Category:Team Ferdinand Cohn

Figure 5: Show the rseP mutation changing the function of acid induction of sigma factor e

Table 1 shows conversion of 2-C-methyl-d-eythritol 2,4-cyclodiphosphate into (E)-4-hydroxy-3-methylbut-2-enyl diphosphate by GcpE in the presence of thylakoids and light

Structural and mutational analysis allows us to propose a mechanism of metal cofactor-independent glutamate racemase in which 2 cysteine residues are involved in catalysis.

fig. 3 shows addition of multicopy FtsP suppresses division defects of mutants highlighting its significance in cell division

fig. 3 details effects of apo-ACP concentrations on activities of S.pneumoniae, E. Coli, & M. Pneumoniae ACP enzymes

The effect of the cysteine mutations on enzymatic activity was assessed using a coupled enzyme assay. The kinetic results indicate that mutation of individual cysteine residues 27, 46 and 49 decreases the Vmax only 8- to 11-fold, whereas the Vmax for the C30A variant decreases by over 100-fold. Table 2

Table 1: Shows kinetic constants for mutant compared to wild-type for lactose uptake.