Yoshimoto Naoko, Yabe Ayami, Sugino Yuka, Murakami Soichiro, Sai-Ngam Niti, Sumi Shin-Ichiro, Tsuneyoshi Tadamitsu, Saito Kazuki
Graduate School of Pharmaceutical Sciences, Chiba University Chiba, Japan.
Research Planning Department, Wakunaga Pharmaceutical Company Akitakata, Japan.
Front Plant Sci. 2015 Jan 8;5:758. doi: 10.3389/fpls.2014.00758. eCollection 2014.
S-Alk(en)yl-L-cysteine sulfoxides are pharmaceutically important secondary metabolites produced by plants that belong to the genus Allium. Biosynthesis of S-alk(en)yl-L-cysteine sulfoxides is initiated by S-alk(en)ylation of glutathione, which is followed by the removal of glycyl and γ-glutamyl groups and S-oxygenation. However, most of the enzymes involved in the biosynthesis of S-alk(en)yl-L-cysteine sulfoxides in Allium plants have not been identified. In this study, we identified three genes, AsGGT1, AsGGT2, and AsGGT3, from garlic (Allium sativum) that encode γ-glutamyl transpeptidases (GGTs) catalyzing the removal of the γ-glutamyl moiety from a putative biosynthetic intermediate of S-allyl-L-cysteine sulfoxide (alliin). The recombinant proteins of AsGGT1, AsGGT2, and AsGGT3 exhibited considerable deglutamylation activity toward a putative alliin biosynthetic intermediate, γ-glutamyl-S-allyl-L-cysteine, whereas these proteins showed very low deglutamylation activity toward another possible alliin biosynthetic intermediate, γ-glutamyl-S-allyl-L-cysteine sulfoxide. The deglutamylation activities of AsGGT1, AsGGT2, and AsGGT3 toward γ-glutamyl-S-allyl-L-cysteine were elevated in the presence of the dipeptide glycylglycine as a γ-glutamyl acceptor substrate, although these proteins can act as hydrolases in the absence of a proper acceptor substrate, except water. The apparent K m values of AsGGT1, AsGGT2, and AsGGT3 for γ-glutamyl-S-allyl-L-cysteine were 86 μM, 1.1 mM, and 9.4 mM, respectively. Subcellular distribution of GFP-fusion proteins transiently expressed in onion cells suggested that AsGGT2 localizes in the vacuole, whereas AsGGT1 and AsGGT3 possess no apparent transit peptide for localization to intracellular organelles. The different kinetic properties and subcellular localizations of AsGGT1, AsGGT2, and AsGGT3 suggest that these three GGTs may contribute differently to the biosynthesis of alliin in garlic.
S-烷(烯)基-L-半胱氨酸亚砜是葱属植物产生的具有重要药学意义的次生代谢产物。S-烷(烯)基-L-半胱氨酸亚砜的生物合成起始于谷胱甘肽的S-烷(烯)基化,随后去除甘氨酰基和γ-谷氨酰基并进行S-氧化。然而,葱属植物中参与S-烷(烯)基-L-半胱氨酸亚砜生物合成的大多数酶尚未被鉴定。在本研究中,我们从大蒜(葱属)中鉴定出三个基因,即AsGGT1、AsGGT2和AsGGT3,它们编码γ-谷氨酰转肽酶(GGT),催化从S-烯丙基-L-半胱氨酸亚砜(蒜氨酸)的假定生物合成中间体上去除γ-谷氨酰基部分。AsGGT1、AsGGT2和AsGGT3的重组蛋白对假定的蒜氨酸生物合成中间体γ-谷氨酰-S-烯丙基-L-半胱氨酸表现出相当可观的去谷氨酰化活性,而这些蛋白对另一种可能的蒜氨酸生物合成中间体γ-谷氨酰-S-烯丙基-L-半胱氨酸亚砜的去谷氨酰化活性非常低。在二肽甘氨酰甘氨酸作为γ-谷氨酰受体底物存在的情况下,AsGGT1、AsGGT2和AsGGT3对γ-谷氨酰-S-烯丙基-L-半胱氨酸的去谷氨酰化活性升高,尽管这些蛋白在没有合适受体底物(除水外)的情况下可作为水解酶起作用。AsGGT1、AsGGT2和AsGGT3对γ-谷氨酰-S-烯丙基-L-半胱氨酸的表观K m值分别为86 μM、1.1 mM和9.4 mM。在洋葱细胞中瞬时表达的绿色荧光蛋白融合蛋白的亚细胞定位表明,AsGGT2定位于液泡,而AsGGT1和AsGGT3没有明显的转运肽用于定位于细胞内细胞器。AsGGT1、AsGGT2和AsGGT3不同的动力学性质和亚细胞定位表明,这三种GGT可能对大蒜中蒜氨酸的生物合成有不同的贡献。