2006
DOI: 10.1007/s11274-005-4561-1
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Auxin, Gibberellin, Cytokinin and Abscisic Acid Production in Some Bacteria

Abstract: In this study, auxin (indole-3-acetic acid), gibberellin, cytokinin (zeatin) and abscisic acid production were investigated in the culture medium of the bacteria Proteus mirabilis, P. vulgaris, Klebsiella pneumoniae, Bacillus megaterium, B. cereus, Escherichia coli. To determine the levels of these plant growth regulators, high performance liquid chromatography (HPLC) technique was used. Our findings show that the bacteria used in this study synthesized the plant growth regulators, auxin, gibberellin, cytokini… Show more

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Cited by 177 publications
(87 citation statements)
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“…The cultures were then centrifuged at 3000 x g for 15 min at room temperature. Extraction and detection of the free and the bound forms of abscisic acid, GA, IAA and Z from G. xylinus cell pellets and culture supernatants were performed as previously described 31,38 with minor modifications. Briefly, the culture supernatant was transferred to a separate glass vial whereas the cell pellets were washed in 0.85% sterile saline solution and resuspended in 10 mL sterile water in a glass vial.…”
Section: Pellicle Characteristicsmentioning
confidence: 99%
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“…The cultures were then centrifuged at 3000 x g for 15 min at room temperature. Extraction and detection of the free and the bound forms of abscisic acid, GA, IAA and Z from G. xylinus cell pellets and culture supernatants were performed as previously described 31,38 with minor modifications. Briefly, the culture supernatant was transferred to a separate glass vial whereas the cell pellets were washed in 0.85% sterile saline solution and resuspended in 10 mL sterile water in a glass vial.…”
Section: Pellicle Characteristicsmentioning
confidence: 99%
“…Absorbance was monitored at 265 nm for ABA and Z, 280 nm for IAA and 208 nm for GA as described previously. 31,39 Culture supernatants of G. xylinus grown in either SH or SH amended with 0.05% (w/v) L-tryptophan were assayed for the production of IAA using the method of Gordon and Weber 40 as modified by Sarwar and Kremer 41 in which culture filtrate was reacted with Salkowski reagent in a microplate. A pink-colored product after 30 min was taken to be a positive result.…”
Section: Pellicle Characteristicsmentioning
confidence: 99%
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“…Considering that 1 g of soil may harbor 10 3 -10 6 bacterial species (Torsvik et al, 1990;Curtis et al, 2002;Gans et al, 2005;Roesch et al, 2007), the vast majority would remain undetected. Community richness estimations in fact indicated that most of the diversity in the environment is due to rare members (Hughes et al, 2001;Reeder and Knight, 2009) and these may also have important ecological functions, for example, in cycling of elements, as a supplier of phytohormones or as phytopathogens (Karadeniz et al, 2006;Humbert et al, 2010;Pester et al, 2010;Roper, 2011;Krzmarzick et al, 2012).…”
Section: Introductionmentioning
confidence: 99%
“…Extracted phytohormones were analyzed by HPLC (Model Breeze, Waters, USA). Analytical conditions were as follows; Luna 5µ C18(2) LC column 250 × 4.6 mm (Phenomenex, USA), flow rates of 1 ml/min of 35% methanol (in 1% acetic acid) for IAA, 30% methanol (0.1 M H3PO4) for GA3 and 55% methanol (0.1 M acetic acid) for ABA, wavelengths of UV detector 280, 208, and 265 nm for IAA, GA3, and ABA, respectively (Karadeniz et al, 2006). The amount of bacterial protein was measured by Bradford assay (Bradford, 1976), and the production of phytohormone was also expressed based on bacterial protein.…”
Section: Isolation and Identification Of Rhizobacteriamentioning
confidence: 99%