Microbial-electrode electron transfer is a mechanism by which microbes make their living coupling to electronic circuits, even across long distances. From a chemistry perspective, it represents a model platform that integrates biological metabolism with artificial electronics, and will facilitate the fundamental understanding of charge transport properties within these distinct chemical systems and particularly at their interfaces. From a broad standpoint, this understanding will also open up new possibilities in a wide range of high impact applications in bioelectrochemical system based technologies, which have shown promise in electricity, biochemical, chemical feedstock production but still require many orders of magnitude improvement to lead to viable technologies. Here we review opportunities to understand microbial-electrode electron transfer to improve electrocatalysis (bioelectricity) and electrosynthesis (biochemical and chemical production). We discuss challenges and the ample interdisciplinary research opportunities and suggest paths to take to improve production of fuels and chemicals at high yield and efficiency and the new applications that may result from increased understanding of the microbial-electrode electron transfer mechanism.Bio-electrochemical system (BES) can be expressed as the bidirectional electron transports between biotic and abiotic components, where the redoxactive microorganisms or bio-macromolecules act as the catalysts that facilitate the exchange process 1 . A glossary of important terms is provided in box 1. A model system of BES that has been widely studies is the Microbial Fuel Cell (MFCs). Similar to the conventional fuel cell, the microorganisms can transport electrons to the anodes of MFC after oxidizing the electron donors, thus generating the electrical flow toward the cathode 2 . Meanwhile, certain microorganisms are also known for their capability to reduce the electron acceptors such as nitrate, perchlorate or metals in the cathodes 3 . Other BESs such as Microbial electrolysis cells (MEC), Microbial electrosynthesis (MES),Microbial solar cells (MSCs), and Plant microbial fuel cells (PMFCs) also share similar electron transport strategy. These direct electron transport processes created a novel and promising possibility to bridge the fundamental researches in microbiology, electrochemistry, environmental engineering, material science and the applications in waste remediation & resource recovery, sustainable energy production, and bio-inspired material development. The basic working principles and the applications of these different BESs have been comprehensively reviewed by many different groups [4][5][6][7] . Bioelectrochemcial systemsEnzymatic electron transport process is one of the earliest BES models which received extensive attention due to the interests in development of amperometric biosensors and enzymatic fuel cell in late 20 th century [8][9][10][11][12] . In this system, the electrons generated from specific enzymatic reactions can be either...

Graphite electrodes were modified with reduction of aryl diazonium salts and implemented as anodes in microbial fuel cells. First, reduction of 4-aminophenyl diazonium is considered using increased coulombic charge density from 16.5 to 200 mC/cm(2). This procedure introduced aryl amine functionalities at the surface which are neutral at neutral pH. These electrodes were implemented as anodes in "H" type microbial fuel cells inoculated with waste water, acetate as the substrate and using ferricyanide reduction at the cathode and a 1000 Ω external resistance. When the microbial anode had developed, the performances of the microbial fuel cells were measured under acetate saturation conditions and compared with those of control microbial fuel cells having an unmodified graphite anode. We found that the maximum power density of microbial fuel cell first increased as a function of the extent of modification, reaching an optimum after which it decreased for higher degree of surface modification, becoming even less performing than the control microbial fuel cell. Then, the effect of the introduction of charged groups at the surface was investigated at a low degree of surface modification. It was found that negatively charged groups at the surface (carboxylate) decreased microbial fuel cell power output while the introduction of positively charged groups doubled the power output. Scanning electron microscopy revealed that the microbial anode modified with positively charged groups was covered by a dense and homogeneous biofilm. Fluorescence in situ hybridization analyses showed that this biofilm consisted to a large extent of bacteria from the known electroactive Geobacter genus. In summary, the extent of modification of the anode was found to be critical for the microbial fuel cell performance. The nature of the chemical group introduced at the electrode surface was also found to significantly affect the performance of the microbial fuel cells. The method used for modification is easy to control and can be optimized and implemented for many carbon materials currently used in microbial fuel cells and other bioelectrochemical systems.

Catalyses of electrode reactions by oxidoreductases or living electroactive bacteria are compared and recent advances reviewed. The relation between the biological and nevertheless inert nature of enzymes and the living machinery of electroactive microbes is discussed. The way these biocatalysts may be electrically contacted to anodes or cathodes is considered with a focus on their immobilization at electrodes and on the issue of time stability of these assemblies. Recent improvements in power output of biofuel cells are reviewed together with applications that have appeared in the literature. This account also reviews new approaches for combining enzymes and living microbes in bioelectrochemical systems such as reproducing microbial metabolisms with enzyme cascades and expressing oxidoreductases on genetically engineered microbes. Finally, the use of surface chemistry for studying the microbe-electrode interface and bioelectrodes with cell organelles, such as mitochondria, or with higher organisms, such as yeasts, are discussed. Some perspectives for future research to extend this field are offered as conclusions.