Wallenberg Wood Science Center, Division of Industrial Biotechnology, Department of Biology and Biological Engineering, Chalmers University of Technology, SE-412 96, Gothenburg, Sweden.
Department of Chemistry, University of Copenhagen, DK-2100, Copenhagen, Denmark.
Essays Biochem. 2023 Apr 18;67(3):493-503. doi: 10.1042/EBC20220155.
Glucuronoyl esterases (GEs) are microbial enzymes able to cleave covalent linkages between lignin and carbohydrates in the plant cell wall. GEs are serine hydrolases found in carbohydrate esterase family 15 (CE15), which belongs to the large α/β hydrolase superfamily. GEs have been shown to reduce plant cell wall recalcitrance by hydrolysing the ester bonds found between glucuronic acid moieties on xylan polysaccharides and lignin. In recent years, the exploration of CE15 has broadened significantly and focused more on bacterial enzymes, which are more diverse in terms of sequence and structure to their fungal counterparts. Similar to fungal GEs, the bacterial enzymes are able to improve overall biomass deconstruction but also appear to have less strict substrate preferences for the uronic acid moiety. The structures of bacterial GEs reveal that they often have large inserts close to the active site, with implications for more extensive substrate interactions than the fungal GEs which have more open active sites. In this review, we highlight the recent work on GEs which has predominantly regarded bacterial enzymes, and discuss similarities and differences between bacterial and fungal enzymes in terms of the biochemical properties, diversity in sequence and modularity, and structural variations that have been discovered thus far in CE15.
糖醛酸酯酶(Glucuronoyl esterases,GEs)是能够切断植物细胞壁中木质素和碳水化合物之间共价键的微生物酶。GEs 是属于大型 α/β 水解酶超家族的碳水化合物酯酶家族 15(CE15)中的丝氨酸水解酶。已经证明,GEs 通过水解木聚糖多糖上的糖醛酸部分和木质素之间的酯键来降低植物细胞壁的抗降解性。近年来,CE15 的探索显著拓宽,更多地关注细菌酶,这些酶在序列和结构上比真菌酶更加多样化。与真菌 GEs 相似,细菌酶能够提高整体生物质解构,但对糖醛酸部分的底物偏好似乎也不那么严格。细菌 GEs 的结构表明,它们的活性位点附近通常有较大的插入片段,这意味着它们与真菌 GEs 相比,具有更广泛的底物相互作用,真菌 GEs 的活性位点更开放。在这篇综述中,我们重点介绍了最近主要针对细菌酶的 GEs 研究,并讨论了细菌和真菌酶在生化特性、序列和模块多样性以及迄今为止在 CE15 中发现的结构变化方面的相似性和差异。