The Microbiology of Lean and Obese Soil

Total Page:16

File Type:pdf, Size:1020Kb

The Microbiology of Lean and Obese Soil The microbiology of lean and obese soil Frances Patricia Jones September 2016 Department of Geography and Environmental Science, University of Reading, UK Department of AgroEcology, Rothamsted Research, UK Submitted in partial fulfilment of the requirement for the degree of Doctor of Philosophy Abstract The bacterial genus Bradyrhizobium is biologically important within soils, with different representatives found to perform a range of functions including nitrogen fixation through symbioses, photosynthesis and denitrification. The Highfield experiment at Rothamsted provides an opportunity to study the impact of plants on microbial communities as it has three long-term contrasting regimes; permanent grassland, arable and bare fallow (devoid of plants). The bare fallow plots have a significant reduction in soil carbon and microbial biomass. Bradyrhizobium has been shown by metagenomic studies on soil to be one of the most abundant and active groups including in bare fallow soil indicating that some phenotypes are adapted to survive in the absence of plants. A culture collection was created with isolates obtained from contrasting soil types from Highfield in addition to woodland soil, gorse (Ulex europeaus) and broom (Cytisus scoparius) root nodules. The collection’s phylogeny has been explored by sequencing housekeeping genes to determine whether soil treatment affects the core genome. One grassland and one bare fallow isolate had their genome sequenced and differences have been assessed to establish their potential for a range of functions and to direct future experiments. The functional diversity of the collection has been investigated using carbon metabolism assays to identify key substrates and determine whether the isolates group according to soil treatment. Symbiosis capacity and role in nitrogen cycling has been examined using nodulation tests, anaerobic growth on nitrate and nitrous oxide production and reduction through denitrification. A high level of diversity can be seen throughout the collection with differences being linked to niche adaptation. Understanding more about Bradyrhizobium could give clues on how above ground management impacts a key group within the soil community. Furthermore, the first assembled genomes of two non-symbiotic Bradyrhizobium strains isolated from soil provide an important resource for microbiology and soil ecology. i Table of contents 1 Abstract ................................................................................................................................................ i Table of contents ................................................................................................................................ ii List of tables ........................................................................................................................................ x List of figures ...................................................................................................................................... xi Abbreviation list ............................................................................................................................... xiv Statement of original authorship ..................................................................................................... xvi Acknowledgements ......................................................................................................................... xvii Dedication ...................................................................................................................................... xviii 1 Introduction ............................................................................................................................... 1 1.1 Soil microbial communities ................................................................................................ 1 1.2 Abiotic and biotic effects on soil microbial communities .................................................. 3 1.3 Plant-microbe interactions................................................................................................. 5 1.4 Soil microbial ecology and agriculture ............................................................................... 8 1.5 The Fabaceae plant family ............................................................................................... 11 1.6 Rhizobiales and the Bradyrhizobiaceae ........................................................................... 12 1.7 Nodulation ....................................................................................................................... 16 1.8 The microbial nitrogen cycle ............................................................................................ 22 1.8.1 Nitrogen fixation ...................................................................................................... 22 1.8.2 Denitrification .......................................................................................................... 22 1.9 The Highfield experiment and Bradyrhizobium ............................................................... 23 1.10 Project objectives ............................................................................................................. 25 1.10.1 Aims .......................................................................................................................... 25 2 General materials and methods ............................................................................................... 27 2.1 Culture medium ............................................................................................................... 27 2.2 Growth conditions............................................................................................................ 27 2.3 DNA extraction ................................................................................................................. 27 2.4 Polymerase chain reaction (PCR) mixture ........................................................................ 28 2.5 Agarose gel electrophoresis and PCR product purification ............................................. 28 ii 2.6 DNA sequencing and sequence analysis .......................................................................... 28 2.7 Storage of isolates ............................................................................................................ 29 3 Isolation & identification of Bradyrhizobium from soil and root nodules ............................... 30 3.1 Introduction ..................................................................................................................... 30 3.1.1 Isolation of bacteria from root nodules ................................................................... 30 3.1.2 Isolation of bacteria from soil .................................................................................. 31 3.1.3 Medium design and growth conditions ................................................................... 31 3.1.4 Key characteristics of Bradyrhizobium for the isolation method............................. 32 3.1.5 Culture medium for Bradyrhizobium isolation ......................................................... 32 3.1.6 Use of 16S rRNA gene for identification .................................................................. 33 3.1.7 Aims .......................................................................................................................... 33 3.2 Materials and methods .................................................................................................... 34 3.2.1 Description of study sites ......................................................................................... 34 3.2.2 Isolation of free-living Bradyrhizobium isolates ....................................................... 37 3.2.3 Isolation of symbiotic Bradyrhizobium isolates ....................................................... 37 3.2.4 Bradyrhizobium specific 16S primer design ............................................................. 38 3.2.5 PCR optimisation ...................................................................................................... 41 3.2.6 PCR amplification ..................................................................................................... 42 3.2.7 Reference isolates included in the culture collection .............................................. 42 3.2.8 Sequence analysis .................................................................................................... 43 3.3 Results .............................................................................................................................. 45 3.3.1 Creation of a Rothamsted Bradyrhizobium culture collection ................................. 45 3.3.2 16S sequence analysis .............................................................................................. 51 3.4 Discussion ......................................................................................................................... 55 3.4.1 Summary of the Bradyrhizobium culture collection ................................................ 55 3.4.2 Isolation method of Bradyrhizobium from soil and nodules ................................... 55 3.4.3 Importance of a culture collection ........................................................................... 56 4 Multilocus sequence analysis of the Bradyrhizobium culture collection ................................. 57 iii 4.1 Introduction ....................................................................................................................
Recommended publications
  • Nature Conservation Practical Year 2014
    Polhillia on the brink: Taxonomy, ecophysiology and conservation assessment of a highly threatened Cape legume genus by Brian du Preez Thesis presented in partial fulfilment of the requirements for the degree of Master of Science (Botany) in the Faculty of Science at Stellenbosch University Department of Botany and Zoology, University of Stellenbosch, Private Bag X1, Matieland 7602, South Africa. Supervisors: Prof. L.L. Dreyer, Prof. A.J. Valentine, Prof. M. Muasya April 2019 Stellenbosch University https://scholar.sun.ac.za DECLARATION By submitting this thesis electronically, I declare that the entirety of the work contained therein is my own, original work, that I am the sole author thereof (save to the extent explicitly otherwise stated), that reproduction and publication thereof by Stellenbosch University will not infringe any third-party rights and that I have not previously in its entirety or in part submitted it for obtaining any qualification. Date: ……15 February 2019……… Copyright ©2019 Stellenbosch University All rights reserved. i Stellenbosch University https://scholar.sun.ac.za TABLE OF CONTENTS DECLARATION....................................................................................................................... i LIST OF FIGURES ................................................................................................................ vi LIST OF TABLES ................................................................................................................... x ABSTRACT .........................................................................................................................
    [Show full text]
  • Comparative Genomics of Bradyrhizobium Japonicum CPAC
    Siqueira et al. BMC Genomics 2014, 15:420 http://www.biomedcentral.com/1471-2164/15/420 RESEARCH ARTICLE Open Access Comparative genomics of Bradyrhizobium japonicum CPAC 15 and Bradyrhizobium diazoefficiens CPAC 7: elite model strains for understanding symbiotic performance with soybean Arthur Fernandes Siqueira1,2†, Ernesto Ormeño-Orrillo3†,RangelCelsoSouza4,ElisetePainsRodrigues5, Luiz Gonzaga Paula Almeida4, Fernando Gomes Barcellos5, Jesiane Stefânia Silva Batista6, Andre Shigueyoshi Nakatani2, Esperanza Martínez-Romero3, Ana Tereza Ribeiro Vasconcelos4 and Mariangela Hungria1,2* Abstract Background: The soybean-Bradyrhizobium symbiosis can be highly efficient in fixing nitrogen, but few genomic sequences of elite inoculant strains are available. Here we contribute with information on the genomes of two commercial strains that are broadly applied to soybean crops in the tropics. B. japonicum CPAC 15 (=SEMIA 5079) is outstanding in its saprophytic capacity and competitiveness, whereas B. diazoefficiens CPAC 7 (=SEMIA 5080) is known for its high efficiency in fixing nitrogen. Both are well adapted to tropical soils. The genomes of CPAC 15 and CPAC 7 were compared to each other and also to those of B. japonicum USDA 6T and B. diazoefficiens USDA 110T. Results: Differences in genome size were found between species, with B. japonicum having larger genomes than B. diazoefficiens. Although most of the four genomes were syntenic, genome rearrangements within and between species were observed, including events in the symbiosis island. In addition to the symbiotic region, several genomic islands were identified. Altogether, these features must confer high genomic plasticity that might explain adaptation and differences in symbiotic performance. It was not possible to attribute known functions to half of the predicted genes.
    [Show full text]
  • Azorhizobium Doebereinerae Sp. Nov
    ARTICLE IN PRESS Systematic and Applied Microbiology 29 (2006) 197–206 www.elsevier.de/syapm Azorhizobium doebereinerae sp. Nov. Microsymbiont of Sesbania virgata (Caz.) Pers.$ Fa´tima Maria de Souza Moreiraa,Ã, Leonardo Cruzb,Se´rgio Miana de Fariac, Terence Marshd, Esperanza Martı´nez-Romeroe,Fa´bio de Oliveira Pedrosab, Rosa Maria Pitardc, J. Peter W. Youngf aDepto. Cieˆncia do solo, Universidade Federal de Lavras, C.P. 3037 , 37 200–000, Lavras, MG, Brazil bUniversidade Federal do Parana´, C.P. 19046, 81513-990, PR, Brazil cEmbrapa Agrobiologia, antiga estrada Rio, Sa˜o Paulo km 47, 23 851-970, Serope´dica, RJ, Brazil dCenter for Microbial Ecology, Michigan State University, MI 48824, USA eCentro de Investigacio´n sobre Fijacio´n de Nitro´geno, Universidad Nacional Auto´noma de Mexico, Apdo Postal 565-A, Cuernavaca, Mor, Me´xico fDepartment of Biology, University of York, PO Box 373, York YO10 5YW, UK Received 18 August 2005 Abstract Thirty-four rhizobium strains were isolated from root nodules of the fast-growing woody native species Sesbania virgata in different regions of southeast Brazil (Minas Gerais and Rio de Janeiro States). These isolates had cultural characteristics on YMA quite similar to Azorhizobium caulinodans (alkalinization, scant extracellular polysaccharide production, fast or intermediate growth rate). They exhibited a high similarity of phenotypic and genotypic characteristics among themselves and to a lesser extent with A. caulinodans. DNA:DNA hybridization and 16SrRNA sequences support their inclusion in the genus Azorhizobium, but not in the species A. caulinodans. The name A. doebereinerae is proposed, with isolate UFLA1-100 ( ¼ BR5401, ¼ LMG9993 ¼ SEMIA 6401) as the type strain.
    [Show full text]
  • Proquest Dissertations
    Approaches to assessing microbial communities in soil, two examples: Biosurfactant production and phenanthrene degradation Item Type text; Dissertation-Reproduction (electronic) Authors Bodour, Adria Publisher The University of Arizona. Rights Copyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the author. Download date 01/10/2021 06:55:39 Link to Item http://hdl.handle.net/10150/280136 INFORMATION TO USERS This manuscript has been reproduced from the microfiinn master. UMI films the text directly from the original or copy submitted. Thus, some thesis and dissertation copies are in typewriter face, while others may be from any type of computer printer. The quality of this reproduction is dependent upon the quality of the copy submitted. Broken or indistinct print, colored or poor quality illustrations and photographs, print bleedthrough, substandard margins, and improper alignment can adversely affect reproduction. In the unlikely event that the author did not send UMI a complete manuscript and there are missing pages, these will be noted. Also, if unauthorized copyright material had to be removed, a note will indicate the deletion. Oversize materials (e.g., maps, drawings, charts) are reproduced by sectioning the original, beginning at the upper left-hand corner and continuing from left to right in equal
    [Show full text]
  • Phylogeny and Phylogeography of Rhizobial Symbionts Nodulating Legumes of the Tribe Genisteae
    View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Lincoln University Research Archive G C A T T A C G G C A T genes Review Phylogeny and Phylogeography of Rhizobial Symbionts Nodulating Legumes of the Tribe Genisteae Tomasz St˛epkowski 1,*, Joanna Banasiewicz 1, Camille E. Granada 2, Mitchell Andrews 3 and Luciane M. P. Passaglia 4 1 Autonomous Department of Microbial Biology, Faculty of Agriculture and Biology, Warsaw University of Life Sciences (SGGW), Nowoursynowska 159, 02-776 Warsaw, Poland; [email protected] 2 Universidade do Vale do Taquari—UNIVATES, Rua Avelino Tallini, 171, 95900-000 Lajeado, RS, Brazil; [email protected] 3 Faculty of Agriculture and Life Sciences, Lincoln University, P.O. Box 84, Lincoln 7647, New Zealand; [email protected] 4 Departamento de Genética, Instituto de Biociências, Universidade Federal do Rio Grande do Sul. Av. Bento Gonçalves, 9500, Caixa Postal 15.053, 91501-970 Porto Alegre, RS, Brazil; [email protected] * Correspondence: [email protected]; Tel.: +48-509-453-708 Received: 31 January 2018; Accepted: 5 March 2018; Published: 14 March 2018 Abstract: The legume tribe Genisteae comprises 618, predominantly temperate species, showing an amphi-Atlantic distribution that was caused by several long-distance dispersal events. Seven out of the 16 authenticated rhizobial genera can nodulate particular Genisteae species. Bradyrhizobium predominates among rhizobia nodulating Genisteae legumes. Bradyrhizobium strains that infect Genisteae species belong to both the Bradyrhizobium japonicum and Bradyrhizobium elkanii superclades. In symbiotic gene phylogenies, Genisteae bradyrhizobia are scattered among several distinct clades, comprising strains that originate from phylogenetically distant legumes.
    [Show full text]
  • Phenotypic and Microbial Influences on Dairy Heifer Fertility and Calf Gut Microbial Development
    Phenotypic and microbial influences on dairy heifer fertility and calf gut microbial development Connor E. Owens Dissertation submitted to the faculty of the Virginia Polytechnic Institute and State University in partial fulfillment of the requirements for the degree of Doctor of Philosophy In Animal Science, Dairy Rebecca R. Cockrum Kristy M. Daniels Alan Ealy Katharine F. Knowlton September 17, 2020 Blacksburg, VA Keywords: microbiome, fertility, inoculation Phenotypic and microbial influences on dairy heifer fertility and calf gut microbial development Connor E. Owens ABSTRACT (Academic) Pregnancy loss and calf death can cost dairy producers more than $230 million annually. While methods involving nutrition, climate, and health management to mitigate pregnancy loss and calf death have been developed, one potential influence that has not been well examined is the reproductive microbiome. I hypothesized that the microbiome of the reproductive tract would influence heifer fertility and calf gut microbial development. The objectives of this dissertation were: 1) to examine differences in phenotypes related to reproductive physiology in virgin Holstein heifers based on outcome of first insemination, 2) to characterize the uterine microbiome of virgin Holstein heifers before insemination and examine associations between uterine microbial composition and fertility related phenotypes, insemination outcome, and season of breeding, and 3) to characterize the various maternal and calf fecal microbiomes and predicted metagenomes during peri-partum and post-partum periods and examine the influence of the maternal microbiome on calf gut development during the pre-weaning phase. In the first experiment, virgin Holstein heifers (n = 52) were enrolled over 12 periods, on period per month. On -3 d before insemination, heifers were weighed and the uterus was flushed.
    [Show full text]
  • Specificity in Legume-Rhizobia Symbioses
    International Journal of Molecular Sciences Review Specificity in Legume-Rhizobia Symbioses Mitchell Andrews * and Morag E. Andrews Faculty of Agriculture and Life Sciences, Lincoln University, PO Box 84, Lincoln 7647, New Zealand; [email protected] * Correspondence: [email protected]; Tel.: +64-3-423-0692 Academic Editors: Peter M. Gresshoff and Brett Ferguson Received: 12 February 2017; Accepted: 21 March 2017; Published: 26 March 2017 Abstract: Most species in the Leguminosae (legume family) can fix atmospheric nitrogen (N2) via symbiotic bacteria (rhizobia) in root nodules. Here, the literature on legume-rhizobia symbioses in field soils was reviewed and genotypically characterised rhizobia related to the taxonomy of the legumes from which they were isolated. The Leguminosae was divided into three sub-families, the Caesalpinioideae, Mimosoideae and Papilionoideae. Bradyrhizobium spp. were the exclusive rhizobial symbionts of species in the Caesalpinioideae, but data are limited. Generally, a range of rhizobia genera nodulated legume species across the two Mimosoideae tribes Ingeae and Mimoseae, but Mimosa spp. show specificity towards Burkholderia in central and southern Brazil, Rhizobium/Ensifer in central Mexico and Cupriavidus in southern Uruguay. These specific symbioses are likely to be at least in part related to the relative occurrence of the potential symbionts in soils of the different regions. Generally, Papilionoideae species were promiscuous in relation to rhizobial symbionts, but specificity for rhizobial genus appears to hold at the tribe level for the Fabeae (Rhizobium), the genus level for Cytisus (Bradyrhizobium), Lupinus (Bradyrhizobium) and the New Zealand native Sophora spp. (Mesorhizobium) and species level for Cicer arietinum (Mesorhizobium), Listia bainesii (Methylobacterium) and Listia angolensis (Microvirga).
    [Show full text]
  • Amorpha Canescens Pursh Leadplant
    leadplant, Page 1 Amorpha canescens Pursh leadplant State Distribution Best Survey Period Photo by Susan R. Crispin Jan Feb Mar Apr May Jun Jul Aug Sept Oct Nov Dec Status: State special concern the Mississippi valley through Arkansas to Texas and in the western Great Plains from Montana south Global and state rank: G5/S3 through Wyoming and Colorado to New Mexico. It is considered rare in Arkansas and Wyoming and is known Other common names: lead-plant, downy indigobush only from historical records in Montana and Ontario (NatureServe 2006). Family: Fabaceae (pea family); also known as the Leguminosae. State distribution: Of Michigan’s more than 50 occurrences of this prairie species, the vast majority of Synonym: Amorpha brachycarpa E.J. Palmer sites are concentrated in southwest Lower Michigan, with Kalamazoo, St. Joseph, and Cass counties alone Taxonomy: The Fabaceae is divided into three well accounting for more than 40 of these records. Single known and distinct subfamilies, the Mimosoideae, outlying occurrences have been documented in the Caesalpinioideae, and Papilionoideae, which are last two decades from prairie remnants in Oakland and frequently recognized at the rank of family (the Livingston counties in southeast Michigan. Mimosaceae, Caesalpiniaceae, and Papilionaceae or Fabaceae, respectively). Of the three subfamilies, Recognition: Leadplant is an erect, simple to sparsely Amorpha is placed within the Papilionoideae (Voss branching shrub ranging up to ca. 1 m in height, 1985). Sparsely hairy plants of leadplant with greener characterized by its pale to grayish color derived from leaves have been segregated variously as A. canescens a close pubescence of whitish hairs that cover the plant var.
    [Show full text]
  • Table S5. the Information of the Bacteria Annotated in the Soil Community at Species Level
    Table S5. The information of the bacteria annotated in the soil community at species level No. Phylum Class Order Family Genus Species The number of contigs Abundance(%) 1 Firmicutes Bacilli Bacillales Bacillaceae Bacillus Bacillus cereus 1749 5.145782459 2 Bacteroidetes Cytophagia Cytophagales Hymenobacteraceae Hymenobacter Hymenobacter sedentarius 1538 4.52499338 3 Gemmatimonadetes Gemmatimonadetes Gemmatimonadales Gemmatimonadaceae Gemmatirosa Gemmatirosa kalamazoonesis 1020 3.000970902 4 Proteobacteria Alphaproteobacteria Sphingomonadales Sphingomonadaceae Sphingomonas Sphingomonas indica 797 2.344876284 5 Firmicutes Bacilli Lactobacillales Streptococcaceae Lactococcus Lactococcus piscium 542 1.594633558 6 Actinobacteria Thermoleophilia Solirubrobacterales Conexibacteraceae Conexibacter Conexibacter woesei 471 1.385742446 7 Proteobacteria Alphaproteobacteria Sphingomonadales Sphingomonadaceae Sphingomonas Sphingomonas taxi 430 1.265115184 8 Proteobacteria Alphaproteobacteria Sphingomonadales Sphingomonadaceae Sphingomonas Sphingomonas wittichii 388 1.141545794 9 Proteobacteria Alphaproteobacteria Sphingomonadales Sphingomonadaceae Sphingomonas Sphingomonas sp. FARSPH 298 0.876754244 10 Proteobacteria Alphaproteobacteria Sphingomonadales Sphingomonadaceae Sphingomonas Sorangium cellulosum 260 0.764953367 11 Proteobacteria Deltaproteobacteria Myxococcales Polyangiaceae Sorangium Sphingomonas sp. Cra20 260 0.764953367 12 Proteobacteria Alphaproteobacteria Sphingomonadales Sphingomonadaceae Sphingomonas Sphingomonas panacis 252 0.741416341
    [Show full text]
  • Vegetative Growth and Organogenesis 555
    Vegetative Growth 19 and Organogenesis lthough embryogenesis and seedling establishment play criti- A cal roles in establishing the basic polarity and growth axes of the plant, many other aspects of plant form reflect developmental processes that occur after seedling establishment. For most plants, shoot architecture depends critically on the regulated production of determinate lateral organs, such as leaves, as well as the regulated formation and outgrowth of indeterminate branch systems. Root systems, though typically hidden from view, have comparable levels of complexity that result from the regulated formation and out- growth of indeterminate lateral roots (see Chapter 18). In addition, secondary growth is the defining feature of the vegetative growth of woody perennials, providing the structural support that enables trees to attain great heights. In this chapter we will consider the molecular mechanisms that underpin these growth patterns. Like embryogenesis, vegetative organogenesis and secondary growth rely on local differences in the interactions and regulatory feedback among hormones, which trigger complex programs of gene expres- sion that drive specific aspects of organ development. Leaf Development Morphologically, the leaf is the most variable of all the plant organs. The collective term for any type of leaf on a plant, including struc- tures that evolved from leaves, is phyllome. Phyllomes include the photosynthetic foliage leaves (what we usually mean by “leaves”), protective bud scales, bracts (leaves associated with inflorescences, or flowers), and floral organs. In angiosperms, the main part of the foliage leaf is expanded into a flattened structure, the blade, or lamina. The appearance of a flat lamina in seed plants in the middle to late Devonian was a key event in leaf evolution.
    [Show full text]
  • Prokaryotic Biodiversity of Lonar Meteorite Crater Soda Lake Sediment and Community Dynamics During Microenvironmental Ph Homeostasis by Metagenomics
    Prokaryotic Biodiversity of Lonar Meteorite Crater Soda Lake Sediment and Community Dynamics During Microenvironmental pH Homeostasis by Metagenomics Dissertation for the award of the degree "Doctor of Philosophy" Ph.D. Division of Mathematics and Natural Sciences of the Georg-August-Universität Göttingen within the doctoral program in Biology of the Georg-August University School of Science (GAUSS) Submitted by Soumya Biswas from Ranchi (India) Göttingen, 2016 Thesis Committee Prof. Dr. Rolf Daniel Department of Genomic and Applied Microbiology, Institute of Microbiology and Genetics, Faculty of Biology and Psychology, Georg-August-Universität Göttingen, Germany PD Dr. Michael Hoppert Department of General Microbiology, Institute of Microbiology and Genetics, Faculty of Biology and Psychology, Georg-August-Universität Göttingen, Germany Members of the Examination Board Reviewer: Prof. Dr. Rolf Daniel, Department of Genomic and Applied Microbiology, Institute of Microbiology and Genetics, Faculty of Biology and Psychology, Georg-August-Universität Göttingen, Germany Second Reviewer: PD Dr. Michael Hoppert, Department of General Microbiology, Institute of Microbiology and Genetics, Faculty of Biology and Psychology, Georg-August-Universität Göttingen, Germany Further members of the Examination Board: Prof. Dr. Burkhard Morgenstern, Department of Bioinformatics, Institute of Microbiology and Genetics, Faculty of Biology and Psychology, Georg-August-Universität Göttingen, Germany PD Dr. Fabian Commichau, Department of General Microbiology,
    [Show full text]
  • Bacteria-Inducing Legume Nodules Involved in the Improvement of Plant Growth, Health and Nutrition
    Bacteria-Inducing Legume Nodules Involved in the Improvement of Plant 4 Growth, Health and Nutrition Encarna Velázquez, Lorena Carro, José David Flores-Félix, Esther Menéndez, Martha-Helena Ramírez-Bahena, and Alvaro Peix Abstract Bacteria-inducing legume nodules are known as rhizobia and belong to the class Alphaproteobacteria and Betaproteobacteria. They promote the growth and nutrition of their respective legume hosts through atmospheric nitrogen fixation which takes place in the nodules induced in their roots or stems. In addition, rhizobia have other plant growth-promoting mechanisms, mainly solubilization of phosphate and production of indoleacetic acid, ACC deaminase and sidero- phores. Some of these mechanisms have been reported for strains of rhizobia which are also able to promote the growth of several nonlegumes, such as cere- als, oilseeds and vegetables. Less studied are the mechanisms that have the rhi- zobia to promote the plant health; however, these bacteria are able to exert biocontrol of some phytopathogens and to induce the plant resistance. In this chapter, we revised the available data about the ability of the legume nodule-­ inducing bacteria for improving the plant growth, health and nutrition of both legumes and nonlegumes. These data showed that rhizobia meet all the require- ments of sustainable agriculture to be used as bio-inoculants allowing the total or partial replacement of chemicals used for fertilization or protection of crops. E. Velázquez (*) Departamento de Microbiología y Genética, Universidad de Salamanca, Salamanca, Spain Unidad Asociada Universidad de Salamanca- CSIC ‘Interacción Planta-Microorganismo’, Salamanca, Spain e-mail: [email protected] L. Carro · J. D. Flores-Félix · E. Menéndez · M.-H.
    [Show full text]