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Filamentous Thermosensitive Mutant Z: An Appealing Target for Emerging Pathogens and a Trek on Its Natural Inhibitors
Manisha Gurnani1, Abhishek Chauhan2, Anuj Ranjan3
1Amity Institute of Environmental Science, Amity University, Noida 201301, India.
Abstract:
Antibiotic resistance is a major emerging issue in the health care sector, as highlighted by the WHO. Filamentous Thermosensitive mutant Z (Fts-Z) is gaining significant attention in the scientific community as a potential anti-bacterial target for fighting antibiotic resistance among several pathogenic bacteria. The Fts-Z plays a key role in bacterial cell division by allowing Z ring formation. Several in vitro and in silico experiments have demonstrated that inhibition of Fts-Z can lead to filamentous growth of the cells, and finally, cell death occurs. Many natural compounds that have successfully inhibited Fts-Z are also studied. This review article intended to highlight the structural-functional aspect of Fts-Z that leads to Z-ring formation and its contribution to the biochemistry and physiology of cells. The current trend of natural inhibitors of Fts-Z protein is also covered.
Insights
Antibiotic resistance is a growing global health threat. Targeting Filamentous Thermosensitive mutant Z (Fts-Z), crucial for bacterial cell division, offers a promising strategy against resistant pathogens.
Area of Science:
- Microbiology
- Biochemistry
- Drug Discovery
Background:
- Antibiotic resistance is a critical global health challenge.
- Filamentous Thermosensitive mutant Z (Fts-Z) is essential for bacterial cell division and a potential target for new antibiotics.
- Inhibiting Fts-Z can lead to bacterial cell death.
Purpose of the Study:
- To review the structural and functional aspects of Fts-Z.
- To explore Fts-Z's role in bacterial biochemistry and physiology.
- To cover current natural inhibitors of Fts-Z.
Main Methods:
- Literature review of in vitro and in silico studies.
- Analysis of Fts-Z structure and function.
- Compilation of data on natural Fts-Z inhibitors.
Main Results:
- Fts-Z's critical role in Z-ring formation and bacterial division is highlighted.
- Inhibition of Fts-Z leads to cell filamentation and death.
- Various natural compounds show potential as Fts-Z inhibitors.
Conclusions:
- Fts-Z is a validated target for developing novel antibacterial agents.
- Understanding Fts-Z structure-function is key to designing effective inhibitors.
- Natural compounds represent a promising avenue for combating antibiotic resistance.
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