Introduction Three of the proteins required in the project are cytochrome c proteins (haem proteins). Hence, the heme biosynthesis pathway needs to be modelled. Pathway of heme production in E. coli (C-5 pathway from glutamate)

Mathematical model Pathway of heme production in E. coli (C-5 pathway from glutamate): Also, d-Aminolevulinate (ALA) produced as an intermediate in the above reactions. -Aminolevulinate Synthase (ALA Synthase) is the committed step of the heme synthesis pathway, and is usually rate-limiting for the overall pathway. Regulation occurs through control of gene transcription. Heme functions as a feedback inhibitor, repressing transcription of the gene for -Aminolevulinate Synthase. A non-competitive irreversible feedback inhibition model is assumed for this step with a Ki value of 0.02 mM. Hence, the following equation governs the production of ALA:

The rest of the reactions in this pathway are assumed to proceed via Henri-Michaelis-Menten kinetics:

Km and Vmax values of hydroxymethylbilane synthase:

Stimulation

After putting in the rate laws and the values of various parameters in Copasi software, following graphs were obtained for the concentrations and rate of formation of various species involved (Copasi has been used for obtaining all graphs and mathematical equations):

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Fig 1: Amount of ferroheme b formed in the cytoplasm.	Fig 2: Amount of ferroheme transported to the periplasm
Fig 3: rate of formation of ferroheme in the cytosol	Fig 4: rate of transfer of ferroheme from the cytoplasm to the periplasm.

The following are the differential equations associated with the above processes:

Interpretation

After this, the following reactions take place, depending on the protein produced:
1. Nitrite reduction (nrfA protein; Km = 0.11 mM) NO2- ----> NH3 Differential equations involved: