Oxidants induce Escherichia coli MarR glutathionylation in the presence of glutathione

The results of protein thiols reacting with oxidants may be different in the presence or absence of glutathione (GSH). Upon exposure to oxidants, such as Cu<sup>2+</sup> and polysulfide, the multiple drug resistant regulator MarR dimer in Escherichia coli is believed to form tetramers linked by disulfide bonds between its Cys<sup>80</sup> thiols. We confirmed this observation in the absence of GSH; however, the MarR-Cys<sup>80</sup> thiol was primarily glutathionylated in the presence of GSH after MarR was treated with various oxidants, including octasulfur (S<sub>8</sub>), Cu<sup>2+</sup>, H<sub>2</sub>O<sub>2</sub>, ClO<sup>-</sup>, and a NO donor. When using S<sub>8</sub> as the oxidizing agent, we identified four pathways to induce MarR-Cys<sup>80</sup> glutathionylation. Since E. coli contains high concentrations of GSH, MarR is likely glutathionylated instead of forming tetramers inside the cells. When E. coli was exposed to S<sub>8</sub>, cellular levels of protein glutathionylation were increased and most MarR was glutathionylated, as shown by Western blot and LC-MS analyses. The glutathionylated MarR displayed reduced affinity to its cognate operator, resulting in the expression of its repressed genes. The results highlight the need to consider the wide presence of GSH when investigating protein thiol modification.

Authors

Institutions

Publication Details

Journal
Redox Biology
Published
2025-04-11
DOI
https://doi.org/10.1016/j.redox.2025.103629
Primary Topic
Sulfur Compounds in Biology
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Oxidants induce Escherichia coli MarR glutathionylation in the presence of glutathione

Yongzhen Xia, Luying Xun, Huaiwei Liu, Tianqi Wang
Redox Biology
Sulfur Compounds in Biology
article

Oxidants induce Escherichia coli MarR glutathionylation in the presence of glutathione

Yongzhen Xia, Luying Xun, Huaiwei Liu, Tianqi Wang
article en

Abstract

The results of protein thiols reacting with oxidants may be different in the presence or absence of glutathione (GSH). Upon exposure to oxidants, such as Cu<sup>2+</sup> and polysulfide, the multiple drug resistant regulator MarR dimer in Escherichia coli is believed to form tetramers linked by disulfide bonds between its Cys<sup>80</sup> thiols. We confirmed this observation in the absence of GSH; however, the MarR-Cys<sup>80</sup> thiol was primarily glutathionylated in the presence of GSH after MarR was treated with various oxidants, including octasulfur (S<sub>8</sub>), Cu<sup>2+</sup>, H<sub>2</sub>O<sub>2</sub>, ClO<sup>-</sup>, and a NO donor. When using S<sub>8</sub> as the oxidizing agent, we identified four pathways to induce MarR-Cys<sup>80</sup> glutathionylation. Since E. coli contains high concentrations of GSH, MarR is likely glutathionylated instead of forming tetramers inside the cells. When E. coli was exposed to S<sub>8</sub>, cellular levels of protein glutathionylation were increased and most MarR was glutathionylated, as shown by Western blot and LC-MS analyses. The glutathionylated MarR displayed reduced affinity to its cognate operator, resulting in the expression of its repressed genes. The results highlight the need to consider the wide presence of GSH when investigating protein thiol modification.

Redox BiologyVol. 83
Qingdao University (CN), Shandong University (CN), State Key Laboratory of Microbial Technology, Washington State University (US)
Openalex Percentile: Top 92%
Sulfur Compounds in Biology
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.