Transformation of Carbon Tetrachloride by Reduced Vitamin B 12 in Aqueous Cysteine Solution

Chiu, PC; Reinhard, M

HERO ID

1068271

Reference Type

Journal Article

Year

1996

HERO ID 1068271
In Press No
Year 1996
Title Transformation of Carbon Tetrachloride by Reduced Vitamin B 12 in Aqueous Cysteine Solution
Authors Chiu, PC; Reinhard, M
Journal Environmental Science & Technology
Volume 30
Issue 6
Page Numbers 1882-1889
Abstract Cysteine was studied as a reductant in carbon tetrachloride (CCl4) transformation mediated by vitamin B-12 at room temperature in the pH range of 4-14. The reaction proceeded in two consecutive phases: the initial phase was rapid but lasted only minutes before the slow subsequent phase started as B-12 was inactivated, presumably due to nonreactive alkylcobalamin formation. The reduction of Co(III) to Co(II) was rate-limiting in the fast phase, whereas the decomposition of the alkylcobalamin may control the rate in the slow phase. B-12r was the reduced B-12 species but exhibited little reactivity toward CCl4 in the absence of cysteine; the reactive B-12 species is hypothesized to be the penta coordinated B-12r-cysteinate complex. Most of the CCl4 was transformed to unidentified water-soluble products. The chloroform yield decreased with pH from 20% to nearly zero, whereas the carbon monoxide yield remained constant (3.2 +/- 0.3%) with pH. These findings suggest that (1) the reductant controls both the kinetics and the mechanism of the reaction and should not be viewed simply as an electron donor, and (2) the B-12 species involved in reductive biodehalogenation is likely to be either B-12s Or B-12r-thiolate complexes.
Doi 10.1021/es950477o
Wosid WOS:A1996UM99100033
Url http://pubs.acs.org/doi/abs/10.1021/es950477o
Is Certified Translation No
Dupe Override No
Is Public Yes
Is Qa No