Cadmium Adsorption by Chlamydomonas reinhardtii and its Interaction with the Cell Wall Proteins

2004 ◽  
Vol 1 (3) ◽  
pp. 172 ◽  
Author(s):  
Heliana Kola ◽  
Luis M. Laglera ◽  
Nalini Parthasarathy ◽  
Kevin J. Wilkinson

Environmental Context. In natural waters, trace metals levels are largely controlled by microbiology; organisms take up, metabolize, store, and detoxify the metals. However, aquatic organisms may regulate their own uptake via dynamic processes that result in a system that is far from equilibrium. By examining the model title alga with a battery of techniques, a more realistic assessment of metal uptake and metal regulatory processes could be gained. Abstract. Cadmium adsorption by a wild type strain of Chlamydomonas reinhardtii and a cell wall-less mutant was quantified as a function of Cd speciation in a well-defined aqueous medium. For both strains, Cd adsorption to the cell surface was not predicted by a single-site (Langmuirian) model. Indeed, no saturation of the cell wall was observed, even for Cd concentrations in excess of 5 × 10−3 M. A continual production of Cd binding sites appeared to be responsible for the observed increase of Cd adsorption with time. SDS-page separations and measurements of the protein content of algal supernatants demonstrated that organic matter was released by the algae, both in the presence and absence of Cd. Both the nature (e.g. polysaccharides, proteins) and the quantity of exudate production was influenced by the physicochemistry of the external medium. Measurements using the permeation liquid membrane (PLM) and anodic stripping voltammetry (ASV) demonstrated that dissolved cadmium was rapidly complexed by the organic exudates produced by the algae.

2020 ◽  
Vol 175 ◽  
pp. 115650 ◽  
Author(s):  
Jay C. Bullen ◽  
Aaron Torres-Huerta ◽  
Pascal Salaün ◽  
Jonathan S. Watson ◽  
Swachchha Majumdar ◽  
...  

2011 ◽  
Vol 8 (6) ◽  
pp. 612 ◽  
Author(s):  
Séverine Le Faucheur ◽  
Yvan Tremblay ◽  
Claude Fortin ◽  
Peter G. C. Campbell

Environmental contextMercury is classified as a priority pollutant owing to the biomagnification of its methylated species along food chains and the consequent effects on top consumers. The pH of natural waters affects many of the biogeochemical processes that control mercury accumulation in aquatic organisms. Here, evidence is presented that pH affects mercury uptake by unicellular algae, primary producers in aquatic food chains, thereby providing a new example of the pervasive influence of pH on the mercury biogeochemical cycle. AbstractWe have examined the influence of pH on HgII uptake (mainly in the form of the lipophilic complex HgCl2) by a green, unicellular alga, Chlamydomonas reinhardtii. Uptake of the dichloro complex increased by a factor of 1.6 to 2 when the pH was lowered from 6.5 to 5.5, an unexpected result given that the intracellular hydrolysis rate of fluorescein diacetate (FDA), used as a probe for the passive diffusion of lipophilic solutes through algal membranes, decreased in the studied alga under similar conditions. Several mechanisms were explored to explain the enhanced uptake at pH 5.5, including pH-induced changes in cell surface binding of Hg or in Hg loss rates from cells, but none of them gave completely satisfactory explanations. The present findings imply that inorganic HgII in aqueous solution behaves, in terms of uptake, neither as a lipophilic complex (the uptake of which would be expected to decrease with acidification because of algal membrane packing), nor as a cationic metal (the transport of which by facilitated transport would be expected to diminish with increasing proton concentration because of metal–proton competition at the transporter binding sites). Mercury uptake by algae seems rather to be stimulated by proton addition.


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