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通过高效逆流色谱法从培养的土壤蓝藻(念珠藻属)中两步分离诺斯托菌素6 。

Two-step separation of nostotrebin 6 from cultivated soil cyanobacterium (Nostoc sp.) by high performance countercurrent chromatography.

作者信息

Cheel José, Kučerová Petra, Garrard Ian, Ignatova Svetlana, Hrouzek Pavel, Kopecký Jiří

机构信息

Department of Phototrophic Microorganisms-ALGATECH, Institute of Microbiology, Academy of Sciences of the Czech Republic, Opatovický mlýn, Třebon 379 81, Czech Republic.

Brunel Institute for Bioengineering, Brunel University, Kingston Lane, Uxbridge, Middlesex UB8 3PH, UK.

出版信息

Molecules. 2014 Jun 25;19(7):8773-87. doi: 10.3390/molecules19078773.

Abstract

High performance countercurrent chromatography (HPCCC) was successfully applied for the separation of nostotrebin 6 from cultivated soil cyanobacteria in a two-step operation. A two-phase solvent system composed of n-hexane-ethyl acetate-methanol-water (4:5:4:5, v/v/v/v) was employed for the HPCCC separation. In the first-step operation, its neutral upper phase was used as stationary phase and its basic lower phase (1% NH3 in lower phase) was employed as mobile phase at a flow rate of 1 mL/min. In the second operation step, its neutral upper phase was used as stationary phase, whereas both its neutral lower phase and basic lower phase were employed as mobile phase with a linear gradient elution at a flow rate of 0.8 mL/min. The revolution speed and temperature of the separation column were 1,000 rpm and 30 °C, respectively. Using HPCCC followed by clean-up on Sephadex LH-20 gel, 4 mg of nostotrebin 6 with a purity of 99% as determined by HPLC/DAD-ESI-HRMS was obtained from 100 mg of crude extract. The chemical identity of the isolated compound was confirmed by comparing its spectroscopic data (UV, ESI-HRMS, ESI-HRMS2) with those of an authentic standard and data available in the literature.

摘要

高效逆流色谱法(HPCCC)通过两步操作成功应用于从培养的土壤蓝细菌中分离6-去甲托特罗定。采用正己烷 - 乙酸乙酯 - 甲醇 - 水(4:5:4:5,v/v/v/v)组成的两相溶剂系统进行HPCCC分离。在第一步操作中,其中性上相用作固定相,碱性下相(下相中含1% NH₃)用作流动相,流速为1 mL/min。在第二步操作中,其中性上相用作固定相,而中性下相和碱性下相均用作流动相,以0.8 mL/min的流速进行线性梯度洗脱。分离柱的转速和温度分别为1000 rpm和30℃。通过HPCCC分离,随后在Sephadex LH - 20凝胶上进行纯化,从100 mg粗提物中获得了4 mg纯度为99%的6-去甲托特罗定(通过HPLC/DAD - ESI - HRMS测定)。通过将分离得到的化合物的光谱数据(UV、ESI - HRMS、ESI - HRMS²)与标准品的光谱数据以及文献中的数据进行比较,确认了该分离化合物的化学结构。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1ed/6271089/0bebbe17f16f/molecules-19-08773-g001.jpg

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