2010
DOI: 10.1016/j.phytochem.2010.08.013
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Vacuolar and cytosolic cytokinin dehydrogenases of Arabidopsis thaliana: Heterologous expression, purification and properties

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Cited by 78 publications
(71 citation statements)
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“…This is consistent with data indicating that increased cytokinin signaling in Ljsnf2 or through ectopic MtLog overexpression reduces nodulation (Tirichine et al, 2007;Mortier et al, 2014). Most Arabidopsis CKX have predicted signal peptides and are proposed to localize to the apoplast or vacuoles Kowalska et al, 2010). We also found LjCKX3 has a predicted secretion signal and is therefore likely degrading cytokinin in the extracellular space.…”
Section: Local Restriction Of Cytokinin Accumulation Is Required For supporting
confidence: 91%
“…This is consistent with data indicating that increased cytokinin signaling in Ljsnf2 or through ectopic MtLog overexpression reduces nodulation (Tirichine et al, 2007;Mortier et al, 2014). Most Arabidopsis CKX have predicted signal peptides and are proposed to localize to the apoplast or vacuoles Kowalska et al, 2010). We also found LjCKX3 has a predicted secretion signal and is therefore likely degrading cytokinin in the extracellular space.…”
Section: Local Restriction Of Cytokinin Accumulation Is Required For supporting
confidence: 91%
“…Cytokinin levels are also regulated by cytokinin oxidases, copper-dependent amine oxidase enzymes that cleave the N 6 -side chains from tZ-and iP-type cytokinins, thus irreversibly inactivating them Werner et al, 2006). In most plant species, cytokinin oxidase is encoded by a multigene family whose members show distinct patterns of expression, intracellular locations, and enzymatic properties Kowalska et al, 2010). Several genes encoding cytokinin oxidases are induced rapidly upon cytokinin and auxin treatment in rice (Oryza sativa) and Arabidopsis (Tsai et al, 2012;Bhargava et al, 2013;Gao et al, 2014).…”
Section: Cytokininsmentioning
confidence: 99%
“…With the exception of N-3 glucosides, N-glucosides are generally not active in bioassays and it has been assumed that N-7 and N-9 glucosylation irreversibly inactivates CKs , whereas N-3 glucoside can be converted to the free base by b-glucosidases (Brzobohatý et al 1993). Recently, CK N-9 glucosides were found to be the preferred substrates of some CKX isoforms (Galuszka et al 2007;Kowalska et al 2010).…”
Section: Ck Metabolismmentioning
confidence: 99%
“…The substrate binds above the isoalloxazine plane of the FAD cofactor and its amino group forms a hydrogen bond with an aspartic acid-glutamic acid (Asp-Glu) pair that facilitates the oxidation (Malito et al 2004). Studies on the substrate specificity of Arabidopsis thaliana and maize CKX isoforms revealed that not only free bases and ribosides of isoprenoid CKs, including cis-zeatin (Šmehilová et al 2009;Pertry et al 2010;Gajdošová et al 2011), but also CK 9-glucosides and nucleotides are effectively cleaved by individual isoforms (Galuszka et al 2007;Kowalska et al 2010). It was also presented that aromatic CKs are degraded by CKX as well, although with lower reaction rates (Frébortová et al 2004;Galuszka et al 2007).…”
Section: Ck Metabolismmentioning
confidence: 99%