2003
DOI: 10.1034/j.1399-3054.2003.00086.x
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Methods for isolating and characterizing ACC deaminase‐containing plant growth‐promoting rhizobacteria

Abstract: One of the major mechanisms utilized by plant growth-promoting rhizobacteria (PGPR) to facilitate plant growth and development is the lowering of ethylene levels by deamination of 1-aminocyclopropane-1-carboxylic acid (ACC) the immediate precursor of ethylene in plants. The enzyme catalysing this reaction, ACC deaminase, hydrolyses ACC to alpha-ketobutyrate and ammonia. Several bacterial strains that can utilize ACC as a sole source of nitrogen have been isolated from rhizosphere soil samples. All of these str… Show more

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Cited by 1,278 publications
(831 citation statements)
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“…The isolates were further screened for their ACC deaminase activity with and without salt supplementation, by measuring the amount of a-ketobutyrate produced by ACC using 2,4-dinitrophenylhydrazine reagent (Honma and Shimomura 1978;Penrose and Glick 2003). The bacterial cells were grown in a tryptone soya broth up to late log phase and later grown and induced in minimal media (with and without supplemented salt) with additional 3.0 mM ACC as sole nitrogen source.…”
Section: Assessment Of Salt Tolerance Of Isolatesmentioning
confidence: 99%
“…The isolates were further screened for their ACC deaminase activity with and without salt supplementation, by measuring the amount of a-ketobutyrate produced by ACC using 2,4-dinitrophenylhydrazine reagent (Honma and Shimomura 1978;Penrose and Glick 2003). The bacterial cells were grown in a tryptone soya broth up to late log phase and later grown and induced in minimal media (with and without supplemented salt) with additional 3.0 mM ACC as sole nitrogen source.…”
Section: Assessment Of Salt Tolerance Of Isolatesmentioning
confidence: 99%
“…The ability of the isolates to produce ACC deaminase was also screened on minimal media containing ACC as their sole nitrogen source as described by Penrose and Glick (2003). Optical density (OD) was measured after 48 h at 540 nm by spectrophotometer (Specord 200, Analytic Jena, Germany) and considered as an index for evaluating ACC deaminaseproducing isolates.…”
Section: Isolation Of Endophytic Bacterial Strainsmentioning
confidence: 99%
“…Growth was determined by measuring the OD at 600 nm after incubation at 30°C for 72 h. The ACCD activity of cell-free extracts was determined by monitoring the amount of a-ketobutyrate generated by the hydrolysis of ACC (Saleh and Glick 2001), by comparing the absorbance (540 nm) of a sample to a standard curve of a-ketobutyrate ranging between 0.1 and 1.0 mmol L -1 according to Penrose and Glick (2003) and Dell'Amico et al (2008). The mixtures containing no cell suspension or no ACC were used as controls.…”
Section: Acc Deaminase Activitymentioning
confidence: 99%