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研究AA9家族的木质素过氧化物酶在不同蒸汽预处理云杉酶解过程中的作用。

Investigating the role of AA9 LPMOs in enzymatic hydrolysis of differentially steam-pretreated spruce.

作者信息

Caputo Fabio, Tõlgo Monika, Naidjonoka Polina, Krogh Kristian B R M, Novy Vera, Olsson Lisbeth

机构信息

Division of Industrial Biotechnology, Department of Biology and Biological Engineering, Chalmers University of Technology, Kemivägen 10, 412 96, Gothenburg, Sweden.

Wallenberg Wood Science Center, Chalmers University of Technology, Kemigården 4, 412 96, Gothenburg, Sweden.

出版信息

Biotechnol Biofuels Bioprod. 2023 Apr 19;16(1):68. doi: 10.1186/s13068-023-02316-0.

Abstract

BACKGROUND

To realize the full potential of softwood-based forest biorefineries, the bottlenecks of enzymatic saccharification of softwood need to be better understood. Here, we investigated the potential of lytic polysaccharide monooxygenases (LPMO9s) in softwood saccharification. Norway spruce was steam-pretreated at three different severities, leading to varying hemicellulose retention, lignin condensation, and cellulose ultrastructure. Hydrolyzability of the three substrates was assessed after pretreatment and after an additional knife-milling step, comparing the efficiency of cellulolytic Celluclast + Novozym 188 and LPMO-containing Cellic CTec2 cocktails. The role of Thermoascus aurantiacus TaLPMO9 in saccharification was assessed through time-course analysis of sugar release and accumulation of oxidized sugars, as well as wide-angle X-ray scattering analysis of cellulose ultrastructural changes.

RESULTS

Glucose yield was 6% (w/w) with the mildest pretreatment (steam pretreatment at 210 °C without catalyst) and 66% (w/w) with the harshest (steam pretreatment at 210 °C with 3%(w/w) SO) when using Celluclast + Novozym 188. Surprisingly, the yield was lower with all substrates when Cellic CTec2 was used. Therefore, the conditions for optimal LPMO activity were tested and it was found that enough O was present over the headspace and that the reducing power of the lignin of all three substrates was sufficient for the LPMOs in Cellic CTec2 to be active. Supplementation of Celluclast + Novozym 188 with TaLPMO9 increased the conversion of glucan by 1.6-fold and xylan by 1.5-fold, which was evident primarily in the later stages of saccharification (24-72 h). Improved glucan conversion could be explained by drastically reduced cellulose crystallinity of spruce substrates upon TaLPMO9 supplementation.

CONCLUSION

Our study demonstrated that LPMO addition to hydrolytic enzymes improves the release of glucose and xylose from steam-pretreated softwood substrates. Furthermore, softwood lignin provides enough reducing power for LPMOs, irrespective of pretreatment severity. These results provided new insights into the potential role of LPMOs in saccharification of industrially relevant softwood substrates.

摘要

背景

为充分发挥针叶材基森林生物精炼厂的潜力,需要更好地了解针叶材酶解糖化的瓶颈。在此,我们研究了裂解多糖单加氧酶(LPMO9s)在针叶材糖化中的潜力。挪威云杉在三种不同的严苛程度下进行蒸汽预处理,导致半纤维素保留、木质素缩合和纤维素超微结构各不相同。在预处理后以及额外的刀磨步骤后,评估了三种底物的可水解性,比较了纤维素酶Celluclast + Novozym 188和含LPMO的Cellic CTec2酶混合物的效率。通过糖释放和氧化糖积累的时间进程分析以及纤维素超微结构变化的广角X射线散射分析,评估了嗜热栖热菌TaLPMO9在糖化中的作用。

结果

使用Celluclast + Novozym 188时,最温和预处理(210°C无催化剂蒸汽预处理)的葡萄糖产率为6%(w/w),最严苛预处理(210°C含3%(w/w)SO的蒸汽预处理)的葡萄糖产率为66%(w/w)。令人惊讶的是,使用Cellic CTec2时,所有底物的产率都较低。因此,测试了LPMO最佳活性的条件,发现顶空存在足够的O,并且所有三种底物的木质素的还原能力足以使Cellic CTec2中的LPMO具有活性。用TaLPMO9补充Celluclast + Novozym 188使葡聚糖转化率提高了1.6倍,木聚糖转化率提高了1.5倍,这主要在糖化后期(24 - 72小时)表现明显。补充TaLPMO9后云杉底物的纤维素结晶度大幅降低,可以解释葡聚糖转化率的提高。

结论

我们的研究表明,向水解酶中添加LPMO可提高蒸汽预处理针叶材底物中葡萄糖和木糖的释放。此外,针叶材木质素为LPMO提供了足够的还原能力,与预处理的严苛程度无关。这些结果为LPMO在工业相关针叶材底物糖化中的潜在作用提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb31/10114483/df89258ab0fc/13068_2023_2316_Fig1_HTML.jpg

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