2010
DOI: 10.1016/j.biochi.2010.05.006
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Phenyl- and benzylurea cytokinins as competitive inhibitors of cytokinin oxidase/dehydrogenase: A structural study

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Cited by 58 publications
(50 citation statements)
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“…The enhanced fruit enlargement due to CPPU treatments is thought to be derived from a direct stimulation of cell division and/or activation of plant responses typically induced by naturally occurring adeninesubstituted cytokinins [2], combined with an inhibition of cytokinin oxidase/dehydrogenase enzymes that are responsible of cell homeostasis, thus increasing the effective concentration of the endogenous phytohormones [3]. CPPU is commercially available as 1% or 0.1% emulsifiable concentrates under different trade names, i.e.…”
mentioning
confidence: 99%
“…The enhanced fruit enlargement due to CPPU treatments is thought to be derived from a direct stimulation of cell division and/or activation of plant responses typically induced by naturally occurring adeninesubstituted cytokinins [2], combined with an inhibition of cytokinin oxidase/dehydrogenase enzymes that are responsible of cell homeostasis, thus increasing the effective concentration of the endogenous phytohormones [3]. CPPU is commercially available as 1% or 0.1% emulsifiable concentrates under different trade names, i.e.…”
mentioning
confidence: 99%
“…It is worth noting that FCF targets at least three distinct proteins in plants (23,63), and it may be naive to imagine that for none of these would there be a nonplant protein sharing high structural similarity at the site of FCF binding. In principle, the same kind of biochemical approach used to identify CSBP as the major FCF-binding protein in plants (63,64) could be applied to other organisms to isolate FCF-binding proteins.…”
Section: Discussionmentioning
confidence: 99%
“…FCF binds and competitively inhibits the catabolic cytokinin dehydrogenase CKO (23), resulting in prolonged elevation of intracellular cytokinin levels and, ultimately, larger fruits (23). In 2004, Iwase et al reported that treatment of the budding yeast Saccharomyces cerevisiae with FCF inhibits growth and causes the formation of ectopic septin structures (24).…”
mentioning
confidence: 99%
“…Several synthetic urea-derived CKs that competitively inhibit CKX activity have been reported, including thidiazuron, CPPU, and CBPU (Hare and Van Staden 1994;Laloue and Fox 1989;Burch and Horgan 1989;Kopečný et al 2010). In the most cases, their modes of binding to CKX have been clarified by structural analysis (Kopečný et al 2010).…”
Section: Chemical Tools To Modulate Cytokinin Statusmentioning
confidence: 99%
“…In the most cases, their modes of binding to CKX have been clarified by structural analysis (Kopečný et al 2010). The activity of CKX was shown to be strongly inhibited by unsaturated allenic (HA-1, HA-8) and alkyne substrate analogues (Houba-Hérin et al 1999;Suttle and Mornet 2005;Kopečný et al 2008).…”
Section: Chemical Tools To Modulate Cytokinin Statusmentioning
confidence: 99%