Rapid-Scan Time-Resolved ATR-FTIR Study on the Photoassembly of the Water-Oxidizing Mn4CaO5 Cluster in Photosystem II
The catalytic center of photosynthetic water oxidation, the Mn4CaO5 cluster, is assembled in photosystem II (PSII) through a light-driven process called photoactivation, whose mechanism remains elusive. Here, we used rapid-scan time-resolved Fourier transform infrared (FTIR) spectroscopy combined wi...
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Veröffentlicht in: | The journal of physical chemistry. B 2021-04, Vol.125 (16), p.4031-4045 |
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description | The catalytic center of photosynthetic water oxidation, the Mn4CaO5 cluster, is assembled in photosystem II (PSII) through a light-driven process called photoactivation, whose mechanism remains elusive. Here, we used rapid-scan time-resolved Fourier transform infrared (FTIR) spectroscopy combined with the attenuated total reflection (ATR) technique to monitor the photoactivation process. Rapid-scan ATR-FTIR spectra of apo-PSII with Mn2+ upon flash illumination showed spectral features typical of carboxylate stretching vibrations, which were attributed to two carboxylate ligands, D1-D170 and D1-E189, by quantum chemical calculations. The FTIR signal decayed with a time constant of ∼0.7 s, showing that the subsequent “dark rearrangement” step occurred with a low quantum yield and Mn3+ ions were mostly released during this decay. Simulation of the kinetic process provided a slow intrinsic rate of the dark rearrangement, which was attributed to a large protein conformational change. The photoassembly mechanism of the Mn4CaO5 cluster is proposed based on these findings. |
doi_str_mv | 10.1021/acs.jpcb.1c01624 |
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Here, we used rapid-scan time-resolved Fourier transform infrared (FTIR) spectroscopy combined with the attenuated total reflection (ATR) technique to monitor the photoactivation process. Rapid-scan ATR-FTIR spectra of apo-PSII with Mn2+ upon flash illumination showed spectral features typical of carboxylate stretching vibrations, which were attributed to two carboxylate ligands, D1-D170 and D1-E189, by quantum chemical calculations. The FTIR signal decayed with a time constant of ∼0.7 s, showing that the subsequent “dark rearrangement” step occurred with a low quantum yield and Mn3+ ions were mostly released during this decay. Simulation of the kinetic process provided a slow intrinsic rate of the dark rearrangement, which was attributed to a large protein conformational change. 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B</title><addtitle>J. Phys. Chem. B</addtitle><description>The catalytic center of photosynthetic water oxidation, the Mn4CaO5 cluster, is assembled in photosystem II (PSII) through a light-driven process called photoactivation, whose mechanism remains elusive. Here, we used rapid-scan time-resolved Fourier transform infrared (FTIR) spectroscopy combined with the attenuated total reflection (ATR) technique to monitor the photoactivation process. Rapid-scan ATR-FTIR spectra of apo-PSII with Mn2+ upon flash illumination showed spectral features typical of carboxylate stretching vibrations, which were attributed to two carboxylate ligands, D1-D170 and D1-E189, by quantum chemical calculations. The FTIR signal decayed with a time constant of ∼0.7 s, showing that the subsequent “dark rearrangement” step occurred with a low quantum yield and Mn3+ ions were mostly released during this decay. Simulation of the kinetic process provided a slow intrinsic rate of the dark rearrangement, which was attributed to a large protein conformational change. The photoassembly mechanism of the Mn4CaO5 cluster is proposed based on these findings.</description><subject>B: Biophysical and Biochemical Systems and Processes</subject><issn>1520-6106</issn><issn>1520-5207</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNotkE1PwzAMhiMEEmNw55gjBzKcpMmS41SxUWloqCviWKVtyjr1YywtYvx6wraDZfv1a8t6ELqnMKHA6JPJ3WS7y7MJzYFKFlygERUMiI_p5bmWFOQ1unFuC8AEU3KEhtjsqoKsc9PipGosia3r6m9b4FkSk3kSxXjdD8UBdy3uNxa_bbq-M87ZJqu9WB7FD9PbPVn9VEX1W7Wf-LUNQrMSOKwH5ye4ak977uDbBkfRLboqTe3s3TmP0fv8OQlfyHK1iMLZkhjGaE-mRguelcC1krmVAJznWgsrlbGqDApmiyxTBkBlXBQlVRpoQLVUQgSCg-Bj9HC6u9t3X4N1fdpULrd1bVrbDS5lggZCC-DKWx9PVg8y3XbDvvWPpRTSf7rpUfR00zNd_gexC22K</recordid><startdate>20210429</startdate><enddate>20210429</enddate><creator>Sato, Akihiko</creator><creator>Nakano, Yuki</creator><creator>Nakamura, Shin</creator><creator>Noguchi, Takumi</creator><general>American Chemical Society</general><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-3281-6827</orcidid></search><sort><creationdate>20210429</creationdate><title>Rapid-Scan Time-Resolved ATR-FTIR Study on the Photoassembly of the Water-Oxidizing Mn4CaO5 Cluster in Photosystem II</title><author>Sato, Akihiko ; Nakano, Yuki ; Nakamura, Shin ; Noguchi, Takumi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a221t-7a953bf03986ce60033c995e68ae8f4d2edbb8a008b35df189014196855453053</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>B: Biophysical and Biochemical Systems and Processes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sato, Akihiko</creatorcontrib><creatorcontrib>Nakano, Yuki</creatorcontrib><creatorcontrib>Nakamura, Shin</creatorcontrib><creatorcontrib>Noguchi, Takumi</creatorcontrib><collection>MEDLINE - Academic</collection><jtitle>The journal of physical chemistry. 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Here, we used rapid-scan time-resolved Fourier transform infrared (FTIR) spectroscopy combined with the attenuated total reflection (ATR) technique to monitor the photoactivation process. Rapid-scan ATR-FTIR spectra of apo-PSII with Mn2+ upon flash illumination showed spectral features typical of carboxylate stretching vibrations, which were attributed to two carboxylate ligands, D1-D170 and D1-E189, by quantum chemical calculations. The FTIR signal decayed with a time constant of ∼0.7 s, showing that the subsequent “dark rearrangement” step occurred with a low quantum yield and Mn3+ ions were mostly released during this decay. Simulation of the kinetic process provided a slow intrinsic rate of the dark rearrangement, which was attributed to a large protein conformational change. The photoassembly mechanism of the Mn4CaO5 cluster is proposed based on these findings.</abstract><pub>American Chemical Society</pub><doi>10.1021/acs.jpcb.1c01624</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0002-3281-6827</orcidid></addata></record> |
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title | Rapid-Scan Time-Resolved ATR-FTIR Study on the Photoassembly of the Water-Oxidizing Mn4CaO5 Cluster in Photosystem II |
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