首页> 外文期刊>Analytical chemistry >FTMS structure elucidation of natural products: Application to muraymycin antibiotics using ESI multi-CHEF SORI-CID FTMSn, the top-down/bottom-up approach, and HPLC ESI capillary-skimmer CID FTMS
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FTMS structure elucidation of natural products: Application to muraymycin antibiotics using ESI multi-CHEF SORI-CID FTMSn, the top-down/bottom-up approach, and HPLC ESI capillary-skimmer CID FTMS

机译:FTMS天然产物的结构解析:使用ESI多CHEF SORI-CID FTMSn,自上而下/自下而上的方法以及HPLC ESI毛细管分离器CID FTMS应用于穆雷霉素抗生素

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The molecular formulas for the structures and substructures of muraymycin antibiotics A1 (C52H90N14O19, MW 1214) and B1 (C49H83N11O18, MW 1113) were determined using electrospray ionization (ESI) Fourier transform mass spectrometry (FTMS). The muraymycin A1 and B1 structures were elucidated by utilizing capillary-skimmer fragmentation with up to five stages of mass spectrometry (MS5). Multi-CHEF, a multiple ion isolation method, was used at each stage of MSn to isolate a parent ion and up to four reference ions, for exact-mass calibration. The parent ions were fragmented by SORI-CID and the product ions internally calibrated with average absolute mass errors less than 1 ppm at each stage in the fragmentation processes. Using the top-down/bottom-up approach, the molecular formulas for the antibiotics were determined by summing the elemental formulas of the neutral losses, obtained by measuring the mass differences (< 500 Da) between the genetically related sequential parent ion masses in the MSn spectra, with the unique elemental formula of the lowest parent ion mass (< 500 Da). The structures of 12 additional compounds in the muraymycin complex were elucidated using HPLC ESI capillary-skimmer CID FTMS by correlating their fragmentation patterns with those of muraymycins A1 and B1. Sequential neutral losses of an aminosugar, a valine, a uridine, and an ester fatty acid from the muraymycin parent ions provided diagnostic fragments for characterization. [References: 27]
机译:使用电喷雾电离(ESI)傅里叶变换质谱(FTMS)确定了穆来霉素抗生素A1(C52H90N14O19,MW 1214)和B1(C49H83N11O18,MW 1113)的结构和亚结构的分子式。通过使用毛细管分离器裂解和多达五个质谱(MS5)阶段来阐明穆雷霉素A1和B1结构。在MSn的每个阶段都使用Multi-CHEF(一种多离子分离方法)来分离母离子和最多四个参考离子,以进行精确质量校准。母离子通过SORI-CID进行裂解,并且在裂解过程的每个阶段内部校正的产物离子的平均绝对质量误差均小于1 ppm。使用自上而下/自下而上的方法,通过对中性损失的元素公式求和来确定抗生素的分子式,这些元素式是通过测量遗传相关顺序母体离子质量之间的质量差(<500 Da)而获得的。 MSn光谱,具有最低母离子质量(<500 Da)的独特元素式。使用HPLC ESI毛细管分离器CID FTMS阐明了穆来霉素复合物中12种其他化合物的结构,方法是将它们的片段化模式与穆来霉素A1和B1的片段化模式相关联。来自穆拉霉素母体离子的氨基糖,缬氨酸,尿苷和酯脂肪酸的连续中性损失提供了表征的诊断片段。 [参考:27]

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