The taxonomic range for the selected organisms is: Brassica oleracea var. botrytis The expected taxonomic range for this enzyme is: Eukaryota, Bacteria
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REACTION
REACTION DIAGRAM
COMMENTARY
ORGANISM
UNIPROT
LITERATURE
breaks a beta-(1->4) bond in the backbone of a xyloglucan and transfers the xyloglucanyl segment on to O-4 of the non-reducing terminal glucose residue of an acceptor, which can be a xyloglucan or an oligosaccharide of xyloglucan
enzyme possesss the catalytic sequence motif EIDFE conserved in the glycosyl hydrolase family 16
certain cold-water-extractable, heat-stable polymers (CHPs), e.g. from cauliflower florets, mung bean shoots, and Arabidopsis cell-suspension cultures, can re-solubilise the bound enzyme, re-activating it
certain cold-water-extractable, heat-stable polymers (CHPs), e.g. from cauliflower florets, mung bean shoots, and Arabidopsis cell-suspension cultures, can re-solubilise the bound enzyme, re-activating it
xyloglucan endotransglucosylase (XET) activity, which cuts and re-joins hemicellulose chains in the plant cell wall, contributing to wall assembly and growth regulation, is the major activity of XTH proteins. During purification, XTHs often lose XET activity which, however, is restored by treatment with certain cold-water-extractable, heat-stable polymers (CHPs), e.g. from cauliflower florets, mung bean shoots, and Arabidopsis cell-suspension cultures
XTHs in dilute solution bind to diverse surfaces (e.g. glass and cellulose), and certain cold-water-extractable, heat-stable polymers (CHPs), e.g. from cauliflower florets, can re-solubilise the bound enzyme, re-activating it. Cell walls prepared from cauliflower florets, mung bean shoots and Arabidopsis cell-suspension cultures each contain endogenous, tightly bound, inactive XTHs, which are likewise rapidly solubilised and thus activated by cauliflower XTH-activating factor (XAF). Analysis of XTH-activating factor (XAF) activity of CHP preparations from diverse plant sources, CHPs from all plants tested possess XAF activity, overview
XTHs in dilute solution bind to diverse surfaces (e.g. glass and cellulose), and certain cold-water-extractable, heat-stable polymers (CHPs), e.g. from cauliflower florets, can re-solubilise the bound enzyme, re-activating it. Cell walls prepared from cauliflower florets, mung bean shoots and Arabidopsis cell-suspension cultures each contain endogenous, tightly bound, inactive XTHs, which are likewise rapidly solubilised and thus activated by cauliflower XTH-activating factor (XAF). Analysis of XTH-activating factor (XAF) activity of CHP preparations from diverse plant sources, CHPs from all plants tested possess XAF activity, overview
one N-glycosylation site situated close to the predicted catalytic residues, enzyme is a high-mannose-type glycan, glycosylation is required for activity, deglycosylation results in 40% loss of activity, overview
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PURIFICATION (Commentary)
ORGANISM
UNIPROT
LITERATURE
native enzyme from florets to homogeneity by adsorption chromatography, 55-140fold purification dependent on different assay methods for quantification
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CLONED (Commentary)
ORGANISM
UNIPROT
LITERATURE
DNA and amino acid sequence determination and analysis, expression in Pichia pastoris resulting in a recombinant enzyme which is more highly mannosylated than the native enzyme without having influence on activity
Xyloglucan endotransglucosylase/hydrolases (XTHs) are inactivated by binding to glass and cellulosic surfaces, and released in active form by a heat-stable polymer from cauliflower florets
J. Plant Physiol.
218
135-143
2017
Arabidopsis thaliana (P24806), Vigna radiata (Q5MB21), Brassica oleracea var. botrytis (Q6YDN9), Brassica oleracea var. botrytis