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以氧化氘为跟踪探针通过拉曼光谱监测微藻细胞中的光合活性

Monitoring Photosynthetic Activity in Microalgal Cells by Raman Spectroscopy with Deuterium Oxide as a Tracking Probe.

作者信息

Yonamine Yusuke, Suzuki Yuta, Ito Takuro, Miura Yoshiko, Goda Keisuke, Ozeki Yasuyuki, Hoshino Yu

机构信息

Department of Chemical Engineering, Kyushu University, 744 Motooka, Fukuoka, 819-0395, Japan.

Department of Electrical Engineering and Information Systems, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8656, Japan.

出版信息

Chembiochem. 2017 Oct 18;18(20):2063-2068. doi: 10.1002/cbic.201700314. Epub 2017 Sep 7.

Abstract

Microalgae offer great potential for the production of biofuel, but high photosynthetic activity is demanded for the practical realisation of microalgal biofuels. To this end, it is essential to evaluate the photosynthetic activity of single microalgal cells in a heterogeneous population. In this study, we present a method to monitor the photosynthetic activity of microalgae (in particular Euglena gracilis, a microalgal species of unicellular, photosynthetic, flagellate protists as our model organism) at single-cell resolution by Raman spectroscopy with deuterium from deuterium oxide (D O) as a tracking probe. Specifically, we replaced H O in culture media with D O up to a concentration of 20 % without disturbing the growth rate of E. gracilis cells and evaluated C-D bond formation as a consequence of photosynthetic reactions by Raman spectroscopy. We used the probe to monitor the kinetics of the C-D bond formation in E. gracilis cells by incubating them in D O media under light irradiation. Furthermore, we demonstrated Raman microscopy imaging of each single E. gracilis cell to discriminate deuterated cells from normal cells. Our results hold great promise for Raman-based screening of E. gracilis and potentially other microalgae with high photosynthetic activity by using D O as a tracking probe.

摘要

微藻在生物燃料生产方面具有巨大潜力,但微藻生物燃料的实际应用需要高光合活性。为此,评估异质群体中单个微藻细胞的光合活性至关重要。在本研究中,我们提出了一种方法,以氧化氘(D₂O)中的氘作为追踪探针,通过拉曼光谱在单细胞分辨率下监测微藻(特别是纤细裸藻,一种单细胞、光合、具鞭毛的原生生物微藻物种作为我们的模式生物)的光合活性。具体而言,我们将培养基中的H₂O用D₂O替代,浓度高达20%,且不影响纤细裸藻细胞的生长速率,并通过拉曼光谱评估光合反应导致的C-D键形成。我们通过在光照下将纤细裸藻细胞置于D₂O培养基中孵育,利用该探针监测其细胞中C-D键形成的动力学。此外,我们展示了对每个单个纤细裸藻细胞的拉曼显微镜成像,以区分氘化细胞和正常细胞。我们的结果对于基于拉曼光谱利用D₂O作为追踪探针筛选纤细裸藻以及潜在地筛选其他具有高光合活性的微藻具有很大的前景。

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