From the Department of Environmental and Plant Biology, Ohio University, Athens, OH, 45701, USA; Molecular and Cellular Biology Program, Ohio University, Athens, OH, 45701, USA.
The Department of Chemistry & Environmental Science, New Jersey Institute of Technology, Newark, NJ, 07102, USA.
Plant Physiol Biochem. 2024 Oct;215:109052. doi: 10.1016/j.plaphy.2024.109052. Epub 2024 Aug 17.
Cellulose and hemicellulose are the major structural β-glycan polysaccharides in cell walls of land plants. They are characterized by a backbone of β-(1,3)- and/or β-(1,4)-linked sugars such as glucose, mannose, or xylose. The backbones of these polymers are produced by processive glycosyltransferases (GTs) called synthases having multiple transmembrane domains anchoring them to the membrane. Thus, they are among the most difficult membrane proteins to test in vitro and to purify. Recently, we developed an in vitro GT-array (i-GTray) platform and showed that non-processive type II membrane GTs could be produced via cell-free system in a soluble and active form and tested in this platform. To determine whether i-GT-ray platform is adequate for the production and testing of β-glycan synthases, we tested five synthases involved in cellulose, xyloglucan, (gluco)mannan, and β-(1,3)(1,4)-mixed-linkage glucan synthesis. Our results revealed unsuspected features of these enzymes. For example, all these synthases could be produced in a soluble and active form and are active in the absence of detergent or membrane lipids, and none of them required a primer for initiation of synthesis. All synthases produced ethanol-insoluble products that were susceptible to the appropriate hydrolases (i.e., cellulase, lichenase, mannanase). Using this platform, we showed that AtCslC4 and AtXXT1 interact directly to form an active xyloglucan synthase that produced xylosylated cello-oligosaccharides (up to three xylosyl residues) when supplied with UDP-Glc and UDP-Xyl. i-GTray platform represents a simple and powerful functional genomics tool for discovery of new insights of synthase activities and can be adapted to other enzymes.
纤维素和半纤维素是陆地植物细胞壁中主要的结构β-糖苷多糖。它们的特征是由β-(1,3)-和/或β-(1,4)-连接的糖组成的骨架,如葡萄糖、甘露糖或木糖。这些聚合物的骨架是由称为合酶的连续糖基转移酶(GT)产生的,合酶具有多个跨膜结构域将其锚定在膜上。因此,它们是最难在体外测试和纯化的膜蛋白之一。最近,我们开发了一种体外 GT 阵列(i-GTray)平台,并表明非连续型 II 型膜 GT 可以通过无细胞系统以可溶性和活性形式产生,并在该平台上进行测试。为了确定 i-GT-ray 平台是否适合生产和测试β-糖苷合酶,我们测试了参与纤维素、木葡聚糖、(葡)甘露聚糖和β-(1,3)(1,4)-混合链接葡聚糖合成的五种合酶。我们的结果揭示了这些酶的意想不到的特征。例如,所有这些合酶都可以以可溶性和活性形式产生,并且在没有去污剂或膜脂的情况下具有活性,它们都不需要引物来启动合成。所有合酶都产生了对适当的水解酶(即纤维素酶、几丁质酶、甘露聚糖酶)敏感的乙醇不溶性产物。使用该平台,我们表明 AtCslC4 和 AtXXT1 直接相互作用形成活性木葡聚糖合酶,当提供 UDP-Glc 和 UDP-Xyl 时,它可以产生木糖基化的纤维寡糖(多达三个木糖残基)。i-GTray 平台代表了一种简单而强大的功能基因组学工具,可用于发现合酶活性的新见解,并且可以适应其他酶。