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Metformin hydrolase is a recently evolved nickel-dependent heteromeric ureohydrolase
by
Funck, D.
, Riede, L.
, Hartig, J. S.
, Bachmann, A.
, Fleming, J. R.
, Lutz, H.
, Mayans, O.
, Sinn, M.
in
631/181/735
/ 631/45/607/1164
/ 704/172/169/896
/ 82/83
/ Anthropogenic factors
/ Antidiabetics
/ Bacterial Proteins - chemistry
/ Bacterial Proteins - genetics
/ Bacterial Proteins - metabolism
/ Biodegradation
/ Biodegradation, Environmental
/ Catalytic Domain
/ Contaminants
/ Crystal structure
/ Crystallography, X-Ray
/ Degradation
/ Diabetes mellitus
/ Enzymes
/ Evolution
/ Genes
/ Humanities and Social Sciences
/ Hydrolysis
/ Medicinal plants
/ Metformin
/ Metformin - chemistry
/ Metformin - metabolism
/ Models, Molecular
/ multidisciplinary
/ Nickel
/ Nickel - chemistry
/ Nickel - metabolism
/ Nickel compounds
/ Pharmaceutical industry wastes
/ Pharmaceuticals
/ Proteins
/ Pseudomonas - enzymology
/ Pseudomonas - genetics
/ Science
/ Science (multidisciplinary)
/ Stoichiometry
/ Surface water
/ Ureohydrolases - chemistry
/ Ureohydrolases - genetics
/ Ureohydrolases - metabolism
/ Wastewater treatment
/ Wastewater treatment plants
2024
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Metformin hydrolase is a recently evolved nickel-dependent heteromeric ureohydrolase
by
Funck, D.
, Riede, L.
, Hartig, J. S.
, Bachmann, A.
, Fleming, J. R.
, Lutz, H.
, Mayans, O.
, Sinn, M.
in
631/181/735
/ 631/45/607/1164
/ 704/172/169/896
/ 82/83
/ Anthropogenic factors
/ Antidiabetics
/ Bacterial Proteins - chemistry
/ Bacterial Proteins - genetics
/ Bacterial Proteins - metabolism
/ Biodegradation
/ Biodegradation, Environmental
/ Catalytic Domain
/ Contaminants
/ Crystal structure
/ Crystallography, X-Ray
/ Degradation
/ Diabetes mellitus
/ Enzymes
/ Evolution
/ Genes
/ Humanities and Social Sciences
/ Hydrolysis
/ Medicinal plants
/ Metformin
/ Metformin - chemistry
/ Metformin - metabolism
/ Models, Molecular
/ multidisciplinary
/ Nickel
/ Nickel - chemistry
/ Nickel - metabolism
/ Nickel compounds
/ Pharmaceutical industry wastes
/ Pharmaceuticals
/ Proteins
/ Pseudomonas - enzymology
/ Pseudomonas - genetics
/ Science
/ Science (multidisciplinary)
/ Stoichiometry
/ Surface water
/ Ureohydrolases - chemistry
/ Ureohydrolases - genetics
/ Ureohydrolases - metabolism
/ Wastewater treatment
/ Wastewater treatment plants
2024
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Metformin hydrolase is a recently evolved nickel-dependent heteromeric ureohydrolase
by
Funck, D.
, Riede, L.
, Hartig, J. S.
, Bachmann, A.
, Fleming, J. R.
, Lutz, H.
, Mayans, O.
, Sinn, M.
in
631/181/735
/ 631/45/607/1164
/ 704/172/169/896
/ 82/83
/ Anthropogenic factors
/ Antidiabetics
/ Bacterial Proteins - chemistry
/ Bacterial Proteins - genetics
/ Bacterial Proteins - metabolism
/ Biodegradation
/ Biodegradation, Environmental
/ Catalytic Domain
/ Contaminants
/ Crystal structure
/ Crystallography, X-Ray
/ Degradation
/ Diabetes mellitus
/ Enzymes
/ Evolution
/ Genes
/ Humanities and Social Sciences
/ Hydrolysis
/ Medicinal plants
/ Metformin
/ Metformin - chemistry
/ Metformin - metabolism
/ Models, Molecular
/ multidisciplinary
/ Nickel
/ Nickel - chemistry
/ Nickel - metabolism
/ Nickel compounds
/ Pharmaceutical industry wastes
/ Pharmaceuticals
/ Proteins
/ Pseudomonas - enzymology
/ Pseudomonas - genetics
/ Science
/ Science (multidisciplinary)
/ Stoichiometry
/ Surface water
/ Ureohydrolases - chemistry
/ Ureohydrolases - genetics
/ Ureohydrolases - metabolism
/ Wastewater treatment
/ Wastewater treatment plants
2024
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Metformin hydrolase is a recently evolved nickel-dependent heteromeric ureohydrolase
Journal Article
Metformin hydrolase is a recently evolved nickel-dependent heteromeric ureohydrolase
2024
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Overview
The anti-diabetic drug metformin is one of the most widely prescribed medicines in the world. Together with its degradation product guanylurea, it is a major pharmaceutical pollutant in wastewater treatment plants and surface waters. An operon comprising two genes of the ureohydrolase family in
Pseudomonas
and
Aminobacter
species has recently been implicated in metformin degradation. However, the corresponding proteins have not been characterized. Here we show that these genes encode a Ni
2+
-dependent enzyme that efficiently and specifically hydrolyzes metformin to guanylurea and dimethylamine. The active enzyme is a heteromeric complex of α- and β- subunits in which only the α-subunits contain the conserved His and Asp residues for the coordination of two Ni
2+
ions in the active site. A crystal structure of metformin hydrolase reveals an α
2
β
4
stoichiometry of the hexameric complex, which is unprecedented in the ureohydrolase family. By studying a closely related but more widely distributed enzyme, we find that the putative predecessor specifically hydrolyzes dimethylguanidine instead of metformin. Our findings establish the molecular basis for metformin hydrolysis to guanylurea as the primary pathway for metformin biodegradation and provide insight into the recent evolution of ureohydrolase family proteins in response to an anthropogenic compound.
The diabetes drug metformin and its degradation product guanylurea are major pharmaceutical contaminants in waste and surface water. Here, a Ni2+-dependent enzyme that hydrolysed metformin to guanylurea and its evolutionary predecessor are presented.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
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