Krivi G G, Brown G M
Biochem Genet. 1979 Apr;17(3-4):371-90. doi: 10.1007/BF00498976.
Sepiapterin synthase, the enzyme system responsible for the synthesis of sepiapterin from dihydroneopterin triphosphate, has been partially purified from extracts of the heads of young adult fruit flies (Drosophila melanogaster). The sepiapterin synthase system consists of two components, termed "enzyme A" (MW 82,000) and "enzyme B" (MW 36,000). Some of the properties of the enzyme system are as follows: NADPH and a divalent cation, supplied most effectively as MgCl2, are required for activity; optimal activity occurs are pH 7.4 and 30 C; the Km for dihydroneopterin triphosphate is 10 microM; and a number of unconjugated pterins, including biopterin and sepiapterin, are inhibitory. Dihydroneopterin cannot be used as substrate in place of dihydroneopterin triphosphate. Evidence is presented in support of a proposed reaction mechanism for the enzymatic conversion of dihydroneopterin triphosphate to sepiapterin in which enzyme A catalyzes the production of a labile intermediate by nonhydrolytic elimination of the phosphates of dihydroneopterin triphosphate, and enzyme B catalyzes the conversion of this intermediate, in the presence of NADPH, to sepiapterin. An analysis of the activity of sepiapterin synthase during development in Drosophila revealed the presence of a small amount of activity in eggs and young larvae and a much larger amount in late pupae and young adults. Sepiapterin synthase activity during development corresponds with the appearance of sepiapterin in the flies. Of a variety of eye color mutants of Drosophila melanogaster tested for sepiapterin synthase activity, only purple (pr) flies contained activity that was significantly lower than that found in the wild-type flies (22% of the wild-type activity). Further studies indicated that the amount of enzyme A activity is low in purple flies, whereas the amount of enzyme B activity is equal to that present in wild-type flies.
蝶啶合酶是一种负责从三磷酸二氢新蝶呤合成蝶啶的酶系统,已从成年果蝇(黑腹果蝇)头部提取物中部分纯化出来。蝶啶合酶系统由两个组分组成,分别称为“酶A”(分子量82,000)和“酶B”(分子量36,000)。该酶系统的一些特性如下:活性需要NADPH和最有效的二价阳离子MgCl₂;最佳活性出现在pH 7.4和30℃;三磷酸二氢新蝶呤的Km为10微摩尔;包括生物蝶呤和蝶啶在内的许多未结合的蝶呤具有抑制作用。二氢新蝶呤不能替代三磷酸二氢新蝶呤用作底物。有证据支持三磷酸二氢新蝶呤酶促转化为蝶啶的反应机制,其中酶A通过非水解去除三磷酸二氢新蝶呤的磷酸基团催化产生不稳定中间体,酶B在NADPH存在下催化该中间体转化为蝶啶。对果蝇发育过程中蝶啶合酶活性的分析表明,卵和幼虫早期存在少量活性,而蛹后期和成年果蝇中活性要高得多。果蝇发育过程中的蝶啶合酶活性与果蝇中蝶啶的出现相对应。在测试蝶啶合酶活性的各种黑腹果蝇眼色突变体中,只有紫色(pr)果蝇的活性明显低于野生型果蝇(为野生型活性的22%)。进一步研究表明,紫色果蝇中酶A的活性较低,而酶B的活性与野生型果蝇中的相等。