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首页> 外文期刊>BMC Biotechnology >Cloning, overexpression, purification, and characterization of a polyextremophilic β-galactosidase from the Antarctic haloarchaeon Halorubrum lacusprofundi
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Cloning, overexpression, purification, and characterization of a polyextremophilic β-galactosidase from the Antarctic haloarchaeon Halorubrum lacusprofundi

机译:南极嗜盐古菌Halorubrum lacusprofundi的多嗜性β-半乳糖苷酶的克隆,过表达,纯化和鉴定

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Background Halorubrum lacusprofundi is a cold-adapted halophilic archaeon isolated from Deep Lake, a perennially cold and hypersaline lake in Antarctica. Its genome sequencing project was recently completed, providing access to many genes predicted to encode polyextremophilic enzymes active in both extremely high salinity and cold temperatures. Results Analysis of the genome sequence of H. lacusprofundi showed a gene cluster for carbohydrate utilization containing a glycoside hydrolase family 42 β-galactosidase gene, named bga . In order to study the biochemical properties of the β-galactosidase enzyme, the bga gene was PCR amplified, cloned, and expressed in the genetically tractable haloarchaeon Halobacterium sp. NRC-1 under the control of a cold shock protein ( csp D2) gene promoter. The recombinant β-galactosidase protein was produced at 20-fold higher levels compared to H. lacusprofundi , purified using gel filtration and hydrophobic interaction chromatography, and identified by SDS-PAGE , LC-MS /MS, and ONPG hydrolysis activity. The purified enzyme was found to be active over a wide temperature range (?5 to 60°C) with an optimum of 50°C, and 10% of its maximum activity at 4°C. The enzyme also exhibited extremely halophilic character, with maximal activity in either 4?M NaCl or KCl. The polyextremophilic β-galactosidase was also stable and active in 10–20% alcohol-aqueous solutions, containing methanol, ethanol, n -butanol, or isoamyl alcohol. Conclusion The H. lacusprofundi β-galactosidase is a polyextremophilic enzyme active in high salt concentrations and low and high temperature. The enzyme is also active in aqueous-organic mixed solvents, with potential applications in synthetic chemistry. H. lacuprofundi proteins represent a significant biotechnology resource and for developing insights into enzyme catalysis under water limiting conditions. This study provides a system for better understanding how H. lacusprofundi is successful in a perennially cold, hypersaline environment, with relevance to astrobiology.
机译:背景Halorubrum lacusprofundi是一种冷适应的嗜盐古细菌,从深湖(深湖,南极的常年寒冷和高盐湖)中分离出来。它的基因组测序项目最近完成,提供了许多预计可编码在极高盐度和低温下均具有活性的极端嗜热菌酶基因的基因。结果对H. lacusprofundi基因组序列的分析表明,利用碳水化合物的基因簇含有一个糖苷水解酶家族的42β-半乳糖苷酶基因,称为bga。为了研究β-半乳糖苷酶的生化特性,对bga基因进行了PCR扩增,克隆并在可遗传处理的卤代古细菌Halobacterium sp。中表达。 NRC-1受冷休克蛋白(csp D2)基因启动子的控制。重组β-半乳糖苷酶蛋白的生产量比幽门螺杆菌高20倍,使用凝胶过滤和疏水相互作用色谱法纯化,并通过SDS-PAGE,LC-MS / MS和ONPG水解活性鉴定。发现纯化的酶在很宽的温度范围内(约5至60℃)有活性,最适温度为50℃,最大酶活性在4℃时为10%。该酶还具有极强的嗜盐性,在4?M NaCl或KCl中具有最大的活性。多嗜极端β-半乳糖苷酶在含有甲醇,乙醇,正丁醇或异戊醇的10-20%醇水溶液中也很稳定且有活性。结论幽门螺杆菌β-半乳糖苷酶是一种多极端性酶,在高盐浓度,低温和高温下均具有活性。该酶在水性有机混合溶剂中也具有活性,在合成化学中具有潜在的应用。 H. lacuprofundi蛋白代表着重要的生物技术资源,可用于开发在水限制条件下对酶催化的见解。这项研究提供了一个系统,可以更好地了解在常年寒冷,高盐环境下与天体生物学相关的幽门螺杆菌如何成功。

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