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Protein stable isotope probing with (H2O)-O-18 differentiated cold stress response at permissive temperatures from general growth at optimal conditions in Escherichia coli K12
- 1.0542371 - MBÚ 2022 RIV US eng J - Journal Article
Starke, Robert - Schape, S. S. - Jehmlich, N. - von Bergen, M.
Protein stable isotope probing with (H2O)-O-18 differentiated cold stress response at permissive temperatures from general growth at optimal conditions in Escherichia coli K12.
Rapid Communications in Mass Spectrometry. Roč. 35, č. 1 (2021), č. článku e8941. ISSN 0951-4198. E-ISSN 1097-0231
R&D Projects: GA ČR(CZ) GJ20-02022Y
Institutional support: RVO:61388971
Keywords : mass-spectrometry * sip * carbon
OECD category: Microbiology
Impact factor: 2.586, year: 2021
Method of publishing: Limited access
https://analyticalsciencejournals.onlinelibrary.wiley.com/doi/epdf/10.1002/rcm.8941
Rationale Tracing isotopically labeled water into proteins allows for the detection of species-specific metabolic activity in complex communities. However, a stress response may alter the newly synthesized proteins.
Methods We traced 18-oxygen from heavy water into proteins of Escherichia coli K12 grown from permissive to retardant temperatures. All samples were analyzed using UPLC/Orbitrap Q-Exactive-MS/MS operating in positive electrospray ionization mode.
Results We found that warmer temperatures resulted in significantly (P-value < 0.05) higher incorporation of 18-oxygen as seen by both substrate utilization as relative isotope abundance (RIA) and growth as labeling ratio (LR). However, the absolute number of peptides with incorporation of 18-oxygen showed no significant correlation to temperature, potentially caused by the synthesis of different proteins at low temperatures, namely, proteins related to cold stress response.
Conclusions Our results unveil the species-specific cold stress response of E. coli K12 that could be misinterpreted as general growth, this is why the quantity as RIA and LR but also the quality as absolute number of peptides with incorporation (relative abundance, RA) and their function must be considered to fully understand the activity of microbial communities.
Permanent Link: http://hdl.handle.net/11104/0319796
Number of the records: 1