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. 2000 Mar;122(3):721–730. doi: 10.1104/pp.122.3.721

Table III.

Cytokinin content of mutant line c1 compared to wild-type (WT) seedlings

Cytokinin Metabolite WT Seedling c1 Callus Increaseb
pmol g−1 fresh wt
iP 7.6a 1.2 ± 0.1 0.2
iP Riboside 3.7 ± 3.3 22.7 ± 5.4 6
iP Riboside 5′-monophosphate 1.5 ± 0.1 12.5 ± 0.4 8
iP 9-Glucoside 4.7 ± 2.2 25.7 ± 4.3 6
trans-Zeatin 0.8a 0.65 ± 0.0 1
Zeatin riboside 2.2 ± 1.7 42.9 ± 5.4 20
Zeatin riboside 5′-monophosphate 2.4 ± 1.3 11.4 ± 2.0 5
Zeatin O-glucoside 6.5 ± 1.0 525 ± 105 81
Zeatin riboside O-glucoside 2.3 ± 0.3 14.8 ± 0.0 6
Zeatin 7-glucoside 148 ± 26 751 ± 25 5
Zeatin 9-glucoside 21 ± 20 257 ± 50 12
Dihydrozeatin 1.4a 0.2 ± 0.1 0.2
Dihydrozeatin riboside 1.1 ± 0.7 2.8 ± 0.3 3
Dihydrozeatin riboside 5′-monophosphate 1.0 ± 0.3 1.4 ± 0.0 1
Dihydrozeatin O-glucoside 7.1 ± 2.5 322 ± 46 45
Dihydrozeatin riboside O-glucoside 2.3 ± 0.3 11.7 ± 3.1 5
Dihydrozeatin 7-glucoside 2.8 ± 1.6 15.1 ± 7.2 5
Dihydrozeatin 9-glucoside 9.7 ± 9.1 13.9 ± 0.0 1

Mutant calli and wild-type seedlings (wt, s) were grown in vitro on solidified hormone-free MS medium. Cytokinin concentrations were determined by micro liquid chromatography with column switch configuration coupled to positive ion electrospray tandem mass spectrometry using multiple reactant monitoring as described in “Materials and Methods.” The data are the means ± se of two biological independent replications.

a

Data from a single sample. 

b

Increase in c1 callus compared with wild-type seedlings.