Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/59872
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Type: Journal article
Title: The genetics, transcriptional profiles, and catalytic properties of UDP-α-D-xylose 4-epimerases from barley
Other Titles: The genetics, transcriptional profiles, and catalytic properties of UDP-alpha-D-xylose 4-epimerases from barley
Author: Zhang, Q.
Shirley, N.
Burton, R.
Lahnstein, J.
Hrmova, M.
Fincher, G.
Citation: Plant Physiology, 2010; 153(2):555-568
Publisher: Amer Soc Plant Physiologists
Issue Date: 2010
ISSN: 0032-0889
1532-2548
Statement of
Responsibility: 
Qisen Zhang, Neil J. Shirley, Rachel A. Burton, Jelle Lahnstein, Maria Hrmova and Geoffrey B. Fincher
Abstract: Cell walls in the grasses contain relatively high levels of heteroxylans and, in particular, arabinoxylans. Enzymes and corresponding genes that are involved in the provision of sugar nucleotide substrates represent potential control points for arabinoxylan biosynthesis. Following expressed sequence tag database analyses, three genes encoding barley (Hordeum vulgare) UDP-D-xylose 4-epimerases (UXE; EC 5.1.3.5), designated HvUXE1, HvUXE2, and HvUXE3, were cloned and their positions on genetic maps defined. To confirm the identity of the genes, a cDNA construct encoding HvUXE1 was expressed in Pichia pastoris. The purified, recombinant HvUXE1 catalyzed the freely reversible interconversion of UDP-{alpha}-D-xylopyranose and UDP-β-L-arabinopyranose, with Km values of 1.8 and 1.4 mM, respectively. At equilibrium, the ratio of substrate to product was approximately 1:1. Each molecule of heterologously expressed HvUXE1 enzyme contained about one molecule of noncovalently bound NAD+. Molecular modeling provided a structural rationale for the substrate specificity of the UDP-D-xylose 4-epimerase and, in particular, explained its tight specificity for UDP-xylose compared with other sugar nucleotide epimerases. Quantitative transcript analyses performed for each of the three genes in a range of organs showed, inter alia, that in developing barley endosperm HvUXE1 and HvUXE3 mRNA levels peaked at a time when UDP-{alpha}-D-xylopyranose synthase (UXS) transcripts also reached a maximum and when arabinoxylan biosynthesis was initiated. Furthermore, the data revealed that the transcription of HvUXE and HvUXS gene family members is coordinated with the incorporation of pentose sugars onto cell walls in barley leaves, roots, and developing endosperm.
Keywords: Cell Wall; Hordeum; Carbohydrate Epimerases; Uridine Diphosphate Sugars; Xylose; Plant Proteins; RNA, Plant; Chromosome Mapping; Cloning, Molecular; Gene Expression Profiling; Sequence Alignment; Phylogeny; Gene Expression Regulation, Plant; Amino Acid Sequence; Substrate Specificity; Models, Molecular; Molecular Sequence Data; Endosperm
Rights: © 2010 American Society of Plant Biologists. OPEN ACCESS ARTICLE
RMID: 0020098052
DOI: 10.1104/pp.110.157644
Appears in Collections:Agriculture, Food and Wine publications

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