In recent history, efforts towards the construction of a transcription regulatory network for Geobacter sulfurreducens have been made in order to model, and ultimately optimize its metabolic activity for bioremediation and clean energy production applications. To contribute to this effort, Fnr-1, a transcription regulator in G. sulfurreducens, was investigated via chromatin immunoprecipitation coupled to microarray analysis (ChIP-chip) and high throughput sequencing (ChIP- seq). 368 genes were identified to be regulated by Fnr-1 via ChIP-chip, and 118 genes were identified via ChIP- seq.73 genes were overlapped between both methods. Results of this study suggest that Fnr-1 functions as a global regulator since controlled genes spanned a wide array of cellular functions. However, Fnr-1 activity is not critical to G. sulfurreducens metabolism since gene deletion has no effect on growth rates. Finally, the observed variation between ChIP-chip and ChIP-seq Fnr-1 binding profiles of this study has brought into question the methods currently used for genome-wide analysis of transcription regulator function