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光诱导部分还原氧物种的形成限制了基于光系统 1 的生物阴极的寿命。

Light-induced formation of partially reduced oxygen species limits the lifetime of photosystem 1-based biocathodes.

机构信息

Analytical Chemistry - Center for Electrochemical Sciences (CES), Ruhr-Universität Bochum, Universitätsstr. 150, Bochum, 44780, Germany.

Center for Electrochemical Sciences - Molecular Nanostructures, Ruhr-Universität Bochum, Universitätsstr. 150, Bochum, 44780, Germany.

出版信息

Nat Commun. 2018 May 17;9(1):1973. doi: 10.1038/s41467-018-04433-z.

Abstract

Interfacing photosynthetic proteins specifically photosystem 1 (PS1) with electrodes enables light-induced charge separation processes for powering semiartificial photobiodevices with, however, limited long-term stability. Here, we present the in-depth evaluation of a PS1/Os-complex-modified redox polymer-based biocathode by means of scanning photoelectrochemical microscopy. Focalized local illumination of the bioelectrode and concomitant collection of HO at the closely positioned microelectrode provide evidence for the formation of partially reduced oxygen species under light conditions. Long-term evaluation of the photocathode at different O concentrations as well as after incorporating catalase and superoxide dismutase reveals the particularly challenging issue of avoiding the generation of reactive species. Moreover, the evaluation of films prepared with inactivated PS1 and free chlorophyll points out additional possible pathways for the generation of oxygen radicals. To avoid degradation of PS1 during illumination and hence to enhance the long-term stability, the operation of biophotocathodes under anaerobic conditions is indispensable.

摘要

将光合蛋白(尤其是光系统 1(PS1))与电极进行界面连接,可实现用于半人工光电设备的光诱导电荷分离过程,但长期稳定性有限。在这里,我们通过扫描光电化学显微镜对 PS1/Os 复合物修饰的氧化还原聚合物基生物阴极进行了深入评估。生物电极的聚焦局部照明和紧密定位的微电极上 HO 的伴随收集为在光照条件下形成部分还原氧物种提供了证据。在不同 O 浓度下以及在加入过氧化氢酶和超氧化物歧化酶后对光电阴极进行的长期评估揭示了避免生成活性物质这一特别具有挑战性的问题。此外,对用失活的 PS1 和游离叶绿素制备的薄膜进行的评估指出了生成氧自由基的其他可能途径。为了避免 PS1 在光照下的降解并因此提高长期稳定性,在厌氧条件下操作生物光电阴极是必不可少的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fbe/5958124/3158eeb12eab/41467_2018_4433_Fig1_HTML.jpg

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