结构域间连接区影响 GH5_34 阿拉伯木聚糖酶中 CBM6 的特性,并改变寡糖的产物特征。

IF 3.4 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Glycobiology Pub Date : 2024-06-22 DOI:10.1093/glycob/cwae048
Siri Norlander, Andrius Jasilionis, Leila Allahgholi, Christina Wennerberg, Carl Grey, Patrick Adlercreutz, Eva Nordberg Karlsson
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引用次数: 0

摘要

了解酶域结构与催化活性之间的关系对于木质纤维素生物转化新型酶的优化工程至关重要。具有不同特异性的木聚糖酶通常用于半纤维素阿拉伯木聚糖(AX)的价值化,但特异性阿拉伯木聚糖酶的表征仍然有限。两个同源的 GH5_34 阿拉伯木聚糖酶(HhXyn5A 和 CtXyn5A)的两个结构域由一个 40 位氨基酸的连接体连接,它们在 AX 上表现出不同的活性,产生不同的反应产物模式,尽管它们具有高度的序列同一性、保守的活性位点和相似的结构域组成。本研究将碳水化合物结合模块 6(CBM6)或结构域间连接器与 CBM6 互换,以研究它们对谷物 AX 的水解活性和寡糖产物模式的影响。与原始酶相比,只交换了 CBM6 的变体在商业小麦和黑麦 AX 以及提取的燕麦纤维上的活性降低。此外,交换连接子和 CBM6 导致在大肠杆菌培养中以可溶形式产生的酶比例降低,从而导致 HhXyn5A 和 CtXyn5A 变体失去活性。应用 HPAEC-PAD 分析寡糖产物模式发现,CBM6 被置换的 CtXyn5A 的反应产物数量减少,这与 HhXyn5A 的产物模式相似。这些发现强调了 CBM6 与连接体和催化结构域的相互作用对酶活性和特异性的重要性,并强调了连接体在酶结构组织和产物形成中的作用,其中连接体与催化结构域和/或 CBM6 结构域相互作用的改变会影响酶与底物的结合和特异性。
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Inter domain linker region affects properties of CBM6 in GH5_34 arabinoxylanases and alters oligosaccharide product profile.

Understanding the relation between enzyme domain structure and catalytic activity is crucial for optimal engineering of novel enzymes for lignocellulose bioconversion. Xylanases with varying specificities are commonly used to valorise the hemicellulose arabinoxylan (AX), yet characterization of specific arabinoxylanases remain limited. Two homologous GH5_34 arabinoxylanases, HhXyn5A and CtXyn5A, in which the two domains are connected by a 40-residue linker, exhibit distinct activity on AX, yielding different reaction product patterns, despite high sequence identity, conserved active sites and similar domain composition. In this study, the carbohydrate binding module 6 (CBM6), or the inter domain linker together with CBM6, were swapped to investigate their influence on hydrolytic activity and oligosaccharide product pattern on cereal AXs. The variants, with only CBM6 swapped, displayed reduced activity on commercial wheat and rye AX, as well as on extracted oat fibre, compared to the original enzymes. Additionally, exchange of both linker and CBM6 resulted in a reduced ratio of enzyme produced in soluble form in Escherichia coli cultivations, causing loss of activity of both HhXyn5A and CtXyn5A variants. Analysis of oligosaccharide product patterns applying HPAEC-PAD revealed a decreased number of reaction products for CtXyn5A with swapped CBM6, which resembled the product pattern of HhXyn5A. These findings emphasize the importance of the CBM6 interactions with the linker and the catalytic domain for enzyme activity and specificity, and underlines the role of the linker in enzyme structure organisation and product formation, where alterations in linker interactions with the catalytic and/or CBM6 domains, influence enzyme-substrate association and specificity.

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来源期刊
Glycobiology
Glycobiology 生物-生化与分子生物学
CiteScore
7.50
自引率
4.70%
发文量
73
审稿时长
3 months
期刊介绍: Established as the leading journal in the field, Glycobiology provides a unique forum dedicated to research into the biological functions of glycans, including glycoproteins, glycolipids, proteoglycans and free oligosaccharides, and on proteins that specifically interact with glycans (including lectins, glycosyltransferases, and glycosidases). Glycobiology is essential reading for researchers in biomedicine, basic science, and the biotechnology industries. By providing a single forum, the journal aims to improve communication between glycobiologists working in different disciplines and to increase the overall visibility of the field.
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