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提高热稳定性古菌内酯酶对神经毒剂的广谱水解酶活性。

Improving the promiscuous nerve agent hydrolase activity of a thermostable archaeal lactonase.

机构信息

Istituto di Biochimica delle Proteine, Consiglio Nazionale delle Ricerche, Via P. Castellino 111, 80131 Naples, Italy.

出版信息

Bioresour Technol. 2010 Dec;101(23):9204-12. doi: 10.1016/j.biortech.2010.06.102. Epub 2010 Jul 27.

Abstract

The thermostable Phosphotriesterase-Like Lactonase from Sulfolobus solfataricus (SsoPox) hydrolyzes lactones and, at a lower rate, neurotoxic organophosphorus compounds. The persistent demand of detoxification tools in the field of agricultural wastes and restoring of conditions after terrorist acts prompted us to exploit SsoPox as a "starter" to evolve its ancillary nerve agents hydrolytic capability. A directed evolution strategy yielded, among several variants, the single mutant W263F with k(cat) and specificity constant against paraoxon 16- and 6-fold enhanced, respectively, compared to the wild type. Furthermore, a phenomenon of enzyme activation by SDS has been observed, which allowed to increase those values 150- and 28-fold, respectively. The activity of SsoPox against the deadly nerve gas Cyclosarin has been reported for the first time and proved to be substantially unaffected for variant W263F. Finally, outperforming efficiency of W263F was demonstrated, under severe stressing conditions, with respect to the best known phosphotriesterase PTE from Brevundimonas diminuta.

摘要

来自嗜热硫磺酸杆菌(SsoPox)的热稳定磷酸三酯酶样内酯酶(Phosphotriesterase-Like Lactonase)能够水解内酯,并且以较低的速率水解神经毒性有机磷化合物。农业废物处理领域和恐怖袭击后环境恢复对解毒工具的持续需求促使我们利用 SsoPox 作为“起始”酶来进化其辅助神经毒剂水解能力。一种定向进化策略产生了几个变体,其中 W263F 突变体的 k(cat)和对 paraoxon 的特异性常数分别比野生型提高了 16 倍和 6 倍。此外,还观察到 SDS 激活酶的现象,这使得这些值分别提高了 150 倍和 28 倍。这是首次报道 SsoPox 对致命神经毒气环沙林的活性,并证明变体 W263F 的活性基本不受影响。最后,在苛刻的应激条件下,与最著名的 Brevundimonas diminuta 的 PTE 相比,W263F 的表现效率更高。

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