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Todoroki, Y.

Publications and source records attributed to Todoroki, Y..

3 recordsLinked to original sources

Stable isotope-assisted computational mass spectrometry reveals root-specific alkaloids in Glycyrrhiza species

Licorice (Glycyrrhiza) is a medicinal plant widely used in approximately 70% of traditional Japanese Kampo formulations and is known to produce a wide array of specialized metabolites with diverse pharmacological properties. Although hundreds of metabolites have been reported, the overall chemical diversity of Glycyrrhiza remains poorly characterized. Here, using mass spectrometry data obtained from fully 13C-labeled leaves and roots of Glycyrrhiza uralensis and Glycyrrhiza glabra, we determined the carbon number, followed by molecular formula and substructure prediction in combination with MS/MS similarity-based molecular networking. After excluding redundant ions, including isotopic peaks, adducts, and in-source fragments, we extracted 3,060 unique metabolite features with assigned carbon numbers. Among these, substructure information was assigned to 1,015 features (33%) across the four plant tissues, revealing the tissue-specific metabolome profiles. Furthermore, we discovered five previously unreported alkaloids, homopipecolic acid-conjugated flavonoids, in the roots of G. uralensis and G. glabra, and Glycine max, another member of the Fabaceae family. Two of these structures were validated using nuclear magnetic resonance spectroscopy. We further proposed a biosynthetic route involving a spontaneous reaction between 1-piperideine and malonyl glycoside substrates and confirmed the formation of the conjugated product using authentic standards.

biochemistry↗

The submergence-induced drastic morphological plasticity of root in the amphibious plant Callitriche palustris

Amphibious plants can thrive in both terrestrial and submerged environments, which are fundamentally distinct. Although morphological plasticity of leaf known as heterophylly has been well investigated, the morphological plasticity of root in amphibious plants remains poorly understood. In this study, we discovered that an amphibious plant Callitriche palustris (Plantaginaceae), which has significant heterophylly, has a remarkable morphological plasticity also in root in response to submergence. This species develops thin roots with abundant root hairs, fewer cortical and epidermal cells, and smaller aerenchyma in the terrestrial condition. On the other hand, it develops thicker roots with few root hairs, more cortical and epidermal cells, and larger aerenchyma in the submerged condition. We call this morphological plasticity of root as "heterorhizy". Phytohormone perturbation experiments revealed that abscisic acid (ABA) and gibberellin regulate root hair development and root cell division respectively. We also found the possibility that heterorhizy was acquired in the genus Callitriche. Additionally, a similar form of root hair plasticity was also observed in the phylogenetically distinct amphibious species Ludwigia arcuata (Onagraceae). Furthermore, the absence of root hair development underwater and the similar structure of aerenchyma to C. palustris were broadly seen across diverse aquatic plants. This study provides new insights into the root morphological responses to submerged environments in aquatic plants.

plant biology↗

MS-DIAL 5 multimodal mass spectrometry data mining unveils lipidome complexities

Lipidomics and metabolomics communities comprise various informatics tools; however, software programs that can handle multimodal mass spectrometry (MS) data with structural annotations guided by the Lipidomics Standards Initiative are limited. Here, we provide MS-DIAL 5 to facilitate the in-depth structural elucidation of lipids through electron-activated dissociation (EAD)-based tandem MS, as well as determine their molecular localization through MS imaging (MSI) data using a species/tissue-specific lipidome database containing the predicted collision-cross section (CCS) values. With the optimized EAD settings using 14 eV kinetic energy conditions, the program correctly delineated the lipid structures based on EAD-MS/MS data from 96.4% of authentic standards. Our workflow was showcased by annotating the sn- and double-bond positions of eye-specific phosphatidylcholine molecules containing very-long-chain polyunsaturated fatty acids (VLC-PUFAs), characterized as PC n-3-VLC-PUFA/FA. Using MSI data from the eye and HeLa cells supplemented with n-3-VLC-PUFA, we identified glycerol 3-phosphate (G3P) acyltransferase (GPAT) as an enzyme candidate responsible for incorporating n-3 VLC-PUFAs into the sn-1 position of phospholipids in mammalian cells, which was confirmed using recombinant proteins in a cell-free system. Therefore, the MS-DIAL 5 environment, combined with optimized MS data acquisition methods, facilitates a better understanding of lipid structures and their localization, offering novel insights into lipid biology.

bioinformatics↗