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Rapid identification of cytokinins by an immunological method

Journal Article · · Plant Physiology; (United States)
DOI:https://doi.org/10.1104/pp.95.4.1156· OSTI ID:5265135
; ;  [1];  [2]
  1. Univ. of Missouri-Columbia (USA)
  2. Centre Nationale de la Recherche Scientifique, Gif-sur-Yvette (France)
A method for rapid identification of bacterial cytokinins has been developed in which cultures are fed ({sup 3}H)adenine, the cytokinins (including, {sup 3}H-labeled cytokinins) are isolated by immunoaffinity chromatography, and analyzed by HPLC with on-line scintillation counting. Analysis of Agrobacterium tumefaciens strains showed that some produced primarily trans-zeatin, whereas others produced primarily trans-zeatin riboside. Pseudomonas syringae pv savastanoi produced mixtures of transzeatin, dihydrozeatin, 1{double prime}-methyl-trans-zeatin riboside, and other unknown cytokinin-like substances. Corynebacterium fascians, produced cis-zeatin, isopentenyladenine and isopentenyladenosine. The technique is designed for qualitative rather than quantitative studies and allows ready identification of bacterial cytokinins. It may also have utility in the study of plant cytokinins if adequate incorporation of label into cytokinin precursor pools can be achieved.
OSTI ID:
5265135
Journal Information:
Plant Physiology; (United States), Journal Name: Plant Physiology; (United States) Vol. 95:4; ISSN 0032-0889; ISSN PLPHA
Country of Publication:
United States
Language:
English