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(异)黄酮7-和3'-O-糖基转移酶可被氯化铜诱导。

(iso)flavone 7- and 3'-O-Glycosyltransferases Can Be Induced by CuCl.

作者信息

Zhang Xiang, Zhu Yan, Ye Jun, Ye Ziyu, Zhu Ruirui, Xie Guoyong, Zhao Yucheng, Qin Minjian

机构信息

Department of Resources Science of Traditional Chinese Medicines, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing, China.

Key Laboratory of Modern Traditional Chinese Medicines (Ministry of Education), China Pharmaceutical University, Nanjing, China.

出版信息

Front Plant Sci. 2021 Feb 9;12:632557. doi: 10.3389/fpls.2021.632557. eCollection 2021.

DOI:10.3389/fpls.2021.632557
PMID:33633770
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7900552/
Abstract

In many plants, isoflavones are the main secondary metabolites that have various pharmacological activities, but the low water solubility of aglycones limits their usage. The O-glycosylation of (iso)flavones is a promising way to overcome this barrier. O-glycosyltransferases (UGTs) are key enzymes in the biosynthesis of (iso)flavonoid O-glycosides in plants. However, limited investigations on isoflavonoid O-UGTs have been reported, and they mainly focused on legumes. Goldblatt et Mabberley is a non-legume plant rich in various isoflavonoid glycosides. However, there are no reports regarding its glycosylation mechanism, despite the transcriptome previously being annotated as having non-active isoflavone 7-O-UGTs. Our previous experiments indicated that isoflavonoid glycosides were induced by CuCl in calli; therefore, we hypothesized that isoflavone O-UGTs may be induced by Cu. Thus, a comparative transcriptome analysis was performed using seedlings treated with CuCl, and eight new active BcUGTs were obtained. Biochemical analyses showed that most of the active BcUGTs had broad substrate spectra; however, substrates lacking 5-OH were rarely catalyzed. Real-time quantitative PCR results further indicated that the transcriptional levels of BcUGTs were remarkably induced by Cu. Our study increases the understanding of UGTs and isoflavone biosynthesis in non-legume plants.

摘要

在许多植物中,异黄酮是具有多种药理活性的主要次生代谢产物,但苷元的低水溶性限制了它们的应用。(异)黄酮的O-糖基化是克服这一障碍的一种有前景的方法。O-糖基转移酶(UGTs)是植物中(异)黄酮类O-糖苷生物合成的关键酶。然而,关于异黄酮O-UGTs的研究报道有限,且主要集中在豆科植物上。戈德布拉特和马伯利是一种富含各种异黄酮苷的非豆科植物。然而,尽管其转录组先前被注释为具有无活性的异黄酮7-O-UGTs,但关于其糖基化机制尚无报道。我们之前的实验表明,在愈伤组织中,异黄酮苷受氯化铜诱导;因此,我们推测异黄酮O-UGTs可能受铜诱导。于是,我们对用氯化铜处理的幼苗进行了比较转录组分析,获得了8个新的有活性的BcUGTs。生化分析表明,大多数有活性的BcUGTs具有广泛的底物谱;然而,缺乏5-羟基的底物很少被催化。实时定量PCR结果进一步表明,BcUGTs的转录水平受铜显著诱导。我们的研究增进了对非豆科植物中UGTs和异黄酮生物合成的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f61f/7900552/1f54b09fba22/fpls-12-632557-g0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f61f/7900552/b33b4a34edbb/fpls-12-632557-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f61f/7900552/82f77788ef27/fpls-12-632557-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f61f/7900552/8f35b8ea90cc/fpls-12-632557-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f61f/7900552/8900a6334ac8/fpls-12-632557-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f61f/7900552/1b6b04d38ebe/fpls-12-632557-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f61f/7900552/494bcaac026c/fpls-12-632557-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f61f/7900552/ccb1354c566a/fpls-12-632557-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f61f/7900552/36a2af74d27e/fpls-12-632557-g0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f61f/7900552/1f54b09fba22/fpls-12-632557-g0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f61f/7900552/b33b4a34edbb/fpls-12-632557-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f61f/7900552/82f77788ef27/fpls-12-632557-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f61f/7900552/8f35b8ea90cc/fpls-12-632557-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f61f/7900552/8900a6334ac8/fpls-12-632557-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f61f/7900552/1b6b04d38ebe/fpls-12-632557-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f61f/7900552/494bcaac026c/fpls-12-632557-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f61f/7900552/ccb1354c566a/fpls-12-632557-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f61f/7900552/36a2af74d27e/fpls-12-632557-g0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f61f/7900552/1f54b09fba22/fpls-12-632557-g0009.jpg

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