推进连续酶解改善生物质糖化。

IF 6.1 1区 工程技术 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Roman Brunecky, Yudong Li, Stephen R. Decker, Michael E. Himmel
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引用次数: 0

摘要

背景:一种可部署的、连续的酶解(CEH)工艺可以解决与第二代(Gen2)生物炼制糖/木质素/乙醇生产相关的成本和商业化风险,同时有助于能源供应和安全。针对Gen2预处理生物质(如去乙酰化机械精制(DMR)生物质)的商业酶解配方的发展,需要对现有的混合同步糖化和发酵(SSF)方法进行重新评估。值得注意的是,随着将氧化酶(如水解多糖单加氧酶(LPMOs))引入到商业纤维素酶配方中,SSF中的“精加工水解”实践已经成为问题,因为这些酶需要特定的氧化还原条件和辅助因子。此外,持续的SSF尚未在商业规模上得到证明,这限制了农民、生产商和支持行业的部署和相关的经济效益。结果:连续酶解(CEH)在实验规模上证明了脱乙酰化机械精制(DMR)预处理生物质的最佳糖化性能。经证实,滤除可以保留预处理过的生物质固体和酶进行连续反应,同时原位去除溶解产物糖。CEH工艺带来的一个重大突破是它能够在酶负荷降低约50%的情况下实现等效的端点转化。通过批量水解,葡萄糖和木糖的收率分别提高了~ 15%和~ 4%。与使用酵母或单胞菌的SSF不同,CEH可以精确优化pH值、温度、氧张力、LPMO介质浓度和最终产物抑制剂的去除。结论:先进的CEH有望成为生产可溶性澄清生物质糖和不溶性富木质素流的一种转型、过程强化和成本效益高的方法。提高糖化性能、优化操作参数和采用膜过滤将有助于克服现有的挑战,并使木质纤维素生物质高效生产有价值的生物材料成为可能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Advancing continuous enzymatic hydrolysis for improved biomass saccharification

Advancing continuous enzymatic hydrolysis for improved biomass saccharification

Advancing continuous enzymatic hydrolysis for improved biomass saccharification

Advancing continuous enzymatic hydrolysis for improved biomass saccharification

Background

A deployable, continuous enzymatic hydrolysis (CEH) process can address cost and commercialization risks associated with second-generation (Gen2) biorefinery sugar/lignin/ethanol production while contributing to energy supply and security. Developments in commercial enzymatic hydrolysis formulations targeting Gen2 pretreated biomass such as deacetylated mechanically refined (DMR) biomass necessitate a reassessment of the existing hybrid simultaneous saccharification and fermentation (SSF) approach. Notably, the practice of "finishing hydrolysis" in SSF has become problematic with the introduction of oxidative enzymes, such as lytic polysaccharide monooxygenases (LPMOs), into commercial cellulase formulations as these require specific redox conditions and cofactor. Moreover, continuous SSF has not been demonstrated at commercial scale, limiting deployment and the associated economic benefits to farmers, producers, and support industries.

Results

Continuous enzymatic hydrolysis (CEH) was demonstrated at bench scale to enable optimal saccharification performance of deacetylated mechanically refined (DMR) pretreated biomass. Diafiltration was demonstrated to retain pretreated biomass solids and enzymes for continuous reaction while removing solubilized product sugars in situ. A significant breakthrough afforded by the CEH process is its ability to achieve equivalent endpoint conversions with approximately 50% lower enzyme loading. Yields of glucose and xylose were increased ~ 15% and ~ 4%, respectively, over batch hydrolysis. Unlike SSF using yeast or Zymomonas, CEH allows precise optimization of pH, temperature, oxygen tension, LPMO mediator concentration, and removal of end-product inhibitors.

Conclusions

Advanced CEH holds promise as a transformational, process-intensified, and cost-effective method for producing soluble clarified biomass sugars and insoluble lignin-rich streams. Enhancing saccharification performance, optimizing operating parameters, and employing membrane filtration will help overcome existing challenges and enable the efficient production of valuable biomaterials from lignocellulosic biomass.

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来源期刊
Biotechnology for Biofuels
Biotechnology for Biofuels 工程技术-生物工程与应用微生物
自引率
0.00%
发文量
0
审稿时长
2.7 months
期刊介绍: Biotechnology for Biofuels is an open access peer-reviewed journal featuring high-quality studies describing technological and operational advances in the production of biofuels, chemicals and other bioproducts. The journal emphasizes understanding and advancing the application of biotechnology and synergistic operations to improve plants and biological conversion systems for the biological production of these products from biomass, intermediates derived from biomass, or CO2, as well as upstream or downstream operations that are integral to biological conversion of biomass. Biotechnology for Biofuels focuses on the following areas: • Development of terrestrial plant feedstocks • Development of algal feedstocks • Biomass pretreatment, fractionation and extraction for biological conversion • Enzyme engineering, production and analysis • Bacterial genetics, physiology and metabolic engineering • Fungal/yeast genetics, physiology and metabolic engineering • Fermentation, biocatalytic conversion and reaction dynamics • Biological production of chemicals and bioproducts from biomass • Anaerobic digestion, biohydrogen and bioelectricity • Bioprocess integration, techno-economic analysis, modelling and policy • Life cycle assessment and environmental impact analysis
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