Binding specificity and thermodynamics of a family 9 carbohydrate-binding module from Thermotoga maritima xylanase 10A

被引:107
作者
Boraston, AB
Creagh, AL
Alam, MM
Kormos, JM
Tomme, P
Haynes, CA
Warren, RAJ
Kilburn, DG
机构
[1] Univ British Columbia, Biotechnol Lab, Vancouver, BC V6T 1Z3, Canada
[2] Univ British Columbia, Prot Engn Network Ctr Excellence, Vancouver, BC V6T 1Z3, Canada
[3] Univ British Columbia, Dept Microbiol & Immunol, Vancouver, BC V6T 1Z3, Canada
[4] Univ British Columbia, Dept Biol & Chem Engn, Vancouver, BC V6T 1Z3, Canada
关键词
D O I
10.1021/bi0101695
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 C-terminal family 9 carbohydrate-binding module of xylanase 10A from Thermotoga maritima (CBM9-2) binds to amorphous cellulose, crystalline cellulose, and the insoluble fraction of oat spelt xylan, The association constants (K-a) for adsorption to insoluble polysaccharides are 1 x 10(5) to 3 x 10(5) M-1. Of the soluble polysaccharides tested, CBM9-2 binds to barley beta -glucan, xyloglucan, and xylan. CBM9-2 binds specifically to the reducing ends of cellulose and soluble polysaccharides, a property that is currently unique to this CBM. CBM9-2 also binds glucose, xylose, galactose, arabinose, cellooligosaccharides, xylooligosaccharides, maltose, and lactose, with affinities ranging from 10(3) M-1 for monosaccharides to 10(6) M-1 for disaccharides and oligosaccharides. Cellooligosaccharides longer than two glucose units do not bind with improved affinity, indicating that cellobiose is sufficient to occupy the entire binding site. In general, the binding reaction is dominated by favorable changes in enthalpy, which are partially compensated by unfavorable entropy changes.
引用
收藏
页码:6240 / 6247
页数:8
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