Related Experiment Video
Updated: May 8, 2026
Immobilization of Multi-biocatalysts in Alginate Beads for Cofactor Regeneration and Improved Reusability
Published on: April 22, 2016
[Gene cloning and characterization of a solvent-resistant glucose dehydrogenase from Bacillus sp. YX-1]
Botao Zhang1, Rongzhen Zhang, Lei Wang
1Key Laboratory of Industrial Biotechnology, Ministry of Education, School of Biotechnology, Jiangnan University, Wuxi 214122, China. zhangbotao1986@yahoo.com.cn
Objective:
A gene encoding solvent-resistant glucose dehydrogenase was cloned from Bacillus sp. YX-1 and expressed in Escherichia coli. The recombinant enzyme was then characterized.
Methods:
The glucose dehydrogenase gene was amplified from Bacillus sp. YX-1 genome according to its conserved sequences in Bacillus sp. The recombinant enzyme was over-expressed in E. coli and purified by HisTrap HP affinity chromatography. The purified enzyme were characterized.
Results:
The glucose dehydrogenase gene contains an open reading frame of 786 bp encoding 261 amino acids. The maximum activity was observed at 45 degrees C and pH 8.0. The recombinant enzyme was highly resistant to several organic solvents. More than 90% of the activity was maintained when the enzyme was incubated in 50% cyclohexane, octane, decane at home temperature for 1 h. In addition, the enzyme displayed broad substrate spectrum and has catalytic activity for several sugars to afford reduced coenzymes. It exhibits similar capability to regenerate either NADH or NADPH with specific activity of 8.37 U/mg and 8.62 U/mg for NAD+ and NADP+.
Conclusion:
The organic solvent-tolerant glucose dehydrogenase was explored successfully on the basis of bioinformatics analysis. The work supplied a new biocatalyst for the cofactor-regeneration during the reaction in organic phases catalyzed by oxidoreductases.
