Anomalous Temperature Dependence of the Triplet-Triplet Energy Transfer in Cereibacter sphaeroides I(L177)H Mutant Reaction Centers
In photosynthetic reaction centers, quenching of the primary donor triplet state by energy transfer to the carotenoid molecule provides efficient suppression of generation of singlet-excited oxygen, potent chemical oxidant. This process in the Cereibacter sphaeroides reaction centers is thermoactiva...
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Veröffentlicht in: | Biochemistry (Moscow) 2024-09, Vol.89 (9), p.1573-1581 |
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creator | Fufina, Tatiana Yu Vasilieva, Lyudmila G. Klenina, Irina B. Proskuryakov, Ivan I. |
description | In photosynthetic reaction centers, quenching of the primary donor triplet state by energy transfer to the carotenoid molecule provides efficient suppression of generation of singlet-excited oxygen, potent chemical oxidant. This process in the
Cereibacter sphaeroides
reaction centers is thermoactivated, and discontinues at temperatures below 40 K. In these reaction centers, substitution of amino acid residue isoleucine at the 177 position of the L-subunit with histidine results in the sharp decrease of activation energy, so that the carotenoid triplets are populated even at 10 K. Activation energy of the
T-T
energy transfer was estimated as 7.5 cm
–1
, which is more than 10-fold lower than activation energy in the wild type reaction centers. At certain temperatures, the energy transfer in the mutant is decelerated, which is related to the increase of effective distance of the triplet-triplet transfer. To the best of our knowledge, the described mutation presents the first reaction center modification leading to the significant decrease in activation energy of the
T-T
energy transfer to carotenoid molecule. The I(L177)H mutant reaction centers present a considerable interest for further studies of the triplet state quenching mechanisms, and of other photophysical and photochemical processes in the reaction centers of bacterial photosynthesis. |
doi_str_mv | 10.1134/S0006297924090049 |
format | Article |
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Cereibacter sphaeroides
reaction centers is thermoactivated, and discontinues at temperatures below 40 K. In these reaction centers, substitution of amino acid residue isoleucine at the 177 position of the L-subunit with histidine results in the sharp decrease of activation energy, so that the carotenoid triplets are populated even at 10 K. Activation energy of the
T-T
energy transfer was estimated as 7.5 cm
–1
, which is more than 10-fold lower than activation energy in the wild type reaction centers. At certain temperatures, the energy transfer in the mutant is decelerated, which is related to the increase of effective distance of the triplet-triplet transfer. To the best of our knowledge, the described mutation presents the first reaction center modification leading to the significant decrease in activation energy of the
T-T
energy transfer to carotenoid molecule. The I(L177)H mutant reaction centers present a considerable interest for further studies of the triplet state quenching mechanisms, and of other photophysical and photochemical processes in the reaction centers of bacterial photosynthesis.</description><identifier>ISSN: 0006-2979</identifier><identifier>ISSN: 1608-3040</identifier><identifier>EISSN: 1608-3040</identifier><identifier>DOI: 10.1134/S0006297924090049</identifier><identifier>PMID: 39418516</identifier><language>eng</language><publisher>Moscow: Pleiades Publishing</publisher><subject>Activation energy ; Amino acid substitution ; Amino acids ; Atomic energy levels ; Bacterial Proteins - chemistry ; Bacterial Proteins - genetics ; Bacterial Proteins - metabolism ; Biochemistry ; Biomedical and Life Sciences ; Biomedicine ; Bioorganic Chemistry ; Carotenoids ; Carotenoids - chemistry ; Carotenoids - metabolism ; Energy ; Energy Transfer ; Histidine ; Isoleucine ; Knowledge management ; Life Sciences ; Microbiology ; Mutants ; Mutation ; Oxidants ; Oxidizing agents ; Photochemical reactions ; Photochemicals ; Photosynthesis ; Photosynthetic Reaction Center Complex Proteins - chemistry ; Photosynthetic Reaction Center Complex Proteins - genetics ; Photosynthetic Reaction Center Complex Proteins - metabolism ; Quenching ; Reaction centers ; Rhodobacter sphaeroides - genetics ; Rhodobacter sphaeroides - metabolism ; Substitution reactions ; Temperature ; Temperature dependence ; Triplet state</subject><ispartof>Biochemistry (Moscow), 2024-09, Vol.89 (9), p.1573-1581</ispartof><rights>Pleiades Publishing, Ltd. 2024</rights><rights>Pleiades Publishing, Ltd. 2024.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c254t-e398a2345b6459807e5b27fe36d3f888082017d131705b8cdb8deab5039ead9f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1134/S0006297924090049$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1134/S0006297924090049$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39418516$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fufina, Tatiana Yu</creatorcontrib><creatorcontrib>Vasilieva, Lyudmila G.</creatorcontrib><creatorcontrib>Klenina, Irina B.</creatorcontrib><creatorcontrib>Proskuryakov, Ivan I.</creatorcontrib><title>Anomalous Temperature Dependence of the Triplet-Triplet Energy Transfer in Cereibacter sphaeroides I(L177)H Mutant Reaction Centers</title><title>Biochemistry (Moscow)</title><addtitle>Biochemistry Moscow</addtitle><addtitle>Biochemistry (Mosc)</addtitle><description>In photosynthetic reaction centers, quenching of the primary donor triplet state by energy transfer to the carotenoid molecule provides efficient suppression of generation of singlet-excited oxygen, potent chemical oxidant. This process in the
Cereibacter sphaeroides
reaction centers is thermoactivated, and discontinues at temperatures below 40 K. In these reaction centers, substitution of amino acid residue isoleucine at the 177 position of the L-subunit with histidine results in the sharp decrease of activation energy, so that the carotenoid triplets are populated even at 10 K. Activation energy of the
T-T
energy transfer was estimated as 7.5 cm
–1
, which is more than 10-fold lower than activation energy in the wild type reaction centers. At certain temperatures, the energy transfer in the mutant is decelerated, which is related to the increase of effective distance of the triplet-triplet transfer. To the best of our knowledge, the described mutation presents the first reaction center modification leading to the significant decrease in activation energy of the
T-T
energy transfer to carotenoid molecule. The I(L177)H mutant reaction centers present a considerable interest for further studies of the triplet state quenching mechanisms, and of other photophysical and photochemical processes in the reaction centers of bacterial photosynthesis.</description><subject>Activation energy</subject><subject>Amino acid substitution</subject><subject>Amino acids</subject><subject>Atomic energy levels</subject><subject>Bacterial Proteins - chemistry</subject><subject>Bacterial Proteins - genetics</subject><subject>Bacterial Proteins - metabolism</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Bioorganic Chemistry</subject><subject>Carotenoids</subject><subject>Carotenoids - chemistry</subject><subject>Carotenoids - metabolism</subject><subject>Energy</subject><subject>Energy Transfer</subject><subject>Histidine</subject><subject>Isoleucine</subject><subject>Knowledge management</subject><subject>Life Sciences</subject><subject>Microbiology</subject><subject>Mutants</subject><subject>Mutation</subject><subject>Oxidants</subject><subject>Oxidizing agents</subject><subject>Photochemical reactions</subject><subject>Photochemicals</subject><subject>Photosynthesis</subject><subject>Photosynthetic Reaction Center Complex Proteins - chemistry</subject><subject>Photosynthetic Reaction Center Complex Proteins - genetics</subject><subject>Photosynthetic Reaction Center Complex Proteins - metabolism</subject><subject>Quenching</subject><subject>Reaction centers</subject><subject>Rhodobacter sphaeroides - genetics</subject><subject>Rhodobacter sphaeroides - metabolism</subject><subject>Substitution reactions</subject><subject>Temperature</subject><subject>Temperature dependence</subject><subject>Triplet state</subject><issn>0006-2979</issn><issn>1608-3040</issn><issn>1608-3040</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kU1LxDAQhoMoun78AC8S8LIeqpOmbZKjrB-7sCLoei5pO9VKm9akPXj2j5uyq4LiaZi8zzsz5CXkmME5Yzy6eASAJFRChREogEhtkQlLQAYcItgmk1EORn2P7Dv36tsQFN8le1xFTMYsmZCPS9M2um4HR1fYdGh1P1ikV9ihKdDkSNuS9i9IV7bqauyDTaXXBu3zu3_WxpVoaWXoDC1Wmc5737ruRaNtqwIdXUyXTIizOb0bem16-oCeqdrRYDzrDslOqWuHR5t6QJ5urlezebC8v13MLpdBHsZRHyBXUoc8irMkipUEgXEWihJ5UvBSSgkyBCYKxpmAOJN5kckCdRYDV6gLVfIDMl3P7Wz7NqDr06ZyOda1Nug_IOWMCaU4CO7R01_oaztY468bqXE958xTbE3ltnXOYpl2tmq0fU8ZpGNC6Z-EvOdkM3nIGiy-HV-ReCBcA85L5hntz-r_p34CEFiZ8A</recordid><startdate>20240901</startdate><enddate>20240901</enddate><creator>Fufina, Tatiana Yu</creator><creator>Vasilieva, Lyudmila G.</creator><creator>Klenina, Irina B.</creator><creator>Proskuryakov, Ivan I.</creator><general>Pleiades Publishing</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7TM</scope><scope>7U9</scope><scope>C1K</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>7X8</scope></search><sort><creationdate>20240901</creationdate><title>Anomalous Temperature Dependence of the Triplet-Triplet Energy Transfer in Cereibacter sphaeroides I(L177)H Mutant Reaction Centers</title><author>Fufina, Tatiana Yu ; Vasilieva, Lyudmila G. ; Klenina, Irina B. ; Proskuryakov, Ivan I.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c254t-e398a2345b6459807e5b27fe36d3f888082017d131705b8cdb8deab5039ead9f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Activation energy</topic><topic>Amino acid substitution</topic><topic>Amino acids</topic><topic>Atomic energy levels</topic><topic>Bacterial Proteins - chemistry</topic><topic>Bacterial Proteins - genetics</topic><topic>Bacterial Proteins - metabolism</topic><topic>Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Bioorganic Chemistry</topic><topic>Carotenoids</topic><topic>Carotenoids - chemistry</topic><topic>Carotenoids - metabolism</topic><topic>Energy</topic><topic>Energy Transfer</topic><topic>Histidine</topic><topic>Isoleucine</topic><topic>Knowledge management</topic><topic>Life Sciences</topic><topic>Microbiology</topic><topic>Mutants</topic><topic>Mutation</topic><topic>Oxidants</topic><topic>Oxidizing agents</topic><topic>Photochemical reactions</topic><topic>Photochemicals</topic><topic>Photosynthesis</topic><topic>Photosynthetic Reaction Center Complex Proteins - chemistry</topic><topic>Photosynthetic Reaction Center Complex Proteins - genetics</topic><topic>Photosynthetic Reaction Center Complex Proteins - metabolism</topic><topic>Quenching</topic><topic>Reaction centers</topic><topic>Rhodobacter sphaeroides - genetics</topic><topic>Rhodobacter sphaeroides - metabolism</topic><topic>Substitution reactions</topic><topic>Temperature</topic><topic>Temperature dependence</topic><topic>Triplet state</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fufina, Tatiana Yu</creatorcontrib><creatorcontrib>Vasilieva, Lyudmila G.</creatorcontrib><creatorcontrib>Klenina, Irina B.</creatorcontrib><creatorcontrib>Proskuryakov, Ivan I.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>MEDLINE - Academic</collection><jtitle>Biochemistry (Moscow)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fufina, Tatiana Yu</au><au>Vasilieva, Lyudmila G.</au><au>Klenina, Irina B.</au><au>Proskuryakov, Ivan I.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Anomalous Temperature Dependence of the Triplet-Triplet Energy Transfer in Cereibacter sphaeroides I(L177)H Mutant Reaction Centers</atitle><jtitle>Biochemistry (Moscow)</jtitle><stitle>Biochemistry Moscow</stitle><addtitle>Biochemistry (Mosc)</addtitle><date>2024-09-01</date><risdate>2024</risdate><volume>89</volume><issue>9</issue><spage>1573</spage><epage>1581</epage><pages>1573-1581</pages><issn>0006-2979</issn><issn>1608-3040</issn><eissn>1608-3040</eissn><abstract>In photosynthetic reaction centers, quenching of the primary donor triplet state by energy transfer to the carotenoid molecule provides efficient suppression of generation of singlet-excited oxygen, potent chemical oxidant. This process in the
Cereibacter sphaeroides
reaction centers is thermoactivated, and discontinues at temperatures below 40 K. In these reaction centers, substitution of amino acid residue isoleucine at the 177 position of the L-subunit with histidine results in the sharp decrease of activation energy, so that the carotenoid triplets are populated even at 10 K. Activation energy of the
T-T
energy transfer was estimated as 7.5 cm
–1
, which is more than 10-fold lower than activation energy in the wild type reaction centers. At certain temperatures, the energy transfer in the mutant is decelerated, which is related to the increase of effective distance of the triplet-triplet transfer. To the best of our knowledge, the described mutation presents the first reaction center modification leading to the significant decrease in activation energy of the
T-T
energy transfer to carotenoid molecule. The I(L177)H mutant reaction centers present a considerable interest for further studies of the triplet state quenching mechanisms, and of other photophysical and photochemical processes in the reaction centers of bacterial photosynthesis.</abstract><cop>Moscow</cop><pub>Pleiades Publishing</pub><pmid>39418516</pmid><doi>10.1134/S0006297924090049</doi><tpages>9</tpages></addata></record> |
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subjects | Activation energy Amino acid substitution Amino acids Atomic energy levels Bacterial Proteins - chemistry Bacterial Proteins - genetics Bacterial Proteins - metabolism Biochemistry Biomedical and Life Sciences Biomedicine Bioorganic Chemistry Carotenoids Carotenoids - chemistry Carotenoids - metabolism Energy Energy Transfer Histidine Isoleucine Knowledge management Life Sciences Microbiology Mutants Mutation Oxidants Oxidizing agents Photochemical reactions Photochemicals Photosynthesis Photosynthetic Reaction Center Complex Proteins - chemistry Photosynthetic Reaction Center Complex Proteins - genetics Photosynthetic Reaction Center Complex Proteins - metabolism Quenching Reaction centers Rhodobacter sphaeroides - genetics Rhodobacter sphaeroides - metabolism Substitution reactions Temperature Temperature dependence Triplet state |
title | Anomalous Temperature Dependence of the Triplet-Triplet Energy Transfer in Cereibacter sphaeroides I(L177)H Mutant Reaction Centers |
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