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一种新型系统,结合了 L-抗坏血酸 2-磷酸的生物催化去磷酸化和生成的抗坏血酸的电化学氧化。

A novel system combining biocatalytic dephosphorylation of L-ascorbic acid 2-phosphate and electrochemical oxidation of resulting ascorbic acid.

机构信息

Department of Bioengineering, Faculty of Engineering, Nagaoka University of Technology, Nagaoka, Japan.

出版信息

Biosens Bioelectron. 2011 Mar 15;26(7):3382-5. doi: 10.1016/j.bios.2010.12.041. Epub 2011 Jan 4.

Abstract

An enzyme electrode was prepared with acid phosphatase (ACP) for development of a new electric power generation system using ascorbic acid 2-phosphate (AA2P) as a fuel. The properties of the electrode were investigated with respect to biocatalytic dephosphorylation of AA2P and electrochemical oxidation of resulting ascorbic acid (AA). The enzyme electrode was fabricated by immobilization of ACP through amide linkage onto a self-assembled monolayer of 3-mercaptopropionic acid on a gold electrode. AA2P was not oxidized on a bare gold electrode in the potential sweep range from -0.1 to +0.5 V vs. Ag/AgCl. However, the enzyme electrode gave an oxidation current in citric buffer solution of pH 5 containing 10 mM of AA2P. The oxidation current began to increase at +0.2V, and reached to 5.0 μA cm(-2) at +0.5 V. The potential +0.2 V corresponded to the onset of oxidation of ascorbic acid (AA). These results suggest that the oxidation current observed with the enzyme electrode is due to AA resulting from dephosphorylation of AA2P. The oxidation current increased with increasing concentration of AA2P and almost leveled off at around the concentration of 5mM. Thus the enzyme electrode brought about biocatalytic conversion of AA2P to AA, followed by electrochemical oxidation of the AA. The oxidation current is likely to be controlled by the biocatalytic reaction.

摘要

用酸性磷酸酶(ACP)制备了酶电极,以开发一种使用抗坏血酸 2-磷酸(AA2P)作为燃料的新型发电系统。研究了电极的生物催化去磷酸化 AA2P 和电化学氧化生成的抗坏血酸(AA)的性能。酶电极通过酰胺键将 ACP 固定在金电极上的 3-巯基丙酸自组装单层上制备。在 pH 5 的柠檬酸缓冲溶液中,在 -0.1 至 +0.5 V 相对于 Ag/AgCl 的电势范围内,裸金电极上不会氧化 AA2P。然而,在含有 10 mM AA2P 的酶电极在 +0.2 V 时给出氧化电流。氧化电流在 +0.2 V 时开始增加,并在 +0.5 V 时达到 5.0 μA cm(-2)。+0.2 V 的电势对应于 AA 的氧化起始点。这些结果表明,酶电极观察到的氧化电流归因于 AA2P 去磷酸化生成的 AA。随着 AA2P 浓度的增加,氧化电流增加,在约 5mM 左右几乎达到稳定。因此,酶电极将 AA2P 生物催化转化为 AA,然后进行 AA 的电化学氧化。氧化电流可能受生物催化反应控制。

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