Glycobiology vol 5 no 8 pp. 783-789, 1995
© 1995
research-article |
The backbone of the pectic polysaccharide rhamnogalacturonan I is cleaved by an endohydrolase and an endolyase
Complex Carbohydrate Research Center and Department of Biochemistry and Molecular Biology, The University of Georgia 220 Riverbend Road, Athens, GA 30602-4712, USA
1To whom correspondence should be addressed
Received on June 14, 1995; revised on July 27, 1995; accepted on July 31, 1995
Rhamnogalacturonan I (RG-I), a major pectic component of the primary walls of plant cells, is believed to play an important role in determining both the structure and functions of the walls. A more detailed structural description of RG-I is likely to lead to a greater understanding of the biological roles of this polysaccharide. Two enzymes secreted by Aspergillus aculeatus that have been cloned and expressed in a fungal system (Kofod et al., J. Biol Chem., 269, 29182-29189, 1994) cleave the RG-I backbone in an endo fashion and should assist in the further structural characterization of this polysaccharide. We found that both of the available preparations of the cloned enzymes were contaminated with exoglycanases, reducing their utility in structurally characterizing RG-I. We purified the enzymes to apparent homogeneity by ion-exchange chromatography and then used the purified enzymes to generate backbone oligosaccharide fragments from partially debranched sycamore RG-I. The backbone oligosaccharides, which were separated from larger pieces of partially debranched RG-I by gel-permeation chromatography, have been structurally characterized by 1H-NMR spectroscopy, electrospray MS, GC-MS, high-performance anion-exchange chromatography with pulsed amperometric detection (HPAEC-PAD) and UV spectroscopy. The results of these analyses establish that rhamnogalact-uronase A (RGase A) is an endohydrolase that cleaves the -4)-
-D-GaJpA-(1-2)-
-L-Rhqp glycosidic linkage. However, the purported rhamnogalacturonase B (RGase B) is, in fact, an endolyase that cleaves the -2)-
-L-Rhap-(1-4)-
-D-GalpA glycosidic linkage, thereby generating oligosaccharides terminating at the non-reducing end with a hex-4-enopyranosyluronic acid residue.
pectin rhamnogalacturonan I rhamnogalacturonase rhamnogalacturonolyase
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
J. Janecka, M. B. Jenkins, N. S. Brackett, L. W. Lion, and W. C. Ghiorse Characterization of a Sinorhizobium Isolate and Its Extracellular Polymer Implicated in Pollutant Transport in Soil Appl. Envir. Microbiol., January 1, 2002; 68(1): 423 - 426. [Abstract] [Full Text] [PDF] |
||||
![]() |
Z. C. Chen, M. Tanemura, and U. Galili Synthesis of {{alpha}}-gal epitopes (Gal{{alpha}}1-3Gal{beta}1-4GlcNAc-R) on human tumor cells by recombinant {{alpha}}1,3galactosyltransferase produced in Pichia pastoris Glycobiology, July 1, 2001; 11(7): 577 - 586. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Mutter, I. J. Colquhoun, G. Beldman, H. A. Schols, E. J. Bakx, and A. G.J. Voragen Characterization of Recombinant Rhamnogalacturonan alpha -l-Rhamnopyranosyl-(1,4)-alpha -d-Galactopyranosyluronide Lyase from Aspergillus aculeatus . An Enzyme That Fragments Rhamnogalacturonan I Regions of Pectin Plant Physiology, May 1, 1998; 117(1): 141 - 152. [Abstract] [Full Text] |
||||
![]() |
M. Mutter, G. Beldman, S. M. Pitson, H. A. Schols, and A. G.J. Voragen Rhamnogalacturonan alpha -d-Galactopyranosyluronohydrolase . An Enzyme That Specifically Removes the Terminal Nonreducing Galacturonosyl Residue in Rhamnogalacturonan Regions of Pectin Plant Physiology, May 1, 1998; 117(1): 153 - 163. [Abstract] [Full Text] |
||||


