| Autor: |
Yu H; College of Horticulture, Hunan Agricultural University, Changsha 410128, China., Zhou J; College of Horticulture, Hunan Agricultural University, Changsha 410128, China., Zhang J; College of Horticulture, Hunan Agricultural University, Changsha 410128, China., He X; College of Horticulture, Hunan Agricultural University, Changsha 410128, China., Peng S; College of Horticulture, Hunan Agricultural University, Changsha 410128, China., Ling H; College of Horticulture, Hunan Agricultural University, Changsha 410128, China., Dong Z; College of Horticulture, Hunan Agricultural University, Changsha 410128, China., Lu X; College of Bioscience and Biotechnology, Hunan Agricultural University, Changsha 410128, China., Tian Y; College of Bioscience and Biotechnology, Hunan Agricultural University, Changsha 410128, China., Guan G; College of Bioscience and Biotechnology, Hunan Agricultural University, Changsha 410128, China., Tang Q; College of Horticulture, Hunan Agricultural University, Changsha 410128, China., Zhong X; College of Horticulture, Hunan Agricultural University, Changsha 410128, China., He Y; College of Bioscience and Biotechnology, Hunan Agricultural University, Changsha 410128, China. |
| Abstrakt: |
Hedera helix is a traditional medicinal plant. Its primary active ingredients are oleanane-type saponins, which have extensive pharmacological effects such as gastric mucosal protection, autophagy regulation actions, and antiviral properties. However, the glycosylation-modifying enzymes responsible for catalyzing oleanane-type saponin biosynthesis remain unidentified. Through transcriptome, cluster analysis, and PSPG structural domain, this study preliminarily screened four candidate UDP-glycosyltransferases (UGTs), including Unigene26859, Unigene31717, CL11391.Contig2, and CL144.Contig9. In in vitro enzymatic reactions, it has been observed that Unigene26859 ( HhUGT74AG11 ) has the ability to facilitate the conversion of oleanolic acid, resulting in the production of oleanolic acid 28- O -glucopyranosyl ester. Moreover, HhUGT74AG11 exhibits extensive substrate hybridity and specific stereoselectivity and can transfer glycosyl donors to the C -28 site of various oleanane-type triterpenoids (hederagenin and calenduloside E) and the C -7 site of flavonoids (tectorigenin). Cluster analysis found that HhUGT74AG11 is clustered together with functionally identified genes AeUGT74AG6 , CaUGT74AG2 , and PgUGT74AE2 , further verifying the possible reason for HhUGT74AG11 catalyzing substrate generalization. In this study, a novel glycosyltransferase, HhUGT74AG11 , was characterized that plays a role in oleanane-type saponins biosynthesis in H. helix, providing a theoretical basis for the production of rare and valuable triterpenoid saponins. |
