发布: 2017年04月05日第7卷第7期 DOI: 10.21769/BioProtoc.2206 浏览次数: 8483
评审: Valentine V TrotterPetru-Iulian TrasneaAnonymous reviewer(s)
Abstract
The activity of the endo-β-1,4-galactanase GanB from B. subtilis on the high molecular weight β-1,4-galactan was determined quantitatively by the measurement of the increase of the reducing power or with the dyed substrate Azo-galactan. The generated degradation products were analyzed using thinlayer-chromatography (TLC) or high-performance anion-exchange chromatography (HPAEC).
Keywords: Galactanase-assay (半乳聚糖酶分析)Background
Bacillus subtilis possesses comprehensive systems for the utilization of plant cell wall polysaccharides including the gene cluster ganSPQAB which encodes galactan utilization elements (Watzlawick et al., 2016). Galactans are high molecular weight galacto-saccharides and are found as side chains of rhamnogalacturonan type I in pectin. Its degradation is carried out by endo-beta1,4 galactanases (EC 3.2.1.89). The utilization of galactan by B. subtilis involves the extracellular galactanase GanB, cleaving the high molecular galactan inside the chain and resulting short oligomers that enter the cell wall to get there further degraded. The ganB gene from B. subtilis was cloned and expressed in E.coli (Watzlawick et al., 2016) and the enzymatic properties of the purified His-tagged mature protein were characterized by galactanase assays.
Materials and Reagents
Equipment
Procedure
文章信息
版权信息
© 2017 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
Watzlawick, H. (2017). Measurement of the Galactanase Activity of the GanB Galactanase Protein from Bacillus subtilis. Bio-protocol 7(7): e2206. DOI: 10.21769/BioProtoc.2206.
分类
微生物学 > 微生物生物化学 > 蛋白质
微生物学 > 微生物生物化学 > 糖类
生物化学 > 蛋白质 > 活性
您对这篇实验方法有问题吗?
在此处发布您的问题,我们将邀请本文作者来回答。同时,我们会将您的问题发布到Bio-protocol Exchange,以便寻求社区成员的帮助。
提问指南
+ 问题描述
写下详细的问题描述,包括所有有助于他人回答您问题的信息(例如实验过程、条件和相关图像等)。
Share
Bluesky
X
Copy link