Regulation of chondroitin sulfate biosynthesis by specific sulfation: Acceptor specificity of serum beta-GalNAc transferase revealed by structurally defined oligosaccharides

被引:54
作者
Kitagawa, H
Tsutsumi, K
Ujikawa, M
Goto, F
Tamura, J
Neumann, KW
Ogawa, T
Sugahara, K
机构
[1] KOBE PHARMACEUT UNIV,DEPT BIOCHEM,KOBE,HYOGO 658,JAPAN
[2] RIKEN,INST PHYS & CHEM RES,WAKO,SAITAMA 35101,JAPAN
[3] UNIV TOKYO,GRAD SCH AGR & LIFE SCI,TOKYO 113,JAPAN
关键词
chondroitin sulfate; GalNAc transferase; glycosaminoglycan; proteoglycan; sulfated oligosaccharides;
D O I
10.1093/glycob/7.4.531
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The relationship between sulfation and polymerization in chondroitin sulfate (CS) biosynthesis has been poorly understood, In this study, we investigated the specificity of bovine serum UDP-GalNAc: CS beta-GalNAc transferase responsible for chain elongation using structurally defined acceptor substrates, They consisted of tetra- and hexasaecharide-serines that were chemically synthesized and various regular oligosaccharides with a GlcA residue at the nonreducing terminus, prepared from chondroitin and CS using testicular hyaluronidase. The enzyme preparation was obtained from fetal bovine serum by means of heparin-Sepharose affinity chromatography, The preparation did not contain the alpha-GalNAc transferase recently demonstrated in fetal bovine serum (Kitagawa et at, J, Biol., Chem,, 270, 22190-22195, 1995), that utilizes common acceptor substrates, The beta-GalNAc transferase used as accepters, two hexasaccharide-serines GlcA beta 1-3GalNAc beta 1-4GlcA beta 1-3Gal beta 1-3Gal beta 1-4Xyl beta 1-O-Ser and GlcA beta 1-3GalNAc(4-sulfate)beta 1-4GlcA beta 1-3Gal(4-sulfate)beta 1- 3Gal beta 1-4Xyl beta 1-O-Ser, but neither the monosulfated hexasaccharide-serine GlcA beta 1-3GalNAc(4-sulfate)beta 1-4GlcA beta 1-3Gal beta 1-3Gal beta 1-4Xyl beta 1-O-Ser nor tetrasaccharide-serines with or without a sulfate group at C-4 of the third sugar residue Gal-3 from the reducing end. The results indicated that the sulfate group at the Gal-3 C-4 markedly affected the transfer of GalNAc to the terminal GlcA, In addition, a sulfate group at C-4 of the reducing terminal GalNAc of regular tetrasaccharides remarkably enhanced the GalNAc transfer, suggesting that the enzyme recognizes up to the fourth saccharide residue from the nonreducing end, The level of incorporation into a tetra- or hexasaccharide containing a terminal 2-O-sulfated GlcA residue was significant, whereas there was no apparent incorporation into tetra- or hexasaccharides containing a terminal 3-O-sulfated GlcA or penultimate 4,6-O-disulfated GalNAc residue, These results indicated that sulfation reactions play important roles in chain elongation and termination.
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页码:531 / 537
页数:7
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