Langkilde AE

References (1)

Title : The structural basis of fungal glucuronoyl esterase activity on natural substrates - Ernst_2020_Nat.Commun_11_1026
Author(s) : Ernst HA , Mosbech C , Langkilde AE , Westh P , Meyer AS , Agger JW , Larsen S
Ref : Nat Commun , 11 :1026 , 2020
Abstract : Structural and functional studies were conducted of the glucuronoyl esterase (GE) from Cerrena unicolor (CuGE), an enzyme catalyzing cleavage of lignin-carbohydrate ester bonds. CuGE is an alpha/beta-hydrolase belonging to carbohydrate esterase family 15 (CE15). The enzyme is modular, comprised of a catalytic and a carbohydrate-binding domain. SAXS data show CuGE as an elongated rigid molecule where the two domains are connected by a rigid linker. Detailed structural information of the catalytic domain in its apo- and inactivated form and complexes with aldouronic acids reveal well-defined binding of the 4-O-methyl-a-D-glucuronoyl moiety, not influenced by the nature of the attached xylo-oligosaccharide. Structural and sequence comparisons within CE15 enzymes reveal two distinct structural subgroups. CuGE belongs to the group of fungal CE15-B enzymes with an open and flat substrate-binding site. The interactions between CuGE and its natural substrates are explained and rationalized by the structural results, microscale thermophoresis and isothermal calorimetry.
ESTHER : Ernst_2020_Nat.Commun_11_1026
PubMedSearch : Ernst_2020_Nat.Commun_11_1026
PubMedID: 32094331
Gene_locus related to this paper: cerui-gce