Chalak Amani, Villares Ana, Moreau Celine, Haon Mireille, Grisel Sacha, d'Orlando Angélina, Herpoël-Gimbert Isabelle, Labourel Aurore, Cathala Bernard, Berrin Jean-Guy
1Biopolymères Interactions Assemblages, INRA, Nantes, France.
2Biodiversité et Biotechnologie Fongiques, UMR1163, INRA, Aix Marseille Université, Marseille, France.
Biotechnol Biofuels. 2019 Sep 3;12:206. doi: 10.1186/s13068-019-1548-y. eCollection 2019.
Cellulose-active lytic polysaccharide monooxygenases (LPMOs) secreted by filamentous fungi play a key role in the degradation of recalcitrant lignocellulosic biomass. They can occur as multidomain proteins fused to a carbohydrate-binding module (CBM). From a biotech perspective, LPMOs are promising innovative tools for producing nanocelluloses and biofuels, but their direct action on cellulosic substrates is not fully understood.
In this study, we probed the role of the CBM from family 1 (CBM1) appended to the LPMO9H from (LPMO9H) using model cellulosic substrates. Deletion of the CBM1 weakened the binding to cellulose nanofibrils, amorphous and crystalline cellulose. Although the release of soluble sugars from cellulose was drastically reduced under standard conditions, the truncated LPMO retained some activity on soluble oligosaccharides. The cellulolytic action of the truncated LPMO was demonstrated using synergy experiments with a cellobiohydrolase (CBH). The truncated LPMO was still able to improve the efficiency of the CBH on cellulose nanofibrils in the same range as the full-length LPMO. Increasing the substrate concentration enhanced the performance of LPMO9H without CBM in terms of product release. Interestingly, removing the CBM also altered the regioselectivity of LPMO9H, significantly increasing cleavage at the C1 position. Analysis of the insoluble fraction of cellulosic substrates evaluated by optical and atomic force microscopy confirmed that the CBM1 module was not strictly required to promote disruption of the cellulose network.
Absence of the CBM1 does not preclude the activity of the LPMO on cellulose but its presence has an important role in driving the enzyme to the substrate and releasing more soluble sugars (both oxidized and non-oxidized), thus facilitating the detection of LPMO activity at low substrate concentration. These results provide insights into the mechanism of action of fungal LPMOs on cellulose to produce nanocelluloses and biofuels.
丝状真菌分泌的纤维素活性溶菌多糖单加氧酶(LPMOs)在难降解木质纤维素生物质的降解中起关键作用。它们可以作为与碳水化合物结合模块(CBM)融合的多结构域蛋白存在。从生物技术的角度来看,LPMOs是生产纳米纤维素和生物燃料的有前途的创新工具,但其对纤维素底物的直接作用尚未完全了解。
在本研究中,我们使用模型纤维素底物探究了附着于(LPMO9H)的1型家族CBM(CBM1)的作用。CBM1的缺失减弱了与纤维素纳米原纤维、无定形和结晶纤维素的结合。尽管在标准条件下从纤维素中释放的可溶性糖大幅减少,但截短的LPMO对可溶性寡糖仍保留一些活性。通过与纤维二糖水解酶(CBH)的协同实验证明了截短的LPMO的纤维素分解作用。截短的LPMO仍能够在与全长LPMO相同的范围内提高CBH对纤维素纳米原纤维的效率。增加底物浓度提高了无CBM的LPMO9H在产物释放方面的性能。有趣的是,去除CBM也改变了LPMO9H的区域选择性,显著增加了C1位置的裂解。通过光学和原子力显微镜对纤维素底物不溶性部分的分析证实,CBM1模块并非促进纤维素网络破坏所严格必需的。
CBM1的缺失并不排除LPMO对纤维素的活性,但其存在对于将酶导向底物并释放更多可溶性糖(氧化和未氧化的)具有重要作用,从而便于在低底物浓度下检测LPMO活性。这些结果为真菌LPMOs对纤维素产生纳米纤维素和生物燃料的作用机制提供了见解。