This technology enhances control over the function of the protein electron carrier, Ferredoxin, via fragmentation and fusion to proteins that assist with fragment complementation upon chemical binding.
Electron flow is an important consideration when engineering metabolism for the microbial production of high value chemicals (fuels, alcohols, saturated hydrocarbons, chiral bioactive molecules, and pharmaceutical compounds), because the amount and timing of electrons transferred between different donor and acceptor proteins determine the ratio of biomass accumulation versus chemical production. However, the accumulation of reduced and oxidized cofactors in genetically-engineered microbes can result in global redox imbalances that limit chemical production. Moreover, current approaches to solve the redox imbalance are limited to regulating transcription of protein electron carriers via the “on/off” molecular switch controlled by the promoter.
Ferredoxin is one of the most intensively studies families of protein electron carriers important for transferring electrons from a wide range of donor proteins to a diverse range of acceptor proteins. This technology enhances control over the function of the protein electron carrier, Ferredoxin, via fragmentation and fusion to proteins that assist with fragment complementation upon chemical binding. The design of this technology can be used to improve the control over electron flow into and out of cells for the production of chemicals and biosensing applications, such as those found in bioelectronics.
This technology has several designs that introduced multiple new protein electron carriers who’s activities can be switched on and off by either multiple transcriptional inputs, a post-translational input, or combinations of these two mechanisms. This technology can be used during late-stage fermentation when cells are no longer actively growing and have more limited capacity for transcription.
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chiral bioactive molecules
molecular switch controlled
intensively studies families
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link metabolic pathways