1974
DOI: 10.1073/pnas.71.2.536
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Detection and Quantitation of Octopine in Normal Plant Tissue and in Crown Gall Tumors

Abstract: Octopine has been detected in normal tobacco leaf and stem tissue, normal sunflower stem tissue, pinto bean leaves, and normal tobacco callus tissue in culture. Octopine was identified in extracts by means of electrophoresis and chromatography in several solvent systems. Tobacco and sunflower tumor lines induced by various strains of Agrobacterium tumefaciens were found to contain from 1 to 240 times as much octopine as the normal plant tissues examined. Several strains of A. tumefaciens produce undifferentiat… Show more

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Cited by 54 publications
(15 citation statements)
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“…Interestingly, both bacteria induce galls on their host through elevated levels of cytokinins and auxins. Nevertheless, the mechanisms resulting in the hormone imbalance in the infected plant are completely different, and generally A. tumefaciens-induced tumors consist only of undifferentiated cells (Johnson et al, 1974).…”
Section: Discussionmentioning
confidence: 99%
“…Interestingly, both bacteria induce galls on their host through elevated levels of cytokinins and auxins. Nevertheless, the mechanisms resulting in the hormone imbalance in the infected plant are completely different, and generally A. tumefaciens-induced tumors consist only of undifferentiated cells (Johnson et al, 1974).…”
Section: Discussionmentioning
confidence: 99%
“…It is generally accepted that opines are synthesized in transformed cells following infection by Agrobacterium and they serve as carbon-nitrogen source for the invading bacteria (7,16 (2-4, 11, 14, 15, 17). Contrary to the conclusions reached by the above investigators, there have been scattered reports that certain opines could be detected in normal cells (13,21,23). One of these claims however, was withdrawn in a subsequent publication (18 (9).…”
mentioning
confidence: 66%
“…Cultures of A. tumefaciens in midlogarithmic phase were obtained by suspending a single colony in nutrient broth (beef extract 1 g dm -3 , yeast extract 2 g dm -3 ; peptone 5 g dm -3 ; and NaCl 5 g dm -3 ) for 48 h at 28 ºC followed by subculturing in the same medium for another 24 h (Johnson et al 1974).…”
Section: Methodsmentioning
confidence: 99%