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Exploring Bacterial Heparinase II Activities with Defined Substrates
Author(s) -
Bohlmann Lisa,
Chang ChihWei,
Beacham Ifor,
von Itzstein Mark
Publication year - 2015
Publication title -
chembiochem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.05
H-Index - 126
eISSN - 1439-7633
pISSN - 1439-4227
DOI - 10.1002/cbic.201500081
Subject(s) - chemistry , heparin , biochemistry , substrate (aquarium) , heparan sulfate , flavobacterium , bacteria , biology , pseudomonas , ecology , genetics
Bacterial heparinases that cleave heparan sulfate (HS) and heparin are widely used to generate low‐molecular‐weight heparins (LMWHs) and to structurally and functionally characterise heparin and HS biomolecules. We provide novel insights into the substrate specificity of heparinase II from two different bacteria: Pedobacter heparinus (formerly Flavobacterium heparinum ) and Bacteroides eggerthii . The activity towards various well‐defined HS oligosaccharides was investigated by 1 H NMR spectroscopy; this revealed distinct specificities for the two heparinases. Heparinase II from P. heparinus appears to be more active and displays a broader substrate specificity than B. eggerthii heparinase II. Furthermore, HS di‐ and tetrasaccharides inhibited B. eggerthii heparinase II activity. A better understanding of heparinase substrate specificity will contribute to the production of homogenous LMWHs, provide better characterisation of heparin and HS and assist therapeutic applications.