Abstract

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. Mucuna sempervirens (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 Arabidopsis thaliana, which was suggested to be involved in the pathway of ascorbate biosynthesis; however, both MsGulLO and AtGulLO5 are divergent from animal L-gulonolactone oxidases. MsGulLO 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.

Highlights

  • IntroductionL-Ascorbic acid (ascorbate, L-ascorbic acid (AsA)), is a naturally occurring organic compound belonging to the family of monosaccharides

  • L-Ascorbic acid, is a naturally occurring organic compound belonging to the family of monosaccharides

  • For the first time, we identified an AtGulLO homolog in the nectar from Mucuna sempervirens Hemsl (Fabaceae), a perennial woody climber bean species that is widely distributed in subtropical regions of China, Bhutan, North East India (West Bengal, Manipur, Sikkim), Japan and Myanmar

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Summary

Introduction

L-Ascorbic acid (ascorbate, AsA), is a naturally occurring organic compound belonging to the family of monosaccharides. This compound has antioxidant properties, which help protect against reactive oxygen species (ROS) derived from metabolic activity. Non-human primates, guinea pigs, bats, and some birds cannot synthesize AsA because L-gulono-1,4-lactone oxidase (GulLO), the terminal enzyme in the biosynthesis process, does not function due to mutation (Chatterjee, 1973). These animals including humans need to acquire this vitamin from fresh fruits and green vegetables. Plant-derived AsA is the major source of AsA in the human diet

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