Year: 2025
Type: article
Abstract: Atrazine (2-chloro-4-ethylamino-6-isopropylamino-s-triazine CAS: 1912-24-9) is a widely used herbicide that has been connected to a variety of negative human health and environmental effects. Various bacterial strains utilize a six-step enzyme cascade to fully degrade atrazine. The third step in this pathway, N-isopropylammelide aminohydrolase (AtzC), produces the first non-toxic intermediate, cyanuric acid. As such, AtzC, paired with enzymes catalyzing the first two steps in this pathway, triazine hydrolase (TrzN) and hydroxyatrazine (2-(N-ethylamino)-4-hydroxy-6-(N-isopropylamino)-1,3,5-triazine) N-ethylaminohydrolase (AtzB), can effectively degrade atrazine. All three of these enzymes were successfully encapsulated in tetramethyl orthosilicate (TMOS) gels using the sol–gel method, producing active biomaterials. These materials showed increased protection against proteolytic digestion by the endopeptidase trypsin, as well as increased thermal and pH stability when compared to their non-encapsulated counterparts. AtzB:sol and AtzC:sol also showed increased stability over time compared to soluble enzyme. A combination of all three biomaterials, TrzN:sol, AtzB:sol, and AtzC:sol, was shown to be effective at fully degrading 50 µM atrazine to cyanuric acid in just over an hour and a half, thus establishing a potential bioremediation enzyme cascade for atrazine.
Source: Catalysts
Institution: Colorado School of Mines
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $2,654
OpenAlex ID: W4415907114