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高速逆流色谱法从稻曲球中制备分离主要曲菌素

Preparative Separation of Main Ustilaginoidins from Rice False Smut Balls by High-Speed Counter-Current Chromatography.

作者信息

Sun Weibo, Dong Xuejiao, Xu Dan, Meng Jiajia, Fu Xiaoxiang, Wang Xiaohan, Lai Daowan, Zhou Ligang, Liu Yang

机构信息

Key Laboratory of Plant Pathology, Ministry of Agriculture/Department of Plant Pathology, College of Plant Protection, China Agricultural University, Beijing 100193, China.

Institute of Food Science and Technology, Chinese Academy of Agricultural Sciences/Key Laboratory of Agro-products Processing, Ministry of Agriculture, Beijing 100193, China.

出版信息

Toxins (Basel). 2016 Jan 12;8(1):20. doi: 10.3390/toxins8010020.

Abstract

Ustilaginoidins are bis-naphtho-γ-pyrone mycotoxins isolated from the rice false smut balls (FSBs) infected by the pathogen Villosiclava virens in rice spikelets on panicles. In order to obtain large amounts of pure ustilaginoidins to further evaluate their biological activities and functions, phytotoxicity on rice, security to human and animals as well as to accelerate their applications as pharmaceuticals, preparative high-speed counter-current chromatography (HSCCC) was successfully applied to the isolation and purification of seven bis-naphtho-γ-pyrone mycotoxins, namely ustilaginoidins A (1), G (2), B (3), H (4), I (5), C (6), and J (7) from the ethyl acetate crude extract of rice FSBs. Both 1 and 2 were prepared by HSCCC from the low-polarity fraction of the crude extract using the two-phase solvent system composed of n-hexane-ethyl acetate-methanol-water at the volume ratio of 6.5:3.5:5.0:5.0. Similarly, 3, 4 and 5 were prepared from the medium-polarity fraction using the system at the volume ratio of 4.0:5.0:5.0:6.0, and 6 and 7 were prepared from the higher-polarity fraction using the system at volume ratio of 3.0:5.0:4.0:6.7. A total of 6.2 mg of 1, 5.1 mg of 2, 3.9 mg of 3, 1.2 mg of 4, 5.7 mg of 5, 3.5 mg of 6, and 6.1 mg of 7 with purities of 88%, 82%, 91%, 80%, 92%, 81% and 83%, respectively, were yielded from total 62 mg fraction samples in three independent HSCCC runs. The structures of the purified ustilaginoidins were characterized by means of physicochemical and spectrometric analysis.

摘要

黑粉菌毒素是一类双萘并-γ-吡喃型霉菌毒素,从水稻穗部小穗上受病原菌稻绿核菌感染的稻曲球中分离得到。为了获得大量纯的黑粉菌毒素以进一步评估其生物活性和功能、对水稻的植物毒性、对人和动物的安全性,并加速其作为药物的应用,制备型高速逆流色谱(HSCCC)成功应用于从稻曲球的乙酸乙酯粗提物中分离纯化7种双萘并-γ-吡喃型霉菌毒素,即黑粉菌毒素A(1)、G(2)、B(3)、H(4)、I(5)、C(6)和J(7)。1和2通过HSCCC从粗提物的低极性部分制备,使用正己烷-乙酸乙酯-甲醇-水体积比为6.5:3.5:5.0:5.0的两相溶剂系统。同样,3、4和5从中等极性部分使用体积比为4.0:5.0:5.0:6.0的系统制备,6和7从高极性部分使用体积比为3.0:5.0:4.0:6.7的系统制备。在三次独立的HSCCC运行中,从总共62 mg的馏分样品中分别得到了纯度为88%的6.2 mg的1、纯度为82%的5.1 mg的2、纯度为91%的3.9 mg的3、纯度为80%的1.2 mg的4、纯度为92%的5.7 mg的5、纯度为81%的3.5 mg的6和纯度为83%的6.1 mg的7。纯化后的黑粉菌毒素的结构通过物理化学和光谱分析进行了表征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8504/4728542/bd28c904c475/toxins-08-00020-g001.jpg

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