Construction and Performance Assessment of an Enzymatic Reactor for Xylulose Synthesis from Hemicellulose

IF 2.3 4区 化学 Q3 CHEMISTRY, PHYSICAL
Zhongliang Su, Shenghu Hao, Yue Ji, Jiantong Fan, Qiuyue Zhang, Yanju Lu, Xiao Liu
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引用次数: 0

Abstract

Xylulose has broad application prospects in fields such as biomanufacturing, bioenergy, pharmaceuticals, and materials. Enzyme-catalyzed synthesis of xylulose from hemicellulose faces challenges such as enzyme deactivation, low reusability, and high industrial costs. To address these issues, our study employed large-pore resin Amberlyst-15(A-15) as a carrier to immobilize both xylanase and xylose isomerase enzymes. The method involved amino-functionalization of the resin using a Macroporous Ion Exchange Resins A-15’s catalytic properties towards hemicellulose for xylose. The immobilization of xylanase and xylose isomerase was achieved through adsorption-crosslinking, successfully combining organic and enzymatic catalysis. By optimizing the enzyme-catalyzed conditions and immobilization methods, stable and active immobilized enzymes were prepared, with investigations into the effects of crosslinkers, crosslinker concentrations, and crosslinking times, leading to the identification of optimal production conditions. The reaction was conducted at 50 °C in a pH 5.5 buffer system for 12 h, the immobilized dual-enzyme prepared by the adsorption-crosslinking method achieved a hemicellulose conversion rate of 56.60%, significantly higher than that of free enzymes. The immobilized enzyme exhibited higher relative activity than the free enzyme at 80 °C and maintained significantly higher relative activity after 15 days of storage.

Graphical Abstract

半纤维素合成木糖酶法反应器的构建及性能评价
木质素糖在生物制造、生物能源、医药、材料等领域具有广阔的应用前景。酶催化半纤维素合成木糖面临着酶失活、低可重复利用性和高工业成本等挑战。为了解决这些问题,本研究采用大孔树脂Amberlyst-15(a -15)作为载体固定化木聚糖酶和木糖异构酶。该方法利用大孔离子交换树脂a -15对半纤维素的催化性能对木糖进行氨基功能化。通过吸附交联的方法实现了木聚糖酶和木糖异构酶的固定化,成功地将有机催化和酶催化结合起来。通过优化酶催化条件和固定化方法,制备了稳定、活性的固定化酶,考察了交联剂、交联剂浓度和交联次数对固定化酶的影响,确定了最佳生产条件。在pH 5.5的缓冲体系中,在50℃条件下反应12 h,吸附交联法制备的固定化双酶的半纤维素转化率达到56.60%,明显高于游离酶。在80℃条件下,固定化酶的相对活性高于游离酶,贮藏15 d后,固定化酶的相对活性显著高于游离酶。图形抽象
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来源期刊
Catalysis Letters
Catalysis Letters 化学-物理化学
CiteScore
5.70
自引率
3.60%
发文量
327
审稿时长
1 months
期刊介绍: Catalysis Letters aim is the rapid publication of outstanding and high-impact original research articles in catalysis. The scope of the journal covers a broad range of topics in all fields of both applied and theoretical catalysis, including heterogeneous, homogeneous and biocatalysis. The high-quality original research articles published in Catalysis Letters are subject to rigorous peer review. Accepted papers are published online first and subsequently in print issues. All contributions must include a graphical abstract. Manuscripts should be written in English and the responsibility lies with the authors to ensure that they are grammatically and linguistically correct. Authors for whom English is not the working language are encouraged to consider using a professional language-editing service before submitting their manuscripts.
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