TY - JOUR
T1 - An antibiotic-destructase-activated Fenton-like catalyst for synergistic removal of tetracycline residues from aquatic environment
AU - Ren, Hao
AU - Pan, Yuanwei
AU - Zhong, Jiahao
AU - Wang, Jiayi
AU - Lu, Zhaoxiang
AU - He, Qian
AU - Zhou, Shiying
AU - Liao, Xiaoping
AU - Liu, Yahong
AU - An, Taicheng
AU - Sun, Jian
PY - 2023/3/1
Y1 - 2023/3/1
N2 - Environmental tetracycline (TC) residues are deemed as persistent contamination that threats to public health, underlining the necessity for innovative remediation technologies. Herein, TET(X), a TC destructase we identified previously, was found to produce H2O2 during degrading TC. Therefore, a Cu-based metal − organic framework (Cu-MOF) was incorporated with TET(X) to catalyze the Fenton-like reaction in response to TET(X)-produced H2O2, which eminently promoted non-enzymatic breakdown of TC. The designed composite (TET(X)-MOF) was functionally characterized to produce reactive radicals in presence of TC and be able to eradicate 50 ppm TC rapidly in a synergistic manner. The response surface method identified environmental pH as critical factor to TET(X)-MOF efficiency, suggesting that enzymatic activity of TET(X) controlled the degradation catalysis. To verify the in situ efficiency, the TET(X)-MOF was utilized to remove the TC from various environmental matrices including pond water, livestock sewage, urine and pharmaceutic effluent. High efficiency of the composite was observed as 47.9 %-100 % TC was eliminated in matrices within 3 h. Moreover, the degradation pathways of TC were proposed according to the intermediates. Eventually, the in vivo toxicity assessment indicated that the TET(X)-MOF enjoys desirable biosafety without further introduction of hazardous substance. Overall, this is the first study reporting the Fenton-like catalyst activated by and synergistically collaborated with antibiotic destructase for antibiotic decontamination. Such composite, as concept-of-principle, is of great potential to eradicate TC residues and opens up novel perspectives to develop strategies for environmental remediation.
AB - Environmental tetracycline (TC) residues are deemed as persistent contamination that threats to public health, underlining the necessity for innovative remediation technologies. Herein, TET(X), a TC destructase we identified previously, was found to produce H2O2 during degrading TC. Therefore, a Cu-based metal − organic framework (Cu-MOF) was incorporated with TET(X) to catalyze the Fenton-like reaction in response to TET(X)-produced H2O2, which eminently promoted non-enzymatic breakdown of TC. The designed composite (TET(X)-MOF) was functionally characterized to produce reactive radicals in presence of TC and be able to eradicate 50 ppm TC rapidly in a synergistic manner. The response surface method identified environmental pH as critical factor to TET(X)-MOF efficiency, suggesting that enzymatic activity of TET(X) controlled the degradation catalysis. To verify the in situ efficiency, the TET(X)-MOF was utilized to remove the TC from various environmental matrices including pond water, livestock sewage, urine and pharmaceutic effluent. High efficiency of the composite was observed as 47.9 %-100 % TC was eliminated in matrices within 3 h. Moreover, the degradation pathways of TC were proposed according to the intermediates. Eventually, the in vivo toxicity assessment indicated that the TET(X)-MOF enjoys desirable biosafety without further introduction of hazardous substance. Overall, this is the first study reporting the Fenton-like catalyst activated by and synergistically collaborated with antibiotic destructase for antibiotic decontamination. Such composite, as concept-of-principle, is of great potential to eradicate TC residues and opens up novel perspectives to develop strategies for environmental remediation.
KW - Antibiotic-destructase
KW - TET(X)-MOF composite
KW - Fenton-like reaction
KW - Synergistic antibiotic degradation
KW - Response surface method
U2 - 10.1016/j.cej.2023.141576
DO - 10.1016/j.cej.2023.141576
M3 - Article
SN - 1385-8947
VL - 459
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
M1 - 141576
ER -