A. Gutenkauf et al., Fate of substituted benzoates in the freshwater green alga, Chlamydomonas reinhardtii 11-32b, BIODEGRADAT, 9(5), 1998, pp. 359-368
The removal of chlorinated, nitrated, and sulfonated benzoic acids in cultu
res of the unicellular green alga, Chlamydomonas reinhardtii 11-32b, was in
vestigated, and the metabolic fate of a model compound, 4-chloro-3,5,-dinit
robenzoic acid, was determined. The freshwater alga was able to remove a wi
de variety of benzoic compounds from the incubation medium. Chlamydomonas d
iscriminated very specifically between the benzoic acids, indicated by the
varying degrees of which the test compounds disappeared from the culture me
dium. Moreover, the alga was capable of transforming 4-chloro-3,5-dinitrobe
nzoic acid to several metabolites. A release of chloride ions was ob served
, and 3,5-dinitro-4-hydroxybenzoic acid was identified as a major transient
pro duct in the algal metabolism of 4-chloro-3,5-dinitrobenzoic acid.