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HPLC-fluorescence detection method for determination of key intermediates of the lincomycin biosynthesis in fermentation broth

机译:高效液相色谱-荧光检测法测定发酵液中林可霉素生物合成关键中间体

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摘要

The biosynthetic pathway of the clinically important antibiotic lincomycin is not known in details. The precise knowledge of the lincomycin biosynthesis is a prerequisite for generation of improved derivatives by means of combinatorial genetics. Methods allowing determination of the key intermediates are very important tools of the pathway investigation. Two new high-performance liquid chromatography methods with fluorescence detection for determination of lincomycin precursors in fermentation broth of Streptomyces lincolnensis and its lincomycin nonproducing mutants were developed. The first one enables simultaneous analysis of methylthiolincosamide (MTL) and N-demethyllincomycin (NDL), whereas the second one is suitable for 4-propyl-l-proline (PPL) assay. Both methods are based on the pre-column derivatization: MTL and NDL with 4-chloro-7-nitrobenzofurazan; PPL with o-phthaldialdehyde. The methods were validated with lower limit of quantification values of 2.50, 3.75, and 3.75 μg ml?1 for MTL, NDL, and PPL, respectively. The inter- and intra-day accuracies and precisions were all within 12%. Stability of oxidized and derivatized analytes was investigated.
机译:临床上重要的抗生素林可霉素的生物合成途径尚不清楚。对林可霉素生物合成的精确了解是通过组合遗传学产生改良衍生物的前提。允许确定关键中间体的方法是途径研究中非常重要的工具。开发了两种用于荧光检测的高效液相色谱法,用于测定林肯链霉菌及其不产生林可霉素的突变体的发酵液中的林可霉素前体。第一个能够同时分析甲基硫代林可酰胺(MTL)和N-去甲基林可霉素(NDL),而第二个则适用于4-丙基-1-脯氨酸(PPL)分析。两种方法均基于柱前衍生:MTL和NDL与4-氯-7-硝基苯并呋喃; PPL与邻苯二甲醛。对MTL,NDL和PPL的定量限分别为2.50、3.75和3.75μgml?1 进行了验证。日间和日内精确度均在12%以内。研究了氧化和衍生化分析物的稳定性。

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