Structural and functional snapshots of a broad-specificity endoglucanase from Thermogutta terrifontis for biomass saccharification

IF 3.8 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Archives of biochemistry and biophysics Pub Date : 2025-02-01 DOI:10.1016/j.abb.2024.110274
Naveed Hussain , Halina Mikolajek , Peter J. Harrison , Neil Paterson , Muhammad W. Akhtar , Saima Sadaf , James H. Naismith
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Abstract

Multifunctionality, processivity, and thermostability are critical for the cost-effective enzymatic saccharification of non-food plant biomass polymers such as β-glucans, celluloses, and xylans to generate biofuels and other valuable products. We present molecular insights into a processive multifunctional endo-1,3-1,4-β-d-glucanase (Tt_End5A) from the hyperthermophilic bacterium Thermogutta terrifontis. Tt_End5A demonstrated activities against a broad spectrum of β-polysaccharides, including barley glucan, lichenan, carboxymethyl cellulose, regenerated amorphous cellulose (RAC), Avicel, xylan, laminarin, mannan, curdlan, xanthan, and various chromogenic substrates at pH 7 and temperatures ranging from 70 to 80°C. The enzyme exhibited a high level of processivity on RAC and retained over 90% activity at 80°C for an extended period, indicating exceptional thermal stability. The 1.20 Å crystal structure of the Tt_End5A catalytic domain revealed an archetypal glycoside hydrolase family 5 (GH5) catalytic TIM-(β/α)8-barrel, supplemented with additional β-strands, elongated α-helices, and a rare cis-non-Pro (His481-cis-Ala482) peptide. A large central cleft was observed in the 3D structure, which is likely related to the enzyme's multifunctionality and processivity. The catalytic domain is preceded by a novel N-terminal multivalent carbohydrate-binding module (CBM) that enhances the enzymatic degradation of insoluble polysaccharides. Mutagenesis studies, ligand interaction analyses, and the structurally conserved positions of E329 and E448 in Tt_End5A suggest that these residues function as the proton donor and nucleophile in the catalytic mechanism. Owing to its multifunctionality and processivity, Tt_End5A can reduce the need for multiple saccharification enzymes to generate fermentable sugars from plant biomass for bioethanol production. Additionally, it holds promise for applications in the pharmaceutical, feed, and food industries.

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用于生物质糖化的 Thermogutta terrifontis 广特异性内切葡聚糖酶的结构和功能快照
多功能性、加工能力和热稳定性对于具有成本效益的非食用植物生物质聚合物(如β-葡聚糖、纤维素和木聚糖)酶糖化生产生物燃料和其他有价值的产品至关重要。我们介绍了来自超嗜热细菌Thermogutta terrifontis的一种过程多功能内切-1,3-1,4-β- d -葡聚糖酶(Tt_End5A)的分子见解。Tt_End5A在pH值为7、温度为70-80℃的条件下,对广谱β-多糖(包括大麦葡聚糖、地衣聚糖、羧甲基纤维素、再生无定形纤维素(RAC)、Avicel、木聚糖、层粘连素、甘露聚糖、凝乳聚糖、黄原胶和各种显色底物)具有抑制活性。该酶在RAC上表现出高水平的加工能力,并在80℃下长时间保持90%以上的活性,表明了优异的热稳定性。Tt_End5A催化结构域的1.20 Å晶体结构揭示了一个典型的糖苷水解酶家族5 (GH5)催化TIM-(β/α)8桶,补充了额外的β-链,细长的α-螺旋和罕见的顺式-非pro (His481-cis-Ala482)肽。在三维结构中观察到一个大的中央裂缝,这可能与酶的多功能性和加工性有关。催化结构域之前是一个新型的n端多价碳水化合物结合模块(CBM),可以增强不溶性多糖的酶降解。突变研究、配体相互作用分析以及E329和E448在Tt_End5A中的结构保守位置表明,这些残基在催化机制中起到质子供体和亲核试剂的作用。由于Tt_End5A的多功能性和加工性,它可以减少对多种糖化酶的需求,从而从植物生物质中产生可发酵糖用于生物乙醇生产。此外,它还有望应用于制药、饲料和食品工业。
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来源期刊
Archives of biochemistry and biophysics
Archives of biochemistry and biophysics 生物-生化与分子生物学
CiteScore
7.40
自引率
0.00%
发文量
245
审稿时长
26 days
期刊介绍: Archives of Biochemistry and Biophysics publishes quality original articles and reviews in the developing areas of biochemistry and biophysics. Research Areas Include: • Enzyme and protein structure, function, regulation. Folding, turnover, and post-translational processing • Biological oxidations, free radical reactions, redox signaling, oxygenases, P450 reactions • Signal transduction, receptors, membrane transport, intracellular signals. Cellular and integrated metabolism.
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