植物生物合成类异戊二烯的1-脱氧-d -木醛糖-5-磷酸途径

H. Lichtenthaler
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引用次数: 68

摘要

植物类异戊二烯的生物合成通过两个独立的途径进行:1)胞质经典醋酸/甲戊酸途径(甾醇、倍半萜、三萜的生物合成)和2)非甲戊酸1-脱氧-d -木醛糖-5-磷酸(DOX-P)途径,用于生物合成可塑性类异戊二烯,如类胡萝卜素、叶绿醇(叶绿素侧链)、质体醌-9、异戊二烯、单萜和二萜。这两种途径都形成二磷酸异戊基(IPP)作为前体,所有其他类异戊二烯通过头尾加成形成。目前对异戊烯基二磷酸生物合成的新型1-脱氧-d -木醛糖-5-磷酸(DOX-P)途径的了解,显然位于质体中,在这一贡献中进行了回顾。它为叶绿体代谢提供了新的视角。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The plants' 1-deoxy-D-xylulose-5-phosphate pathway for biosynthesis of isoprenoids
Isoprenoid biosynthesis in plants proceeds via two independent pathways: 1) the cytosolic classical acetate/mevalonate pathway (biosynthesis of sterols, sesquiterpenes, triterpenoids) and 2) via the non-mevalonate 1-deoxy-D-xylulose-5-phosphate (DOX-P) pathway for the biosynthesis of plastidic isoprenoids such as carotenoids, phytol (side-chain of chlorophylls), plastoquinone-9, isoprene, mono- and diterpenes. Both pathways form isopentenyl-diphosphate (IPP) as precursors, from which all other isoprenoids are formed via head-to-tail addition. The present knowledge of the novel 1-deoxy-D-xylulose-5-phosphate (DOX-P) pathways for isopentenyl-diphosphate biosynthesis, which is apparently located in plastids, is reviewed in this contribution. It provides a new insight into chloroplast metabolism.
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