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1.
Microb Cell Fact ; 16(1): 146, 2017 Aug 18.
Artigo em Inglês | MEDLINE | ID: mdl-28821247

RESUMO

BACKGROUND: The use of enriched stable isotopes is of outstanding importance in chemical metrology as it allows the application of isotope dilution mass spectrometry (IDMS). Primary methods based on IDMS ensure the quality of the analytical measurements and traceability of the results to the international system of units. However, the synthesis of isotopically labelled molecules from enriched stable isotopes is an expensive and a difficult task. Either chemical and biochemical methods to produce labelled molecules have been proposed, but so far, few cost-effective methods have been described. RESULTS: The aim of this study was to use the microalgae Chlamydomonas reinhardtii to produce, at laboratory scale, 15N-labelled amino acids with a high isotopic enrichment. To do that, a culture media containing 15NH4Cl was used. No kinetic isotope effect (KIE) was observed. The labelled proteins biosynthesized by the microorganism were extracted from the biomass and the 15N-labelled amino acids were obtained after a protein hydrolysis with HCl. The use of the wall deficient strain CC503 cw92 mt+ is fit for purpose, as it only assimilates ammonia as nitrogen source, avoiding isotope contamination with nitrogen from the atmosphere or the reagents used in the culture medium, and enhancing the protein extraction efficiency compared to cell-walled wild type Chlamydomonas. The isotopic enrichment of the labelled amino acids was calculated from their isotopic composition measured by gas chromatography mass spectrometry (GC-MS). The average isotopic enrichment for the 16 amino acids characterized was 99.56 ± 0.05% and the concentration of the amino acids in the hydrolysate ranged from 18 to 90 µg/mL. CONCLUSIONS: Previously reported biochemical methods to produce isotopically labelled proteins have been applied in the fields of proteomics and fluxomics. For these approaches, low amounts of products are required and the isotopic enrichment of the molecules has never been properly determined. So far, only 13C-labelled fatty acids have been isolated from labelled microalga biomass as valuable industrial products. In this study, we propose Chlamydomonas reinhardtii CC503 as a feasible microorganism and strain to produce labelled biomass from which a standard containing sixteen 15N-labelled amino acids could be obtained.


Assuntos
Aminoácidos/metabolismo , Chlamydomonas reinhardtii/metabolismo , Proteínas de Algas/química , Proteínas de Algas/metabolismo , Aminoácidos/análise , Cloreto de Amônio/química , Cloreto de Amônio/metabolismo , Chlamydomonas reinhardtii/crescimento & desenvolvimento , Meios de Cultura/química , Cromatografia Gasosa-Espectrometria de Massas , Marcação por Isótopo , Isótopos de Nitrogênio/química
2.
J Hazard Mater ; 448: 130997, 2023 04 15.
Artigo em Inglês | MEDLINE | ID: mdl-36860062

RESUMO

Microplastics are one of the major pollutants in aquatic environments. Among their components, Bisphenol A (BPA) is one of the most abundant and dangerous, leading to endocrine disorders deriving even in different types of cancer in mammals. However, despite this evidence, the xenobiotic effects of BPA over plantae and microalgae still need to be better understood at the molecular level. To fill this gap, we characterized the physiological and proteomic response of Chlamydomonas reinhardtii during long-term BPA exposure by analyzing physiological and biochemical parameters combined with proteomics. BPA imbalanced iron and redox homeostasis, disrupting cell function and triggering ferroptosis. Intriguingly, this microalgae defense against this pollutant is recovering at both molecular and physiological levels while starch accumulation at 72 h of BPA exposure. In this work, we addressed the molecular mechanisms involved in BPA exposure, demonstrating for the first time the induction of ferroptosis in a eukaryotic alga and how ROS detoxification mechanisms and other specific proteomic rearrangements reverted this situation. These results are of great significance not only for understanding the BPA toxicology or exploring the molecular mechanisms of ferroptosis in microalgae but also for defining novel target genes for microplastic bioremediation efficient strain development.


Assuntos
Chlamydomonas , Poluentes Ambientais , Ferroptose , Microalgas , Animais , Biodegradação Ambiental , Plásticos , Proteômica , Microplásticos , Mamíferos
3.
Bull Environ Contam Toxicol ; 86(5): 531-4, 2011 May.
Artigo em Inglês | MEDLINE | ID: mdl-21437786

RESUMO

Imposex and tributyltin (TBT) body burden were quantified in the gastropod Hexaplex trunculus collected from the Bizerta channel between 2002 and 2010. Except for the imposex frequency that remained maximal (100%), all the other imposex indices decreased throughout the study period. Similarly, TBT levels also decreased over time, being the less frequent compound among butyltins, with a proportion of 22.2%, against 42.9% for dibutyltin (DBT) and 34.9% for monobutyltin (MBT). These findings reflect the effectiveness of new generation of TBT-free antifouling paint introduced in the Tunisian market and global ban of TBT on reducing the environmental impact of this biocide.


Assuntos
Gastrópodes/metabolismo , Compostos de Trialquitina/metabolismo , Poluentes Químicos da Água/metabolismo , Poluição Química da Água/estatística & dados numéricos , Animais , Carga Corporal (Radioterapia) , Disruptores Endócrinos/análise , Disruptores Endócrinos/metabolismo , Gastrópodes/fisiologia , Estações do Ano , Água do Mar/química , Compostos de Trialquitina/análise , Tunísia , Poluentes Químicos da Água/análise
4.
Sci Total Environ ; 672: 314-323, 2019 Jul 01.
Artigo em Inglês | MEDLINE | ID: mdl-30959298

RESUMO

Between November 19th, 2012 and December 3rd, 2012, 50 workers were intoxicated with gaseous Hg in San Juan de Nieva (Asturias, Spain) during the maintenance of a heat exchanger of a zinc manufacturer. We have quantified the concentration of methylmercury (MeHg), ethylmercury (EtHg) and Hg(II) in blood, hair and urine samples of those individuals taken three years after the accident. Blood, hair and urine of their closest relatives were also analyzed to assess whether the mercury burden present in the intoxicated individuals was due to the occupational exposure or to environmental or lifestyle-related factors. The determination of the mercury species in the samples was carried out applying multiple spiking Isotope Dilution GC-ICP-MS. This procedure corrects for possible interconversion reactions between the Hg species during the sample preparation procedure. Linear correlations were observed for both groups when plotting MeHg in blood vs MeHg in hair, and MeHg in hair vs Hg (II) in urine. The concentrations of Hg species in the intoxicated individuals were not significantly different from those obtained in the control group except for MeHg in blood. Significantly higher levels of MeHg in blood were obtained in some of the intoxicated individuals who had not consumed fish or seafood since the accident. A different correlation between MeHg in hair and MeHg in blood was obtained for these individuals compared to the control group who showed a hair-to-blood ratio consistent with the reported value for people exposed to Hg via fish consumption. Our results suggest that ingested MeHg followed the same pathway of deposition in hair in exposed and non-exposed individuals. However, the exposed individuals with high MeHg levels in blood showed a significantly different extent of MeHg deposition in hair compared to the control group.


Assuntos
Poluentes Atmosféricos/metabolismo , Exposição Ambiental/análise , Poluentes Ambientais/metabolismo , Cabelo/metabolismo , Mercúrio/metabolismo , Poluentes Atmosféricos/sangue , Poluentes Atmosféricos/urina , Monitoramento Ambiental , Poluentes Ambientais/sangue , Poluentes Ambientais/urina , Cabelo/química , Humanos , Mercúrio/análise , Mercúrio/sangue , Mercúrio/urina , Espanha
5.
Environ Toxicol Chem ; 30(2): 337-44, 2011 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-21038431

RESUMO

The use of species-specific isotopic tracers for inorganic and methyl mercury has allowed the simultaneous determination of the methylation and demethylation potentials of pure culture of isolated sulfate-reducing (SR) bacterial strains using low Hg species concentration levels (7 µg/L (199)Hg(II), 1 µg/L Me(201)Hg). A major advantage of the method reported here is that it can be used to follow simultaneously both the degradation of the species added but also the formation of their degradation products and thus the determination during the same incubation of the specific methylation/demethylation yields and rate constants. Methylation/demethylation capacities and extents have been found to differ between the tested strains and the tested conditions. The methylating/demethylating capacities of bacteria appear to be strain specific. All the methylating strains were found to demethylate methylmercury (MeHg). The active mechanism responsible for Hg methylation appears directly dependent on the bacterial activity but is not dependent on the metabolism used by the tested bacteria (sulfate reduction, fermentation, or nitrate respiration). The results provide confirmation that SR strains contribute to MeHg demethylation under anoxic conditions, leading to Hg(II) as the end product, consistent with the oxidative degradation pathway. Kinetic experiments have allowed specific transformation rate constants to be addressed for the two reversible processes and the reactivity of each isotopic tracer to be compared. The differential reactivity highlighted the different steps involved in the two apparent processes (i.e., uptake plus internal transformation of mercury species). Methylation appears as the slowest process, mainly controlled by the assimilation of Hg(II), whereas demethylation is faster and not dependent on the MeHg concentration.


Assuntos
Deltaproteobacteria/metabolismo , Mercúrio/metabolismo , Compostos de Metilmercúrio/metabolismo , Desulfovibrio/metabolismo , Cinética , Mercúrio/análise , Metilação , Compostos de Metilmercúrio/análise , Filogenia
6.
Anal Bioanal Chem ; 373(6): 432-40, 2002 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-12172678

RESUMO

Isotope-dilution analysis in combination with GC-ICP-MS detection has been applied to the determination of butyltin species in environmental samples. Different spikes containing the isotopically labeled butyltin species have been synthesized in the laboratory after optimization of the reaction conditions. The isotopic compositions of the tin species in the different spike solutions were determined by GC-ICP-MS after derivatization by aqueous ethylation with sodium tetraethylborate. Reverse isotope-dilution analysis was used for quantitation of the spike solutions by means of natural MBT, DBT, and TBT standards. The mixed spikes were used for simultaneous analysis of MBT, DBT and TBT in the certified reference materials, PACS-2, CRM 462, and CRM 646, with satisfactory results. The excellent agreement of the different speciation results obtained by use of the different spikes is a good indicator of the precision, accuracy, and reliability which can be achieved by using isotope-dilution analysis for trace metal speciation. Application of a double spike containing (119)Sn-enriched MBT (79.7 At%), (118)Sn-enriched DBT (86.7 At%), and (119)Sn-enriched TBT (83.1 At%) also enabled evaluation of the conditions resulting in quantitative extraction of the species from the solid matrix, in combination with possible alterations depending on the different extraction procedures used (mechanical shaking, ultrasounds, and microwaves). Mathematical equations used for this purpose computed the correct species concentrations directly and, additionally, the decomposition factors (from TBT to DBT and from DBT to MBT) after precise measurement of the (119)Sn/(120)Sn and (118)Sn/(120)Sn ratios for all butyltin species by GC-ICP-MS.


Assuntos
Poluição Ambiental/análise , Compostos Orgânicos de Estanho/análise , Cromatografia Líquida de Alta Pressão/métodos , Cromatografia Gasosa-Espectrometria de Massas/métodos , Compostos de Trialquitina/análise
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