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1 lyze the conversion of UDP-D-xylose to UDP-D-apiose.
2 selectively from di-O-isopropylidene-alpha-D-apiose.
3 discernible amounts of cell wall-associated apiose.
4 ermit insights into the mechanism by which d-apiose and other branched monosaccharides are formed.
5 n of UDP-d-glucuronate to a mixture of UDP-d-apiose and UDP-d-xylose with a turnover number of 0.3 mi
8 nts of aqueous methanol-acetonitrile-soluble apiose but did not result in discernible amounts of cell
13 to provide evidence that the ability to form apiose existed prior to the appearance of rhamnogalactur
16 ed that uridine 5'-diphospho-d-apiose (UDP-d-apiose) is formed from UDP-d-glucuronate by decarboxylat
17 r-bound galacturonate, xylose, arabinose and apiose residues (all produced via UDP-glucuronate) stemm
20 have established that uridine 5'-diphospho-d-apiose (UDP-d-apiose) is formed from UDP-d-glucuronate b
23 estral enzyme of UDP-xylose synthase and UDP-apiose/UDP-xylose synthase was diverged to two distinct
26 etyl-protected phosphonate analogue of UDP-D-apiose was synthesized and used in an in situ HPLC assay
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