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.对三萜皂苷甘草酸转运的表征

Characterization of Triterpene Saponin Glycyrrhizin Transport by .

作者信息

Kato Kakuki, Horiba Asako, Hayashi Hiroaki, Mizukami Hajime, Terasaka Kazuyoshi

机构信息

Graduate School of Pharmaceutical Sciences, Nagoya City University, 3-1 Tanabe-Dori, Mizuho-Ku, Nagoya 467-8603, Japan.

College of Pharmaceutical Sciences, Ritsumeikan University, 1-1-1 Noji-Higashi, Kusatsu 525-8577, Japan.

出版信息

Plants (Basel). 2022 May 5;11(9):1250. doi: 10.3390/plants11091250.

Abstract

Glycyrrhizin (GL), a triterpene compound produced by species, is a crucial pharmacologically active component of crude drugs. In contrast to the biosynthesis of GL in plants, little is known about GL transport and accumulation in plants. The transport mechanism of GL was characterized using cultured cells of . Cultured cells of efficiently incorporated exogenously supplied GL. Proton pump inhibitors, such as probenecid and niflumic acid, as well as a protonophore (carbonylcyanide -chlorophenylhydrazone), markedly inhibited GL uptake by cultured cells, whereas vanadate exhibited a moderate inhibition. Furthermore, GL transport by tonoplast vesicles is dependent not on a H-electrochemical gradient but MgATP and is markedly inhibited by vanadate. These results suggest that GL uptake by cultured cells is mediated by a H-symporter in the plasma membrane and an ATP-binding cassette transporter, which has high specificity for the aglycone structure of GL on the tonoplast.

摘要

甘草酸(GL)是由多种植物产生的三萜类化合物,是粗药材中一种关键的药理活性成分。与植物中GL的生物合成相比,人们对GL在植物中的转运和积累知之甚少。利用[植物名称]的培养细胞对GL的转运机制进行了表征。[植物名称]的培养细胞能有效摄取外源供应的GL。丙磺舒和尼氟酸等质子泵抑制剂以及质子载体(羰基氰化物-对氯苯腙)显著抑制培养细胞对GL的摄取,而钒酸盐则表现出中等程度的抑制作用。此外,[植物名称]液泡膜囊泡对GL的转运不依赖于H电化学梯度,而是依赖于MgATP,并且被钒酸盐显著抑制。这些结果表明,培养细胞对GL的摄取是由质膜中的H同向转运体和ATP结合盒转运体介导的,该转运体对液泡膜上GL的苷元结构具有高度特异性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd99/9102456/677dccffb777/plants-11-01250-g001.jpg

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