Basically you need to carry out the following protocols: (1) Making gene construct involving required promoter (inducible/constitutive/heterologous/organism specific); (2) Inserting the gene construct to commercially available vectors to make recombinant vectors; (3) To Transform the C. glutamicum with the recombinant vector. Standardize/optimize the fermentation/growth conditions for the transformed bacteria.
For the exact protocol, you can refer manual on "Molecular Cloning". Written by Maniatis OR the one by Sambrook