江西嗜酸链霉菌去铁胺E及金属络合物的分离鉴定与生物活性研究
收稿日期: 2024-01-30
修回日期: 2024-03-11
网络出版日期: 2024-04-10
基金资助
科技部重大专项(2022YFC2303100); 国家自然科学基金(22193070); 国家自然科学基金(32030002)
Study on Isolation, Identification and Bioactivity of Desferrioxamine E and Its Metal-Complexes from Streptacidiphilus jiangxiensis
Received date: 2024-01-30
Revised date: 2024-03-11
Online published: 2024-04-10
Supported by
National Key Research and Development Program of China(2022YFC2303100); National Natural Science Foundation of China(22193070); National Natural Science Foundation of China(32030002)
嗜酸链霉菌属细菌的研究主要集中在新物种的分离和鉴定上, 而其次级代谢产物的研究则相对较少. 从江西嗜酸链霉菌的发酵液中分离得到一个新的铝配合物铝草铵(alumioxamine, 3)和两个已知化合物去铁胺E (desferrioxamine E, 1)和铁草铵E (ferrioxamine E, 2), 并通过MS、IR、NMR以及单晶X射线衍射技术对其结构进行鉴定. 从结构上来看, 化合物3以铝为中心, 与配体的六个O原子相连, 形成六齿配合物. 此外, 体外细胞毒活性实验表明, 在100 μmol/L浓度时化合物1对4种人肿瘤细胞(Hela、PANC1、A375和MHCC-97H)均具有一定的抑制活性, 细胞存活率为4.8%~66.4%.
李金达 , 程伯涛 , 黄积武 , 刘文 . 江西嗜酸链霉菌去铁胺E及金属络合物的分离鉴定与生物活性研究[J]. 有机化学, 2024 , 44(7) : 2377 -2380 . DOI: 10.6023/cjoc202401038
Research on the genus Streptacidiphilus was mainly focused on the isolation and identification of new species, with relatively less emphasis on the study of secondary metabolites. A new aluminium-complex alumioxamine (3), and two known compounds desferrioxamine E (1) and ferrioxamine E (2) were isolated from the fermentation broth of Streptacidiphilus jiangxiensis CGMCC 4.1857. Their structures were elucidated by MS, IR, NMR and single crystal X-ray diffraction technologies. Structurally, compound 3 features aluminum(III) as the central atom, which is bonded to six oxygen atoms of the ligand, forming a hexadentate complex. Furthermore, in vitro cytotoxicity assays showed that compound 1 exhibited potential inhibitory activity against four human tumor cell lines (Hela, PANC1, A375 and MHCC-97H) at a concentration of 100 μmol/L with cell viability ranging from 4.8% to 66.4%.
| [1] | Kim, S. B.; Lonsdale, J.; Seong, C.; Goodfellow, M. Antonie van Leeuwenhoek 2003, 83, 107. |
| [2] | Huang, Y.; Cui, Q. F.; Wang, L. M.; Rodriguez, C.; Quintana, E.; Goodfellow, M.; Liu, Z. H. Antonie van Leeuwenhoek 2004, 86, 159. |
| [3] | Wang, L. M.; Huang, Y.; Liu, Z. H.; Goodfellow, M.; Rodriguez, C. Int. J. Syst. Evol. Microbiol. 2006, 56, 1257. |
| [4] | Golinska, P.; Kim, B. Y.; Dahm, H.; Goodfellow, M. Antonie van Leeuwenhoek 2013, 104, 965. |
| [5] | Song, W.; Duan, L. P.; Jin, L. Y.; Zhao, J. W.; Jiang, S. W.; Sun, T. Y.; Guo, X. W.; Xiang, W. S.; Wang, X. J. Int. J. Syst. Evol. Microbiol. 2018, 68, 1757. |
| [6] | Roh, S. G.; Kim, M. K.; Park, S.; Yun, B. R.; Park, J.; Kim, M. J.; Kim, Y. S.; Kim, S. B. Int. J. Syst. Evol. Microbiol. 2018, 68, 3149. |
| [7] | Nouioui, I.; Klenk, H. P.; Igual, J. M.; Gulvik, C. A.; Lasker, B. A.; McQuiston, J. R. Int. J. Syst. Evol. Microbiol. 2019, 69, 1047. |
| [8] | Yu, B.; Han, C. Y.; Zhao, J. W.; Zhang, Y. T.; Shan, Q. Q.; Wu, Y.; Ju, H. X.; Xiang, W. S.; Wang, X. J. Int. J. Syst. Evol. Microbiol. 2021, 71, 004824. |
| [9] | Hwang, S.; Yun, Y.; Choi, W. H.; Kim, S. B.; Shin, J.; Lee, M. J.; Oh, D. C. J. Nat. Prod. 2019, 82, 341. |
| [10] | Elsayed, S. S.; Genta-Jouve, G.; Carrión, V. J.; Nibbering, P. H.; Siegler, M. A.; de Boer, W.; Hankemeier, T.; van Wezel, G. P. J. Org. Chem. 2020, 85, 10648. |
| [11] | Koo, M. H.; Kim, E. J.; Lee, J. H.; Han, S. J.; Lee, Y. M.; Lee, S.; Youn, U. J. Biochem. Syst. Ecol. 2023, 110, 104709. |
| [12] | Blin, K.; Shaw, S.; Augustijn, H. E.; Reitz, Z. L.; Biermann, F.; Alanjary, M.; Fetter, A.; Terlouw, B. R.; Metcalf, W. W.; Helfrich, E. J. N.; van Wezel, G. P.; Medema, M. H.; Weber, T. Nucleic Acids Res. 2023, 51, W46. |
| [13] | Kalaitzis, J. A.; Ingrey, S. D.; Chau, R.; Simon, Y.; Neilan, B. A. Aust. J. Chem. 2016, 69, 129. |
| [14] | Van der Helm, D.; Poling, M. J. Am. Chem. Soc. 1976, 98, 82. |
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