Co-operative binding of triplicate carbohydrate-binding modules from a thermophilic xylanase.

Article Details

Citation

Boraston AB, McLean BW, Chen G, Li A, Warren RA, Kilburn DG

Co-operative binding of triplicate carbohydrate-binding modules from a thermophilic xylanase.

Mol Microbiol. 2002 Jan;43(1):187-94.

PubMed ID
11849546 [ View in PubMed
]
Abstract

Family 6 carbohydrate-binding modules were amplified by polymerase chain reaction (PCR) from Clostridium stercorarium strain NCIB11754 genomic DNA as a triplet. Individually, these modules bound to xylooligosaccharides and cellooligosaccharides with affinities varying from approximately 3 x 10(3) M(-1) to approximately 1 x 10(5) M(-1). Tandem and triplet combinations of these modules bound co-operatively to soluble xylan and insoluble cellulose to give approximately 20- to approximately 40-fold increases in affinity relative to the individual modules. This co-operativity was an avidity effect resulting from the modules within the tandems and triplet interacting simultaneously with proximal binding sites on the polysaccharides. This occurred by both intrachain and interchain interactions. The duplication or triplication of modules appears to be linked to the growth temperature of the organism; co-operativity in these multiplets may compensate for the loss of affinity at higher temperatures.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Endo-1,4-beta-xylanase AQ8GJ44Details