Genetics and Biotechnology Laboratory, Embrapa-Agroenergy, Brasília, DF, Brazil.
Department of Cellular Biology, Laboratory of Enzymology, Universidade de Brasília, Brasília, DF, Brazil.
PLoS One. 2021 Jan 15;16(1):e0245118. doi: 10.1371/journal.pone.0245118. eCollection 2021.
Functional screening of metagenomic libraries is an effective approach for identification of novel enzymes. A Caatinga biome goat rumen metagenomic library was screened using esculin as a substrate, and a gene from an unknown bacterium encoding a novel GH3 enzyme, BGL11, was identified. None of the BGL11 closely related genes have been previously characterized. Recombinant BGL11 was obtained and kinetically characterized. Substrate specificity of the purified protein was assessed using seven synthetic aryl substrates. Activity towards nitrophenyl-β-D-glucopyranoside (pNPG), 4-nitrophenyl-β-D-xylopyranoside (pNPX) and 4-nitrophenyl-β-D-cellobioside (pNPC) suggested that BGL11 is a multifunctional enzyme with β-glucosidase, β-xylosidase, and cellobiohydrolase activities. However, further testing with five natural substrates revealed that, although BGL11 has multiple substrate specificity, it is most active towards xylobiose. Thus, in its native goat rumen environment, BGL11 most likely functions as an extracellular β-xylosidase acting on hemicellulose. Biochemical characterization of BGL11 showed an optimal pH of 5.6, and an optimal temperature of 50°C. Enzyme stability, an important parameter for industrial application, was also investigated. At 40°C purified BGL11 remained active for more than 15 hours without reduction in activity, and at 50°C, after 7 hours of incubation, BGL11 remained 60% active. The enzyme kinetic parameters of Km and Vmax using xylobiose were determined to be 3.88 mM and 38.53 μmol.min-1.mg-1, respectively, and the Kcat was 57.79 s-1. In contrast to BLG11, most β-xylosidases kinetically studied belong to the GH43 family and have been characterized only using synthetic substrates. In industry, β-xylosidases can be used for plant biomass deconstruction, and the released sugars can be fermented into valuable bio-products, ranging from the biofuel ethanol to the sugar substitute xylitol.
功能筛选宏基因组文库是鉴定新酶的有效方法。使用表儿茶素作为底物筛选卡汀加生物群落山羊瘤胃宏基因组文库,鉴定出一种来自未知细菌的新型 GH3 酶基因 BGL11。以前没有对 BGL11 的密切相关基因进行过特征描述。获得了重组 BGL11 并对其进行了动力学表征。使用七种合成芳基底物评估了纯化蛋白的底物特异性。对硝基苯基-β-D-吡喃葡萄糖苷(pNPG)、4-硝基苯基-β-D-木吡喃糖苷(pNPX)和 4-硝基苯基-β-D-纤维二糖苷(pNPC)的活性表明,BGL11 是一种多功能酶,具有β-葡萄糖苷酶、β-木糖苷酶和纤维二糖水解酶活性。然而,用五种天然底物进一步测试表明,尽管 BGL11 具有多种底物特异性,但它对纤维二糖的活性最高。因此,在其天然山羊瘤胃环境中,BGL11 很可能作为作用于半纤维素的细胞外β-木糖苷酶发挥作用。BGL11 的生化特性研究表明,其最适 pH 值为 5.6,最适温度为 50°C。酶稳定性是工业应用的一个重要参数,也进行了研究。在 40°C 下,纯化的 BGL11 在 15 小时以上的时间内保持活性,没有活性降低,在 50°C 下孵育 7 小时后,BGL11 的活性保持 60%。使用木二糖测定的 Km 和 Vmax 的酶动力学参数分别为 3.88 mM 和 38.53 μmol.min-1.mg-1,而 Kcat 为 57.79 s-1。与 BLG11 相比,大多数动力学研究的β-木糖苷酶属于 GH43 家族,仅使用合成底物进行了特征描述。在工业中,β-木糖苷酶可用于植物生物质的解构,释放的糖可发酵成有价值的生物产品,从生物燃料乙醇到糖替代品木糖醇。