Effect of HP-β-CD on the biodegradation of nitrobenzene at high concentration by Acinetobacter sp.
Yun Shao
Abstract
Yun Shao
Abstract
The present study investigated the effect of Hydroxypropylβcyclodextrin (HPβCD) on the cell growth, removal of nitrobenzene and the transformation of intermediates during the biodegradation process of nitrobenzene at high concentration by Acinetobacter sp. 2aminophenol was identified as an intermediates using direct acetylation of biodegraded samples of nitrobenzene by acetic anhydride followed by GCMS analysis. When the initial concentration of nitrobenzene was about 400?mg·L-1 (optimal concentration for degrading bacteria to grow vigorously), HPβCD added at 250?mg·L-1 or 500?mg·L-1 had no effect on the biomass and the degradation of nitrobenzene. However, the addition of HPβCD at above 2000?mg·L-1, significantly enhanced the cell growth, the biodegradation of nitrobenzene and the transformation of intermediates when the initial concentration of nitrobenzene was about 850?mg·L-1. The promoting effect was increased proportionally with the dosage of HPβCD, which was mainly due to the detoxification ability of HPβCD through the formation inclusion complexes with nitrobenzene and 2aminophenol. The biodegradation kinetics of 850?mg·L-1 nitrobenzene followed firstorder reaction when HPβCD was added at 0, 2000, 4000?mg·L-1, and the kinetic constant was increased from 00077?h-1 to 00089 and 00161?h-1. However, when HPβCD was added at 8000?mg·L-1, the kinetics was changed to zeroorder reaction and the kinetic constant was 161162?mg·L-1·h-1.
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The present study investigated the effect of Hydroxypropylβcyclodextrin (HPβCD) on the cell growth, removal of nitrobenzene and the transformation of intermediates during the biodegradation process of nitrobenzene at high concentration by Acinetobacter sp. 2aminophenol was identified as an intermediates using direct acetylation of biodegraded samples of nitrobenzene by acetic anhydride followed by GCMS analysis. When the initial concentration of nitrobenzene was about 400?mg·L-1 (optimal concentration for degrading bacteria to grow vigorously), HPβCD added at 250?mg·L-1 or 500?mg·L-1 had no effect on the biomass and the degradation of nitrobenzene. However, the addition of HPβCD at above 2000?mg·L-1, significantly enhanced the cell growth, the biodegradation of nitrobenzene and the transformation of intermediates when the initial concentration of nitrobenzene was about 850?mg·L-1. The promoting effect was increased proportionally with the dosage of HPβCD, which was mainly due to the detoxification ability of HPβCD through the formation inclusion complexes with nitrobenzene and 2aminophenol. The biodegradation kinetics of 850?mg·L-1 nitrobenzene followed firstorder reaction when HPβCD was added at 0, 2000, 4000?mg·L-1, and the kinetic constant was increased from 00077?h-1 to 00089 and 00161?h-1. However, when HPβCD was added at 8000?mg·L-1, the kinetics was changed to zeroorder reaction and the kinetic constant was 161162?mg·L-1·h-1.
Key concepts: Nitrobenzene, Biodegradation, Chemistry, Kinetics, Nuclear chemistry, Aniline, Reaction rate constant, Chromatography