Identification of a Xylogalacturonan Xylosyltransferase Involved in Pectin Biosynthesis inArabidopsis
Author(s) -
Jacob Krüger Jensen,
Susanne Oxenbøll Sørensen,
Jesper Harholt,
Naomi Geshi,
Yumiko Sakuragi,
Isabel Møller,
Joris Zandleven,
Adriana Bernal,
Niels Bjerg Jensen,
Charlotte Sörensen,
Markus Pauly,
G. Beldman,
William G. T. Willats,
Henrik Vibe Scheller
Publication year - 2008
Publication title -
the plant cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.324
H-Index - 341
eISSN - 1532-298X
pISSN - 1040-4651
DOI - 10.1105/tpc.107.050906
Subject(s) - nicotiana benthamiana , mutant , biochemistry , biology , arabidopsis , glycosylation , cell wall , wild type , xyloglucan , glycosyltransferase , golgi apparatus , gene , cell
Xylogalacturonan (XGA) is a class of pectic polysaccharide found in plant cell walls. The Arabidopsis thaliana locus At5g33290 encodes a predicted Type II membrane protein, and insertion mutants of the At5g33290 locus had decreased cell wall xylose. Immunological studies, enzymatic extraction of polysaccharides, monosaccharide linkage analysis, and oligosaccharide mass profiling were employed to identify the affected cell wall polymer. Pectic XGA was reduced to much lower levels in mutant than in wild-type leaves, indicating a role of At5g33290 in XGA biosynthesis. The mutated gene was designated xylogalacturonan deficient1 (xgd1). Transformation of the xgd1-1 mutant with the wild-type gene restored XGA to wild-type levels. XGD1 protein heterologously expressed in Nicotiana benthamiana catalyzed the transfer of xylose from UDP-xylose onto oligogalacturonides and endogenous acceptors. The products formed could be hydrolyzed with an XGA-specific hydrolase. These results confirm that the XGD1 protein is a XGA xylosyltransferase. The protein was shown by expression of a fluorescent fusion protein in N. benthamiana to be localized in the Golgi vesicles as expected for a glycosyltransferase involved in pectin biosynthesis.
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