Deep oxidation of glucose in enzymatic fuel cells through a synthetic enzymatic pathway containing a cascade of two thermostable dehydrogenases

详细信息	查看全文 | 推荐本文 |

• 作者：Zhiguang Zhu^a ; Fangfang Sun^a ; Xiaozhou Zhang^a ; ^d ; Y.-H. Percival Zhang^a ; ^b ; ^c ; ^d ; ^{ypzhang@vt.edu}
• 关键词：Deep oxidation ; Enzymatic fuel cell ; Glucose biobattery ; Thermoenzyme ; Synthetic enzymatic pathway
• 刊名：Biosensors and Bioelectronics
• 出版年：2012
• 期刊代码：12_09565663
• 类别：ch
• 出版时间：June-July, 2012
• 卷：36
• 期：1
• 页码：110-115
• 文件大小：568 K

摘要

A synthetic enzymatic pathway was designed for the deep oxidation of glucose in enzymatic fuel cells (EFCs). Polyphosphate glucokinase converts glucose to glucose-6-phosphate using low-cost, stable polyphosphate rather than costly ATP. Two NAD-dependent dehydrogenases (glucose-6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase) that were immobilized on the bioanode were responsible for generating two NADH per glucose-6-phosphate (i.e., four electrons were generated per glucose via a diaphorase-vitamin K₃ electron shuttle system at the anode). Additionally, to prolong the enzyme lifetime and increase the power output, all of the recombinant enzymes that originated from thermophiles were expressed in Escherichia coli and purified to homogeneity. The maximum power density of the EFC with two dehydrogenases was 0.0203 mW cm^鈭? in 10 mM glucose at room temperature, which was 32%higher than that of an EFC with one dehydrogenase, suggesting that the deep oxidation of glucose had occurred. When the temperature was increased to 50 掳C, the maximum power density increased to 0.322 mW cm^鈭?, which was approximately eight times higher than that based on mesophilic enzymes at the same temperature. Our results suggest that the deep oxidation of glucose could be achieved by using multiple dehydrogenases in synthetic cascade pathways and that high power output could be achieved by using thermostable enzymes at elevated temperatures.