TOXICOLOGICAL HIGHLIGHT Arsenolysis and Thiol-Dependent Arsenate Reduction
نویسنده
چکیده
Conversion of arsenate to arsenite is a critical event in the pathway that leads from inorganic arsenic to a variety of methylated metabolites. The formation of methylated metabolites influences distribution and retention of arsenic and affects the reactivity and toxicity of these intermediates. Indeed, some of the toxic and carcinogenic effects associated with exposure to arsenate or arsenite are probably mediated by methylated arsenicals. Recent work has demonstrated a biologically plausible role for phosphorolytic-arsenolytic enzymes in a reaction scheme in which an ‘‘activated’’ arsenate ester is readily reduced by thiols to arsenite. Thiol-dependent reduction of arsenate esters formed by arsenolysis may be one of several functionally reductant processes that control the flux of arsenic into the cellular pathway for arsenic methylation. Integrating these reductive processes into a conceptual model for arsenic metabolism may provide new insights into the cellular machinery for handling this toxic metalloid.
منابع مشابه
Mechanism of thiol-supported arsenate reduction mediated by phosphorolytic-arsenolytic enzymes: I. The role of arsenolysis.
Several mammalian enzymes catalyzing the phosphorolytic-arsenolytic cleavage of their substrates (thus yielding arsenylated metabolites) have been shown to facilitate reduction of arsenate (AsV) to the more toxic arsenite (AsIII) in presence of their substrate and a thiol. These include purine nucleoside phosphorylase (PNP), glyceraldehyde-3-phosphate dehydrogenase (GAPDH), and glycogen phospho...
متن کاملPurification and role of phosphotransbutyrylase.
In recent years acyl phosphates have received much attention. For example, acetyl (1, 2), propionyl (3, 4), butyryl (5, 6), carbamyl (7, 8), and aspartyl (9) phosphates have been studied in detail. In fermentative bacteria the role of phosphotransacetylase, which facilitates an interconversion of acetyl phosphate and acetyl coenzyme A has been well documented (1,2,10-12). An enzyme capable of c...
متن کاملSuccinic Thiokinase. Ii. Kinetic Studies: Initial Velocity, Product Inhibition, and Effect of Arsenate.
The proposed reaction mechanisms for succinic thiokinases from various sources are well summarized in recent reviews by Jaenicke and Lynen (2) and by Hager (3). On the basis of various isotope exchange studies with the succinic thiokinase from spinach, Kaufman (4) proposed a reaction sequence that includes phosphoryl coenzyme A as an enzyme-bound int’ermediate. This mechanism was supported by M...
متن کاملPolynucleotide phosphorylase of Micrococcus lysodeiktpcus. III. The apparent arsenolysis of nucleoside diphosphates by polynucleotide phosphorylase.
The enzyme, polynucleotide phosphorylase, catalyzes the polymerization of nucleoside diphosphates to polyribonucleotides with the formation of inorganic orthophosphate (1, 2). The reaction is readily reversible, and the phosphorolysis of polyribonucleotides has been studied extensively (3-6). Several recent reviews (7-9) afford extensive summaries of the literature. In the accompanying paper (l...
متن کاملCoenzyme A function in and acetyl transfer by the phosphotransacetylase system.
Lipmann and Tuttle (1) discovered that certain bacterial extracts catalyze a rapid interchange of inorganic and acetyl-bound phosphate. They suggested that this exchange might be due in part to a reversibility of the phosphoroclastic decomposition of pyruvate; however, the observation that the exchange was surprisingly unaffected by addition of acetyl acceptors like formate led them to suspect ...
متن کامل