Ortiz Gastón E, Guitart María E, Albertó Edgardo, Fernández Lahore Héctor M, Blasco Martin
Instituto de Investigaciones Biotecnológicas-Instituto Tecnológico Chascomús (IIB-INTECH, UNSAM-CONICET), Universidad de San Martín, San Martín, Buenos Aires 1650, Argentina.
Downstream Processing Laboratory, Jacobs University Bremen, D-28759 Bremen, Germany.
Anal Biochem. 2014 Jun 1;454:33-5. doi: 10.1016/j.ab.2014.02.028. Epub 2014 Mar 5.
Endo-polygalacturonase (endo-PGase) activity determinations generally rely on viscosity changes or reducing sugar ends produced by this activity over polygalacturonic acid. Torres and coworkers [Enzyme Microb. Technol. 48 (2011) 123-128] showed that ruthenium red (RR) is useful for endo-PGase determination. In this article, we present a high-throughput liquid-based endo-PGase assay based on the RR method and compare it with the viscosity determination method. The reduced assay uses a small volume of enzyme solution, 40 μg of polygalacturonic acid, and 45 μg of RR for each sample determination. Furthermore, we obtained an interconversion factor for RR and viscosity activities.
内切多聚半乳糖醛酸酶(endo-PGase)活性测定通常依赖于该酶作用于聚半乳糖醛酸产生的粘度变化或还原糖末端。托雷斯及其同事[《酶与微生物技术》48(2011)123 - 128]表明,钌红(RR)可用于endo-PGase的测定。在本文中,我们提出了一种基于RR法的高通量液相endo-PGase检测方法,并将其与粘度测定法进行比较。简化后的检测方法在每次样品测定时使用少量酶溶液、40μg聚半乳糖醛酸和45μg RR。此外,我们还获得了RR活性与粘度活性的相互转换因子。