期刊
BIOTECHNOLOGY AND BIOENGINEERING
卷 110, 期 1, 页码 275-285出版社
WILEY
DOI: 10.1002/bit.24609
关键词
xylanosome; hydrolysis; yeast; surface-expression; xylanolytic enzymes; carbohydrate binding module
资金
- National Science Foundation [CBET-0903894]
- Div Of Chem, Bioeng, Env, & Transp Sys
- Directorate For Engineering [0903894] Funding Source: National Science Foundation
Five trimeric xylanosomes were successfully assembled on the cell surface of Saccharomyces cerevisiae. Three dockerin-tagged fungal enzymes, an endoxylanase (XynAc) from Thermomyces lanuginosus, a beta-xylosidase (XlnDt) from Aspergillus niger and an acetylxylan esterase (AwAXEf) from Aspergillus awamori, were displayed for the synergistic saccharification of birchwood xylan. The surface-expression scaffoldins were modular constructs with or without carbohydrate binding modules from Thermotoga maritima (family 22) or Clostridium thermocellum (family 3). The synergy due to enzymeenzyme and enzymesubstrate proximity, and the effects of binding domain choice and position on xylan hydrolysis were determined. The scaffoldin-based enzymes (with no binding domain) showed a 1.6-fold increase in hydrolytic activity over free enzymes; this can be attributed to enzymeenzyme proximity within the scaffoldin. The addition of a xylan binding domain from T. maritima improved hydrolysis by 2.1-fold relative to the scaffoldin without a binding domain (signifying enzymesubstrate synergy), and 3.3-fold over free enzymes, with a xylose productivity of 105?mg?g-1 substrate after 72?h hydrolysis. This system was also superior to the xylanosome carrying the cellulose binding module from C. thermocellum by 1.4-fold. Furthermore, swapping the xylan binding module position within the scaffoldin resulted in 1.5-fold more hydrolysis when the binding domain was adjacent to the endoxylanase. These results demonstrate the applicability of designer xylanosomes toward hemicellulose saccharification in yeast, and the importance of the choice and position of the carbohydrate binding module for enhanced synergy. Biotechnol. Bioeng. 2013; 110: 275285. (C) 2012 Wiley Periodicals, Inc.
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