Transgenic hairy roots of Tetrastigma hemsleyanum: induction, propagation, genetic characteristics and medicinal components

• Published in: Plant cell, tissue and organ culture tissue and organ culture, 2015-08, Vol.122 (2), p.373-382
• Main Authors: Du, Surui, Xiang, Taihe, Song, Yaling, Huang, Lianxiang, Sun, Yang, Han, Yixuan
• Format: Article
• Language: English
• Subjects: Biomedical and Life Sciences; Butyric acid; Deoxyribonucleic acid; DNA; fine roots; genes; genetically modified organisms; Growth rate; Hairy root; Herbal medicine; High performance liquid chromatography; indole butyric acid; Indole-3-butyric acid; Insertion; Integration; Kaempferol; Kinetin; Leaves; Life Sciences; Liquid chromatography; Markets; Medicinal plants; medicine; Metabolites; Naphthaleneacetic acid; Organs; Original Paper; Plant Genetics and Genomics; Plant Pathology; Plant Physiology; Plant propagation; Plant Sciences; plasmids; Polymerase chain reaction; Propagation; Rhizobium rhizogenes; Roots; Secondary metabolites; Seedlings; stems; Subculture; Subcultures; Suspension culture; T-DNA; Tetrastigma; transfer DNA; Transgenic plants; Xylem
• ISSN: 0167-6857; 1573-5044
• DOI: 10.1007/s11240-015-0775-6

Tetrastigma hemsleyanum Diels & Gilg ex Diels (T. hemsleyanum) is an important medicinal plant in China. Its bulbous root is the most valuable part for medicine. There is an increasing demand for T. hemsleyanum in the medicinal market. However, the natural slow growth rate of T. hemsleyanum hardly meets the demand of the medicinal market. There is the need of alternative way for rapid and large-scale production of T. hemsleyanum. In this study, we investigated the induction of hairy roots by using Agrobacterium rhizogenes (A. rhizogenes) as an alternative method of increasing production of the secondary metabolites in hairy roots of T. hemsleyanum. Herein, we reported our successful induction of hairy roots of T. hemsleyanum by cucumopine type A. rhizogenes K599 and their rapid propagation. Firstly, we selected the optimal mediums for induction of hairy roots and for subculture of induced hairy roots. We found that when A. rhizogenes K599 carrying both an endogenous plasmid pRi2659 and an exogenous plasmid pRI101-AN-GFP was used to infect the leaves of T. hemsleyanum seedlings, the optimal medium for inducting hairy roots was the medium of MS + 0.4 mg/L 1-naphthaleneacetic acid. The optimal medium for subculture of hairy roots was the combination of MS + 1.0 mg/L indole-3-butyric acid + 0.5 or 1.0 mg/L kinetin. During suspension culture of hairy roots, the rapid growth phase occurred in the period of 15–28 days. Secondly, we employed polymerase chain reaction (PCR) assays to examine the integration of T-DNA of A. rhizogenes. The PCR results revealed the existence of a phenomenon of lacking of integration of one or more of 11 genes within T-DNA of plasmid pRi2659 into the genomic DNA of hairy roots. Thirdly, we conducted histocytological analysis to examine the structural features of the induced hairy roots and observed that xylem structures of the hairy roots were simplified as compared to those of the bulbous roots and ordinary fine roots of non-transgenic plant. Finally, we applied high performance liquid chromatography to analyze the medicinal components in several organs of the T. hemsleyanum plants. The results showed that the contents of kaempferol in all hairy root lines were significantly higher than those in bulbous roots, fine roots, stems and leaves. These results suggest that insertion and integration of T-DNA from A. rhizogenes can significantly increase the kaempferol content in hairy roots of T. hemsleyanum.