Shimomura O, Teranishi K
Marine Biological Laboratory, Woods Hole, MA 02543, USA.
Luminescence. 2000 Jan-Feb;15(1):51-8. doi: 10.1002/(SICI)1522-7243(200001/02)15:1<51::AID-BIO555>3.0.CO;2-J.
Coelenterazine emits light by chemi-and bioluminescence reactions, decomposing into coelenteramide and CO(2). To ascertain the light emitters involved, the fluorescence of coelenteramide and five analogues were studies in four kinds of solvent. The results showed that coelenteramides can form five kinds of light emitters, ie unionized (lambda(max) 386-423 nm), phenolate anion (lambda(max) 480-490 nm), phenolate anion temporarily formed from the ion-pair state (lambda(max) 465-479 nm), amide anion (lambda(max) 435-458 nm) and pyrazine-N(4) anion (lambda(max) 530-565 nm). The chemiluminescence light emitter of coelenterazine in the presence of alkali (lambda(max) 530-550 nm) was found to be the pyrazine-N(4) anion and not the dianion (ie phenolate anion/amide anion), as previously believed. In chemiluminescence, the normal light emitter is the amide anion, and the pyrazine-N(4) anion emission may occur in the presence of alkali, but light emission from any other emitters has not been observed. In the bioluminescence reaction, the normal light emitter is the amide anion, but no other light emitter was observed except the unionized form found in the Ca-triggered luminescence of semisynthetic aequorins prepared with an e-type coelenterazine instead of coelenterazine.
腔肠素通过化学发光和生物发光反应发光,分解为腔肠酰胺和二氧化碳。为了确定其中涉及的发光体,研究了腔肠酰胺及其五种类似物在四种溶剂中的荧光。结果表明,腔肠酰胺可形成五种发光体,即未电离形式(最大波长386 - 423 nm)、酚盐阴离子(最大波长480 - 490 nm)、由离子对状态临时形成的酚盐阴离子(最大波长465 - 479 nm)、酰胺阴离子(最大波长435 - 458 nm)和吡嗪 - N(4)阴离子(最大波长530 - 565 nm)。已发现,在碱存在下,腔肠素的化学发光发光体(最大波长530 - 550 nm)是吡嗪 - N(4)阴离子,而不是如先前认为的二价阴离子(即酚盐阴离子/酰胺阴离子)。在化学发光中,正常的发光体是酰胺阴离子,吡嗪 - N(4)阴离子发射可能在碱存在时发生,但未观察到来自任何其他发光体的发光。在生物发光反应中,正常的发光体是酰胺阴离子,但除了在用e型腔肠素而非腔肠素制备的半合成水母发光蛋白的钙触发发光中发现的未电离形式外,未观察到其他发光体。