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Novel Function of CtXyn5A from Acetivibrio thermocellus: Dual Arabinoxylanase and Feruloyl Esterase Activity Occur in the Same Active Site

Research Portal at Lubd University. 2022-05; 
Eva Schmitz, Savvina Leontakianakou, Patrick Adlercreutz, Eva Nordberg Karlsson, Javier A. Linares-Pastén
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Gene Synthesis Production and Purification of CtXyn5A-E279S. The truncated gene encoding the two-domain construct (GH5-CBM6) corresponding to CtXyn5A from A. thermocellus, with the catalytic nucleophile Glu279replaced by Ser (E279S) was chemically synthesized (GenScript USA Inc., Piscataway, NJ, USA) with native codons and cloned into the expression vector pET21b (+) with a His-tag introduced to the C-terminus. Get A Quote

摘要

Uncharacterized side activities of enzymes can have significant negative effects on reaction products and yields. Hence, their identification and characterization is crucial for the development of successful reaction systems. Here, we report the presence of feruloyl esterase activity in CtXyn5A from Acetivibrio thermocellus besides its well-known arabinoxylanase activity for the first time. Both reaction types appear to be catalysed in the same active site in two subsequential steps. The ferulic acid substituent is cleaved off first, followed by the hydrolysis of the xylan backbone. The esterase activity on complex carbohydrates was found to be higher than the one of a designated ferulic acid esterase (E-FAERU)... More

关键词

Enzyme catalysis,Multifunctional enzymes,Arabino-xylanase,Feruloyl esterase,Carbohydrates
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