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      Recent Understanding of Soil Acidobacteria and Their Ecological Significance: A Critical Review

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          Abstract

          Acidobacteria represents an underrepresented soil bacterial phylum whose members are pervasive and copiously distributed across nearly all ecosystems. Acidobacterial sequences are abundant in soils and represent a significant fraction of soil microbial community. Being recalcitrant and difficult-to-cultivate under laboratory conditions, holistic, polyphasic approaches are required to study these refractive bacteria extensively. Acidobacteria possesses an inventory of genes involved in diverse metabolic pathways, as evidenced by their pan-genomic profiles. Because of their preponderance and ubiquity in the soil, speculations have been made regarding their dynamic roles in vital ecological processes viz., regulation of biogeochemical cycles, decomposition of biopolymers, exopolysaccharide secretion, and plant growth promotion. These bacteria are expected to have genes that might help in survival and competitive colonization in the rhizosphere, leading to the establishment of beneficial relationships with plants. Exploration of these genetic attributes and more in-depth insights into the belowground mechanics and dynamics would lead to a better understanding of the functions and ecological significance of this enigmatic phylum in the soil-plant environment. This review is an effort to provide a recent update into the diversity of genes in Acidobacteria useful for characterization, understanding ecological roles, and future biotechnological perspectives.

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          Most cited references136

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          dbCAN2: a meta server for automated carbohydrate-active enzyme annotation

          Abstract Complex carbohydrates of plants are the main food sources of animals and microbes, and serve as promising renewable feedstock for biofuel and biomaterial production. Carbohydrate active enzymes (CAZymes) are the most important enzymes for complex carbohydrate metabolism. With an increasing number of plant and plant-associated microbial genomes and metagenomes being sequenced, there is an urgent need of automatic tools for genomic data mining of CAZymes. We developed the dbCAN web server in 2012 to provide a public service for automated CAZyme annotation for newly sequenced genomes. Here, dbCAN2 (http://cys.bios.niu.edu/dbCAN2) is presented as an updated meta server, which integrates three state-of-the-art tools for CAZome (all CAZymes of a genome) annotation: (i) HMMER search against the dbCAN HMM (hidden Markov model) database; (ii) DIAMOND search against the CAZy pre-annotated CAZyme sequence database and (iii) Hotpep search against the conserved CAZyme short peptide database. Combining the three outputs and removing CAZymes found by only one tool can significantly improve the CAZome annotation accuracy. In addition, dbCAN2 now also accepts nucleotide sequence submission, and offers the service to predict physically linked CAZyme gene clusters (CGCs), which will be a very useful online tool for identifying putative polysaccharide utilization loci (PULs) in microbial genomes or metagenomes.
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            Community structure and metabolism through reconstruction of microbial genomes from the environment.

            Microbial communities are vital in the functioning of all ecosystems; however, most microorganisms are uncultivated, and their roles in natural systems are unclear. Here, using random shotgun sequencing of DNA from a natural acidophilic biofilm, we report reconstruction of near-complete genomes of Leptospirillum group II and Ferroplasma type II, and partial recovery of three other genomes. This was possible because the biofilm was dominated by a small number of species populations and the frequency of genomic rearrangements and gene insertions or deletions was relatively low. Because each sequence read came from a different individual, we could determine that single-nucleotide polymorphisms are the predominant form of heterogeneity at the strain level. The Leptospirillum group II genome had remarkably few nucleotide polymorphisms, despite the existence of low-abundance variants. The Ferroplasma type II genome seems to be a composite from three ancestral strains that have undergone homologous recombination to form a large population of mosaic genomes. Analysis of the gene complement for each organism revealed the pathways for carbon and nitrogen fixation and energy generation, and provided insights into survival strategies in an extreme environment.
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              Structure and functions of the bacterial microbiota of plants.

              Plants host distinct bacterial communities on and inside various plant organs, of which those associated with roots and the leaf surface are best characterized. The phylogenetic composition of these communities is defined by relatively few bacterial phyla, including Actinobacteria, Bacteroidetes, Firmicutes, and Proteobacteria. A synthesis of available data suggests a two-step selection process by which the bacterial microbiota of roots is differentiated from the surrounding soil biome. Rhizodeposition appears to fuel an initial substrate-driven community shift in the rhizosphere, which converges with host genotype-dependent fine-tuning of microbiota profiles in the selection of root endophyte assemblages. Substrate-driven selection also underlies the establishment of phyllosphere communities but takes place solely at the immediate leaf surface. Both the leaf and root microbiota contain bacteria that provide indirect pathogen protection, but root microbiota members appear to serve additional host functions through the acquisition of nutrients from soil for plant growth. Thus, the plant microbiota emerges as a fundamental trait that includes mutualism enabled through diverse biochemical mechanisms, as revealed by studies on plant growth-promoting and plant health-promoting bacteria.
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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
                30 October 2020
                2020
                : 11
                : 580024
                Affiliations
                [1] 1Department of Biochemistry, St. Ann’s College for Women , Hyderabad, India
                [2] 2Department of Plant Sciences, School of Life Sciences, University of Hyderabad , Hyderabad, India
                [3] 3Department of Agricultural Microbiology, Aligarh Muslim University , Aligarh, India
                [4] 4Department of Microbiology, PSGVP Mandal’s, Arts, Science and Commerce College , Shahada, India
                [5] 5Institute of Bioproduct Development, Universiti Teknologi Malaysia (UTM) , Skudai, Malaysia
                [6] 6School of Chemical and Energy Engineering, Faculty of Engineering, Universiti Teknologi Malaysia (UTM) , Skudai, Malaysia
                [7] 7City of Scientific Research and Technological Applications , New Borg El-Arab, Egypt
                [8] 8Biology Department, Faculty of Mathematics and Natural Science, Udayana University , Bali, Indonesia
                Author notes

                Edited by: Byung-Kwan Cho, Korea Advanced Institute of Science and Technology, South Korea

                Reviewed by: Vasvi Chaudhry, University of Tübingen, Germany; Sheree J. Finley, Alabama State University, United States; Namil Lee, Korea Advanced Institute of Science and Technology, South Korea

                *Correspondence: Iqbal Ahmad, ahmadiqbal8@ 123456yahoo.co.in

                These authors have contributed equally to this work and share first authorship

                These authors have contributed equally to this work

                This article was submitted to Systems Microbiology, a section of the journal Frontiers in Microbiology

                Article
                10.3389/fmicb.2020.580024
                7661733
                33193209
                0c714827-4c23-452c-abbe-221463d45002
                Copyright © 2020 Kalam, Basu, Ahmad, Sayyed, El-Enshasy, Dailin and Suriani.

                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
                : 04 July 2020
                : 08 October 2020
                Page count
                Figures: 3, Tables: 2, Equations: 0, References: 136, Pages: 15, Words: 0
                Funding
                Funded by: Ministry of Higher Education, Malaysia 10.13039/501100003093
                Funded by: University Grants Commission 10.13039/501100001501
                Categories
                Microbiology
                Review

                Microbiology & Virology
                acidobacteria,biogeochemical cycles,ecological roles,metagenomics,molecular characterization,plant growth-promoting activities,soil

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