Related Experiment Video
Updated: May 26, 2026

Fluorescence Live-cell Imaging of the Complete Vegetative Cell Cycle of the Slow-growing Social Bacterium Myxococcus xanthus
Published on: June 20, 2018
Characterization of the partitioning system of Myxococcus plasmid pMF1
Xia Sun1, Xiao-jing Chen, Jing Feng
1State Key Laboratory of Microbial Technology, School of Life Science, Shandong University, Jinan, China.
Abstract:
pMF1 is the only autonomously replicating plasmid that has been recently identified in myxobacteria. This study characterized the partitioning (par) system of this plasmid. The fragment that significantly increased the retaining stability of plasmids in Myxococcus cells in the absence of selective antibiotics contained three open reading frames (ORFs) pMF1.21-pMF1.23 (parCAB). The pMF1.22 ORF (parA) is homologous to members of the parA ATPase family, with the highest similarity (56%) to the Sphingobium japonicum ParA-like protein, while the other two ORFs had no homologs in GenBank. DNase I footprinting and electrophoretic mobility shift assays showed that the pMF1.23 (parB) product is a DNA-binding protein of iteron DNA sequences, while the product of pMF1.21 (parC) has no binding activity but is able to enhance the DNA-binding activity of ParB to iterons. The ParB protein autogenously repressed the expression of the par genes, consistent with the type Ib par pattern, while the ParC protein has less repressive activity. The ParB-binding iteron sequences are distributed not only near the partitioning gene loci but also along pMF1. These results indicate that the pMF1 par system has novel structural and functional characteristics.
Insights
Researchers characterized the partitioning (par) system of the myxobacterial plasmid pMF1. The study identified novel structural and functional characteristics of the parCAB genes, crucial for plasmid stability.
Area of Science:
- Microbiology
- Molecular Biology
- Genetics
Background:
- pMF1 is the only known autonomously replicating plasmid in myxobacteria.
- Plasmid stability is crucial for genetic studies and biotechnological applications.
Purpose of the Study:
- To characterize the partitioning (par) system of the myxobacterial plasmid pMF1.
- To understand the molecular mechanisms underlying pMF1 plasmid stability in Myxococcus cells.
Main Methods:
- Identification and characterization of open reading frames (ORFs) within the pMF1 par region.
- DNase I footprinting and electrophoretic mobility shift assays (EMSAs) to study protein-DNA interactions.
- Analysis of gene expression regulation by the par proteins.
Main Results:
- A three-ORF fragment (pMF1.21-pMF1.23), named parCAB, was identified and significantly enhanced plasmid stability.
- The ParA protein (pMF1.22) showed homology to the parA ATPase family.
- ParB (pMF1.23) is a DNA-binding protein recognizing iteron sequences, while ParC (pMF1.21) enhances ParB binding.
- ParB autogenously repressed par gene expression, consistent with a type Ib partitioning pattern.
Conclusions:
- The pMF1 par system exhibits novel structural and functional features.
- The parCAB system plays a critical role in maintaining pMF1 plasmid stability in myxobacteria.
- Iteron sequences recognized by ParB are broadly distributed on the pMF1 plasmid.
Related Concept Videos
Bacterial Phylum Tenericutes
Plasmids
Bacterial Phylum Planctomycetes
DNA Bacteriophages

