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      Unintended Laboratory-Driven Evolution Reveals Genetic Requirements for Biofilm Formation by Desulfovibrio vulgaris Hildenborough

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          ABSTRACT

          Biofilms of sulfate-reducing bacteria (SRB) are of particular interest as members of this group are culprits in corrosion of industrial metal and concrete pipelines as well as being key players in subsurface metal cycling. Yet the mechanism of biofilm formation by these bacteria has not been determined. Here we show that two supposedly identical wild-type cultures of the SRB Desulfovibrio vulgaris Hildenborough maintained in different laboratories have diverged in biofilm formation. From genome resequencing and subsequent mutant analyses, we discovered that a single nucleotide change within DVU1017, the ABC transporter of a type I secretion system (T1SS), was sufficient to eliminate biofilm formation in D. vulgaris Hildenborough. Two T1SS cargo proteins were identified as likely biofilm structural proteins, and the presence of at least one (with either being sufficient) was shown to be required for biofilm formation. Antibodies specific to these biofilm structural proteins confirmed that DVU1017, and thus the T1SS, is essential for localization of these adhesion proteins on the cell surface. We propose that DVU1017 is a member of the lapB category of microbial surface proteins because of its phenotypic similarity to the adhesin export system described for biofilm formation in the environmental pseudomonads. These findings have led to the identification of two functions required for biofilm formation in D. vulgaris Hildenborough and focus attention on the importance of monitoring laboratory-driven evolution, as phenotypes as fundamental as biofilm formation can be altered.

          IMPORTANCE

          The growth of bacteria attached to a surface (i.e., biofilm), specifically biofilms of sulfate-reducing bacteria, has a profound impact on the economy of developed nations due to steel and concrete corrosion in industrial pipelines and processing facilities. Furthermore, the presence of sulfate-reducing bacteria in oil wells causes oil souring from sulfide production, resulting in product loss, a health hazard to workers, and ultimately abandonment of wells. Identification of the required genes is a critical step for determining the mechanism of biofilm formation by sulfate reducers. Here, the transporter by which putative biofilm structural proteins are exported from sulfate-reducing Desulfovibrio vulgaris Hildenborough cells was discovered, and a single nucleotide change within the gene coding for this transporter was found to be sufficient to completely stop formation of biofilm.

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          Scalable web services for the PSIPRED Protein Analysis Workbench

          Here, we present the new UCL Bioinformatics Group’s PSIPRED Protein Analysis Workbench. The Workbench unites all of our previously available analysis methods into a single web-based framework. The new web portal provides a greatly streamlined user interface with a number of new features to allow users to better explore their results. We offer a number of additional services to enable computationally scalable execution of our prediction methods; these include SOAP and XML-RPC web server access and new HADOOP packages. All software and services are available via the UCL Bioinformatics Group website at http://bioinf.cs.ucl.ac.uk/.
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            Harnessing homologous recombination in vitro to generate recombinant DNA via SLIC.

            We describe a new cloning method, sequence and ligation-independent cloning (SLIC), which allows the assembly of multiple DNA fragments in a single reaction using in vitro homologous recombination and single-strand annealing. SLIC mimics in vivo homologous recombination by relying on exonuclease-generated ssDNA overhangs in insert and vector fragments, and the assembly of these fragments by recombination in vitro. SLIC inserts can also be prepared by incomplete PCR (iPCR) or mixed PCR. SLIC allows efficient and reproducible assembly of recombinant DNA with as many as 5 and 10 fragments simultaneously. SLIC circumvents the sequence requirements of traditional methods and functions much more efficiently at very low DNA concentrations when combined with RecA to catalyze homologous recombination. This flexibility allows much greater versatility in the generation of recombinant DNA for the purposes of synthetic biology.
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              Complete genome sequence and comparative analysis of the metabolically versatile Pseudomonas putida KT2440.

              Pseudomonas putida is a metabolically versatile saprophytic soil bacterium that has been certified as a biosafety host for the cloning of foreign genes. The bacterium also has considerable potential for biotechnological applications. Sequence analysis of the 6.18 Mb genome of strain KT2440 reveals diverse transport and metabolic systems. Although there is a high level of genome conservation with the pathogenic Pseudomonad Pseudomonas aeruginosa (85% of the predicted coding regions are shared), key virulence factors including exotoxin A and type III secretion systems are absent. Analysis of the genome gives insight into the non-pathogenic nature of P. putida and points to potential new applications in agriculture, biocatalysis, bioremediation and bioplastic production.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                mBio
                MBio
                mbio
                mbio
                mBio
                mBio
                American Society for Microbiology (1752 N St., N.W., Washington, DC )
                2150-7511
                17 October 2017
                Sep-Oct 2017
                : 8
                : 5
                : e01696-17
                Affiliations
                [a ]Department of Biochemistry, University of Missouri, Columbia, Missouri, USA
                [b ]Environmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, Berkeley, California, USA
                [c ]Department of Microbiology and Immunology, Montana State University, Bozeman, Montana, USA
                [d ]Center for Biofilm Engineering, Montana State University, Bozeman, Montana, USA
                [e ]Department of Bioengineering, University of California, Berkeley, California, USA
                [f ]Molecular Biophysics and Integrated Bioimaging Division, Lawrence Berkeley National Laboratory, Berkeley, California, USA
                University of Washington
                Author notes
                Address correspondence to Judy D. Wall, wallj@ 123456missouri.edu .

                This article is a direct contribution from a Fellow of the American Academy of Microbiology. Solicited external reviewers: Alfred Spormann, Stanford University; Steven Finkel, University of Southern California.

                Author information
                http://orcid.org/0000-0002-2499-5650
                http://orcid.org/0000-0002-3357-3097
                http://orcid.org/0000-0001-7405-902X
                http://orcid.org/0000-0001-9053-1849
                Article
                mBio01696-17
                10.1128/mBio.01696-17
                5646257
                29042504
                657bec5b-feaf-4ecf-b7b5-d845c3a59da8
                Copyright © 2017 De León et al.

                This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license.

                History
                : 14 September 2017
                : 18 September 2017
                Page count
                supplementary-material: 4, Figures: 6, Tables: 2, Equations: 0, References: 43, Pages: 16, Words: 10372
                Funding
                Funded by: U.S. Department of Energy (DOE) https://doi.org/10.13039/100000015
                Award ID: DE-AC02-05CH11231
                Award Recipient : Kara B. De Leon Award Recipient : Grant M. Zane Award Recipient : Valentine V. Trotter Award Recipient : Gregory P. Krantz Award Recipient : Adam P. Arkin Award Recipient : Gareth P. Butland Award Recipient : Peter J. Walian Award Recipient : Matthew W. Fields Award Recipient : Judy D. Wall
                Funded by: University of Missouri (MU) https://doi.org/10.13039/100007165
                Award Recipient : Kara B De Leon
                Categories
                Research Article
                Custom metadata
                September/October 2017

                Life sciences
                desulfovibrio vulgaris,biofilms,genetic polymorphisms,secretion systems,sulfate reduction

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