Skip to main content

The Bacterial Nucleoid



The dynamics of the chromosomal DNA of bacteria is arguably simpler than that of eukaryotic cells. Indeed, it is not separated from the rest of the cytoplasm by the nuclear envelope, and its compaction requires fewer levels than the complex hierarchy of mechanisms observed for eukaryotic DNA. Nonetheless, the organization of the bacterial nucleoid (the region of the cell that contains the genomic DNA, as well as several thousands of associated proteins) is still poorly understood and fundamental questions lack an answer, despite the long-lasting efforts of many groups. For example, the nature of the mechanism leading to the 1000-fold compaction of the DNA inside the nucleoid and its separation from the rest of the cytoplasm is still poorly understood. Moreover, the DNA of most bacteria is circular and negatively supercoiled, but the role of supercoiling and its interferences with fundamental biological processes, like DNA compaction, replication or transcription, are the matter of ongoing debates.

The purpose of the proposed internship is precisely to better understand the dynamics of the bacterial nucleoid through coarse-grained molecular modeling and simulations. We recently demonstrated that such models suggest that the principal mechanism for the formation of the bacterial nucleoid is a segregative phase separation driven by the demixing of the DNA and other non-interacting globular macromolecules present in the cytoplasm, presumably ribosomes. The proposed work aims at elaborating further on these results and refining the current models, in order to gain deeper insight into the formation of the nucleoid, the role of supercoiling, and the unavoidable interactions between all mechanisms that take place in the cell. It will therefore consist in building a coarse-grained model of the cytoplasm with all mandatory ingredients, namely supercoiled DNA, non-interacting crowding macromolecules, and DNA-bound proteins, and launching simulations over the long time scales needed to investigate these mechanisms.

Related Publications:

[1] In vivo compaction dynamics of bacterial DNA : A fingerprint of DNA/RNA demixing ? M. Joyeux, Current Opinion in Colloid & Interface Science, 26, 17-27 (2016)

[2] Role of salt valency in the switch of H-NS proteins between DNA-bridging and DNA-stiffening modes. M. Joyeux, Biophysical Journal, 114, 2317-2325 (2018)

[3] Bacterial nucleoid : Interplay of DNA demixing and supercoiling. M. Joyeux, Biophysical Journal, 118 (2020) 2141-2150

Background and skills expected:

The proposed internship involves writing/modifying computer codes (essentially in C language + openMP parallelization) to implement the model of the bacterial cell, launching simulations and exploiting the outcome of these simulations. The applicant should have a good background in physics and be used to working with computers. The relevant knowledge in biology/biophysics may be acquired during the first weeks of the internship.


PSM team
Office 220
Tel: 04 76 51 47 51 (marc[dot]joyeux[at]univ-grenoble-alpes[dot]fr)

Submitted on February 13, 2024

Updated on February 13, 2024