Zhou Hong-Xia, Milne Richard I, Ma Xue-Long, Song Yue-Qin, Fang Jian-Yu, Sun Hang, Zha Hong-Guang
College of Life and Environment Sciences, Huangshan University, Huangshan, China.
Institute of Molecular Plant Sciences, University of Edinburgh, Edinburgh, United Kingdom.
Front Plant Sci. 2018 Jul 30;9:1109. doi: 10.3389/fpls.2018.01109. eCollection 2018.
Floral nectar plays important roles in the interaction between animal-pollinated plants and pollinators. Its components include water, sugars, amino acids, vitamins, and proteins. Growing empirical evidence shows that most of the proteins secreted in nectar (nectarines) are enzymes that can tailor nectar chemistry for their animal mutualists or reduce the growth of microorganisms in nectar. However, to date, the function of many nectarines remains unknown, and very few plant species have had their nectar proteome thoroughly investigated. (Fabaceae) is a perennial woody vine native to China. Nectarines from this species were separated using two-dimensional gel electrophoresis, and analyzed using mass spectrometry. A L-gulonolactone oxidase like protein (MsGulLO) was detected, and the full length cDNA was cloned: it codes for a protein of 573 amino acids with a predicted signal peptide. MsGulLO has high similarity to L-gulonolactone oxidase 5 (AtGulLO5) in , which was suggested to be involved in the pathway of ascorbate biosynthesis; however, both MsGulLO and AtGulLO5 are divergent from animal L-gulonolactone oxidases. was expressed mainly in flowers, and especially in nectary before blooming. However, cloning and gene expression analysis showed that L-galactonolactone dehydrogenase (MsGLDH), a vital enzyme in plant ascorbate biosynthesis, was expressed in all of flowers, roots, stems, and especially leaves. MsGulLO was purified to near homogeneity from raw MS nectar by gel filtration chromatography. The enzyme was determined to be a neutral monomeric protein with an apparent molecular mass of 70 kDa. MsGulLO is not a flavin-containing protein, and has neither L-galactonolactone dehydrogenase activity, nor the L-gulonolactone activity that is usual in animal GulLOs. However, it has weak oxidase activity with the following substrates: L-gulono-1,4-lactone, L -galactono-1,4-lactone, D-gluconic acid-δ-lactone, glucose, and fructose. MsGulLO is suggested to function in hydrogen peroxide generation in nectar but not in plant ascorbate biosynthesis.
花蜜在虫媒植物与传粉者之间的相互作用中起着重要作用。其成分包括水、糖类、氨基酸、维生素和蛋白质。越来越多的实验证据表明,花蜜中分泌的大多数蛋白质(花蜜蛋白)都是酶,这些酶可以为其动物共生伙伴调整花蜜化学成分,或减少花蜜中微生物的生长。然而,迄今为止,许多花蜜蛋白的功能仍然未知,并且很少有植物物种的花蜜蛋白质组得到彻底研究。(豆科)是一种原产于中国的多年生木质藤本植物。使用二维凝胶电泳分离该物种的花蜜蛋白,并通过质谱分析。检测到一种类似L-古洛糖酸内酯氧化酶的蛋白质(MsGulLO),并克隆了其全长cDNA:它编码一种含有预测信号肽的573个氨基酸的蛋白质。MsGulLO与(某植物)中的L-古洛糖酸内酯氧化酶5(AtGulLO5)具有高度相似性,后者被认为参与抗坏血酸生物合成途径;然而,MsGulLO和AtGulLO5都与动物L-古洛糖酸内酯氧化酶不同。(MsGulLO)主要在花中表达,尤其是在开花前的蜜腺中。然而,克隆和基因表达分析表明,L-半乳糖酸内酯脱氢酶(MsGLDH)是植物抗坏血酸生物合成中的一种关键酶,在所有的花、根、茎中都有表达,尤其是在叶中。通过凝胶过滤色谱法从原始的MS花蜜中纯化MsGulLO至接近均一。该酶被确定为一种中性单体蛋白,表观分子量为70 kDa。MsGulLO不是一种含黄素的蛋白质,既没有L-半乳糖酸内酯脱氢酶活性,也没有动物GulLOs中常见的L-古洛糖酸内酯活性。然而,它对以下底物具有微弱的氧化酶活性:L-古洛糖-1,4-内酯、L-半乳糖-1,4-内酯、D-葡萄糖酸-δ-内酯、葡萄糖和果糖。MsGulLO被认为在花蜜中产生过氧化氢方面起作用,但在植物抗坏血酸生物合成中不起作用。