Tuning Promoter Strengths for Improved Synthesis and Function of Electron Conduits in <i>Escherichia coli</i>

Abstract

Introduction of the electron transfer complex MtrCAB from <i>Shewanella oneidensis</i> MR-1 into a heterologous host provides a modular and molecularly defined route for electrons to be transferred to an extracellular inorganic solid. However, an <i>Escherichia coli</i> strain expressing this pathway displayed limited control of MtrCAB expression and impaired cell growth. To overcome these limitations and to improve heterologous extracellular electron transfer, we used an <i>E. coli</i> host with a more tunable induction system and a panel of constitutive promoters to generate a library of strains that separately transcribe the <i>mtr</i> and cytochrome <i>c</i> maturation (<i>ccm</i>) operons over 3 orders of magnitude. From this library, we identified strains that show 2.2 times higher levels of MtrC and MtrA and that have improved cell growth. We find that a ∼300-fold decrease in the efficiency of MtrC and MtrA synthesis with increasing <i>mtr</i> promoter activity critically limits the maximum expression level of MtrC and MtrA. We also tested the extracellular electron transfer capabilities of a subset of the strains using a three-electrode microbial electrochemical system. Interestingly, the strain with improved cell growth and fewer morphological changes generated the largest maximal current per cfu, rather than the strain with more MtrC and MtrA. This strain also showed ∼30-fold greater maximal current per cfu than its <i>ccm</i>-only control strain. Thus, the conditions for optimal MtrCAB expression and anode reduction are distinct, and minimal perturbations to cell morphology are correlated with improved extracellular electron transfer in <i>E. coli</i>