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邻苯二甲酸酐与壳聚糖的化学修饰:稳定来自炭黑曲霉的生淀粉消化淀粉酶的可行选择。

Chemical modification with phthalic anhydride and chitosan: Viable options for the stabilization of raw starch digesting amylase from Aspergillus carbonarius.

作者信息

Nwagu Tochukwu Nwamaka, Okolo Bartholomew, Aoyagi Hideki, Yoshida Shigeki

机构信息

Department of Microbiology, Faculty of Biological Sciences, University of Nigeria, Nsukka, Nigeria.

Department of Microbiology, Faculty of Biological Sciences, University of Nigeria, Nsukka, Nigeria.

出版信息

Int J Biol Macromol. 2017 Jun;99:641-647. doi: 10.1016/j.ijbiomac.2017.03.022. Epub 2017 Mar 6.

DOI:10.1016/j.ijbiomac.2017.03.022
PMID:28279767
Abstract

The raw starch digesting type of amylase (RSDA) presents greater opportunities for process efficiency at cheaper cost and shorter time compared to regular amylases. Chemical modification is a simple and rapid method toward their stabilization for a wider application. RSDA from Aspergillus carbonarius was modified with either phthalic anhydride (PA) or chitosan. Activity retention was 87.3% for PA-modified and 80.9% for chitosan-modified RSDA. Optimum pH shifted from 5 to 7 after PA-modification. Optimum temperature changed from 30°C (native) to 30-40°C and 60°C for PA-modified and chitosan-modified, respectively. Activation energy (kJmol) for hydrolysis was 13.5, 12.7, and 10.2 while the activation energy for thermal denaturation was 32.8, 80.3, 81.9 for free, PA-modified and chitosan-modified, respectively. The specificity constants (V/K) were 73.2 for PA-modified, 63.1 for chitosan-modified and 77.1 for native RSDA. The half-life (h) of the RSDA at 80°C was increased from 6.1 to 25.7 for the PA-modified and 138.6 for the chitosan derivative. Modification also led to increase in D value, activation enthalpy and Gibbs free energy of enzyme deactivation. Fluorescence spectra showed that center of spectral mass decreased for the PA-modified RSDA but increased for chitosan modified RSDA.

摘要

与常规淀粉酶相比,生淀粉消化型淀粉酶(RSDA)在以更低成本和更短时间实现工艺效率方面具有更大的机会。化学修饰是一种简单快速的方法,可使其稳定化以实现更广泛的应用。用邻苯二甲酸酐(PA)或壳聚糖对黑曲霉的RSDA进行了修饰。PA修饰的RSDA活性保留率为87.3%,壳聚糖修饰的为80.9%。PA修饰后,最佳pH从5变为7。最佳温度分别从30°C(天然)变为PA修饰的30 - 40°C和壳聚糖修饰的60°C。水解的活化能(kJ/mol)分别为13.5、12.7和10.2,而热变性的活化能分别为游离的32.8、PA修饰的80.3、壳聚糖修饰的81.9。特异性常数(V/K)分别为PA修饰的73.2、壳聚糖修饰的63.1和天然RSDA的77.1。PA修饰的RSDA在80°C下的半衰期(h)从6.1增加到25.7,壳聚糖衍生物的半衰期为138.6。修饰还导致酶失活的D值、活化焓和吉布斯自由能增加。荧光光谱表明,PA修饰的RSDA光谱质量中心降低,而壳聚糖修饰的RSDA光谱质量中心增加。

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