Norris S R, Barrette T R, DellaPenna D
Department of Biochemistry, University of Arizona, Tucson 85721, USA.
Plant Cell. 1995 Dec;7(12):2139-49. doi: 10.1105/tpc.7.12.2139.
Carotenoids are C40 tetraterpenoids synthesized by nuclear-encoded multienzyme complexes located in the plastids of higher plants. To understand further the components and mechanisms involved in carotenoid synthesis, we screened Arabidopsis for mutations that disrupt this pathway and cause accumulation of biosynthetic intermediates. Here, we report the identification and characterization of two nonallelic albino mutations, pds1 and pds2 (for phytoene desaturation), that are disrupted in phytoene desaturation and as a result accumulate phytoene, the first C40 compound of the pathway. Surprisingly, neither mutation maps to the locus encoding the phytoene desaturase enzyme, indicating that the products of at least three loci are required for phytoene desaturation in higher plants. Because phytoene desaturase catalyzes an oxidation reaction, it has been suggested that components of an electron transport chain may be involved in this reaction. Analysis of pds1 and pds2 shows that both mutants are plastoquinone and tocopherol deficient, in addition to their inability to desaturate phytoene. Separate steps of the plastoquinone/tocopherol biosynthetic pathway are affected by these two mutations. The pds1 mutation affects the enzyme 4-hydroxyphenylpyruvate dioxygenase because it can be rescued by growth on the product but not the substrate of this enzyme, homogentisic acid and 4-hydroxyphenylpyruvate, respectively. The pds2 mutation most likely affects the prenyl/phytyl transferase enzyme of this pathway. Because tocopherol-deficient mutants in the green alga Scenedesmus obliquus can synthesize carotenoids, our findings demonstrate conclusively that plastoquinone is an essential component in carotenoid synthesis. We propose a model for carotenoid synthesis in photosynthetic tissue whereby plastoquinone acts as an intermediate electron carrier between carotenoid desaturases and the photosynthetic electron transport chain.
类胡萝卜素是由位于高等植物质体中的核编码多酶复合物合成的C40四萜类化合物。为了进一步了解类胡萝卜素合成所涉及的成分和机制,我们在拟南芥中筛选了破坏该途径并导致生物合成中间体积累的突变体。在此,我们报告了两个非等位白化突变体pds1和pds2(八氢番茄红素去饱和)的鉴定和特征,它们在八氢番茄红素去饱和过程中被破坏,结果积累了该途径的第一个C40化合物八氢番茄红素。令人惊讶的是,这两个突变都不定位到编码八氢番茄红素去饱和酶的基因座,这表明高等植物中八氢番茄红素去饱和至少需要三个基因座的产物。由于八氢番茄红素去饱和酶催化氧化反应,有人提出电子传递链的成分可能参与该反应。对pds1和pds2的分析表明,除了无法使八氢番茄红素去饱和外,这两个突变体都缺乏质体醌和生育酚。质体醌/生育酚生物合成途径的不同步骤受这两个突变的影响。pds1突变影响4-羟基苯丙酮酸双加氧酶,因为它可以通过在该酶的产物上生长而不是底物上生长来挽救,分别是尿黑酸和4-羟基苯丙酮酸。pds2突变很可能影响该途径的异戊烯基/植基转移酶。由于绿藻斜生栅藻中缺乏生育酚的突变体可以合成类胡萝卜素,我们的研究结果确凿地证明质体醌是类胡萝卜素合成中的必需成分。我们提出了一个光合组织中类胡萝卜素合成的模型,其中质体醌作为类胡萝卜素去饱和酶和光合电子传递链之间的中间电子载体。