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首页> 外文期刊>Journal of Chemical Technology & Biotechnology >A flow injection analysis system for on-line monitoring of cutinase activity at outlet of an expanded bed adsorption column almost in real time
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A flow injection analysis system for on-line monitoring of cutinase activity at outlet of an expanded bed adsorption column almost in real time

机译:流动注射分析系统,用于实时实时监测膨胀床吸附塔出口的角质酶活性

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Expanded bed adsorption (EBA) was used to recover, concentrate and purify Fusarium solani pisi cutinase, secreted by a recombinant Saccharomyces cerevisiae strain, directly from a whole fermentation culture. A flow injection analysis (FIA) system for monitoring Fusarium solani pisi cutinase based on microencapsulation of p-nitrophenylbutyrate (p-NPB) in a micellar system (sodium cholate, tetrahydrofuran, phosphate buffer) was developed for monitoring this target enzyme at the outlet tube of the EBA column. Slight differences in yeast cultivation conditions during cutinase production may influence the fermentation performance, which affects directly the adsorption of cutinase during the loading step and consequently the efficiency of the EBA process. This effect can be especially relevant when it is necessary to stop the application of feedstock to the EBA column when the outlet concentration (A) of the desired product is lower than 5% of the feed concentration (A.). Excellent correlations between the FIA system and the off-line analytical method for monitoring cutinase activity during the different EBA steps were obtained. Additionally, the blocking/fouling of the sample injector and tubes of the FIA system initially observed were eliminated due to the excellent surfactant properties of the sodium cholate contained in the phosphate buffer and used to dilute the enzyme samples. This FIA system was shown to be a powerful analytical tool for monitoring cutinase activity almost in real time (45-60 s), maximizing enzyme adsorption while minimizing product loss and consequently maximizing the recovery yield of the product. (c) 2006 Society of Chemical Industry.
机译:膨胀床吸附(EBA)用于直接从整个发酵培养物中回收,浓缩和纯化由重组酿酒酵母菌株分泌的茄形镰刀菌角质酶。开发了一种基于对硝基苯基丁酸(p-NPB)微囊化胶束系统(胆酸钠,四氢呋喃,磷酸盐缓冲液)的微囊化镰刀菌角质酶的流动注射分析(FIA)系统,用于在出口管上监测该目标酶EBA列。角质酶生产过程中酵母培养条件的细微差异可能会影响发酵性能,从而直接影响角质酶在上样步骤中的吸附,从而影响EBA过程的效率。当所需产品的出口浓度(A)低于进料浓度(A.)的5%时,有必要停止将原料施加到EBA色谱柱上时,此效果尤其重要。获得了FIA系统与离线分析方法之间的极好的相关性,该离线分析方法用于监视不同EBA步骤中的角质酶活性。此外,由于磷酸盐缓冲液中所含的用于稀释酶样品的胆酸钠具有出色的表面活性剂性质,因此消除了最初观察到的FIA系统的进样器和试管的堵塞/结垢。该FIA系统被证明是一种强大的分析工具,可几乎实时(45-60 s)监测角质酶的活性,在最大程度地吸收酶的同时最大程度地减少产品损失,从而最大程度地提高产品的回收率。 (c)2006年化学工业协会。

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