The bacterial biodegradation of a secondary sulphonate, sulphosuccinat
e, has been shown to occur by direct desulphonation. A bacterium, desi
gnated Pseudomonas sp. BS1, was isolated from activated sewage sludge,
for its capacity to grow on sulphosuccinate as the sole source of car
bon and energy. Cultures grown on sulphosuccinate were able to convert
this substrate to sulphite which was subsequently oxidized rapidly to
sulphate. The sequence of desulphonation and carbon-chain catabolism
of sulphosuccinate was determined from measurements of the kinetics of
sulphite and (CO2)-C-14 release from specifically radiolabelled sulph
o[1,4-C-14]succinate and sulpho[2,3-C-14]succinate, which were synthes
ized from the corresponding maleic anhydrides. When each radiolabelled
compound was incubated separately with washed-cell suspensions of Pse
udomonas BS1, sulphite was released before (CO2)-C-14, as shown by che
mical assay and radiorespirometry, respectively. Differences in the ki
netics and extent of (CO2)-C-14 release from the 1,4- and 2,3-labelled
substrates were consistent with entry of the intact C-4 chain into th
e citric acid cycle. When carrier oxaloacetate was added to incubation
mixtures containing resting-cell suspensions and radiolabelled sulpho
succinate, a radiolabelled metabolite with the same HPLC retention tim
e as oxaloacetate accumulated. No radioactive metabolites accumulated
when carrier oxaloacetate was replaced with succinate, fumarate or mal
ate. Collectively, the data indicated co-production of sulphite and ox
aloacetate from sulphosuccinate, which is interpreted in terms of an o
xidative desulphonation mechanism.