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测定吸水链霉菌发酵液中井冈霉素A的新型分光光度法。

Novel spectrophotometric approach for determination of validamycin A in fermentation of Streptomyces hygroscopicus.

作者信息

Li Wei, Feng Jinsong, Liu Yan, Jiang Jing, Zheng Xiaodong, Zhou Wen-Wen

机构信息

College of Biosystems Engineering and Food Science, Fuli Institute of Food Science, Zhejiang Key Laboratory for Agro-Food Processing, Zhejiang University, Hangzhou 310058, Zhejiang, China.

出版信息

J Biosci Bioeng. 2016 Dec;122(6):736-739. doi: 10.1016/j.jbiosc.2016.05.007. Epub 2016 Jun 11.

DOI:10.1016/j.jbiosc.2016.05.007
PMID:27296090
Abstract

Validamycin A (Val-A), produced by Streptomyces hygroscopicus 5008 in industrial fermentation, is one of the most widely used anti-fungal agro-antibiotics in Asia and high performance liquid chromatography (HPLC) assay is usually used to determine the production of Val-A. A new approach to determine Val-A by spectrophotometer is developed. During the fermentation of S. hygroscopicus 5008, a pigment secretion was found along with the Val-A biosynthesis. There was a stable relationship between the concentration of Val-A and spectral absorption (SA) value of this pigment at 450 nm, even in different fermentation cultures or conditions. Using SA value as interior label, a rapid spectrophotometric method for determining Val-A production was established. In comparing Val-A productivity by HPLC method with that by SA method, the relative standard deviation (R.S.D.) was 0.007 (less than 0.05, no variation) and the conditional probability [Pr(T < t)] was 0.3491 (greater than 0.05, no difference) at the optimal time point of Val-A fermentation, which demonstrated SA method was as stable and accurate as standard HPLC method. It was applied successfully to finding positive strains with high Val-A productivity and short fermentation time. SA assay is an accurate and cost-effective method for measuring Val-A and screening high-producing strains, and this work provides a new insight for rapid quantitative analysis of antibiotics in fermentation of pigment-producing strains.

摘要

有效霉素A(Val-A)由吸水链霉菌5008在工业发酵中产生,是亚洲使用最广泛的抗真菌农用抗生素之一,通常采用高效液相色谱(HPLC)分析法来测定Val-A的产量。本文开发了一种用分光光度计测定Val-A的新方法。在吸水链霉菌5008的发酵过程中,发现伴随着Val-A的生物合成有色素分泌。即使在不同的发酵培养物或条件下,Val-A的浓度与该色素在450nm处的光谱吸收(SA)值之间也存在稳定的关系。以SA值为内部标记,建立了一种快速分光光度法测定Val-A产量。在比较HPLC法和SA法测定Val-A的生产率时,在Val-A发酵的最佳时间点,相对标准偏差(R.S.D.)为0.007(小于0.05,无变化),条件概率[Pr(T < t)]为0.3491(大于0.05,无差异),这表明SA法与标准HPLC法一样稳定和准确。它已成功应用于筛选具有高Val-A生产率和短发酵时间的阳性菌株。SA分析法是一种准确且经济高效的测定Val-A和筛选高产菌株的方法,这项工作为色素产生菌株发酵中抗生素的快速定量分析提供了新的见解。

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