{"title":"Renilla renformis的生物发光研究","authors":"Milton J. Cormier , Kazuo Hori","doi":"10.1016/0926-6577(64)90157-3","DOIUrl":null,"url":null,"abstract":"<div><p></p><ul><li><span>1.</span><span><p>1. During the bioluminescent reaction of the sea pansy, <em>Renilla reniformis</em>, an activated intermediate had previously been described which forms upon incubating Renilla luciferin, Ado-3′-5′-<em>P</em><sub>2</sub>, Ca<sup>2+</sup>, and Renilla lucidferase under anaerobic conditions. A chemically identical intermediate can be formed in the absence of Ado-3′-5′-<em>P</em><sub>2</sub> and luciferase by treating luciferin at pH 1.0 for 2 min at 100°, during which time a quantitative conversion to the intermediate occurs as judged by total light measurements. Once the intermediate is formed it can be oxidized rapidly by O<sub>2</sub> or H<sub>2</sub>O<sub>2</sub>, in the absence of luciferase, via a non-luminescent pathway.</p></span></li><li><span>2.</span><span><p>2. Since a relatively slow conversion of luciferin to the activated intermediate occurs at high pH at 100° or at pH 7.0 at 130° the suggestion is made that the mechanism of the <em>Ado</em>-3′,5′-<em>P</em><sub>2</sub>-dependent activation of Renilla luciferin involves the cleavage of an unidentified group from the luciferin molecule.</p></span></li></ul></div>","PeriodicalId":100169,"journal":{"name":"Biochimica et Biophysica Acta (BBA) - Specialized Section on Biophysical Subjects","volume":"88 1","pages":"Pages 99-104"},"PeriodicalIF":0.0000,"publicationDate":"1964-07-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0926-6577(64)90157-3","citationCount":"21","resultStr":"{\"title\":\"Studies on the bioluminescence of Renilla renoformis\",\"authors\":\"Milton J. Cormier , Kazuo Hori\",\"doi\":\"10.1016/0926-6577(64)90157-3\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p></p><ul><li><span>1.</span><span><p>1. During the bioluminescent reaction of the sea pansy, <em>Renilla reniformis</em>, an activated intermediate had previously been described which forms upon incubating Renilla luciferin, Ado-3′-5′-<em>P</em><sub>2</sub>, Ca<sup>2+</sup>, and Renilla lucidferase under anaerobic conditions. A chemically identical intermediate can be formed in the absence of Ado-3′-5′-<em>P</em><sub>2</sub> and luciferase by treating luciferin at pH 1.0 for 2 min at 100°, during which time a quantitative conversion to the intermediate occurs as judged by total light measurements. Once the intermediate is formed it can be oxidized rapidly by O<sub>2</sub> or H<sub>2</sub>O<sub>2</sub>, in the absence of luciferase, via a non-luminescent pathway.</p></span></li><li><span>2.</span><span><p>2. Since a relatively slow conversion of luciferin to the activated intermediate occurs at high pH at 100° or at pH 7.0 at 130° the suggestion is made that the mechanism of the <em>Ado</em>-3′,5′-<em>P</em><sub>2</sub>-dependent activation of Renilla luciferin involves the cleavage of an unidentified group from the luciferin molecule.</p></span></li></ul></div>\",\"PeriodicalId\":100169,\"journal\":{\"name\":\"Biochimica et Biophysica Acta (BBA) - Specialized Section on Biophysical Subjects\",\"volume\":\"88 1\",\"pages\":\"Pages 99-104\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1964-07-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/0926-6577(64)90157-3\",\"citationCount\":\"21\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biochimica et Biophysica Acta (BBA) - Specialized Section on Biophysical Subjects\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/0926657764901573\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biochimica et Biophysica Acta (BBA) - Specialized Section on Biophysical Subjects","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0926657764901573","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Studies on the bioluminescence of Renilla renoformis
1.
1. During the bioluminescent reaction of the sea pansy, Renilla reniformis, an activated intermediate had previously been described which forms upon incubating Renilla luciferin, Ado-3′-5′-P2, Ca2+, and Renilla lucidferase under anaerobic conditions. A chemically identical intermediate can be formed in the absence of Ado-3′-5′-P2 and luciferase by treating luciferin at pH 1.0 for 2 min at 100°, during which time a quantitative conversion to the intermediate occurs as judged by total light measurements. Once the intermediate is formed it can be oxidized rapidly by O2 or H2O2, in the absence of luciferase, via a non-luminescent pathway.
2.
2. Since a relatively slow conversion of luciferin to the activated intermediate occurs at high pH at 100° or at pH 7.0 at 130° the suggestion is made that the mechanism of the Ado-3′,5′-P2-dependent activation of Renilla luciferin involves the cleavage of an unidentified group from the luciferin molecule.