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      Comparative genomics of the Komagataeibacter strains—Efficient bionanocellulose producers

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          Abstract

          Komagataeibacter species are well‐recognized bionanocellulose ( BNC) producers. This bacterial genus, formerly assigned to Gluconacetobacter, is known for its phenotypic diversity manifested by strain‐dependent carbon source preference, BNC production rate, pellicle structure, and strain stability. Here, we performed a comparative study of nineteen Komagataeibacter genomes, three of which were newly contributed in this work. We defined the core genome of the genus, clarified phylogenetic relationships among strains, and provided genetic evidence for the distinction between the two major clades, the Kxylinus and the K. hansenii. We found genomic traits, which likely contribute to the phenotypic diversity between the Komagataeibacter strains. These features include genome flexibility, carbohydrate uptake and regulation of its metabolism, exopolysaccharides synthesis, and the c‐di‐ GMP signaling network. In addition, this work provides a comprehensive functional annotation of carbohydrate metabolism pathways, such as those related to glucose, glycerol, acetan, levan, and cellulose. Findings of this multi‐genomic study expand understanding of the genetic variation within the Komagataeibacter genus and facilitate exploiting of its full potential for bionanocellulose production at the industrial scale.

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          Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing

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            Bacterial Extracellular Polysaccharides in Biofilm Formation and Function.

            Microbes produce a biofilm matrix consisting of proteins, extracellular DNA, and polysaccharides that is integral in the formation of bacterial communities. Historical studies of polysaccharides revealed that their overproduction often alters the colony morphology and can be diagnostic in identifying certain species. The polysaccharide component of the matrix can provide many diverse benefits to the cells in the biofilm, including adhesion, protection, and structure. Aggregative polysaccharides act as molecular glue, allowing the bacterial cells to adhere to each other as well as surfaces. Adhesion facilitates the colonization of both biotic and abiotic surfaces by allowing the bacteria to resist physical stresses imposed by fluid movement that could separate the cells from a nutrient source. Polysaccharides can also provide protection from a wide range of stresses, such as desiccation, immune effectors, and predators such as phagocytic cells and amoebae. Finally, polysaccharides can provide structure to biofilms, allowing stratification of the bacterial community and establishing gradients of nutrients and waste products. This can be advantageous for the bacteria by establishing a heterogeneous population that is prepared to endure stresses created by the rapidly changing environments that many bacteria encounter. The diverse range of polysaccharide structures, properties, and roles highlight the importance of this matrix constituent to the successful adaptation of bacteria to nearly every niche. Here, we present an overview of the current knowledge regarding the diversity and benefits that polysaccharide production provides to bacterial communities within biofilms.
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              Synthesis of cellulose by Acetobacter xylinum. II. Preparation of freeze-dried cells capable of polymerizing glucose to cellulose.

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                Author and article information

                Contributors
                malgorzata.ryngajllo@p.lodz.pl
                Journal
                Microbiologyopen
                Microbiologyopen
                10.1002/(ISSN)2045-8827
                MBO3
                MicrobiologyOpen
                John Wiley and Sons Inc. (Hoboken )
                2045-8827
                26 October 2018
                May 2019
                : 8
                : 5 ( doiID: 10.1002/mbo3.2019.8.issue-5 )
                : e00731
                Affiliations
                [ 1 ] Institute of Technical Biochemistry Lodz University of Technology Lodz Poland
                Author notes
                [*] [* ] Correspondence

                Małgorzata Ryngajłło, Institute of Technical Biochemistry, Lodz University of Technology, Lodz, Poland.

                Email: malgorzata.ryngajllo@ 123456p.lodz.pl

                Author information
                http://orcid.org/0000-0002-0430-0102
                Article
                MBO3731
                10.1002/mbo3.731
                6528568
                30365246
                e73b7c84-1fd9-4674-8ac4-2d2b3845a3e6
                © 2018 The Authors. MicrobiologyOpen published by John Wiley & Sons Ltd.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 06 June 2018
                : 13 August 2018
                : 21 August 2018
                Page count
                Figures: 7, Tables: 1, Pages: 25, Words: 17264
                Categories
                Original Article
                Original Articles
                Custom metadata
                2.0
                mbo3731
                May 2019
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.6.3 mode:remove_FC converted:21.05.2019

                Microbiology & Virology
                bacterial cellulose,c‐di‐gmp network,comparative genomics,exopolysaccharides,genome flexibility,komagataeibacter

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