This tool will take a set of genes as input, and for each, optimize the CDS nucleotide sequence, append a synthetic 5' UTR/Ribosome Binding Site, and optionally append a synthetic yeast promoter and terminator. These redesigned genes are recompiled into an operon, flanked by a T7 promoter and Terminator. This synthetic operon can then be functionally mobilized and expressed across highly diverse microbial taxa using the methodology outlined in [Citation to be appended upon acceptance].