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Rhizobium

About: Rhizobium is a research topic. Over the lifetime, 7442 publications have been published within this topic receiving 234976 citations.


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Journal ArticleDOI
TL;DR: Genetic manipulation of phosphate-solubilizing bacteria to improve their ability to improve plant growth may include cloning genes involved in both mineral and organic phosphate solubilization, followed by their expression in selected rhizobacterial strains.

2,761 citations

Journal ArticleDOI
TL;DR: In some areas of Latin America, inoculation which normally promotes nodulation and nitrogen fixation is hampered by the prevalence of native strains such as R. etli and R. giardinii as discussed by the authors.
Abstract: Common bean (Phaseolus vulgaris) has become a cosmopolitan crop, but was originally domesticated in the Americas and has been grown in Latin America for several thousand years. Consequently an enormous diversity of bean nodulating bacteria have developed and in the centers of origin the predominant species in bean nodules is R. etli. In some areas of Latin America, inoculation, which normally promotes nodulation and nitrogen fixation is hampered by the prevalence of native strains. Many other species in addition to R. etli have been found in bean nodules in regions where bean has been introduced. Some of these species such as R. leguminosarum bv. phaseoli, R. gallicum bv. phaseoli and R. giardinii bv. phaseoli might have arisen by acquiring the phaseoli plasmid from R. etli. Others, like R. tropici, are well adapted to acid soils and high temperatures and are good inoculants for bean under these conditions. The large number of rhizobia species capable of nodulating bean supports that bean is a promiscuous host and a diversity of bean-rhizobia interactions exists. Large ranges of dinitrogen fixing capabilities have been documented among bean cultivars and commercial beans have the lowest values among legume crops. Knowledge on bean symbiosis is still incipient but could help to improve bean biological nitrogen fixation.

1,641 citations

Journal ArticleDOI
Nevin D. Young1, Frédéric Debellé2, Frédéric Debellé3, Giles E. D. Oldroyd4, René Geurts5, Steven B. Cannon6, Steven B. Cannon7, Michael K. Udvardi, Vagner A. Benedito8, Klaus F. X. Mayer, Jérôme Gouzy2, Jérôme Gouzy3, Heiko Schoof9, Yves Van de Peer10, Sebastian Proost10, Douglas R. Cook11, Blake C. Meyers12, Manuel Spannagl, Foo Cheung13, Stéphane De Mita5, Vivek Krishnakumar13, Heidrun Gundlach, Shiguo Zhou14, Joann Mudge15, Arvind K. Bharti15, Jeremy D. Murray4, Marina Naoumkina, Benjamin D. Rosen11, Kevin A. T. Silverstein1, Haibao Tang13, Stephane Rombauts10, Patrick X. Zhao, Peng Zhou1, Valérie Barbe, Philippe Bardou2, Philippe Bardou3, Michael Bechner14, Arnaud Bellec3, Anne Berger, Hélène Bergès3, Shelby L. Bidwell13, Ton Bisseling16, Ton Bisseling5, Nathalie Choisne, Arnaud Couloux, Roxanne Denny1, Shweta Deshpande17, Xinbin Dai, Jeff J. Doyle18, Anne Marie Dudez2, Anne Marie Dudez3, Andrew Farmer15, Stéphanie Fouteau, Carolien Franken5, Chrystel Gibelin3, Chrystel Gibelin2, John Gish11, Steven A. Goldstein14, Alvaro J. González12, Pamela J. Green12, Asis Hallab19, Marijke Hartog5, Axin Hua17, Sean Humphray20, Dong-Hoon Jeong12, Yi Jing17, Anika Jöcker19, Steve Kenton17, Dong-Jin Kim21, Dong-Jin Kim11, Kathrin Klee19, Hongshing Lai17, Chunting Lang5, Shaoping Lin17, Simone L. Macmil17, Ghislaine Magdelenat, Lucy Matthews20, Jamison McCorrison13, Erin L. Monaghan13, Jeong Hwan Mun22, Jeong Hwan Mun11, Fares Z. Najar17, Christine Nicholson20, Céline Noirot3, Majesta O'Bleness17, Charles Paule1, Julie Poulain, Florent Prion3, Florent Prion2, Baifang Qin17, Chunmei Qu17, Ernest F. Retzel15, Claire Riddle20, Erika Sallet2, Erika Sallet3, Sylvie Samain, Nicolas Samson2, Nicolas Samson3, Iryna Sanders17, Olivier Saurat3, Olivier Saurat2, Claude Scarpelli, Thomas Schiex3, Béatrice Segurens, Andrew J. Severin6, D. Janine Sherrier12, Ruihua Shi17, Sarah Sims20, Susan R. Singer23, Senjuti Sinharoy, Lieven Sterck10, Agnès Viollet, Bing Bing Wang1, Keqin Wang17, Mingyi Wang, Xiaohong Wang1, Jens Warfsmann19, Jean Weissenbach, Doug White17, James D. White17, Graham B. Wiley17, Patrick Wincker, Yanbo Xing17, Limei Yang17, Ziyun Yao17, Fu Ying17, Jixian Zhai12, Liping Zhou17, Antoine Zuber3, Antoine Zuber2, Jean Dénarié3, Jean Dénarié2, Richard A. Dixon, Gregory D. May15, David C. Schwartz14, Jane Rogers24, Francis Quetier, Christopher D. Town13, Bruce A. Roe17 
22 Dec 2011-Nature
TL;DR: The draft sequence of the M. truncatula genome sequence is described, a close relative of alfalfa (Medicago sativa), a widely cultivated crop with limited genomics tools and complex autotetraploid genetics, which provides significant opportunities to expand al falfa’s genomic toolbox.
Abstract: Legumes (Fabaceae or Leguminosae) are unique among cultivated plants for their ability to carry out endosymbiotic nitrogen fixation with rhizobial bacteria, a process that takes place in a specialized structure known as the nodule. Legumes belong to one of the two main groups of eurosids, the Fabidae, which includes most species capable of endosymbiotic nitrogen fixation. Legumes comprise several evolutionary lineages derived from a common ancestor 60 million years ago (Myr ago). Papilionoids are the largest clade, dating nearly to the origin of legumes and containing most cultivated species. Medicago truncatula is a long-established model for the study of legume biology. Here we describe the draft sequence of the M. truncatula euchromatin based on a recently completed BAC assembly supplemented with Illumina shotgun sequence, together capturing ∼94% of all M. truncatula genes. A whole-genome duplication (WGD) approximately 58 Myr ago had a major role in shaping the M. truncatula genome and thereby contributed to the evolution of endosymbiotic nitrogen fixation. Subsequent to the WGD, the M. truncatula genome experienced higher levels of rearrangement than two other sequenced legumes, Glycine max and Lotus japonicus. M. truncatula is a close relative of alfalfa (Medicago sativa), a widely cultivated crop with limited genomics tools and complex autotetraploid genetics. As such, the M. truncatula genome sequence provides significant opportunities to expand alfalfa's genomic toolbox.

1,153 citations

Journal ArticleDOI
19 Apr 1990-Nature
TL;DR: Using R. meliloti strains overproducing symbiotic Nod factors, the major alfalfa-specific signal, NodRm-1, is purified by gel permeation, ion exchange and C18 reverse-phase high performance liquid chromatography and elicited root hair deformation on the homologous host when added in nanomolar concentration.
Abstract: Rhizobia are symbiotic bacteria that elicit the formation on leguminous plants of specialized organs, root nodules, in which they fix nitrogen. In various Rhizobium species, such as R. leguminosarum and R. meliloti, common and host-specific nodulation (nod) genes have been identified which determine infection and nodulation of specific hosts. Common nodABC genes as well as host-specific nodH and nodQ genes were shown recently, using bioassays, to be involved in the production of extracellular Nod signals. Using R. meliloti strains overproducing symbiotic Nod factors, we have purified the major alfalfa-specific signal, NodRm-1, by gel permeation, ion exchange and C18 reverse-phase high performance liquid chromatography. From mass spectrometry, nuclear magnetic resonance, (35)S-labelling and chemical modification studies, NodRm-1 was shown to be a sulphated beta-1,4-tetrasaccharide of D-glucosamine (Mr 1,102) in which three amino groups were acetylated and one was acylated with a C16 bis-unsaturated fatty acid. This purified Nod signal specifically elicited root hair deformation on the homologous host when added in nanomolar concentration.

1,086 citations

Journal ArticleDOI
TL;DR: The mechanisms by which the plant allows bacterial infection and promotes the formation of the nodule are reviewed, as well as the details of how a complex interchange of metabolites and regulatory peptides force the bacteria into a nitrogen-fixing organelle-like state are reviewed.
Abstract: Rhizobial bacteria enter a symbiotic association with leguminous plants, resulting in differentiated bacteria enclosed in intracellular compartments called symbiosomes within nodules on the root. The nodules and associated symbiosomes are structured for efficient nitrogen fixation. Although the interaction is beneficial to both partners, it comes with rigid rules that are strictly enforced by the plant. Entry into root cells requires appropriate recognition of the rhizobial Nod factor signaling molecule, and this recognition activates a series of events, including polarized root-hair tip growth, invagination associated with bacterial infection, and the promotion of cell division in the cortex leading to the nodule meristem. The plant's command of the infection process has been highlighted by its enforcement of terminal differentiation upon the bacteria within nodules of some legumes, and this can result in a loss of bacterial viability while permitting effective nitrogen fixation. Here, we review the mechanisms by which the plant allows bacterial infection and promotes the formation of the nodule, as well as the details of how this intimate association plays out inside the cells of the nodule where a complex interchange of metabolites and regulatory peptides force the bacteria into a nitrogen-fixing organelle-like state.

987 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
2023139
2022300
2021143
2020195
2019177
2018154