Energy cost of intracellular metal and metalloid detoxification in wild-type eukaryotic phytoplankton
- PMID: 27465106
- DOI: 10.1039/c6mt00049e
Energy cost of intracellular metal and metalloid detoxification in wild-type eukaryotic phytoplankton
Abstract
Microalgae use various cellular mechanisms to detoxify both non-essential and excess essential metals or metalloids. There exists however, a threshold in intracellular metal(loid) concentrations beyond which detoxification mechanisms are no longer effective and inhibition of cell division inevitably occurs. It is therefore important to determine whether the availability of energy in the cell could constrain metal(loid) detoxification capacity and to better define the thresholds beyond which a metal(loid) becomes toxic. To do this we performed the first extensive bioenergetics analysis of intracellular metal(loid) detoxification mechanisms (e.g., metal-binding peptides, polyphosphate granules, metal efflux, metal and metalloid reduction, metalloid methylation, enzymatic and non-enzymatic antioxidants) in wild-type eukaryotic phytoplankton based on the biochemical mechanisms of each detoxification strategy and on experimental measurements of detoxifying biomolecules in the literature. The results show that at the onset of metal(loid) toxicity to growth, all the detoxification strategies considered required only a small fraction of the total cellular energy available for growth indicating that intracellular detoxification ability in wild-type eukaryotic phytoplankton species is not constrained by the availability of cellular energy. The present study brings new insights into metal(loid) toxicity mechanisms and detoxification strategies in wild-type eukaryotic phytoplankton.
Similar articles
-
Cadmium detoxification strategies in two phytoplankton species: metal binding by newly synthesized thiolated peptides and metal sequestration in granules.Aquat Toxicol. 2009 Apr 9;92(2):65-75. doi: 10.1016/j.aquatox.2008.12.007. Epub 2008 Dec 27. Aquat Toxicol. 2009. PMID: 19201040
-
Contribution of glutathione to the control of cellular redox homeostasis under toxic metal and metalloid stress.J Exp Bot. 2015 May;66(10):2901-11. doi: 10.1093/jxb/erv063. Epub 2015 Mar 5. J Exp Bot. 2015. PMID: 25750419 Review.
-
Effects of metal(loid)-based nanomaterials on essential element homeostasis: the central role of nanometallomics for nanotoxicology.Metallomics. 2014 Apr;6(4):729-47. doi: 10.1039/c3mt00167a. Metallomics. 2014. PMID: 24576883 Review.
-
The role of roots and rhizosphere in providing tolerance to toxic metals and metalloids.Plant Cell Environ. 2022 Mar;45(3):719-736. doi: 10.1111/pce.14188. Epub 2021 Oct 7. Plant Cell Environ. 2022. PMID: 34622470 Review.
-
A Cd/Fe/Zn-responsive phytochelatin synthase is constitutively present in the ancient liverwort Lunularia cruciata (L.) dumort.Plant Cell Physiol. 2014 Nov;55(11):1884-91. doi: 10.1093/pcp/pcu117. Epub 2014 Sep 3. Plant Cell Physiol. 2014. PMID: 25189342
Cited by
-
1 billion-year-old cell contents preserved in monazite and xenotime.Sci Rep. 2019 Jun 21;9(1):9068. doi: 10.1038/s41598-019-45575-4. Sci Rep. 2019. PMID: 31227773 Free PMC article.
-
The maximum growth rate hypothesis is correct for eukaryotic photosynthetic organisms, but not cyanobacteria.New Phytol. 2021 Apr;230(2):601-611. doi: 10.1111/nph.17190. Epub 2021 Feb 24. New Phytol. 2021. PMID: 33449358 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources