Abteilung Biologie, Lehrstuhl für Biochemie der Pflanzen, Gebäude ND 3/130, Postfach 102148, D-4630, Bochum 1, Germany.
Planta. 1983 Aug;158(6):540-9. doi: 10.1007/BF00397245.
Plant cell suspension cultures from Catharanthus roseus were investigated for their capability to dissimilate methionine or its analogs in order to reutilize the sulphane group for cysteine biosynthesis. Three steps have been described as prerequisites of this process: (a) oxidative degradation by the amino-acid oxidase of methionine giving rise to methanethiol production; (b) demethylation by methyltransferases leading to homocysteine and S-methylmethionine (c) replacement of the homocysteine sulphane sulphur by alkylthiol yielding methionine and free hydrogen sulphide. A reversal of the cystathionine pathway as a source of cysteine was ruled out because the cells lack cystathionine γ-lyase. The absence of this enzyme is compensated by the S-alkyl exchange of homocysteine with methylmercaptan. Hydrogen sulphide thus liberated is used for de novo synthesis of cysteine. The complete pathway can be catalyzed by the constitutive set of enzymes present in the higher plant.
长春花细胞悬浮培养物被研究其同化蛋氨酸或其类似物的能力,以便将硫烷基团重新用于半胱氨酸生物合成。这个过程有三个步骤被描述为前提条件:(a)蛋氨酸的氨基酸氧化酶氧化降解,产生甲硫醇;(b)甲基转移酶的去甲基化导致同型半胱氨酸和 S-甲基蛋氨酸;(c)用烷基硫醇取代同型半胱氨酸硫烷硫,生成蛋氨酸和游离硫化氢。胱硫醚途径作为半胱氨酸的来源被排除,因为细胞缺乏胱硫醚 γ-裂解酶。这种酶的缺失通过同型半胱氨酸与甲硫醇的 S-烷基交换得到补偿。因此释放的硫化氢用于半胱氨酸的从头合成。完整的途径可以由高等植物中存在的组成性酶系催化。