Perchlorate

About: Perchlorate is a research topic. Over the lifetime, 12101 publications have been published within this topic receiving 188766 citations.

The origin of naturally occurring perchlorate: the role of atmospheric processes.

Abstract: Perchlorate, an iodide uptake inhibitor, is increasingly being detected in new places and new matrices. Perchlorate contamination has been attributed largely to the manufacture and use of ammonium perchlorate (the oxidizer in solid fuel rockets) and/or the earlier use of Chilean nitrate as fertilizer (∼0.1% perchlorate). However, there are regions such as the southern high plains (Texas Panhandle) where there is no clear historical or current evidence of the extensive presence of rocket fuel or Chilean fertilizer sources. The occurrence of easily measurable concentrations of perchlorate in such places is difficult to understand. In the southern high plains groundwater, perchlorate is better correlated with iodate, known to be of atmospheric origin, compared to any other species. We show that perchlorate is readily formed by a variety of simulated atmospheric processes. For example, it is formed from chloride aerosol by electrical discharge and by exposing aqueous chloride to high concentrations of ozone. ...

Endocytic sorting of lipid analogues differing solely in the chemistry of their hydrophobic tails.

Abstract: To understand the mechanisms for endocytic sorting of lipids, we investigated the trafficking of three lipid-mimetic dialkylindocarbocyanine (DiI) derivatives, DiIC16(3) (1,1′-dihexadecyl-3,3,3′,3′-tetramethylindocarbocyanine perchlorate), DiIC12(3) (1,1′- didodecyl-3,3,3′,3′-tetramethylindocarbocyanine perchlorate), and FAST DiI (1,1′-dilinoleyl-3,3,3′,3′-tetramethylindocarbocyanine perchlorate), in CHO cells by quantitative fluorescence microscopy. All three DiIs have the same head group, but differ in their alkyl tail length or unsaturation; these differences are expected to affect their distribution in membrane domains of varying fluidity or curvature. All three DiIs initially enter sorting endosomes containing endocytosed transferrin. DiIC16(3), with two long 16-carbon saturated tails is then delivered to late endosomes, whereas FAST DiI, with two cis double bonds in each tail, and DiIC12(3), with saturated but shorter (12-carbon) tails, are mainly found in the endocytic recycling compartment. We also find that DiOC16(3) (3,3′- dihexadecyloxacarbocyanine perchlorate) and FAST DiO (3,3′-dilinoleyloxacarbocyanine perchlorate) behave similarly to their DiI counterparts. Furthermore, whereas a phosphatidylcholine analogue with a BODIPY (4,4-difluoro-4-bora-3a,4a-diaza-s-indacene) fluorophore attached at the end of a 5-carbon acyl chain is delivered efficiently to the endocytic recycling compartment, a significant fraction of another derivative with BODIPY attached to a 12-carbon acyl chain entered late endosomes. Our results thus suggest that endocytic organelles can sort membrane components efficiently based on their preference for association with domains of varying characteristics.

A fluorescent anion sensor that works in neutral aqueous solution for bioanalytical application.

Abstract: Anion recognition and anion sensing are of interest because anions play many important roles in living organisms. Most currently known anion sensors work only in organic solution, but sensors for biological applications are required to function in neutral aqueous solution. We have designed and synthesized a novel fluorescent sensor for anions. The sensor molecule 1-CdII contains 7-amino-4-trifluoromethylcoumarin as a fluorescent reporter and CdII-cyclen (1,4,7,10-tetraazacyclododecane) as an anion host. In neutral aqueous solution, CdII of 1-CdII is coordinated by the four nitrogen atoms of cyclen and the aromatic amino group of coumarin. When various anions are added to 100 mM HEPES buffer solution (pH 7.4) containing 1-CdII, the aromatic amino group of coumarin is displaced from CdII, causing a change of the excitation spectrum. While pyrophosphate and citrate were detected with high sensitivity, fluoride and perchlorate produced no response. Among organic anions, ATP and ADP gave strong signals, while ...

Transformation of (per)chlorate into chloride by a newly isolated bacterium: reduction and dismutation

Abstract: Bacterial strain GR-1 was isolated from activated sludge for its ability to oxidize acetate with perchlorate as electron acceptor. Sequencing of 16S rDNA revealed the isolate to belong to the β subgroup of Proteobacteria. When strain GR-1 was grown on acetate and perchlorate, the release of chloride was proportional to the disappearance of perchlorate, showing that this compound was completely reduced. In addition to perchlorate, strain GR-1 used chlorate, oxygen, nitrate and Mn(IV) as electron acceptor. The oxidation of acetate is coupled to the reduction of perchlorate and chlorate, whereas chlorite reduction is not affected by the addition of acetate. Strain GR-1 disproportionates chlorite into molecular oxygen and chloride. As a consequence, the strain oxidizes acetate by simultaneously reducing perchlorate to chlorite and molecular oxygen to water. Comparison of growth yields with oxygen, chlorate and perchlorate and calculated ΔG 0′ values confirms this finding.