Azospirillum-plant relationships: Physiological, molecular, agricultural, and environmental advances, Can. J. Microbiol, vol.521, p.577, 2004. ,
Azospirillum, a free-living nitrogen-fixing bacterium closely associated with grasses: Genetic, biochemical and ecological aspects, FEMS Microbiol. Rev, vol.487, p.506, 2000. ,
Physiological and cytological studies on the inhibition of Striga seed germination by the plant growth-promoting bacterium Azospirillum brasilense, Eur. J. Plant Pathol, vol.106, p.351, 2000. ,
Protection of tomato seedlings against infection by Pseudomonas syringae pv. tomato by using the plant growth-promoting bacterium Azospirillum brasilense, Appl. Environ. Microbiol, p.68, 2002. ,
Effects of colonization of a bacterial endophyte, Azospirillum sp. B510, on disease resistance in rice, Biosci. Biotechnol. Biochem, p.73, 2009. ,
Alginate beads provide a beneficial physical barrier against native microorganisms in wastewater treated with immobilized bacteria and microalgae, Appl. Environ. Microbiol, p.93, 2012. ,
Key physiological properties contributing to rhizosphere adaptation and plant growth promotion abilities of Azospirillum brasilense, FEMS Microbiol. Lett, vol.99, p.108, 2012. ,
Presence of 16S rRNA genes in multiple replicons in Azospirillum brasilense, FEMS Microbiol. Lett, vol.283, p.288, 1999. ,
Genome structure of the genus Azospirillum, J. Bacteriol, vol.4113, p.4116, 2000. ,
Complete genomic structure of the cultivated rice endophyte Azospirillum sp. B510, DNA Res, vol.37, p.50, 2010. ,
Genomic insights into the versatility of the plant growth-promoting bacterium Azospirillum amazonense, BMC Genomics, vol.12, p.409, 2011. ,
Azospirillum genomes reveal transition of bacteria from aquatic to terrestrial environments, PLoS Genet, 2011. ,
Introducing the bacterial 'chromid': not a chromosome, not a plasmid, Trends Microbiol, vol.141, p.148, 2010. ,
Phase variation and genomic architecture changes in Azospirillum, J. Bacteriol, vol.5364, p.5373, 2006. ,
URL : https://hal.archives-ouvertes.fr/hal-00112563
Bacteriophage prevalence in the genus Azospirillum and analysis of the first genome sequence of an Azospirillum brasilense integrative phage, Appl. Environ. Microbiol, vol.861, p.874, 2008. ,
URL : https://hal.archives-ouvertes.fr/halsde-00259504
Efecto de cepas de Azospirillum brasilense en el crecimiento y rendimiento de grano del maiz, Rev. Fitotec. Mex, vol.305, p.310, 2007. ,
Bacterias que incrementan la producción agrícola y procedimientos para aislar y producir con ellas un biofertilizante y para aplicarlo sobre cultivos y suelos similares a su origen, Instituto Politechnico Nacional, p.2005008322, 2005. ,
Insights into the 1.59-Mbp largest plasmid of Azospirillum brasilense CBG497, Arch. Microbiol, vol.725, p.736, 2012. ,
URL : https://hal.archives-ouvertes.fr/hal-02532814
A common genomic framework for a diverse assembly of plasmids in the symbiotic nitrogen fixing bacteria, PLoS One, vol.3, p.2567, 2008. ,
Endophytic colonization and in planta nitrogen fixation by a Herbaspirillum sp isolated from wild rice species, Appl. Environ. Microbiol, vol.5285, p.5293, 2001. ,
DNA-DNA hybridization values and their relationship to whole-genome sequence similarities, Int. J. Syst. Evol. Microbiol, vol.57, p.91, 2007. ,
An efficient algorithm for large-scale detection of protein families, Nucleic Acids Res, 2002. ,
Comparative genome analysis of four magnetotactic bacteria reveals a complex set of group-specific genes implicated in magnetosome biomineralization and function, J. Bacteriol, vol.4899, p.4910, 2007. ,
Evolution of the core and pan-genome of Streptococcus: positive selection, recombination, and genome composition, Genome Biol, vol.8, p.71, 2007. ,
Pyrroloquinoline quinone is a plant growth promotion factor produced by Pseudomonas fluorescens B16, Plant Physiol, vol.657, p.668, 2008. ,
Extracellular polysaccharide composition of Azospirillum brasilense and its relation with cell aggregation, FEMS Microbiol. Lett, vol.259, p.264, 2000. ,
Extracellular polysaccharides and polysaccharide-containing biopolymers from Azospirillum species: Properties and the possible role in interaction with plant roots, FEMS Microbiol. Lett, vol.223, p.229, 1998. ,
The Azospirillum brasilense Sp7 noeJ and noeL genes are involved in extracellular polysaccharide biosynthesis, Microbiology, vol.4058, p.4068, 2009. ,
Surface properties and motility of Rhizobium and Azospirillum in relation to plant root attachment, Microb. Ecol, vol.149, p.169, 1996. ,
The tad locus: Postcards from the widespread colonization island, Nat. Rev. Microbiol, vol.5, p.375, 2007. ,
Attachment of bacteria to the roots of higher plants, FEMS Microbiol. Lett, vol.127, p.136, 2007. ,
In-situ localization of Azospirillum brasilense in the rhizosphere of wheat with fluorescently labeled, ribosomal-RNA-targeted oligonucleotide probes and scanning confocal laser microscopy, Appl. Environ. Microbiol, p.61, 1995. ,
Acquisition of phosphorus and nitrogen in the rhizosphere and plant growth promotion by microorganisms, Plant Soil, vol.305, p.339, 2009. ,
URL : https://hal.archives-ouvertes.fr/halsde-00525548
Role of gluconic acid production in the regulation of biocontrol traits of Pseudomonas fluorescens CHA0, Appl. Environ. Microbiol, vol.4162, p.4174, 2009. ,
Gluconic acid production and phosphate solubilization by the plant growth-promoting bacterium Azospirillum spp, Naturwissenschaften, vol.552, p.555, 2004. ,
How the plant growth-promoting bacterium Azospirillum promotes plant growth -A critical assessment, Adv. Agron, vol.77, p.135, 2010. ,
Molecularcloning and sequence analysis of an Azospirillum brasilense indole 3-pyruvate decarboxylase gene, Mol. Gen. Genet, vol.463, p.472, 1994. ,
Growth and indole 3-acetic acid biosynthesis of Azospirillum brasilense Sp245 is environmentally controlled, FEMS Microbiol. Lett, vol.125, p.132, 2005. ,
Characterization of phenylpyruvate decarboxylase, involved in auxin production of Azospirillum brasilense, J. Bacteriol, vol.7626, p.7633, 2007. ,
The hisC1 gene, encoding aromatic amino acid aminotransferase 1 in Azospirillum brasilense Sp7, expressed in wheat, Plant Soil, 2011. ,
Associative and endophytic nitrogen-fixing bacteria and cyanobacterial associations, 2003. ,
Physiological evidence for differently regulated tryptophan-dependent pathways for indole 3-acetic acid synthesis in Azospirillum brasilense, Mol. Gen. Genet, vol.264, p.530, 2000. ,
Cytochrome P450 CYP79B2 from Arabidopsis catalyzes the conversion of tryptophan to indole-3-acetaldoxime, a precursor of indole glucosinolates and indole-3-acetic acid, J. Biol. Chem, vol.33712, p.33717, 2000. ,
Discovery of a bacterial gene cluster for catabolism of the plant hormone indole 3-acetic acid, FEMS Microbiol. Ecol, vol.238, p.250, 2008. ,
Utilization of the plant hormone indole 3-acetic acid for growth by Pseudomonas putida strain 1290, Appl. Environ. Microbiol, p.71, 2005. ,
Promotion of plant growth by ACC deaminaseproducing soil bacteria, Eur. J. Plant Pathol, vol.329, p.339, 2007. ,
Phylogeny of the 1-aminocyclopropane-1-carboxylic acid deaminase-encoding gene acdS in phytobeneficial and pathogenic Proteobacteria and relation with strain biogeography, FEMS Microbiol. Ecol, vol.56, p.470, 2006. ,
URL : https://hal.archives-ouvertes.fr/hal-00124530
Physical organization and phylogenetic analysis of acdR as leucineresponsive regulator of the 1-aminocyclopropane-1-carboxylate deaminase gene acdS in phytobeneficial Azospirillum lipoferum 4B and other Proteobacteria, FEMS Microbiol. Ecol, vol.202, p.219, 2008. ,
URL : https://hal.archives-ouvertes.fr/hal-02555008
The origin, composition and rated of organic nitrogen deposition: A missing piece of the nitrogen cycle? Biogeochemistry, vol.99, p.136, 2002. ,
Genetics of the glutamate-mediated methylamine utilization pathway in the facultative methylotrophic beta-proteobacterium Methyloversatilis universalis FAM5, Mol. Microbiol, vol.426, p.439, 2009. ,
Expressed genome of Methylobacillus flagellatus as defined through comprehensive proteomics and new insights into methylotrophy, J. Bacteriol, vol.4859, p.4867, 2010. ,
Genomes of three methylotrophs from a single niche reveal the genetic and metabolic divergence of the methylophilaceae, J. Bacteriol, vol.3757, p.3764, 2011. ,
{gamma}-Glutamylmethylamide is an essential intermediate in the metabolism of methylamine by Methylocella silvestris, Appl. Environ. Microbiol, vol.4530, p.4537, 2010. ,
Microbial degradation of aromatic compounds -from one strategy to four, Nat. Rev. Microbiol, vol.9, p.816, 2011. ,
Characterization of the last step of the aerobic phenylacetic acid degradation pathway, Microbiology, vol.357, p.365, 2007. ,
Identification of the pcaRKF gene cluster from Pseudomonas putida: involvement in chemotaxis, biodegradation, and transport of 4-hydroxybenzoate, J. Bacteriol, vol.6479, p.6488, 1994. ,
Regulation of phenylacetic acid degradation genes of Burkholderia cenocepacia K56-2, BMC Microbiol, vol.9, p.222, 2009. ,
The phenylacetyl-CoA catabolon: a complex catabolic unit with broad biotechnological applications, Mol. Microbiol, pp.39-1434, 2001. ,
Functional analysis of PvdS, an iron starvation sigma factor of Pseudomonas aeruginosa, J. Bacteriol, p.182, 2000. ,
Role of iron and the TonB system in colonization of corn seeds and roots by Pseudomonas putida KT2440, Environ. Microbiol, vol.7, p.449, 2005. ,
The oxidative burst in plant disease resistance, Annu. Rev. Plant Physiol. Plant Mol. Biol, vol.48, p.275, 1997. ,
Oxidative burst in alfalfa-Sinorhizobium meliloti symbiotic interaction, Mol. Plant-Microbe Interac, vol.86, p.89, 2001. ,
Only one catalase, katG, is detectable in Rhizobium etli, and is encoded along with the regulator OxyR on a plasmid replicon, Microbiology, p.149, 2003. ,
What is type VI secretion doing in all those bugs?, Trends Microbiol, vol.531, p.537, 2010. ,
Nooks and crannies in type VI secretion regulation, J. Bacteriol, vol.3850, p.3860, 2010. ,
URL : https://hal.archives-ouvertes.fr/hal-02001273
The Vibrio cholerae type VI secretion system displays antimicrobial properties, Proc. Natl. Acad. Sci, p.107, 2010. ,
Transcriptome Analysis of the Rhizosphere Bacterium Azospirillum brasilense Reveals an Extensive Auxin Response, Microb. Ecol, vol.723, p.728, 2011. ,
Diversity of bacterial laccase-like multicopper oxidase genes in forest and grassland Cambisol soil samples, Soil Biol. Biochem, vol.638, p.648, 2008. ,
Polyphenol Oxidase in Azospirillum lipoferum Isolated from Rice Rhizosphere Evidence for Laccase Activity in Nonmotile Strains of Azospirillum lipoferum, FEMS Microbiol. Lett, vol.205, p.210, 1993. ,
Isolation of Azospirillum lipoferum 4T Tn5 Mutants Affected in Melanization and Laccase Activity, Appl. Environ. Microbiol, vol.3413, p.3415, 1994. ,
Loss of cytochrome c oxidase activity and acquisition of resistance to quinone analogs in a laccase-positive variant of Azospirillum lipoferum, J. Bacteriol, vol.6730, p.6738, 1999. ,
, Bacterial lacases. World J. Microbiol. Biotechnol, vol.823, p.832, 2007.
Duplication of plasmid-borne nitrite reductase gene nirK in the wheat-associated plant growth-promoting rhizobacterium Azospirillum brasilense Sp245, Mol. Plant-Microbe Interact, vol.21, p.842, 2008. ,
URL : https://hal.archives-ouvertes.fr/halsde-00344099
Importance of widespread gene transfer agent genes in alphaproteobacteria, Trends Microbiol, vol.54, p.62, 2007. ,
Identification of a divided genome for VSH 1, the prophage-like gene transfer agent of Brachyspira hyodysenteriae, J. Bacteriol, p.191, 2009. ,
CRISPR provides acquired resistance against viruses in prokaryotes, Science, p.315, 2007. ,
, CRISPI: a CRISPR Interactive database, p.23, 2012.
Versatile and open software for comparing large genomes, Genome Biol, vol.5, p.12, 2004. ,
, , p.23, 2012.
MicroScope: A platform for microbial genome annotation and comparative genomics, p.21, 2009. ,
MUSCLE: multiple sequence alignment with high accuracy and high throughput, Nucleic Acids Res, p.32, 2004. ,
SeaView version 4: A multiplatform graphical user interface for sequence alignment and phylogenetic tree building, Mol. Biol. Evol, vol.221, p.224, 2010. ,
URL : https://hal.archives-ouvertes.fr/lirmm-00511794
Basic local alignment search tool, J. Mol. Biol, vol.403, p.410, 1990. ,
KaKs_Calculator: calculating Ka and Ks through model selection and model averaging, Genom. Proteom. Bioinf, 2006. ,