Abendroth Christian, Simeonov Claudia, Peretó Juli, Antúnez Oreto, Gavidia Raquel, Luschnig Olaf, Porcar Manuel
Cavanilles Institute of Biodiversity and Evolutionary Biology, Universitat de València, C/ José Beltran 2, 46980 Paterna, Spain.
Institute for Integrative Systems Biology (I2SysBio, Universitat de València-CSIC), C/ José Beltran 2, 46980 Paterna, Spain.
Biotechnol Biofuels. 2017 Jul 3;10:171. doi: 10.1186/s13068-017-0859-0. eCollection 2017.
Separating acidification and methanogenic steps in anaerobic digestion processes can help to optimize the process and contribute to producing valuable sub-products such as methane, hydrogen and organic acids. However, the full potential of this technology has not been fully explored yet. To assess the underlying fermentation process in more detail, a combination of high-throughput sequencing and proteomics on the acidification step of plant material (grass) at both mesophilic and thermophilic temperatures (37 and 55 °C, respectively) was applied for the first time.
High-strength liquor from acidified grass biomass exhibited a low biodiversity, which differed greatly depending on temperature. It was dominated by Bacteroidetes and Firmicutes at 37 °C, and by Firmicutes and Proteobacteria at 55 °C. At the methane stage, , and proved to be highly sensitive to environmental changes as their abundance in the seed sludges dropped dramatically after transferring the seed sludges from the respective reactors into the experimental setup. Further, an increase in Actinobacteria coincided with reduced biogas production at the end of the experiment. Over 1700 proteins were quantified from the first cycle of acidification samples using label-free quantitative proteome analysis and searching protein databases. The most abundant proteins included an almost complete set of glycolytic enzymes indicating that the microbial population is basically engaged in the degradation and catabolism of sugars. Differences in protein abundances clearly separated samples into two clusters corresponding to culture temperature. More differentially expressed proteins were found under mesophilic (120) than thermophilic (5) conditions.
Our results are the first multi-omics characterisation of a two-stage biogas production system with separated acidification and suggest that screening approaches targeting specific taxa such as , and could be useful diagnostic tools as indicators of environmental changes such as temperature or oxidative stress or, as in the case of Actinobacteria, they could be used as a proxy of the gas production potential of anaerobic digesters. Metaproteome analyses only detected significant expression differences in mesophilic samples, whereas thermophilic samples showed more stable protein composition with an abundance of chaperones suggesting a role in protein stability under thermal stress.
在厌氧消化过程中分离酸化和产甲烷步骤有助于优化该过程,并有助于生产有价值的副产物,如甲烷、氢气和有机酸。然而,这项技术的全部潜力尚未得到充分探索。为了更详细地评估潜在的发酵过程,首次将高通量测序和蛋白质组学相结合,对中温(37℃)和高温(55℃)下植物材料(草)的酸化步骤进行了研究。
酸化草生物质产生的高强度液体显示出较低的生物多样性,且因温度不同而有很大差异。在37℃时,优势菌群为拟杆菌门和厚壁菌门;在55℃时,优势菌群为厚壁菌门和变形菌门。在甲烷生成阶段,嗜甲基菌属、嗜氢菌属和甲烷八叠球菌属被证明对环境变化高度敏感,因为将种子污泥从各自的反应器转移到实验装置后,它们在种子污泥中的丰度急剧下降。此外,在实验结束时,放线菌门的增加与沼气产量的降低同时出现。使用无标记定量蛋白质组分析和搜索蛋白质数据库,从酸化样品的第一个循环中定量了1700多种蛋白质。最丰富的蛋白质包括几乎完整的糖酵解酶集,表明微生物群体主要参与糖类的降解和分解代谢。蛋白质丰度的差异将样品明显分为对应培养温度的两个簇。在中温条件下(120种)比高温条件下(5种)发现了更多差异表达的蛋白质。
我们的结果是首次对具有分离酸化的两阶段沼气生产系统进行多组学表征,表明针对特定分类群(如嗜甲基菌属、嗜氢菌属和甲烷八叠球菌属)的筛选方法可能是有用的诊断工具,可作为温度或氧化应激等环境变化的指标,或者,就放线菌门而言,它们可作为厌氧消化器产气潜力的替代指标。元蛋白质组分析仅在中温样品中检测到显著的表达差异,而高温样品显示出更稳定的蛋白质组成,有大量伴侣蛋白,表明其在热应激下对蛋白质稳定性起作用。