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藻胆素生物合成:嗜热蓝藻血红素加氧酶的还原剂需求及产物鉴定

Phycobilin biosynthesis: reductant requirements and product identification for heme oxygenase from Cyanidium caldarium.

作者信息

Rhie G, Beale S I

机构信息

Division of Biology and Medicine, Brown University, Providence, Rhode Island 02912, USA.

出版信息

Arch Biochem Biophys. 1995 Jun 20;320(1):182-94. doi: 10.1006/abbi.1995.1358.

Abstract

Algal heme oxygenase is a soluble enzyme from Cyanidium caldarium that catalyzes the first committed step of phycobilin biosynthesis by converting protoheme to biliverdin IX alpha. Although the physiological substrate (protoheme) of algal heme oxygenase is identical to that of microsomal heme oxygenase, which catalyzes heme catabolism in animals, the two enzyme systems differ in several respects including the nature of the required reductants and solubility of the enzymes. Addition of the strong Fe3+ ion chelators, desferrioxamine and Tiron (4,5-dihydroxy-1,3-benzenedisulfonic acid), greatly increased the yield of solvent-extracted bilin product. The effect of the Fe3+ chelators was approximately equal whether they were added during or after the enzyme incubation. Postincubation treatment of the enzyme reaction mixture with strong acid also greatly increased the product yield. Addition of desferrioxamine to the reaction mixture after the incubation was terminated caused the appearance of an absorption spectrum, indicating an increase in the concentration of free bilin product. Acid and Fe3+ chelators are known to cause dissociation of Fe(III)-bilin complexes. These results indicate that the in vitro enzymic reaction product of algal heme oxygenase is a nonenzyme-bound Fe(III)-biliverdin IX alpha complex that is poorly extracted and/or quantitated unless it is first dissociated. Algal heme oxygenase required the simultaneous presence of both reduced ferredoxin and a second reductant such as ascorbate for activity. The requirement for L-ascorbate could be substituted by Trolox (6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid) or D-ascorbate, but not by dehydroascorbate or dithiothreitol. Heme oxygenase was purified over 200-fold from C. caldarium by differential (NH4)2SO4 precipitation and serial column chromatography over reactive blue 2-Sepharose, DEAE-cellulose, Sephadex G-75, and ferredoxin-Sepharose.

摘要

藻类血红素加氧酶是一种来自嗜热蓝藻的可溶性酶,它通过将原血红素转化为胆绿素IXα来催化藻胆素生物合成的第一步关键反应。尽管藻类血红素加氧酶的生理底物(原血红素)与微粒体血红素加氧酶相同,微粒体血红素加氧酶在动物体内催化血红素分解代谢,但这两种酶系统在几个方面存在差异,包括所需还原剂的性质和酶的溶解性。添加强Fe3+离子螯合剂去铁胺和钛铁试剂(4,5 - 二羟基 - 1,3 - 苯二磺酸)可大大提高溶剂萃取的胆素产物的产量。无论在酶孵育期间还是之后添加Fe3+螯合剂,其效果大致相同。用强酸对酶反应混合物进行孵育后处理也可大大提高产物产量。孵育终止后向反应混合物中添加去铁胺会导致出现吸收光谱,表明游离胆素产物浓度增加。已知酸和Fe3+螯合剂会导致Fe(III)-胆素复合物解离。这些结果表明,藻类血红素加氧酶的体外酶促反应产物是一种非酶结合的Fe(III)-胆绿素IXα复合物,除非首先使其解离,否则很难提取和/或定量。藻类血红素加氧酶需要同时存在还原型铁氧还蛋白和第二种还原剂(如抗坏血酸)才能发挥活性。L - 抗坏血酸的需求可以被生育三烯酚(6 - 羟基 - 2,5,7,8 - 四甲基色满 - 2 - 羧酸)或D - 抗坏血酸替代,但不能被脱氢抗坏血酸或二硫苏糖醇替代。通过差示硫酸铵沉淀以及在活性蓝2 - 琼脂糖、DEAE - 纤维素、葡聚糖G - 75和铁氧还蛋白 - 琼脂糖上进行连续柱色谱,从嗜热蓝藻中纯化出了超过200倍的血红素加氧酶。

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