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      Putative Nitrogen-Fixing Bacteria Associated With the Rhizosphere and Root Endosphere of Wheat Plants Grown in an Andisol From Southern Chile

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          Abstract

          Acidic ash derived volcanic soils (Andisols) support 50% of cereal production in Chile. Nitrogen (N) is essential for cereal crops and commonly added as urea with consequent environmental concerns due to leaching. Despite the relevance of N to plant growth, few studies have focused on understanding the application, management and ecological role of N 2-fixing bacterial populations as tool for improve the N nutrition of cereal crops in Chile. It is known that N 2-fixing bacteria commonly inhabits diverse plant compartments (e.g., rhizosphere and root endosphere) where they can supply N for plant growth. Here, we used culture-independent and dependent approaches to characterize and compare the putative N 2-fixing bacteria associated with the rhizosphere and root endosphere of wheat plants grown in an Andisol from southern Chile. Our results showed significantly greater bacterial loads in the rhizosphere than the root endosphere. Quantitative PCR results indicated that the copy number of the 16S rRNA gene ranged from 10 12~10 13 and 10 7~10 8 g −1 sample in rhizosphere and root endosphere, respectively. The nifH gene copy number ranged from 10 5~10 6 and 10 5 g −1 sample in rhizosphere and root endosphere, respectively. The total culturable bacteria number ranged from 10 9~10 10 and 10 7~10 8 CFU g −1 sample in rhizosphere and 10 4~10 5 and 10 4 CFU g −1 sample in root endosphere using LB and NM-1 media, respectively. Indirect counts of putative N 2-fixing bacteria were 10 3 and 10 2~10 3 CFU g −1 sample in rhizosphere and root endosphere using NFb medium, respectively. Sequencing of 16S rRNA genes from randomly selected putative N 2-fixing bacteria revealed the presence of members of Proteobacteria ( Bosea and Roseomonas), Actinobacteria ( Georgenia, Mycobacterium, Microbacterium, Leifsonia, and Arthrobacter), Bacteroidetes ( Chitinophaga) and Firmicutes ( Bacillus and Psychrobacillus) taxa. Differences in 16S rRNA and putative nifH-containing bacterial communities between rhizosphere and root endosphere were shown by denaturing gradient gel electrophoresis (DGGE). This study shows a compartmentalization between rhizosphere and root endosphere for both the abundance and diversity of total (16S rRNA) and putative N 2-fixing bacterial communities on wheat plants grown in Chilean Andisols. This information can be relevant for the design and application of agronomic strategies to enhance sustainable N-utilization in cereal crops in Chile.

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          Distribution of repetitive DNA sequences in eubacteria and application to fingerprinting of bacterial genomes.

          Dispersed repetitive DNA sequences have been described recently in eubacteria. To assess the distribution and evolutionary conservation of two distinct prokaryotic repetitive elements, consensus oligonucleotides were used in polymerase chain reaction [PCR] amplification and slot blot hybridization experiments with genomic DNA from diverse eubacterial species. Oligonucleotides matching Repetitive Extragenic Palindromic [REP] elements and Enterobacterial Repetitive Intergenic Consensus [ERIC] sequences were synthesized and tested as opposing PCR primers in the amplification of eubacterial genomic DNA. REP and ERIC consensus oligonucleotides produced clearly resolvable bands by agarose gel electrophoresis following PCR amplification. These band patterns provided unambiguous DNA fingerprints of different eubacterial species and strains. Both REP and ERIC probes hybridized preferentially to genomic DNA from Gram-negative enteric bacteria and related species. Widespread distribution of these repetitive DNA elements in the genomes of various microorganisms should enable rapid identification of bacterial species and strains, and be useful for the analysis of prokaryotic genomes.
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            Unraveling the plant microbiome: looking back and future perspectives

            Most eukaryotes develop close interactions with microorganisms that are essential for their performance and survival. Thus, eukaryotes and prokaryotes in nature can be considered as meta-organisms or holobionts. Consequently, microorganisms that colonize different plant compartments contain the plant’s second genome. In this respect, many studies in the last decades have shown that plant-microbe interactions are not only crucial for better understanding plant growth and health, but also for sustainable crop production in a changing world. This mini-review acting as editorial presents retrospectives and future perspectives for plant microbiome studies as well as information gaps in this emerging research field. In addition, the contribution of this research topic to the solution of various issues is discussed.
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              Improved culturability of soil bacteria and isolation in pure culture of novel members of the divisions Acidobacteria, Actinobacteria, Proteobacteria, and Verrucomicrobia.

              The culturability of bacteria in the bulk soil of an Australian pasture was investigated by using nutrient broth at 1/100 of its normal concentration (dilute nutrient broth [DNB]) as the growth medium. Three-tube most-probable-number serial dilution culture resulted in a mean viable count that was only 1.4% of the mean microscopically determined total cell count. Plate counts with DNB solidified with agar and with gellan gum resulted in viable counts that were 5.2 and 7.5% of the mean microscopically determined total cell count, respectively. Prior homogenization of the soil sample with an ultrasonic probe increased the viable count obtained by using DNB solidified with gellan gum to 14.1% of the mean microscopically determined cell count. A microscopic examination of the cell aggregates that remained after sonication revealed that the potential CFU count was only 70.4% of the total cell count, due to cells occurring as pairs or in clumps of three or more cells. Staining with SYTO 9 plus propidium iodide indicated that 91.3% of the cells in sonicated soil samples were potentially viable. Together, these findings suggest that the maximum achievable CFU count may be as low as 64.3% of the total cell count. Thirty isolates obtained from plate counting experiments performed with DNB as the growth medium were identified by comparative analysis of partial 16S rRNA gene sequences. A large proportion of these isolates represent the first known isolates of globally distributed groups of soil bacteria belonging to novel lineages within the divisions Actinobacteria, Acidobacteria, Proteobacteria, and Verrucomicrobia.
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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
                20 November 2018
                2018
                : 9
                : 2710
                Affiliations
                [1] 1Applied Microbial Ecology Laboratory, Departamento de Ciencias Químicas y Recursos Naturales, Universidad de La Frontera , Temuco, Chile
                [2] 2Center of Plant, Soil Interaction and Natural Resources Biotechnology, Scientific and Technological Bioresource Nucleus (BIOREN), Universidad de La Frontera , Temuco, Chile
                [3] 3Programa de Doctorado en Ciencias de Recursos Naturales, Universidad de La Frontera , Temuco, Chile
                [4] 4Department of Soil, Water, and Climate, Department of Plant and Microbial Biology, BioTechnology Institute, University of Minnesota , Saint Paul, MN, United States
                Author notes

                Edited by: Benjamin Gourion, Plant Interactions Laboratory Microorganisms (LIPM), France

                Reviewed by: Andrzej Tkacz, University of Oxford, United Kingdom; Feth-el-zahar Haichar, Microbial Ecology, France

                *Correspondence: Milko A. Jorquera milko.jorquera@ 123456ufrontera.cl

                This article was submitted to Plant Microbe Interactions, a section of the journal Frontiers in Microbiology

                Article
                10.3389/fmicb.2018.02710
                6256256
                30524385
                9907f8b7-b608-481c-8a10-ce7d1103ceb8
                Copyright © 2018 Rilling, Acuña, Sadowsky and Jorquera.

                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
                : 26 June 2018
                : 23 October 2018
                Page count
                Figures: 4, Tables: 3, Equations: 0, References: 70, Pages: 13, Words: 9080
                Funding
                Funded by: Consejo Nacional de Innovación, Ciencia y Tecnología 10.13039/501100009068
                Funded by: Fondo Nacional de Desarrollo Científico y Tecnológico 10.13039/501100002850
                Categories
                Microbiology
                Original Research

                Microbiology & Virology
                andisol,root endosphere,n2-fixing bacteria,rhizosphere,wheat
                Microbiology & Virology
                andisol, root endosphere, n2-fixing bacteria, rhizosphere, wheat

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