Centre for Environmental Biotechnology, School of Environmental and Natural Sciences, Bangor University, Bangor, LL57 2UW, United Kingdom.
Department of Plant Pathology and Microbiology, Faculty of Agriculture, Food and Environment, Hebrew University of Jerusalem, Rehovot, 7610001, Israel.
FEMS Microbiol Ecol. 2024 Aug 13;100(9). doi: 10.1093/femsec/fiae114.
Family GH1 glycosyl hydrolases are ubiquitous in prokaryotes and eukaryotes and are utilized in numerous industrial applications, including bioconversion of lignocelluloses. In this study, hyperacidophilic archaeon Cuniculiplasma divulgatum (S5T=JCM 30642T) was explored as a source of novel carbohydrate-active enzymes. The genome of C. divulgatum encodes three GH1 enzyme candidates, from which CIB12 and CIB13 were heterologously expressed and characterized. Phylogenetic analysis of CIB12 and CIB13 clustered them with β-glucosidases from genuinely thermophilic archaea including Thermoplasma acidophilum, Picrophilus torridus, Sulfolobus solfataricus, Pyrococcus furiosus, and Thermococcus kodakarensis. Purified enzymes showed maximal activities at pH 4.5-6.0 (CIB12) and 4.5-5.5 (CIB13) with optimal temperatures at 50°C, suggesting a high-temperature origin of Cuniculiplasma spp. ancestors. Crystal structures of both enzymes revealed a classical (α/β)8 TIM-barrel fold with the active site located inside the barrel close to the C-termini of β-strands including the catalytic residues Glu204 and Glu388 (CIB12), and Glu204 and Glu385 (CIB13). Both enzymes preferred cellobiose over lactose as substrates and were classified as cellobiohydrolases. Cellobiose addition increased the biomass yield of Cuniculiplasma cultures growing on peptides by 50%, suggesting that the cellobiohydrolases expand the carbon substrate range and hence environmental fitness of Cuniculiplasma.
家族 GH1 糖苷水解酶在原核生物和真核生物中普遍存在,并被广泛应用于许多工业应用,包括木质纤维素的生物转化。在这项研究中,嗜酸古菌 Cuniculiplasma divulgatum (S5T=JCM 30642T) 被探索为新型碳水化合物活性酶的来源。C. divulgatum 的基因组编码了三种 GH1 酶候选物,其中 CIB12 和 CIB13 被异源表达和表征。CIB12 和 CIB13 的系统发育分析将它们与真正嗜热古菌的β-葡萄糖苷酶聚类,包括嗜酸热原体、嗜热硫还原球菌、嗜酸硫磺酸、Pyrococcus furiosus 和 Thermococcus kodakarensis。纯化后的酶在 pH4.5-6.0(CIB12)和 4.5-5.5(CIB13)时表现出最大活性,最适温度为 50°C,表明 Cuniculiplasma spp. 祖先起源于高温环境。两种酶的晶体结构均揭示了一个典型的(α/β)8 TIM 桶折叠结构,活性位点位于桶内,靠近包括催化残基 Glu204 和 Glu388(CIB12)和 Glu204 和 Glu385(CIB13)在内的β-链的 C 末端。两种酶都优先选择纤维二糖而不是乳糖作为底物,被归类为纤维二糖水解酶。纤维二糖的添加使以肽为碳源的 Cuniculiplasma 培养物的生物量产量增加了 50%,这表明纤维二糖水解酶扩大了 Cuniculiplasma 的碳底物范围,从而提高了其环境适应性。