Mudd S H, Datko A H
Laboratory of General and Comparative Biochemistry, National Institute of Mental Health, Bethesda, Maryland 20892.
Plant Physiol. 1990 Jun;93(2):623-30. doi: 10.1104/pp.93.2.623.
The metabolism of S-methylmethionine has been studied in cultures of plants of Lemna paucicostata and of cells of carrot (Daucus carota) and soybean (Glycine max). In each system, radiolabeled S-methylmethionine was rapidly formed from labeled l-methionine, consistent with the action of S-adenosyl-l-methionine:methionine S-methyltransferase, an enzyme which was demonstrated during these studies in Lemna homogenates. In Lemna plants and carrot cells radiolabel disappeared rapidly from S-methylmethionine during chase incubations in nonradioactive media. The results of pulse-chase experiments with Lemna strongly suggest that administered radiolabeled S-methylmethionine is metabolized initially to soluble methionine, then to the variety of compounds formed from soluble methionine. An enzyme catalyzing the transfer of a methyl group from S-methylmethionine to homocysteine to form methionine was demonstrated in homogenates of Lemna. The net result of these reactions, together with the hydrolysis of S-adenosylhomocysteine to homocysteine and adenosine, is to convert S-adenosylmethionine to methionine and adenosine. A physiological advantage is postulated for this sequence in that it provides the plant with a means of sustaining the pool of soluble methionine even when overshoot occurs in the conversion of soluble methionine to S-adenosylmethionine. The facts that the pool of soluble methionine is normally very small relative to the flux into S-adenosylmethionine and that the demand for the latter compound may change very markedly under different growth conditions make it plausible that such overshoot may occur unless the rate of synthesis of S-adenosylmethionine is regulated with exquisite precision. The metabolic cost of this apparent safeguard is the consumption of ATP. This S-methylmethionine cycle may well function in plants other than Lemna, but further substantiating evidence is neeeded.
已在少脉浮萍植株培养物以及胡萝卜(胡萝卜属)和大豆(大豆属)细胞中研究了S-甲基蛋氨酸的代谢。在每个系统中,放射性标记的S-甲基蛋氨酸都能从标记的L-蛋氨酸快速形成,这与S-腺苷-L-蛋氨酸:蛋氨酸S-甲基转移酶的作用一致,该酶在这些研究中已在浮萍匀浆中得到证实。在浮萍植株和胡萝卜细胞中,在非放射性培养基的追踪孵育过程中,放射性标记迅速从S-甲基蛋氨酸中消失。用浮萍进行的脉冲追踪实验结果强烈表明,给予的放射性标记S-甲基蛋氨酸最初代谢为可溶性蛋氨酸,然后代谢为从可溶性蛋氨酸形成的各种化合物。在浮萍匀浆中证实了一种催化甲基从S-甲基蛋氨酸转移至同型半胱氨酸以形成蛋氨酸的酶。这些反应的最终结果,连同S-腺苷同型半胱氨酸水解为同型半胱氨酸和腺苷,是将S-腺苷蛋氨酸转化为蛋氨酸和腺苷。推测该序列具有生理优势,因为即使在可溶性蛋氨酸向S-腺苷蛋氨酸的转化出现超调时,它也为植物提供了维持可溶性蛋氨酸库的一种方式。可溶性蛋氨酸库通常相对于进入S-腺苷蛋氨酸的通量非常小,而且在不同生长条件下对后一种化合物的需求可能会发生非常明显的变化,这使得除非S-腺苷蛋氨酸的合成速率受到精确调节,否则很可能会发生这种超调。这种明显保障措施的代谢成本是ATP的消耗。这个S-甲基蛋氨酸循环很可能在除浮萍之外的其他植物中发挥作用,但还需要进一步的确证证据。