Pellaud Sébastien, Mène-Saffrané Laurent
Department of Biology, University of Fribourg, Fribourg, Switzerland.
Front Plant Sci. 2017 Nov 14;8:1959. doi: 10.3389/fpls.2017.01959. eCollection 2017.
Tocochromanols are organic compounds mostly produced by photosynthetic organisms that exhibit vitamin E activity in animals. They result from the condensation of homogentisate with four different polyprenyl side chains derived all from geranylgeranyl pyrophosphate. The core tocochromanol biosynthesis has been investigated in several photosynthetic organisms and is now well-characterized. In contrast, our current knowledge of the biosynthesis and transport of tocochromanol biosynthetic precursors is much more limited. While tocochromanol synthesis occurs in plastids, converging genetic data in Arabidopsis and soybean demonstrate that the synthesis of the polar precursor homogentisate is located in the cytoplasm. These data implies that tocochromanol synthesis involves several plastidic membrane transporter(s) that remain to be identified. In addition, the metabolic origin of the lipophilic isoprenoid precursor is not fully elucidated. While some genetic data exclusively attribute the synthesis of the prenyl component of tocochromanols to the plastidic methyl erythritol phosphate pathway, multiple lines of evidence provided by feeding experiments and metabolic engineering studies indicate that it might partially originate from the cytoplasmic mevalonate pathway. Although this question is still open, these data demonstrate the existence of membrane transporter(s) capable of importing cytosolic polyprenyl pyrophosphate such as farnesyl pyrophosphate into plastids. Since the availability of both homogentisate and polyprenyl pyrophosphates are currently accepted as major mechanisms controlling the type and amount of tocochromanols produced in plant tissues, we summarized our current knowledge and research gaps concerning the biosynthesis, metabolic origins and transport of tocochromanol biosynthetic precursors in plant cells.
生育三烯酚是主要由光合生物产生的有机化合物,在动物体内具有维生素E活性。它们是由尿黑酸与四种不同的聚异戊二烯侧链缩合而成,这些侧链均来源于香叶基香叶基焦磷酸。几种光合生物中已对生育三烯酚的核心生物合成进行了研究,目前已得到充分表征。相比之下,我们目前对生育三烯酚生物合成前体的生物合成和运输的了解要有限得多。虽然生育三烯酚的合成发生在质体中,但拟南芥和大豆中越来越多的遗传数据表明,极性前体尿黑酸的合成位于细胞质中。这些数据表明生育三烯酚的合成涉及几种有待鉴定的质体膜转运蛋白。此外,亲脂性类异戊二烯前体的代谢来源尚未完全阐明。虽然一些遗传数据仅将生育三烯酚的异戊二烯成分的合成归因于质体甲基赤藓糖醇磷酸途径,但饲喂实验和代谢工程研究提供的多条证据表明,它可能部分源自细胞质甲羟戊酸途径。尽管这个问题仍然没有定论,但这些数据证明存在能够将胞质聚异戊二烯焦磷酸(如法呢基焦磷酸)导入质体的膜转运蛋白。由于目前认为尿黑酸和聚异戊二烯焦磷酸的可用性是控制植物组织中产生的生育三烯酚的类型和数量的主要机制,我们总结了我们目前关于植物细胞中生育三烯酚生物合成前体的生物合成、代谢来源和运输的知识以及研究空白。