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      Structure and mechanism of a Hypr GGDEF enzyme that activates cGAMP signaling to control extracellular metal respiration

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          Abstract

          A newfound signaling pathway employs a GGDEF enzyme with unique activity compared to the majority of homologs associated with bacterial cyclic di-GMP signaling. This system provides a rare opportunity to study how signaling proteins natively gain distinct function. Using genetic knockouts, riboswitch reporters, and RNA-Seq, we show that GacA, the Hypr GGDEF in Geobacter sulfurreducens, specifically regulates cyclic GMP-AMP (3′,3′-cGAMP) levels in vivo to stimulate gene expression associated with metal reduction separate from electricity production. To reconcile these in vivo findings with prior in vitro results that showed GacA was promiscuous, we developed a full kinetic model combining experimental data and mathematical modeling to reveal mechanisms that contribute to in vivo specificity. A 1.4 Å-resolution crystal structure of the Geobacter Hypr GGDEF domain was determined to understand the molecular basis for those mechanisms, including key cross-dimer interactions. Together these results demonstrate that specific signaling can result from a promiscuous enzyme.

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          Microscopic organisms known as bacteria are found in virtually every environment on the planet. One reason bacteria are so successful is that they are able to form communities known as biofilms on surfaces in animals and other living things, as well as on rocks and other features in the environment. These biofilms protect the bacteria from fluctuations in the environment and toxins.

          For over 30 years, a class of enzymes called the GGDEF enzymes were thought to make a single signal known as cyclic di-GMP that regulates the formation of biofilms. However, in 2016, a team of researchers reported that some GGDEF enzymes, including one from a bacterium called Geobacter sulfurreducens, were also able to produce two other signals known as cGAMP and cyclic di-AMP. The experiments involved making the enzymes and testing their activity outside the cell. Therefore, it remained unclear whether these enzymes (dubbed ‘Hypr’ GGDEF enzymes) actually produce all three signals inside cells and play a role in forming bacterial biofilms.

          G. sulfurreducens is unusual because it is able to grow on metallic minerals or electrodes to generate electrical energy. As part of a community of microorganisms, they help break down pollutants in contaminated areas and can generate electricity from wastewater. Now, Hallberg, Chan et al. – including many of the researchers involved in the 2016 work – combined several experimental and mathematical approaches to study the Hypr GGDEF enzymes in G. sulfurreducens.

          The experiments show that the Hypr GGDEF enzymes produced cGAMP, but not the other two signals, inside the cells. This cGAMP regulated the ability of G. sulfurreducens to grow by extracting electrical energy from the metallic minerals, which appears to be a new, biofilm-less lifestyle. Further experiments revealed how Hypr GGDEF enzymes have evolved to preferentially make cGAMP over the other two signals.

          Together, these findings demonstrate that enzymes with the ability to make several different signals, are capable of generating specific responses in bacterial cells. By understanding how bacteria make decisions, it may be possible to change their behaviors. The findings of Hallberg, Chan et al. help to identify the signaling pathways involved in this decision-making and provide new tools to study them in the future.

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          Most cited references50

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          Conversion of wastes into bioelectricity and chemicals by using microbial electrochemical technologies.

          Waste biomass is a cheap and relatively abundant source of electrons for microbes capable of producing electrical current outside the cell. Rapidly developing microbial electrochemical technologies, such as microbial fuel cells, are part of a diverse platform of future sustainable energy and chemical production technologies. We review the key advances that will enable the use of exoelectrogenic microorganisms to generate biofuels, hydrogen gas, methane, and other valuable inorganic and organic chemicals. Moreover, we examine the key challenges for implementing these systems and compare them to similar renewable energy technologies. Although commercial development is already underway in several different applications, ranging from wastewater treatment to industrial chemical production, further research is needed regarding efficiency, scalability, system lifetimes, and reliability.
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            Electricity Production by Geobacter sulfurreducens Attached to Electrodes

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              Evolution of two-component signal transduction systems.

              To exist in a wide range of environmental niches, bacteria must sense and respond to a variety of external signals. A primary means by which this occurs is through two-component signal transduction pathways, typically composed of a sensor histidine kinase that receives the input stimuli and then phosphorylates a response regulator that effects an appropriate change in cellular physiology. Histidine kinases and response regulators have an intrinsic modularity that separates signal input, phosphotransfer, and output response; this modularity has allowed bacteria to dramatically expand and diversify their signaling capabilities. Recent work has begun to reveal the molecular basis by which two-component proteins evolve. How and why do orthologous signaling proteins diverge? How do cells gain new pathways and recognize new signals? What changes are needed to insulate a new pathway from existing pathways? What constraints are there on gene duplication and lateral gene transfer? Here, we review progress made in answering these questions, highlighting how the integration of genome sequence data with experimental studies is providing major new insights.
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                Author and article information

                Contributors
                Role: Reviewing Editor
                Role: Senior Editor
                Journal
                eLife
                Elife
                eLife
                eLife
                eLife Sciences Publications, Ltd
                2050-084X
                09 April 2019
                2019
                : 8
                : e43959
                Affiliations
                [1 ]deptDepartment of Chemistry University of California, Berkeley BerkeleyUnited States
                [2 ]deptDepartment of Plant and Microbial Biology and BioTechnology Institute University of Minnesota MinnesotaUnited States
                [3 ]deptDepartment of Microbiology and Immunobiology Harvard Medical School BostonUnited States
                [4 ]deptDepartment of Cancer Immunology and Virology Dana-Farber Cancer Institute BostonUnited States
                [5 ]Parker Institute for Cancer Immunotherapy at Dana-Farber Cancer Institute BostonUnited States
                [6 ]deptBiophysics Graduate Group University of California, Berkeley BerkeleyUnited States
                [7 ]deptDepartment of Molecular & Cell Biology University of California, Berkeley BerkeleyUnited States
                [8 ]deptDepartment of Chemistry University of Utah Salt Lake CityUnited States
                Dartmouth College United States
                National Institute of Child Health and Human Development United States
                Dartmouth College United States
                John Innes Centre/University of East Anglia United Kingdom
                Author notes
                [‡]

                Department of Plant and Microbial Biology, University of California, Berkeley, Berkeley, United States.

                [§]

                Innovative Genomics Institute, University of California, Berkeley, Berkeley, United States.

                [#]

                Henry Eyring Center for Cell & Genome Science, University of Utah, Salt Lake City, United States.

                [¶]

                Department of Chemistry, University of Utah, Salt Lake City, United States.

                8 Department of Plant and Microbial Biology, University of California, Berkeley, CA 94720, USA.

                [†]

                These authors contributed equally to this work.

                Author information
                http://orcid.org/0000-0002-6596-3436
                https://orcid.org/0000-0001-8083-7107
                http://orcid.org/0000-0003-2666-4764
                Article
                43959
                10.7554/eLife.43959
                6456294
                30964001
                af2d79d5-568b-48fa-b4a2-802cb30c0a7b
                © 2019, Hallberg et al

                This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.

                History
                : 27 November 2018
                : 12 March 2019
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100000001, National Science Foundation;
                Award ID: 1716256
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100000006, Office of Naval Research;
                Award ID: N000141612194
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100000002, National Institutes of Health;
                Award ID: R01 GM124589
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100000001, National Science Foundation;
                Award ID: 1714196
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100000001, National Science Foundation;
                Award ID: 1915466
                Award Recipient :
                The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
                Categories
                Research Article
                Biochemistry and Chemical Biology
                Microbiology and Infectious Disease
                Custom metadata
                A newfound signaling enzyme that diverged from a protein family ubiquitous in bacteria provides mechanistic insights into how new signaling activity emerges to control distinct cellular function and physiology.

                Life sciences
                geobacter sulfurreducens,cgamp signaling,cyclic dinucleotide,hypr ggdef,riboswitch,cyclic di-gmp,e. coli,other

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