In Vivo Characterization of Escherichia coli ftsZ Mutants: Effects on Z-Ring Structure and Function
Open Access
- 15 August 2003
- journal article
- Published by American Society for Microbiology in Journal of Bacteriology
- Vol. 185 (16) , 4796-4805
- https://doi.org/10.1128/jb.185.16.4796-4805.2003
Abstract
We have characterized the in vivo phenotypes of 17 mutations of Escherichia coli ftsZ. In particular, we determined whether these mutations can complement a null ftsZ phenotype, and we demonstrated that two noncomplementing mutations show partial dominant-negative behavior. We performed immunofluorescence microscopy to determine whether these mutants could assemble into normal or abnormal structures in vivo. The mutants separated into four classes—those that complemented the null and formed normal FtsZ rings, those that complemented the null but formed aberrant FtsZ structures, those that formed aberrant FtsZ structures and did not complement, and those that were unable to form any FtsZ structures. We did not find any mutations that produced nonfunctional Z rings of normal appearance. Surprisingly, some mutants that produced extensively spiraled Z-ring structures divided and grew with a normal doubling time. The analysis was carried out using a complementation system based on an ftsZ deletion strain, a temperature-sensitive rescue plasmid, and a complementation vector that placed mutated ftsZ alleles under the control of the pBAD promoter, which offered several advantages over previous systems.Keywords
This publication has 38 references indexed in Scilit:
- Asymmetric Cell Division in B. subtilis Involves a Spiral-like Intermediate of the Cytokinetic Protein FtsZCell, 2002
- Colocalization of cell division proteins FtsZ and FtsA to cytoskeletal structures in living Escherichia coli cells by using green fluorescent proteinProceedings of the National Academy of Sciences, 1996
- FtsZ‐spirals and ‐arcs determine the shape of the invaginating septa in some mutants of Escherichia coliMolecular Microbiology, 1996
- Bacterial cell division protein FtsZ assembles into protofilament sheets and minirings, structural homologs of tubulin polymers.Proceedings of the National Academy of Sciences, 1996
- Visualization of the subcellular location of sporulation proteins in Bacillus subtilis using immunofluorescence microscopyMolecular Microbiology, 1995
- GTP-dependent polymerization of Escherichia coli FtsZ protein to form tubules.Proceedings of the National Academy of Sciences, 1994
- FtsZ ring structure associated with division in Escherichia coliNature, 1991
- A pSC101-derived plasmid which shows no sequence homology to other commonly used cloning vectorsGene, 1984
- A 37 × 103 molecular weight plasmid-encoded protein is required for replication and copy number control in the plasmid pSC101 and its temperature-sensitive derivative pHS1Journal of Molecular Biology, 1984
- The 3′-Terminal Sequence of Escherichia coli 16S Ribosomal RNA: Complementarity to Nonsense Triplets and Ribosome Binding SitesProceedings of the National Academy of Sciences, 1974