CAZyme discovery and design for sweet dreams

被引:57
作者
Andre, Isabelle [1 ,2 ,3 ]
Potocki-Veronese, Gabrielle [1 ,2 ,3 ]
Barbe, Sophie [1 ,2 ,3 ]
Moulis, Claire [1 ,2 ,3 ]
Remaud-Simeon, Magali [1 ,2 ,3 ]
机构
[1] Univ Toulouse, LISBP, INP, UPS,INSA, F-31077 Toulouse, France
[2] CNRS, UMR5504, F-31400 Toulouse, France
[3] INRA, UMR792 Ingn Syst Biol & Procedes, F-31400 Toulouse, France
关键词
GLYCOSIDE HYDROLASE; CHEMOENZYMATIC SYNTHESIS; ENZYMATIC GLYCOSYLATION; DIRECTED EVOLUTION; SPECIFICITY; ENZYMES; GLYCOSYNTHASE; EFFICIENT; GLYCOSYLTRANSFERASES; DERIVATIVES;
D O I
10.1016/j.cbpa.2013.11.014
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
Development of synthetic routes to complex carbohydrates and glyco-conjugates is often hampered by the lack of enzymes with requisite properties or specificities. Indeed, assembly or degradation of carbohydrates requires carbohydrate-active enzymes (CAZymes) able to act on a vast range of glycosidic monomers, oligomers or polymers in a regio-specific or stereo-specific manner in order to produce the desired structure. Sequence-based analyses allow finding the most original enzymes. Novel screening methods have emerged that enable a more efficient exploitation of the CAZyme diversity found in the microbial world or generated by protein engineering. Computational biology methods also play a prominent role in the success of CAZyme design. Such progress allows circumventing current limitations of carbohydrate synthesis and opens new opportunities related to the synthetic biology field.
引用
收藏
页码:17 / 24
页数:8
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