Department of Biotechnology, Graduate School of Engineering, Osaka University, 2-1 Yamadaoka, Suita, 565-0871 Japan.
RIKEN Center for Sustainable Resource Science, 1-7-22 Suehiro-cho, Tsurumi-ku, Yokohama, 230-0045 Japan.
Plant Cell Physiol. 2024 Feb 15;65(2):185-198. doi: 10.1093/pcp/pcad161.
Glycyrrhizin, a type of the triterpenoid saponin, is a major active ingredient contained in the roots of the medicinal plant licorice (Glycyrrhiza uralensis, G. glabra and G. inflata), and is used worldwide in diverse applications, such as herbal medicines and sweeteners. The growing demand for licorice threatens wild resources and therefore a sustainable method of supplying glycyrrhizin is required. With the goal of establishing an alternative glycyrrhizin supply method not dependent on wild plants, we attempted to produce glycyrrhizin using hairy root culture. We tried to promote glycyrrhizin production by blocking competing pathways using CRISPR/Cas9-based gene editing. CYP93E3 CYP72A566 double-knockout (KO) and CYP93E3 CYP72A566 CYP716A179 LUS1 quadruple-KO variants were generated, and a substantial amount of glycyrrhizin accumulation was confirmed in both types of hairy root. Furthermore, we evaluated the potential for promoting further glycyrrhizin production by simultaneous CYP93E3 CYP72A566 double-KO and CYP88D6-overexpression. This strategy resulted in a 3-fold increase (∼1.4 mg/g) in glycyrrhizin accumulation in double-KO/CYP88D6-overexpression hairy roots, on average, compared with that of double-KO hairy roots. These findings demonstrate that the combination of blocking competing pathways and overexpression of the biosynthetic gene is important for enhancing glycyrrhizin production in G. uralensis hairy roots. Our findings provide the foundation for sustainable glycyrrhizin production using hairy root culture. Given the widespread use of genome editing technology in hairy roots, this combined with gene knockout and overexpression could be widely applied to the production of valuable substances contained in various plant roots.
甘草酸是一种三萜皂苷,是药用植物甘草(甘草、甘草和甘草)根中的主要活性成分,在草药和甜味剂等多种应用中在全球范围内使用。对甘草的需求不断增长,威胁到野生资源,因此需要一种可持续的供应甘草酸的方法。为了建立一种不依赖野生植物的替代甘草酸供应方法,我们试图使用毛状根培养生产甘草酸。我们试图通过使用基于 CRISPR/Cas9 的基因编辑来阻断竞争途径来促进甘草酸的生产。生成了 CYP93E3 CYP72A566 双敲除 (KO) 和 CYP93E3 CYP72A566 CYP716A179 LUS1 四重敲除 (KO) 变体,并在两种毛状根中均证实了大量甘草酸的积累。此外,我们评估了通过同时 CYP93E3 CYP72A566 双 KO 和 CYP88D6 过表达来促进进一步甘草酸生产的潜力。与双 KO 毛状根相比,这种策略导致双 KO/CYP88D6 过表达毛状根中甘草酸积累平均增加了 3 倍(约 1.4mg/g)。这些发现表明,阻断竞争途径和过表达生物合成基因的组合对于提高甘草毛状根中甘草酸的生产是重要的。我们的发现为利用毛状根培养可持续生产甘草酸提供了基础。鉴于基因组编辑技术在毛状根中的广泛应用,这种与基因敲除和过表达的结合可以广泛应用于各种植物根中所含有价值物质的生产。