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nph12544-sup-0001-FigS1.pptxapplication/pptx98KFig. S1 HopQ1 possesses a well conserved nucleoside hydrolase (NH) domain close to its C-terminus.
nph12544-sup-0002-FigS2.jpgimage/jpg127KFig. S2 HopQ1 and the mutant forms of HopQ1 induce cell death in Nicotiana benthamiana on prolonged expression.
nph12544-sup-0003-FigS3.pptxapplication/pptx1297KFig. S3 Subcellular localization of HopQ1 in Nicotiana benthamiana.
nph12544-sup-0004-FigS4.pptxapplication/pptx1576KFig. S4 HopQ1 expression interferes with root development in Arabidopsis.
nph12544-sup-0005-FigS5.pptxapplication/pptx65KFig. S5 In vivo content of phytohormones related to PRR regulation in Arabidopsis.
nph12544-sup-0006-FigS6.pptxapplication/pptx73KFig. S6 In vivo content of CK variants. Hormone concentrations in leaf tissue of 6-wk-old Arabidopsis Col-0 lines expressing HopQ1 from the β-estradiol-inducible XVE promoter were determined by HPLC-MS analysis.
nph12544-sup-0007-FigS7.pptxapplication/pptx52KFig. S7 Induction of the putative CK responsive gene NbARR5 in HopQ1 expressing transiently transformed Nicotiana benthamiana tissue.
nph12544-sup-0008-FigS8.pptxapplication/pptx619KFig. S8 In vitro CK hydrolysis.
nph12544-sup-0009-FigS9.pptxapplication/pptx147KFig. S9 Exogenous application of trans-zeatin (tZ) CK forms in low concentrations leads to suppression of PTI responses in Nicotiana benthamiana.
nph12544-sup-0010-FigS10.pptxapplication/pptx56KFig. S10 Model for the interaction between CKs and immunity.
nph12544-sup-0011-TableS1-S2.docxWord document22K

Table S1 Strains and plasmids used in this study

Table S2 Primers used in this study