Cellular Morphology and Transcriptome Comparative Analysis of Astragalus membranaceus Bunge Sprouts Cultured In Vitro under Different LED Light

Author:

Seo Ji Won1,Lee Jae Geun2ORCID,Yoo Ji Hye3,Lim Jung Dae4ORCID,Choi Ik Young5ORCID,Kim Myong Jo6,Yu Chang Yeon6,Seong Eun Soo6ORCID

Affiliation:

1. Interdisciplinary Program in Smart Science, Kangwon National University, Chuncheon 24341, Republic of Korea

2. Research Institute of Biotechnology, Hwajin Cosmetics, Hongcheon 25142, Republic of Korea

3. Bioherb Research Institute, Kangwon National University, Chuncheon 24341, Republic of Korea

4. Bio-Health Convergence, Kangwon National University, Chuncheon 24341, Republic of Korea

5. Department of Agriculture and Life Industry, Kangwon National University, Chuncheon 24341, Republic of Korea

6. Division of Bioresource Sciences, Department of Applied Plant Sciences, Kangwon National University, Chuncheon 24341, Republic of Korea

Abstract

Astragalus membranaceus, the major components of which are saponins, flavonoids, and polysaccharides, has been established to have excellent pharmacological activity. After ginseng, it is the second most used medicinal plant. To examine the utility of A. membranaceus as a sprout crop for plant factory cultivation, we sought to establish a functional substance control model by comparing the transcriptomes of sprouts grown in sterile, in vitro culture using LED light sources. Having sown the seeds of A. membranaceus, these were exposed to white LED light (continuous spectrum), red LED light (632 nm, 1.58 μmol/m2/s), or blue LED light (465 nm, 1.44 μmol/m2/s) and grown for 6 weeks; after which, the samples were collected for transcriptome analysis. Scanning electron microscopy analysis of cell morphology in plants exposed to the three light sources revealed that leaf cell size was largest in those plants exposed to red light, where the thickest stem was observed in plants exposed to white light. The total number of genes in A. membranaceus spouts determined via de novo assembly was 45,667. Analysis of differentially expressed genes revealed that for the comparisons of blue LED vs. red LED, blue LED vs. white LED, and red LED vs. white LED, the numbers of upregulated genes were 132, 148, and 144, respectively. Binding, DNA integration, transport, phosphorylation, DNA biosynthetic process, membrane, and plant-type secondary cell wall biogenesis were the most enriched in the comparative analysis of blue LED vs. red LED, whereas Binding, RNA-templated DNA biosynthetic process, DNA metabolic process, and DNA integration were the most enriched in the comparative analysis of blue vs. white LED, and DNA integration and resolution of meiotic recombination intermediates were the most enrichment in the comparison between red LED vs. white LED. The GO term associated with flavonoid biosynthesis, implying the functionality of A. membranaceus, was the flavonoid biosynthetic process, which was enriched in the white LED vs. red LED comparison. The findings of this study thus indicate that different LED light sources can differentially influence the transcriptome expression pattern of A. membranaceus sprouts, which can provide a basis for establishing a flavonoid biosynthesis regulation model and thus, the cultivation of high-functional Astragalus sprouts.

Publisher

MDPI AG

Subject

Plant Science,Ecology,Ecology, Evolution, Behavior and Systematics

Reference31 articles.

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4. Antioxidant and Antidiabetic Effects of Various Sections of Astragalus membranaceus;Yin;Korean J. Pharmacogn.,2009

5. Physicochemical Properties and Antioxidant Activity of Extract from Astragalus membranaceus Bunge Leaf Fermented with Lactic Acid Bacteria;Song;Korean J. Med. Crop Sci.,2020

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