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一种来自解凝胶芽孢杆菌的新型 AA10 及其对结晶和复合多糖的协同作用。

A novel AA10 from Paenibacillus curdlanolyticus and its synergistic action on crystalline and complex polysaccharides.

作者信息

Limsakul Puangpen, Phitsuwan Paripok, Waeonukul Rattiya, Pason Patthra, Tachaapaikoon Chakrit, Poomputsa Kanokwan, Kosugi Akihiko, Sakka Makiko, Sakka Kazuo, Ratanakhanokchai Khanok

机构信息

School of Bioresources and Technology, King Mongkut's University of Technology Thonburi, Bangkok, 10150, Thailand.

Pilot Plant Development and Training Institute, King Mongkut's University of Technology Thonburi, Bangkok, 10150, Thailand.

出版信息

Appl Microbiol Biotechnol. 2020 Sep;104(17):7533-7550. doi: 10.1007/s00253-020-10758-x. Epub 2020 Jul 10.

Abstract

Lytic polysaccharide monooxygenases (LPMOs) play an important role in the degradation of complex polysaccharides in lignocellulosic biomass. In the present study, we characterized a modular LPMO (PcAA10A), consisting of a family 10 auxiliary activity of LPMO (AA10) catalytic domain, and non-catalytic domains including a family 5 carbohydrate-binding module, two fibronectin type-3 domains, and a family 3 carbohydrate-binding module from Paenibacillus curdlanolyticus B-6, which was expressed in a recombinant Escherichia coli. Comparison of activities between full-length PcAA10A and the catalytic domain polypeptide (PcAA10A_CD) indicates that the non-catalytic domains are important for the deconstruction of crystalline cellulose and complex polysaccharides contained in untreated lignocellulosic biomass. Interestingly, PcAA10A_CD acted not only on cellulose and chitin, but also on xylan, mannan, and xylan and cellulose contained in lignocellulosic biomass, which has not been reported for the AA10 family. Mutation of the key residues, Trp51 located at subsite - 2 and Phe171 located at subsite +2, in the substrate-binding site of PcAA10A_CD revealed that these residues are substantially involved in broad substrate specificity toward cellulose, xylan, and mannan, albeit with a low effect toward chitin. Furthermore, PcAA10A had a boosting effect on untreated corn hull degradation by P. curdlanolyticus B-6 endo-xylanase Xyn10D and Clostridium thermocellum endo-glucanase Cel9A. These results suggest that PcAA10A is a unique LPMO capable of cleaving and enhancing lignocellulosic biomass degradation, making it a good candidate for biotechnological applications. KEY POINTS: • PcAA10A is a novel modular LPMO family 10 from Paenibacillus curdlanolyticus. • PcAA10A showed broad substrate specificity on β-1,4 glycosidic linkage substrates. • Non-catalytic domains are important for degrading complex polysaccharides. • PcAA10A is a unique LPMO capable of enhancing lignocellulosic biomass degradation.

摘要

裂解多糖单加氧酶(LPMOs)在木质纤维素生物质中复杂多糖的降解过程中发挥着重要作用。在本研究中,我们对一种模块化LPMO(PcAA10A)进行了表征,它由来自解凝胶芽孢杆菌B - 6的10家族辅助活性的LPMO(AA10)催化结构域以及非催化结构域组成,非催化结构域包括一个5家族碳水化合物结合模块、两个纤连蛋白III型结构域和一个3家族碳水化合物结合模块,该LPMO在重组大肠杆菌中表达。全长PcAA10A与催化结构域多肽(PcAA10A_CD)之间的活性比较表明,非催化结构域对于未处理木质纤维素生物质中结晶纤维素和复杂多糖的解构很重要。有趣的是,PcAA10A_CD不仅作用于纤维素和几丁质,还作用于木聚糖、甘露聚糖以及木质纤维素生物质中含有的木聚糖和纤维素,这在AA10家族中尚未见报道。PcAA10A_CD底物结合位点上关键残基(位于亚位点 - 2的Trp51和位于亚位点 +2的Phe171)的突变表明,这些残基在对纤维素、木聚糖和甘露聚糖的广泛底物特异性中起重要作用,尽管对几丁质的作用较小。此外,PcAA10A对解凝胶芽孢杆菌B - 6内切木聚糖酶Xyn10D和嗜热栖热菌内切葡聚糖酶Cel9A降解未处理的玉米壳有促进作用。这些结果表明,PcAA10A是一种独特的LPMO,能够裂解并增强木质纤维素生物质的降解,使其成为生物技术应用的良好候选者。要点:• PcAA10A是来自解凝胶芽孢杆菌的一种新型模块化10家族LPMO。• PcAA10A对β - 1,4糖苷键底物表现出广泛的底物特异性。• 非催化结构域对于降解复杂多糖很重要。• PcAA10A是一种独特的能够增强木质纤维素生物质降解的LPMO。

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