An enzymatic method for preparation of homopolymannuronate blocks and strictly alternating sequences of mannuronic and guluronic units

被引:15
作者
Heyraud, A
Colin-Morel, P
Gey, C
Chavagnat, F
Guinand, M
Wallach, J
机构
[1] CNRS, Ctr Rech Macromol Vegetales, F-38041 Grenoble, France
[2] Univ Grenoble 1, F-38041 Grenoble, France
[3] Univ Claude Bernard, Lab Biochim Analyt & Synth Bioorgan, F-69622 Villeurbanne, France
关键词
bacterial alginate; Pseudomonas aeruginosa; alginate lyase; mannuronate lyase; poly-M-and poly-MG blocks;
D O I
10.1016/S0008-6215(98)00094-9
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
Two Pseudomonas aeruginosa alginates were lysed by an overexpressed polymannuronate lyase AlxM(B) (only acting on two or more consecutive, nonacetylated mannuronate units) to prepare either mannuronate blocks (poly-M blocks) with dp similar to 30, or strictly alternating sequences of mannuronic and guluronic acid (poly-MG blocks) with dp > 20. The poly-M blocks were obtained by lysis of a P. aeruginosa polymannuronate that has 50% O-acetylation at C-2 and C-3. The poly-MG blocks were obtained from a P. aeruginosa alginate that contained both mannuronate and guluronate residues. The polysaccharide was first deacetylated and then treated with the lyase to excise the mannuronate units from the alternating-MG blocks. Both types of blocks should have potent biological effects and should provide useful specific substrates for characterisation of other alginate lyases. (C) 1998 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:417 / 422
页数:6
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