Selective Desulfurization of Dibenzothiophene by Rhodococcus erythropolis D-1
Yoshikazu Izumi, Takashi Ohshiro, Hiroshi Ogino, Yoshimitsu Hine, Masayuki Shimao
Abstract
Yoshikazu Izumi, Takashi Ohshiro, Hiroshi Ogino, Yoshimitsu Hine, Masayuki Shimao
Abstract
A dibenzothiophene (DBT)-degrading bacterium, Rhodococcus erythropolis D-1, which utilized DBT as a sole source of sulfur, was isolated from soil. DBT was metabolized to 2-hydroxybiphenyl (2-HBP) by the strain, and 2-HBP was almost stoichiometrically accumulated as the dead-end metabolite of DBT degradation. DBT degradation by this strain was shown to proceed as DBT --> DBT sulfone --> 2-HBP. DBT at an initial concentration of 0.125 mM was completely degraded within 2 days of cultivation. DBT at up to 2.2 mM was rapidly degraded by resting cells within only 150 min. It was thought this strain had a higher DBT-desulfurizing ability than other microorganisms reported previously.
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A dibenzothiophene (DBT)-degrading bacterium, Rhodococcus erythropolis D-1, which utilized DBT as a sole source of sulfur, was isolated from soil. DBT was metabolized to 2-hydroxybiphenyl (2-HBP) by the strain, and 2-HBP was almost stoichiometrically accumulated as the dead-end metabolite of DBT degradation. DBT degradation by this strain was shown to proceed as DBT --> DBT sulfone --> 2-HBP. DBT at an initial concentration of 0.125 mM was completely degraded within 2 days of cultivation. DBT at up to 2.2 mM was rapidly degraded by resting cells within only 150 min. It was thought this strain had a higher DBT-desulfurizing ability than other microorganisms reported previously.
Key concepts: Dibenzothiophene, Rhodococcus, Flue-gas desulfurization, Strain (injury), Sulfur, Degradation (telecommunications), Biodegradation, Chemistry