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EC Number
Substrates
Commentary Substrates
Organism
Products
Commentary (Products)
Reversibility
4.99.1.2
alkyl mercuric halides + H+
primary, secondary, tertiary
Escherichia coli
?
-
?
4.99.1.2
alkyl mercuric halides + H+
primary, secondary, tertiary
Escherichia coli overproducing
?
-
?
4.99.1.2
CH3Hg+ + H+
-
Escherichia coli
CH4 + Hg2+
-
?
4.99.1.2
CH3Hg+ + H+
theoretical insights into the mechanism of Hg-C bond protonolysis in methyl mercury coordinated by the tris(2-mercapto-1-tert-butylimidazolyl)hydroborato ligand, the structural and functional analogue of the organomercurial lyase MerB, different cleavage pathways including both frontside and backside attack transition states are systematically studied by the hybrid density functional method B3LYP
Escherichia coli
CH4 + Hg2+
-
?
4.99.1.2
CH3Hg+ + H+
-
Pseudomonas sp. K-62
Hg2+ + CH4
-
?
4.99.1.2
CH3Hg+ + H+
the growth rates of both the wild-type and ppk/merTtransgenic tobacco callus are largely inhibited by CH3Hg+ in a dose-dependent manner
Pseudomonas sp. K-62
Hg2+ + CH4
-
?
4.99.1.2
cis-2-butenylmercuric chloride + H+
-
Escherichia coli
?
-
?
4.99.1.2
crotonyl mercuric bromide + H+
-
Escherichia coli
crotonaldehyde + Hg2+ + Br-
-
?
4.99.1.2
crotonyl mercuric bromide + H+
-
Escherichia coli overproducing
crotonaldehyde + Hg2+ + Br-
-
?
4.99.1.2
diethyllead + H+
-
Escherichia coli
2 ethane + Pb2+
-
?
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