What is the need of studying bacterial growth? Cell division DNA replication and cell elongation Formation of cell division plane Synthesis of petidoglycan Cell division Generation time: time required for one cell to divide and form two cells Binary fission During growth cycle all cellular constituents increases proportionally and each daughter cell receives chromosomes and sufficient copies of ribosomes and other monomers.
What triggers cell division in bacteria? How is it controlled? In Rod shaped bacteria how constriction happens exactly at the center ?
Control of Cell Division : Fts Proteins and divisome Min proteins (minicell locus ) Min C, Min D and Min E) Nucleoid occlusion mechanism Fts Proteins Fts (filamentous temperature-sensitive) Proteins Essential for cell division in all prokaryotes Interact to form the divisome (cell division apparatus) FtsZ: forms ring around center of cell ZipA: anchor that connects FtsZ ring to cytoplasmic membrane FtsA: helps connect FtsZ ring to membrane and also recruits other divisome proteins Related to actin FtsI peptidoglycan biosynthesis proteins FtsK separates chromosome DNA replicates before the FtsZ ring forms
Location of FtsZ ring is facilitated by Min proteins (minicell locus ) MinC, MinD : Inhibits FtsZ anchoring MinE : Inhibitor of MinC and MinD present at the center FtsK protein mediates separation of chromosomes to daughter cells 1. DNA replication and segregation 2. Min system controls the site of division 3. FtsZ ring assembly in the center along with the formation of divisome 4. Z-ring maturation 5. Septal invagination with the constriction of the envelope layers 6. Septum closure and splitting of the daughter cells FtsZ ring assembly 1. First group of proteins assembles and anchor the FtsZ to form Z ring 2. Z ring forms as an arc at several points at the median 3. Arc formed by the self polimerization of FtsZ proteins with the help of GTP utilization 4. FtsA and ZipA proteins anchor the micro arc on the cell membrane Z-ring maturation after orderly recruitment of the divisome components 1. By the ordered recruitment of late divisome components 2. ZapA and ZapC enhance the polymerization of the arc by aggregating the FtsZ and inhibiting GTPase activity. 3. FtsK drag Chromosome from the plane
Septal invagination with the constriction of the envelope layers Constriction is energy dependent Z-ring can exert a constrictive force onto the membrane Simultaneously autolysin hydrolyses peptidoglycan layer and create small opening on the cell wall New wall materials are added across the opening with the help of bactoprenol and PBP
Control of Z ring assemly By Two complementary systems ; Min system and Nucleoid occlusion
Min system prevents aberrant division at the poles Fts inhibitor MinC and MinD organized to form MinCD complex MinCD prevents the lateral assembly of FtsZ Competes with FtsA and ZipA Min E system prevents MinCD complex Regulation of Z ring ASSEMBLY Nucleoid occlusion DNA associated proteins inhibits Z-ring formation This provides a protective mechanism to the DNA, and contributes to the precise temporal and spatial positioning of the division septum. Growth rate dependent Z ring inhibitor UgtP (UDP-glucose diacylglycerol glucosyltransferase) was identified in B. subtilis and may constitute the link between metabolism and cell division Under nutrient rich conditions, in response to high levels of its substrate, UgtP is present in the cytoplasm inhibits FtsZ assembly, by disruption of the lateral protofilaments interactions during growth on a poor carbon source, the levels of UgtP are reduced When DNA is damaged, an SOS response is activated to repair the DNA and cease cell division by inhibiting FtsZ polymerization