Jh. Ansede et Dc. Yoch, COMPARISON OF SELENIUM AND SULFUR VOLATILIZATION BY DIMETHYLSULFONIOPROPIONATE LYASE (DMSP) IN 2 MARINE-BACTERIA AND ESTUARINE SEDIMENTS, FEMS microbiology, ecology, 23(4), 1997, pp. 315-324
The volatile forms of selenium emitted from soils and plants have been
identified by others as dimethylselenide and dimethyldiselenide. Dime
thylselenoniopropionate, a possible precursor of dimethylselenide, is
the selenium analogue of the common marine osmoprotectant, dimethylsul
foniopropionate. Dimethylselenoniopropionate was organically synthesiz
ed from dimethylselenide and acrylate and used in a comparative study
with dimethylsulfoniopropionate as a growth substrate, an inducer and
substrate for dimethylsulfoniopropionate lyase in two marine bacterial
isolates, Alcaligenes sp. strain M3A and Pseudomonas doudoroffii, and
in salt marsh sediments and estuarine creek water samples. In P. doud
oroffii, the rate of dimethylselenoniopropionate transport into cells
was about half that observed with dimethylsulfoniopropionate; Alcalige
nes does not take up these molecules. The rate and extent of induction
of dimethylsulfoniopropionate lyase in P. doudoroffii at low concentr
ations of dimethylselenoniopropionate were similar to that of dimethyl
sulfoniopropionate. In Alcaligenes the low constitutive level of dimet
hylsulfoniopropionate lyase cleaved dimethylselenoniopropionate into d
imethylselenide and acrylate, but induction of dimethylsulfoniopropion
ate lyase by dimethylselenoniopropionate did not follow. Dimethylsulfo
niopropionate lyases from both strains, when induced by dimethylsulfon
iopropionate, utilized dimethylselenoniopropionate as a substrate with
emission of dimethylselenide. Rates of partially purified dimethylsul
foniopropionate lyase activity with dimethylselenoniopropionate were h
alf those with dimethylsulfoniopropionate. Anoxic salt marsh sediments
catalyzed dimethylsulfoniopropionate and dimethylselenoniopropionate
degradation at equal rates. In sediments containing high organic matte
r, both dimethylsulfide and dimethylselenide served as substrates for
methanogenesis. These data support the hypothesis that organic seleniu
m molecules can be volatilized by the same biochemical pathways as org
anic sulfur molecules.