Cell Division in Bacteria
Research Interest:
Increasing bacterial resistance to the existing antibiotics is emerging as one of the major challenge to human health. Cell division is an essential but a complex process in all the living organisms. Bacterial cell division has always been an attraction for the development of antibacterial agents. A greater understanding of bacteria cell division will be highly helpful for the discovery of novel antibacterial agents.
In E. coli cell division is performed by a coordinated assembly of more than a dozen of different proteins, which form a complex structure known as divisome. Assembly of divisome is initiated by the localization of FtsZ at the division site. FtsZ, a bacterial homolog of tubulin, is highly conserved among the prokaryotes. It polymerizes to form protofilaments and bundles that bind to the inner membrane with the help of membrane anchor proteins FtsA or ZipA, to form a ring like structure known as Z ring. The downstream proteins then get recruited to the Z ring in a hierarchy and make it dynamic structure, divisome. The final role of the divisome is to constrict the membrane and form a septum at the division site. Inhibition of the divisome leads to inhibition of the cell division and thus cell division has been considered as an attractive target for the development of antibacterial agents. We are interested to investigate the interactions among the cell division proteins and target these interactions for the discovery of novel antibacterial agents.
PhD position available: Interested candidates having CSIR-UGC JRF or any other fellowship may directly contact me.
Postdoc/ RA/ N-PDF: Candidates submitted their PhD thesis may directly contact me with their updated CV.