Department of Biochemistry, Molecular Biology and Biophysics and Biotechnology Institute, University of Minnesota, Twin Cities, 1479 Gortner Ave, St. Paul, MN, U.S.A.
Department of Environmental Microbiology, Swiss Federal Institute of Aquatic Science and Technology (Eawag), Ueberlandstrasse 133, 8600 Duebendorf, Switzerland.
Biochem J. 2024 Dec 4;481(23):1757-1770. doi: 10.1042/BCJ20240283.
Per- and polyfluorinated chemicals (PFAS) are of rising concern due to environmental persistence and emerging evidence of health risks to humans. Environmental persistence is largely attributed to a failure of microbes to degrade PFAS. PFAS recalcitrance has been proposed to result from chemistry, specifically C-F bond strength, or biology, largely negative selection from fluoride toxicity. Given natural evolution has many hurdles, this review advocates for a strategy of laboratory engineering and evolution. Enzymes identified to participate in defluorination reactions have been discovered in all Enzyme Commission classes, providing a palette for metabolic engineering. In vivo PFAS biodegradation will require multiple types of reactions and powerful fluoride mitigation mechanisms to act in concert. The necessary steps are to: (1) engineer bacteria that survive very high, unnatural levels of fluoride, (2) design, evolve, and screen for enzymes that cleave C-F bonds in a broader array of substrates, and (3) create overall physiological conditions that make for positive selective pressure with PFAS substrates.
由于环境持久性和对人类健康风险的新证据,全氟和多氟化合物 (PFAS) 引起了越来越多的关注。环境持久性在很大程度上归因于微生物未能降解 PFAS。PFAS 的抗降解性据说是由于化学性质,特别是 C-F 键强度,或生物学性质,主要是由于氟化物毒性的负选择。鉴于自然进化有许多障碍,本综述提倡采用实验室工程和进化的策略。已在所有酶委员会类别中发现了参与脱氟反应的酶,为代谢工程提供了一个调色板。体内 PFAS 生物降解将需要多种类型的反应和强大的氟化物缓解机制协同作用。必要的步骤是:(1) 工程化细菌,使其能够在非常高的、非自然的氟化物水平下存活;(2) 设计、进化和筛选能够在更广泛的底物中切割 C-F 键的酶;(3) 创造有利于 PFAS 底物的正向选择压力的整体生理条件。