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PMID: 1554366 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Xyloglucan endotransglycosylase, a new wall-loosening enzyme activity from plants.

The Biochemical journal ·Vol. 282 ( Pt 3) ·1992-03-15 ·Pages 821-8

Fry SC, Smith RC, Renwick KF, Martin DJ, Hodge SK, Matthews KJ

Abstract

1. Cell-free extracts of all plants tested contained a novel enzyme activity (xyloglucan endotransglycosylase, XET) able to transfer a high-Mr portion from a donor xyloglucan to a suitable acceptor such as a xyloglucan-derived nonasaccharide (Glc4Xyl3GalFuc; XG9). 2. A simple assay for the enzyme, using [3H]XG9 and based on the ability of the [3H]polysaccharide product to bind to filter paper, is described. 3. The enzyme was highly specific for xyloglucan as the glycosyl donor, and showed negligible transglycosylation of other polysaccharides, including CM-cellulose. 4. The Km for XG9 was 50 microM; certain other 3H-labelled xyloglucan oligosaccharides also acted as acceptors, and certain non-radioactive xyloglucan oligosaccharides competed with [3H]XG9 as acceptor; the minimum acceptor structure was deduced to be: [formula: see text] 5. The pH optimum was approx. 5.5 and the enzyme was less than half as active at pH 7.0. The enzyme was slightly activated by Ca2+, Mg2+, Mn2+, spermidine, ascorbate and 2-mercaptoethanol, and inhibited by Ag+, Hg2+, Zn2+ and La3+. 6. XET activity was essentially completely extracted by aqueous solutions of low ionic strength; Triton X-100, Ca2+, La3+, and Li+ did not enhance extraction. Negligible activity was left in the unextractable (cell-wall-rich) residue. 7. The enzyme differed from the major cellulases (EC 3.2.1.4) of pea in: (a) susceptibility to inhibition by cello-oligosaccharides, (b) polysaccharide substrate specificity, (c) inducibility by auxin, (d) requirement for salt in the extraction buffer and (e) activation by 2-mercaptoethanol. XET is therefore concluded to be a new enzyme activity (xyloglucan: xyloglucan xyloglucanotransferase; EC 2.4.1.-). 8. XET was detected in extracts of the growing portions of dicotyledons, monocotyledons (graminaceous and liliaceous) and bryophytes. 9. The activity was positively correlated with growth rate in different zones of the pea stem. 10. We propose that XET is responsible for cutting and rejoining intermicrofibrillar xyloglucan chains and that it thus causes the wall-loosening required for plant cell expansion.

MeSH Terms
Carbohydrate Sequence Cell Wall/enzymology Cellulase/metabolism Fabaceae/enzymology Glucans Glycosyltransferases/metabolism Molecular Sequence Data Plant Development Plant Proteins/metabolism Plants/enzymology Plants, Medicinal Polysaccharides/metabolism Substrate Specificity Xylans
Chemicals
Glucans Plant Proteins Polysaccharides Xylans xyloglucan Glycosyltransferases xyloglucan endotransglycosylase Cellulase
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Fry S C
Division of Biological Sciences, University of Edinburgh, U.K.
Smith R C
Renwick K F
Martin D J
Hodge S K
Matthews K J
References (13)
13 references, click to expand
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Article Info
Journal
The Biochemical journal
Abbr.
Biochem J
ISSN
0264-6021
Published
1992-03-15
Pages
821-8
Language
English
Region
England
NLM ID
2984726R
PMCID
PMC1130861
Subset
IM
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