“…First, the reductive potential of alkG (−0.24 V vs SCE) is within the range of many AQ moieties, rendering sequential electron transfer from AQ mediator to alkB via alkG, and thermodynamically feasible. ,, Second, AQ moieties undergo extremely rapid and reversible two-proton-coupled two-electron transfer mechanisms especially in aqueous media (Scheme S1). , Resultantly, the rich redox chemistry of AQs extends to microbial fuel cells, redox flow batteries, solar cell devices, redox-dyes, antioxidants, antitumor agents, molecular electronics, wastewater treatment, and other energy storage systems. ,− Third, quinones, as natural electron acceptors/donors in key biological processes (e.g., photosynthesis, neurotransmission, and cellular signaling), are typically biocompatible and nontoxic to most biocatalysts. , Quinones have good biocatalytic redox active site accessibility because the quinone/hydroquinone redox function occurs across membranes or interfaces . Finally, AQs are relatively small, prototypically hydrophobic, and aromatic polyketide rings .…”