Data on nucleoid-associated proteins isolated from Mycoplasma Gallisepticum in different growth phases

Data in Brief

A. Semashko Tatiana¹  V. Evsyutina Daria²  G. Ladygina Valentina²  Yu. Fisunov Gleb²  I. Kovalchuk Sergey²  I. Zubov Aleksandr²  V. Pobeguts Olga²  H. Ziganshin Rustam³  A. Galyamina Maria³ 

[1] Corresponding author.;Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency, Moscow, Russia;Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Moscow, Russia;

关键词: Mycoplasma gallisepticum;    Synchronous growth;    Nucleoid;    Nucleoid-associated proteins;    Proteomic analysis;    Data-independent acquisition;   

DOI  :  

来源: DOAJ

【 摘 要 】

Mycoplasma gallisepticum (MG) is one of the smallest free-living and self-replicating organisms, it is characterized by lack of cell wall and reduced genome size. As a result of genome reduction, MG has a limited variety of DNA-binding proteins and transcription factors. To investigate the dynamic changes of the proteomic profile of MG nucleoid, that may assist in revealing its mechanisms of functioning, regulation of chromosome organization and stress adaptation, a quantitative proteomic study was performed on MG nucleoids obtained from the cell culture in logarithmic and stationary phases of synchronous growth. MG cells were grown on a liquid medium with a 9 h starvation period. Nucleoids were obtained from the cell culture at the 26th and the 50th hour (logarithmic and stationary growth phases respectively) by sucrose density gradient centrifugation. LC-MS analysis was carried out on an Ultimate 3000 RSLCnano HPLC system connected to a Fusion Lumos mass spectrometer, controlled by XCalibur software (Thermo Fisher Scientific) via a nanoelectrospray source (Thermo Fisher Scientific). For comprehensive peptide library generation one sample from each biological replicate was run in DDA mode. Then, all the samples were run in a single LC-MS DIA run. Identification of DDA files and DIA quantitation was performed with MaxQuant and Skyline software, correspondingly. All raw data generated from IDA and DDA acquisitions are presented in the PRIDE database with identifier PXD019077.

【 授权许可】

Unknown