Studies on the bioluminescence of Renilla renoformis

Milton J. Cormier , Kazuo Hori
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引用次数: 21

Abstract

  • 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.

Renilla renformis的生物发光研究
1.1. 在海三色堇Renilla reniformis的生物发光反应中,一种被激活的中间体在厌氧条件下通过Renilla lucifin、Ado-3 ' -5 ' -P2、Ca2+和Renilla lucidferin酶孵育形成。在pH 1.0条件下,荧光素在100°温度下处理2分钟,可以在没有do-3 ' -5 ' -P2和荧光素酶的情况下形成化学上相同的中间体,在此期间,通过总光测量来判断中间体的定量转化。一旦中间体形成,在没有荧光素酶的情况下,它可以通过非发光途径被O2或H2O2迅速氧化。由于荧光素在高pH(100°)或pH 7.0(130°)下转化为活化中间体的速度相对较慢,因此我们提出了一种建议,即紫丁香荧光素的do-3 ',5 ' - p2依赖性激活的机制涉及从荧光素分子中切割一个未知基团。
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