{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Wyllie S"],"funding":["Wellcome Trust"],"pagination":["529-40"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC2784880"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["74(3)"],"pubmed_abstract":["The bifunctional trypanothione synthetase-amidase (TRYS) comprises two structurally distinct catalytic domains for synthesis and hydrolysis of trypanothione (N(1),N(8)-bis(glutathionyl)spermidine). This unique dithiol plays a pivotal role in thiol-redox homeostasis and in defence against chemical and oxidative stress in trypanosomatids. A tetracycline-dependent conditional double knockout of TRYS (cDKO) was generated in bloodstream Trypanosoma brucei. Culture of cDKO parasites without tetracycline induction resulted in loss of trypanothione and accumulation of glutathione, followed by growth inhibition and cell lysis after 6 days. In the absence of inducer, cDKO cells were unable to infect mice, confirming that this enzyme is essential for virulence in vivo as well as in vitro. To establis"],"journal":["Molecular microbiology"],"pubmed_title":["Dissecting the essentiality of the bifunctional trypanothione synthetase-amidase in Trypanosoma brucei using chemical and genetic methods."],"pmcid":["PMC2784880"],"funding_grant_id":["079838","WT 083481","077705","083481","WT 079838","WT 077705"],"pubmed_authors":["Thompson S","Oza SL","Fairlamb AH","Spinks D","Wyllie S","Patterson S"],"additional_accession":[]},"is_claimable":false,"name":"Dissecting the essentiality of the bifunctional trypanothione synthetase-amidase in Trypanosoma brucei using chemical and genetic methods.","description":"The bifunctional trypanothione synthetase-amidase (TRYS) comprises two structurally distinct catalytic domains for synthesis and hydrolysis of trypanothione (N(1),N(8)-bis(glutathionyl)spermidine). This unique dithiol plays a pivotal role in thiol-redox homeostasis and in defence against chemical and oxidative stress in trypanosomatids. A tetracycline-dependent conditional double knockout of TRYS (cDKO) was generated in bloodstream Trypanosoma brucei. Culture of cDKO parasites without tetracycline induction resulted in loss of trypanothione and accumulation of glutathione, followed by growth inhibition and cell lysis after 6 days. In the absence of inducer, cDKO cells were unable to infect mice, confirming that this enzyme is essential for virulence in vivo as well as in vitro. To establis","dates":{"release":"2009-01-01T00:00:00Z","publication":"2009 Nov","modification":"2025-04-19T01:26:59.259Z","creation":"2019-03-27T00:26:56Z"},"accession":"S-EPMC2784880","cross_references":{"pubmed":["19558432"],"doi":["10.1111/j.1365-2958.2009.06761.x"]}}