酶解分支是a9家族水解多糖单加氧酶木聚糖降解活性的关键决定因素。

Monika Tõlgo, Olav A Hegnar, Johan Larsbrink, Francisco Vilaplana, Vincent G H Eijsink, Lisbeth Olsson
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引用次数: 1

摘要

背景:先前的研究表明,当与木聚糖和纤维素的混合物孵育时,一些辅助活性家族9 (AA9)水解多糖单加氧酶(LPMOs)氧化和降解某些类型的木聚糖。在这里,我们证明了两种具有木聚糖活性的LPMOs TtLPMO9E和TtLPMO9G的木聚糖水解活性强烈依赖于木聚糖取代的存在。结果:使用磷酸膨胀纤维素(PASC)和小麦阿拉伯木聚糖(WAX)的混合物,我们发现用GH62阿拉伯木聚糖苷酶去除阿拉伯木聚糖取代导致木聚糖更好地吸附到纤维素上,并使lpmo催化木聚糖的裂解成为可能。此外,PASC与杉木糖醛酸苷混合的实验表明,木聚糖与GH62阿拉伯糖醛酸苷酶和GH115葡萄糖醛酸苷酶的脱支作用促进了LPMO的活性。与PASC和(非阿拉伯糖基化)山毛榉木葡萄糖醛酸氧酶混合分析表明,GH115的作用也促进了这种木聚糖的LPMO活性。值得注意的是,在GH62存在的情况下,当WAX与Avicel而不是PASC一起培养时,LPMO9对木聚糖和纤维素的降解都受到了损害,这表明纤维素-木聚糖复合物的形成及其对LPMO作用的敏感性也取决于纤维素的性质。这些去支效应不仅与纤维素-木聚糖相互作用的调节有关,这影响了木聚糖的构象和刚性,而且可能也影响了lpmo -木聚糖相互作用,因为去支改变了木聚糖表面的结构。结论:我们的研究结果揭示了木聚糖分解LPMO9的活性,以及复合木质纤维素分解酶鸡尾酒成员之间的功能相互作用和可能的协同作用。这些发现将对未来木质纤维素分解混合物和生物材料的开发具有重要意义。
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Enzymatic debranching is a key determinant of the xylan-degrading activity of family AA9 lytic polysaccharide monooxygenases.

Background: Previous studies have revealed that some Auxiliary Activity family 9 (AA9) lytic polysaccharide monooxygenases (LPMOs) oxidize and degrade certain types of xylans when incubated with mixtures of xylan and cellulose. Here, we demonstrate that the xylanolytic activities of two xylan-active LPMOs, TtLPMO9E and TtLPMO9G from Thermothielavioides terrestris, strongly depend on the presence of xylan substitutions.

Results: Using mixtures of phosphoric acid-swollen cellulose (PASC) and wheat arabinoxylan (WAX), we show that removal of arabinosyl substitutions with a GH62 arabinofuranosidase resulted in better adsorption of xylan to cellulose, and enabled LPMO-catalyzed cleavage of this xylan. Furthermore, experiments with mixtures of PASC and arabinoglucuronoxylan from spruce showed that debranching of xylan with the GH62 arabinofuranosidase and a GH115 glucuronidase promoted LPMO activity. Analyses of mixtures with PASC and (non-arabinosylated) beechwood glucuronoxylan showed that GH115 action promoted LPMO activity also on this xylan. Remarkably, when WAX was incubated with Avicel instead of PASC in the presence of the GH62, both xylan and cellulose degradation by the LPMO9 were impaired, showing that the formation of cellulose-xylan complexes and their susceptibility to LPMO action also depend on the properties of the cellulose. These debranching effects not only relate to modulation of the cellulose-xylan interaction, which influences the conformation and rigidity of the xylan, but likely also affect the LPMO-xylan interaction, because debranching changes the architecture of the xylan surface.

Conclusions: Our results shed new light on xylanolytic LPMO9 activity and on the functional interplay and possible synergies between the members of complex lignocellulolytic enzyme cocktails. These findings will be relevant for the development of future lignocellulolytic cocktails and biomaterials.

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