4.2 Article

Production and characterization of Acidothermus cellulolyticus endoglucanase in Pichia pastoris

期刊

PROTEIN EXPRESSION AND PURIFICATION
卷 77, 期 2, 页码 153-158

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.pep.2011.01.006

关键词

Thermostable endoglucanase; Synthetic gene; Methylumbelliferyl-beta-D-cellobioside; Codon optimization; alpha-Mating factor signal peptide; Michaelis-Menten kinetic parameters

资金

  1. Chevron Technology Ventures, Inc RSO [23]
  2. National Science Foundation (DGE) [0653984]
  3. Direct For Education and Human Resources
  4. Division Of Graduate Education [0653984] Funding Source: National Science Foundation

向作者/读者索取更多资源

The endoglucanase (E1) from Acidothermus cellutolyticus has been used extensively in cellulase research. The goal of this work was to produce high levels of this enzyme in a system that facilitates purification. A codon-optimized synthetic gene for A. cellulolyticus E1 with a C-terminal histidine tag was cloned into the genome of Pichia pastoris. Strain KM71H expressed the most enzyme, with a yield of 550 mg/L culture supernatant. The temperature optimum (80 degrees C) and pH optimum (5.1) of the purified enzyme agree with previously determined values for the enzyme produced in other systems. Michaelis-Menten kinetic parameters were determined, using a fluorescent substrate (methylumbelliferyl-beta-D-cellobioside) at various temperatures. This thermostable enzyme can be used in future cellulosic biofuels-related research. (c) 2011 Elsevier Inc. All rights reserved.

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