomyces cerevisiae)不仅是具有实用潜力的生物吸附剂,也是研究重金属生物吸附机理的良好材料。结合自己的研究成果,总结了酿酒酵母作为生物吸附材料的优点、研究中的表现形式和吸附性能,重点讨论了酿酒酵母生物吸附机理,介绍了等温吸附平衡模型和动力学模型在酵母生物吸附中的应用情况。最后提出生物吸附进一步的研究方向。     

Complementary metal ion specificity of the metal-citrate transporters CitM and CitH of Bacillus subtilis

Citrate uptake in Bacillus subtilis is stimulated by a wide range of divalent metal ions. The metal ions were separated into two groups based on the expression pattern of the uptake system. The two groups correlated with the metal ion specificity of two homologous B. subtilis secondary citrate transporters, CitM and CitH, upon expression in Escherichia coli. CitM transported citrate in complex with Mg(2+), Ni(2+), Mn(2+), Co(2+), and Zn(2+) but not in complex with Ca(2+), Ba(2+), and Sr(2+). CitH transported citrate in complex with Ca(2+), Ba(2+), and Sr(2+) but not in complex with Mg(2+), Ni(2+), Mn(2+), Co(2+), and Zn(2+). Both transporters did not transport free citrate. Nevertheless, free citrate uptake could be demonstrated in B. subtilis, indicating the expression of at least a third citrate transporter, whose identity is not known. For both the CitM and CitH transporters it was demonstrated that the metal ion promoted citrate uptake and, vice versa, that citrate promoted uptake of the metal ion, indicating that the complex is the transported species. The results indicate that CitM and CitH are secondary transporters that transport complexes of divalent metal ions and citrate but with a complementary metal ion specificity. The potential physiological function of the two transporters is discussed.     

ESR characterization and metallokinetic analysis of Cr(V) in the blood of rats given carcinogen chromate(VI) compounds.

It has been shown that bio-trace metal elements are related to many diseases and the aging process. For many years, carcinogen hexavalent chromium (VI) has been known to be toxic to animals, but its dynamic toxicological mechanism is not sufficiently elucidated. Bioinorganic chemistry in terms of metallokinetic analysis of beneficial or toxic metal ions and their complexes is an important investigation for understanding their biochemical and physiological roles. We have tried to examine the real-time behavior of paramagnetic metal ions and complexes in animals, in which electron spin resonance (ESR) was capable of measuring paramagnetic species in chemical and biological systems. On the basis of our previous results on stable nitroxide spin probes, we have developed the in vivo blood circulation monitoring-electron spin resonance (BCM-ESR) method to analyze time-dependent ESR signal changes due to paramagnetic metal ions and their complexes in real time. When K2Cr2O7 or Na2Cr2O7 in saline was intravenously administered to rats, two ESR signals due to pentavalent chromium(V) were detectable in the circulating blood of rats. Cr(V) detected in the blood was indicated to be in the CrO(O4) and CrO(S2O2) coordination modes after the study on model complexes. From the changes of ESR signal intensities due to Cr(V) in the blood, the metallokinetic parameters were obtained using the pharmacokinetic analysis and the curve-fitting methods. The obtained results are important for understanding carcinogen chromate in terms of the formation of Cr(V) in animals. In addition, we propose the BCM-ESR method, which is useful to analyze the disposition of paramagnetic metal species in the blood of living animals.     

Phytochelatins as biomarkers for heavy metal stress in maize (Zea mays L.) and wheat (Triticum aestivum L.): combined effects of copper and cadmium

Heavy metal contaminated soils often show increased levels of more than one metal, e.g. copper (Cu), cadmium (Cd), zinc (Zn), lead (Pb) or nickel (Ni). In case such soils are used for crop production, prediction of yield reduction or quality decline due to heavy metals in the soil is inadequate when based only on chemical soil analysis. The use of biomarkers such as phytochelatins (PC), non-protein thiols specifically induced in plants upon exposure to heavy metals, may be an additional tool or diagnostic criterion in heavy metal research and in practice. In the present work, Cu and Cd uptake and induction of PC synthesis are studied with hydroponically grown maize and wheat plants exposed to mixtures of the two metals. We observed a close positive relationship between the concentrations of Cd and PC in the plant shoot material. A decreased shoot concentration of Cd after addition of Cu, due to metal competition at common root absorption sites, coincided with lower shoot PC levels. Also differences in metal uptake and xylary metal transport among the two plant species were reflected in corresponding differences in PC concentration. The observed direct relationship between shoot PC concentration and the degree of metal-induced growth inhibition makes the use of PC promising for the purpose tested for.     

Interaction of lactic acid bacteria with metal ions: opportunities for improving food safety and quality

Certain species of lactic acid bacteria (LAB), as well as other microorganisms, can bind metal ions to their cells surface or transport and store them inside the cell. Due to this fact, over the past few years interactions of metal ions with LAB have been intensively investigated in order to develop the usage of these bacteria in new biotechnology processes in addition to their health and probiotic aspects. Preliminary studies in model aqueous solutions yielded LAB with high absorption potential for toxic and essential metal ions, which can be used for improving food safety and quality. This paper provides an overview of results obtained by LAB application in toxic metal ions removing from drinking water, food and human body, as well as production of functional foods and nutraceutics. The biosorption abilities of LAB towards metal ions are emphasized. The binding mechanisms, as well as the parameters influencing the passive and active uptake are analyzed.