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      Phototrophic N 2 and CO 2 Fixation Using a Rhodopseudomonas palustris-H 2 Mediated Electrochemical System With Infrared Photons

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          Abstract

          A promising approach for the synthesis of high value reduced compounds is to couple bacteria to the cathode of an electrochemical cell, with delivery of electrons from the electrode driving reductive biosynthesis in the bacteria. Such systems have been used to reduce CO 2 to acetate and other C-based compounds. Here, we report an electrosynthetic system that couples a diazotrophic, photoautotrophic bacterium, Rhodopseudomonas palustris TIE-1, to the cathode of an electrochemical cell through the mediator H 2 that allows reductive capture of both CO 2 and N 2 with all of the energy coming from the electrode and infrared (IR) photons. R. palustris TIE-1 was shown to utilize a narrow band of IR radiation centered around 850 nm to support growth under both photoheterotrophic, non-diazotrophic and photoautotrophic, diazotrophic conditions with growth rates similar to those achieved using broad spectrum incandescent light. The bacteria were also successfully cultured in the cathodic compartment of an electrochemical cell with the sole source of electrons coming from electrochemically generated H 2, supporting reduction of both CO 2 and N 2 using 850 nm photons as an energy source. Growth rates were similar to non-electrochemical conditions, revealing that the electrochemical system can fully support bacterial growth. Faradaic efficiencies for N 2 and CO 2 reduction were 8.5 and 47%, respectively. These results demonstrate that a microbial-electrode hybrid system can be used to achieve reduction and capture of both CO 2 and N 2 using low energy IR radiation and electrons provided by an electrode.

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          Complete genome sequence of the metabolically versatile photosynthetic bacterium Rhodopseudomonas palustris.

          Rhodopseudomonas palustris is among the most metabolically versatile bacteria known. It uses light, inorganic compounds, or organic compounds, for energy. It acquires carbon from many types of green plant-derived compounds or by carbon dioxide fixation, and it fixes nitrogen. Here we describe the genome sequence of R. palustris, which consists of a 5,459,213-base-pair (bp) circular chromosome with 4,836 predicted genes and a plasmid of 8,427 bp. The sequence reveals genes that confer a remarkably large number of options within a given type of metabolism, including three nitrogenases, five benzene ring cleavage pathways and four light harvesting 2 systems. R. palustris encodes 63 signal transduction histidine kinases and 79 response regulator receiver domains. Almost 15% of the genome is devoted to transport. This genome sequence is a starting point to use R. palustris as a model to explore how organisms integrate metabolic modules in response to environmental perturbations.
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            Microbial electrosynthesis - revisiting the electrical route for microbial production.

            Microbial electrocatalysis relies on microorganisms as catalysts for reactions occurring at electrodes. Microbial fuel cells and microbial electrolysis cells are well known in this context; both use microorganisms to oxidize organic or inorganic matter at an anode to generate electrical power or H(2), respectively. The discovery that electrical current can also drive microbial metabolism has recently lead to a plethora of other applications in bioremediation and in the production of fuels and chemicals. Notably, the microbial production of chemicals, called microbial electrosynthesis, provides a highly attractive, novel route for the generation of valuable products from electricity or even wastewater. This Review addresses the principles, challenges and opportunities of microbial electrosynthesis, an exciting new discipline at the nexus of microbiology and electrochemistry.
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              Nanowire-bacteria hybrids for unassisted solar carbon dioxide fixation to value-added chemicals.

              Direct solar-powered production of value-added chemicals from CO2 and H2O, a process that mimics natural photosynthesis, is of fundamental and practical interest. In natural photosynthesis, CO2 is first reduced to common biochemical building blocks using solar energy, which are subsequently used for the synthesis of the complex mixture of molecular products that form biomass. Here we report an artificial photosynthetic scheme that functions via a similar two-step process by developing a biocompatible light-capturing nanowire array that enables a direct interface with microbial systems. As a proof of principle, we demonstrate that a hybrid semiconductor nanowire-bacteria system can reduce CO2 at neutral pH to a wide array of chemical targets, such as fuels, polymers, and complex pharmaceutical precursors, using only solar energy input. The high-surface-area silicon nanowire array harvests light energy to provide reducing equivalents to the anaerobic bacterium, Sporomusa ovata, for the photoelectrochemical production of acetic acid under aerobic conditions (21% O2) with low overpotential (η < 200 mV), high Faradaic efficiency (up to 90%), and long-term stability (up to 200 h). The resulting acetate (∼6 g/L) can be activated to acetyl coenzyme A (acetyl-CoA) by genetically engineered Escherichia coli and used as a building block for a variety of value-added chemicals, such as n-butanol, polyhydroxybutyrate (PHB) polymer, and three different isoprenoid natural products. As such, interfacing biocompatible solid-state nanodevices with living systems provides a starting point for developing a programmable system of chemical synthesis entirely powered by sunlight.
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                Author and article information

                Contributors
                Journal
                Front Microbiol
                Front Microbiol
                Front. Microbiol.
                Frontiers in Microbiology
                Frontiers Media S.A.
                1664-302X
                14 August 2019
                2019
                : 10
                : 1817
                Affiliations
                [1] 1Department of Chemistry and Biochemistry, Utah State University , Logan, UT, United States
                [2] 2Department of Biological Sciences, Idaho State University , Pocatello, ID, United States
                [3] 3Department of Plant, Soils and Climate, Utah State University , Logan, UT, United States
                [4] 4Department of Biology, Southern Methodist University , Dallas, TX, United States
                Author notes

                Edited by: Martin G. Klotz, Washington State University, United States

                Reviewed by: Kathleen Scott, University of South Florida, United States; Jeffrey A. Gralnick, University of Minnesota, Twin Cities, United States

                *Correspondence: Lance C. Seefeldt, lance.seefeldt@ 123456usu.edu

                This article was submitted to Microbial Physiology and Metabolism, a section of the journal Frontiers in Microbiology

                Article
                10.3389/fmicb.2019.01817
                6705187
                31474945
                453ea38c-3483-41ba-8378-23b883589d07
                Copyright © 2019 Soundararajan, Ledbetter, Kusuma, Zhen, Ludden, Bugbee, Ensign and Seefeldt.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 20 December 2018
                : 23 July 2019
                Page count
                Figures: 6, Tables: 0, Equations: 3, References: 26, Pages: 9, Words: 0
                Funding
                Funded by: National Aeronautics and Space Administration 10.13039/100000104
                Award ID: NNX17AJ31G/NNH16ZOA001N-16STRII_B3
                Categories
                Microbiology
                Original Research

                Microbiology & Virology
                microbial electrocatalysis,in situ fertilizer,bioelectrochemical nitrogen reduction,haber–bosch,bioelectrosynthesis,bioelectrochemical carbon dioxide reduction

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