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© Institut Pasteur
Cells infected for 24 hrs with C. Trachomatis. The cell nuclei are labelled in blue, the bacteria appear yellow, within the inclusion lumen. A bacterial protein secreted out the inclusion into the host cytoplasm id labelled in red.
Publication : Biochimica et biophysica acta. Molecular basis of disease

Unraveling the role of thiosulfate sulfurtransferase in metabolic diseases.

Team: Structural Microbiology
Member: Fernando Batista
Scientific Fields
Diseases
Organisms
Applications
Technique

Published in Biochimica et biophysica acta. Molecular basis of disease - 01 Jun 2020

Kruithof PD, Lunev S, Aguilar Lozano SP, de Assis Batista F, Al-Dahmani ZM, Joles JA, Dolga AM, Groves MR, van Goor H,

Link to Pubmed [PMID] – 32061776

Link to DOI – S0925-4439(20)30061-210.1016/j.bbadis.2020.165716

Biochim Biophys Acta Mol Basis Dis 2020 06; 1866(6): 165716

Thiosulfate sulfurtransferase (TST, EC 2.8.1.1), also known as Rhodanese, is a mitochondrial enzyme which catalyzes the transfer of sulfur in several molecular pathways. After its initial identification as a cyanide detoxification enzyme, it was found that its functions also include sulfur metabolism, modification of iron‑sulfur clusters and the reduction of antioxidants glutathione and thioredoxin. TST deficiency was shown to be strongly related to the pathophysiology of metabolic diseases including diabetes and obesity. This review summarizes research related to the enzymatic properties and functions of TST, to then explore the association between the effects of TST on mitochondria and development of diseases such as diabetes and obesity.