James F, Paquet L, Sparace S A, Gage D A, Hanson A D
Horticultural Sciences Department, University of Florida, Gainesville 32611-0690, USA.
Plant Physiol. 1995 Aug;108(4):1439-48. doi: 10.1104/pp.108.4.1439.
3-Dimethylsulfoniopropionate (DMSP) is an osmoprotectant accumulated by certain flowering plants and algae. In Wollastonia biflora (L.) DC. (Compositae) the first intermediate in DMSP biosynthesis has been shown to be S-methylmethionine (SMM) (A.D. Hanson, J. Rivoal, L. Paquet, D.A. Gage [1994] Plant Physiol 105: 103-110). Other possible intermediates were investigated by radiolabeling methods using W. biflora leaf discs. In pulse-chase experiments with [35S]SMM, 3-dimethylsulfoniopropionaldehyde (DMSP-ald) acquired label rapidly and lost it during the chase period. Conversely, 3-dimethylsulfoniopropylamine (DMSP-amine), 3-dimethylsulfoniopropionamide (DMSP-amide), and 4-dimethylsulfonio-2-hydroxybutyrate (DMSHB) labeled slowly and continuously during both pulse and chase. When unlabeled compounds were supplied along with [35S]SMM, DMSP-ald promoted [35S]DMSP-ald accumulation but DMSHB, DMSP-amide, and DMSP-amine had no such trapping effect. These data indicate that DMSP-ald is an intermediate in DMSP biosynthesis and that the other three compounds are not. Consistent with this, [35S]DMSHB was not metabolized to DMSP. Although [14C]DMSP-amine and [14C]DMSP-amide were converted slowly to DMSP, similar or higher conversion rates were found in plants that do not naturally accumulate DMSP, indicating that nonspecific reactions were responsible. These nonaccumulating species did not form [35S]DMSP-ald from [35S]SMM, implying that DMSP-ald is specific to DMSP biosynthesis. W. biflora leaf discs catabolized supplied sulfonium compounds to dimethylsulfide at differing rates, in the order DMSP-ald >> DMSP-amine > SMM > DMSP-amide > DMSHB > DMSP.
3-二甲基巯基丙酸内盐(DMSP)是某些开花植物和藻类积累的一种渗透保护剂。在双花黄鹌菜(菊科)中,DMSP生物合成的第一个中间体已被证明是S-甲基甲硫氨酸(SMM)(A.D. 汉森、J. 里瓦尔、L. 帕凯、D.A. 盖奇[1994]《植物生理学》105: 103 - 110)。使用双花黄鹌菜叶片圆盘通过放射性标记方法研究了其他可能的中间体。在用[35S]SMM进行的脉冲追踪实验中,3-二甲基巯基丙醛(DMSP-ald)迅速获得标记并在追踪期内失去标记。相反,3-二甲基巯基丙胺(DMSP-amine)、3-二甲基巯基丙酰胺(DMSP-amide)和4-二甲基巯基-2-羟基丁酸(DMSHB)在脉冲和追踪期间标记缓慢且持续。当未标记的化合物与[35S]SMM一起供应时,DMSP-ald促进了[35S]DMSP-ald的积累,但DMSHB、DMSP-amide和DMSP-amine没有这种捕获作用。这些数据表明DMSP-ald是DMSP生物合成的中间体,而其他三种化合物不是。与此一致的是,[35S]DMSHB没有代谢为DMSP。尽管[14C]DMSP-amine和[14C]DMSP-amide缓慢转化为DMSP,但在自然不积累DMSP的植物中也发现了相似或更高的转化率,表明是非特异性反应导致的。这些不积累的物种不能从[35S]SMM形成[35S]DMSP-ald,这意味着DMSP-ald对DMSP生物合成具有特异性。双花黄鹌菜叶片圆盘以不同速率将供应的锍化合物分解为二甲基硫醚,顺序为DMSP-ald >> DMSP-amine > SMM > DMSP-amide > DMSHB > DMSP。