Dmitry A. Cherepanov, Anastasiya A. Petrova, Mariya S. Fadeeva, Fedor E. Gostev, Ivan V. Shelaev, Victor A. Nadtochenko, Alexey Yu. Semenov
{"title":"绿色微藻小球藻光系统 I 光化学能量转换的特异性","authors":"Dmitry A. Cherepanov, Anastasiya A. Petrova, Mariya S. Fadeeva, Fedor E. Gostev, Ivan V. Shelaev, Victor A. Nadtochenko, Alexey Yu. Semenov","doi":"10.1134/S0006297924060129","DOIUrl":null,"url":null,"abstract":"<p>Primary excitation energy transfer and charge separation in photosystem I (PSI) from the extremophile desert green alga <i>Chlorella ohadii</i> grown in low light were studied using broadband femtosecond pump-probe spectroscopy in the spectral range from 400 to 850 nm and in the time range from 50 fs to 500 ps. Photochemical reactions were induced by the excitation into the blue and red edges of the chlorophyll Qy absorption band and compared with similar processes in PSI from the cyanobacterium <i>Synechocystis</i> sp. PCC 6803. When PSI from <i>C. ohadii</i> was excited at 660 nm, the processes of energy redistribution in the light-harvesting antenna complex were observed within a time interval of up to 25 ps, while formation of the stable radical ion pair P<sub>700</sub><sup>+</sup>A<sub>1</sub><sup>−</sup> was kinetically heterogeneous with characteristic times of 25 and 120 ps. When PSI was excited into the red edge of the Qy band at 715 nm, primary charge separation reactions occurred within the time range of 7 ps in half of the complexes. In the remaining complexes, formation of the radical ion pair P<sub>700</sub><sup>+</sup>A<sub>1</sub><sup>−</sup> was limited by the energy transfer and occurred with a characteristic time of 70 ps. Similar photochemical reactions in PSI from <i>Synechocystis</i> 6803 were significantly faster: upon excitation at 680 nm, formation of the primary radical ion pairs occurred with a time of 3 ps in ~30% complexes. Excitation at 720 nm resulted in kinetically unresolvable ultrafast primary charge separation in 50% complexes, and subsequent formation of P<sub>700</sub><sup>+</sup>A<sub>1</sub><sup>−</sup> was observed within 25 ps. The photodynamics of PSI from <i>C. ohadii</i> was noticeably similar to the excitation energy transfer and charge separation in PSI from the microalga <i>Chlamydomonas reinhardtii</i>; however, the dynamics of energy transfer in <i>C. ohadii</i> PSI also included slower components.</p>","PeriodicalId":483,"journal":{"name":"Biochemistry (Moscow)","volume":"89 6","pages":"1133 - 1145"},"PeriodicalIF":2.3000,"publicationDate":"2024-07-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Specificity of Photochemical Energy Conversion in Photosystem I from the Green Microalga Chlorella ohadii\",\"authors\":\"Dmitry A. Cherepanov, Anastasiya A. Petrova, Mariya S. 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When PSI from <i>C. ohadii</i> was excited at 660 nm, the processes of energy redistribution in the light-harvesting antenna complex were observed within a time interval of up to 25 ps, while formation of the stable radical ion pair P<sub>700</sub><sup>+</sup>A<sub>1</sub><sup>−</sup> was kinetically heterogeneous with characteristic times of 25 and 120 ps. When PSI was excited into the red edge of the Qy band at 715 nm, primary charge separation reactions occurred within the time range of 7 ps in half of the complexes. In the remaining complexes, formation of the radical ion pair P<sub>700</sub><sup>+</sup>A<sub>1</sub><sup>−</sup> was limited by the energy transfer and occurred with a characteristic time of 70 ps. Similar photochemical reactions in PSI from <i>Synechocystis</i> 6803 were significantly faster: upon excitation at 680 nm, formation of the primary radical ion pairs occurred with a time of 3 ps in ~30% complexes. Excitation at 720 nm resulted in kinetically unresolvable ultrafast primary charge separation in 50% complexes, and subsequent formation of P<sub>700</sub><sup>+</sup>A<sub>1</sub><sup>−</sup> was observed within 25 ps. 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Specificity of Photochemical Energy Conversion in Photosystem I from the Green Microalga Chlorella ohadii
Primary excitation energy transfer and charge separation in photosystem I (PSI) from the extremophile desert green alga Chlorella ohadii grown in low light were studied using broadband femtosecond pump-probe spectroscopy in the spectral range from 400 to 850 nm and in the time range from 50 fs to 500 ps. Photochemical reactions were induced by the excitation into the blue and red edges of the chlorophyll Qy absorption band and compared with similar processes in PSI from the cyanobacterium Synechocystis sp. PCC 6803. When PSI from C. ohadii was excited at 660 nm, the processes of energy redistribution in the light-harvesting antenna complex were observed within a time interval of up to 25 ps, while formation of the stable radical ion pair P700+A1− was kinetically heterogeneous with characteristic times of 25 and 120 ps. When PSI was excited into the red edge of the Qy band at 715 nm, primary charge separation reactions occurred within the time range of 7 ps in half of the complexes. In the remaining complexes, formation of the radical ion pair P700+A1− was limited by the energy transfer and occurred with a characteristic time of 70 ps. Similar photochemical reactions in PSI from Synechocystis 6803 were significantly faster: upon excitation at 680 nm, formation of the primary radical ion pairs occurred with a time of 3 ps in ~30% complexes. Excitation at 720 nm resulted in kinetically unresolvable ultrafast primary charge separation in 50% complexes, and subsequent formation of P700+A1− was observed within 25 ps. The photodynamics of PSI from C. ohadii was noticeably similar to the excitation energy transfer and charge separation in PSI from the microalga Chlamydomonas reinhardtii; however, the dynamics of energy transfer in C. ohadii PSI also included slower components.
期刊介绍:
Biochemistry (Moscow) is the journal that includes research papers in all fields of biochemistry as well as biochemical aspects of molecular biology, bioorganic chemistry, microbiology, immunology, physiology, and biomedical sciences. Coverage also extends to new experimental methods in biochemistry, theoretical contributions of biochemical importance, reviews of contemporary biochemical topics, and mini-reviews (News in Biochemistry).