Title of article :
Cloning and expression in E. coli of an organic solvent-tolerant and alkali-resistant glucose 1-dehydrogenase from Lysinibacillus sphaericus G10
Author/Authors :
Ding، نويسنده , , Hai-Tao and Du، نويسنده , , Yi-Qing and Liu، نويسنده , , Dan Feng and Li، نويسنده , , Ze-Li and Chen، نويسنده , , Xue-Jiao and Zhao، نويسنده , , Yu-Hua، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2011
Abstract :
The gene gdh encoding an organic solvent-tolerant and alkaline-resistant NAD(P)-dependent glucose 1-dehydrogenase (LsGDH) was cloned from Lysinibacillus sphaericus G10 and expressed in Escherichia coli. The recombinant LsGDH exhibited maximum activity at pH 9.5 and 50 °C. LsGDH displayed high stability at a wide pH ranging from 6.5 to 10.0 and was stable after incubation at 30 °C for 1 week in 25 mM sodium phosphate buffer (pH 6.5) in the absence or presence of NaCl. The activity of LsGDH was enhanced by Li+, Na+, K+, NH 4 + , Mg2+, and EDTA at pH 8.0. LsGDH exhibited high tolerance to 60% DMSO, 30% acetone, 30% methanol, 30% ethanol, 10% n-propanol, 30% isopropanol, 60% n-hexanol and 30% n-hexane. The relationship between stability and chain length of the alcohols fit a Gaussian distribution model (R2 ⩾ 0.94), and demonstrated lowest enzyme stability in C4-alcohol. The results suggested that LsGDH was potentially useful for coenzyme regeneration in organic solvents or under alkaline conditions.
Keywords :
Organic solvent-tolerance , Glucose 1-dehydrogenase , Coenzyme regeneration , Alkaline-resistance
Journal title :
Bioresource Technology
Journal title :
Bioresource Technology