The Diversity of Archaea and Bacteria in Association with the Roots of Zea mays L.
By M. Chelius, E. Triplett. Microbial Ecology, 2001
874 citations recorded by the source corpus.
Subfields: Ecology, Molecular Biology, Plant Science
View Paper: https://www.semanticscholar.org/paper/4e105217d4e98e71622f4e8dc254b5dd9ef862e9
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Ecology
- Noah Fierer
- Rob Knight
- Ruth E. Ley
- Omry Koren
- I. Zilber-Rosenberg
- A. Spor
- Eugene Rosenberg
- Ajar Nath Yadav
In Molecular Biology
- Rob Knight
- Noah Fierer
- Ruth E. Ley
- Omry Koren
- A. Spor
- Eugene Rosenberg
- I. Zilber-Rosenberg
- Samir K. Banerjee
In Plant Science
- A. Sessitsch
- S. Compant
- G. Berg
- Anil K. Saxena
- Ajar Nath Yadav
- P. Garbeva
- R. Mendes
- I. Zilber-Rosenberg
Citations in the corpus
- Biological nitrogen fixation in maize (Zea mays L.) by 15N isotope-dilution and identification of associated culturable diazotrophs (2009, background): “Studying the diversity of Archea and bacteria in association with the roots of maize (Chelius and Triplett 2001) found that most of the sequences analyzed were related to proteobacteria with the α-subdivision predominating and β-subdivision in second place.”
- The rhizosphere microbiome: significance of plant beneficial, plant pathogenic, and human pathogenic microorganisms. (2013, background): “For the rhizosphere, an earlier study by Chelius & Triplett (2001) identified six unique archaeal sequences associated with maize roots.”
- Azospirillum inoculation and nitrogen fertilization effect on grain yield and on the diversity of endophytic bacteria in the phyllosphere of rice rainfed crop (2009, methodology): “The amplification of bacterial DNA from plant tissues was performed as suggested by Chelius and Triplett [13] to avoid interference from chloroplasts and mitochondrial DNA.”
- Biodiversity and biotechnological applications of halophilic microbes for sustainable agriculture (2018, background): “Archaea have been reported as unculturable from maize [20] and rice crop [21], whereas culturable archaea have been reported from Abutilon, Cressa, Sporobolus, S.”
- Cropping practices manipulate abundance patterns of root and soil microbiome members paving the way to smart farming (2018, methodology): “The 16S rRNA gene amplicon library was generated using the PCR primers 799F [72] and 1193R [73].”
- Microbial diversity and function in soil: from genes to ecosystems. (2002, background): “Over the past two decades, molecular methods, especially 16S rRNA gene sequencing, have become very popular to help identify unknown bacteria [6,7].”
- Characterization of diazotrophic bacteria associated with maize: effect of plant genotype, ontogeny and nitrogen-supply (2006, background): “It must be noted here that considerable amounts of N2-fixing bacteria exist on the root surface or inside the plant, and diversity of microorganisms in natural environments is higher than that detected by traditional methods (Ueda et al. 1995; Chelius & Triplett, 2001 ).”
- Molecular Phylogenetic Analysis of Archaea and Bacteria in Wind Cave, South Dakota (2004, methodology): “Cloning, amplified rDNA restriction analysis (ARDRA), and PCR amplification of 16S rDNA of archaeal origin followed the procedures Chelius and Triplett (2001) .”
- Structure and Function of the Bacterial Root Microbiota in Wild and Domesticated Barley (2015, background): “We further assessed the variability in abundance estimates for bacterial taxa which could be detected in both analyses (excluding Cyanobacteria) and found several discrepancies, despite the overall high correlation (0.86 Pearson coefficient; p < 1.75E 12).”
- Combined amendment of immobilizers and the plant growth-promoting strain Burkholderia phytofirmans PsJN favours plant growth and reduces heavy metal uptake (2015, methodology): “…amplification, library preparation and pyrotag sequencing For the identification of bacteria, 16S rRNA gene amplicons were obtained by PCR using the fusion primer pairs specific for the V5eV9 region (799-forward) (Chelius and Triplett, 2001) and 1520- reverse pH primer (Massol-Deya et al., 1995).”