F. Baldi et al., METHYLMERCURY RESISTANCE IN DESULFOVIBRIO-DESULFURICANS STRAINS IN RELATION TO METHYLMERCURY DEGRADATION, Applied and environmental microbiology, 59(8), 1993, pp. 2479-2485
Two strains of Desulfovibrio desulfuricans, one known to synthesize mo
nomethylmercury from ionic mercury, were grown to determine methylmerc
ury toxicity and for comparison with an anaerobic strain of Clostridiu
m pasteurianum, a H-2 producer, and with the broad-spectrum mercury-re
sistant Pseudomonas putida strain FB-1, capable of degrading 1 mug of
methylmercury to methane and elemental mercury in 2 h. The CH3HgCl res
istance of D. desulfuricans strains was 10 times that of P. putida FB-
1 and 100 times that of C. pasteurianum. The methylmercury resistance
of D. desulfuricans was related to the disappearance of methylmercury
from cultures by transformation to dimethylmercury, metacinnabar, meth
ane, and traces of ionic mercury. During a 15-day experiment the kinet
ics of the two volatile compounds dimethylmercury (CH3)2Hg! and metha
ne were monitored in the liquid by a specific new technique with purge
-and-trap gas chromatography in line with Fourier transform infrared s
pectroscopy and in the headspace by gas chromatography with flame ioni
zation detection. Insoluble metacinnabar (cubic HgS) of biological ori
gin was detected by X-ray diffractometry in the gray precipitate from
the insoluble residue of the pellet of a 1-liter culture spiked with 1
00 mg of CH3HgCl. This was compared with a 1-liter culture of D. desul
furicans LS spiked with 100 mg of HgCl2. In a further experiment, it w
as demonstrated that insoluble, decomposable, white dimethylmercury su
lfide (CH3Hg)2S! formed instantly in the reaction of methylmercury wi
th hydrogen sulfide. This organomercurial was extracted with chlorofor
m and identified by gas chromatography in tine with mass spectrometry.
The D. desulfuricans strains were resistant to high concentrations of
methylmercury because they produced insoluble dimethylmercury sulfide
, which slowly decomposed under anaerobic conditions to metacinnabar a
nd volatilized to dimethylmercury and methane between pHs 6.2 and 6.5
for high (4.5-g . liter-1) or low (0.09-g . liter-1) sulfate contents.
Methane was produced from CH3HgCl at a lower rate than by the broad-s
pectrum Hg-resistant P. putida strain FB-1.