Zhao Zhi-Qing, Tian Bao-Hu, Zhang Xuan, Ghulam Abbas, Zheng Tu-Cai, Shen Dong-Sheng
College of Environment and Resource Sciences, Zhejiang University, Hangzhou, People's Republic of China.
Biodegradation. 2015 Feb;26(1):1-14. doi: 10.1007/s10532-014-9704-3. Epub 2014 Sep 20.
The fate of fluorinated compounds in the environment, especially polyfluorinated aromatics, is a matter of great concern. In this work, 4-Fluoroaniline (4-FA), 2,4-Difluoroanilines (2,4-DFA), and 2,3,4-Trifluoroanilines (2,3,4-TFA), were chosen as the target pollutants to study their biodegradability under aerobic conditions. The required enriched time of the mixed bacterial culture for degrading 4-FA, 2,4-DFA, and 2,3,4-TFA was 26, 51, and 165 days, respectively, which suggested that the longer enrichment time was required with the increase of fluorine substitution. At the initial concentrations of 100-200 mg L(-1), the 4-FA, 2,4-DFA, and 2,3,4-TFA could be degraded completely by the mixed bacterial culture. The maximum specific degradation rates of 4-FA, 2,4-DFA, and 2,3,4-TFA were 22.48 ± 0.55, 15.27 ± 2.04, and 8.84 ± 0.93 mg FA (g VSS h)(-1), respectively. Also, the three FAs enriched cultures showed certain potential of degrading other two FAs. The results from enzyme assay suggested the expression of meta-cleavage pathways during three FAs degradation. The denaturing gradient gel electrophoresis analysis revealed that unique bacterial communities were formed after FAs enrichment and these were principally composed of β-Proteobacteria, Oscillatoriophycideae, δ-Proteobacteria, α-Proteobacteria, Thermales, Xanthomonadales, Deinococci, Flavobacteriia, and Actinobacteridae. The Shannon-Wiener indexes in three FAs enriched culture decreased with the increase of fluorine substitution, indicating the significant effect of fluorine substitution on the microbial diversity. These findings supply important information on the fate of three FAs under aerobic environment, and the bacterial communities in their degradation systems.
含氟化合物,尤其是多氟芳烃在环境中的归宿是一个备受关注的问题。在本研究中,选择了4-氟苯胺(4-FA)、2,4-二氟苯胺(2,4-DFA)和2,3,4-三氟苯胺(2,3,4-TFA)作为目标污染物,研究它们在好氧条件下的生物降解性。混合细菌培养物降解4-FA、2,4-DFA和2,3,4-TFA所需的富集时间分别为26天、51天和165天,这表明随着氟取代度的增加,需要更长的富集时间。在初始浓度为100 - 200 mg L(-1)时,混合细菌培养物可将4-FA、2,4-DFA和2,3,4-TFA完全降解。4-FA、2,4-DFA和2,3,4-TFA的最大比降解速率分别为22.48 ± 0.55、15.27 ± 2.04和8.84 ± 0.93 mg FA (g VSS h)(-1)。此外,三种富集了相应氟苯胺的培养物显示出降解其他两种氟苯胺的一定潜力。酶活性测定结果表明,三种氟苯胺降解过程中均有间位裂解途径的表达。变性梯度凝胶电泳分析表明,氟苯胺富集后形成了独特的细菌群落,这些群落主要由β-变形菌纲、颤藻纲、δ-变形菌纲、α-变形菌纲、嗜热菌纲、黄单胞菌目、嗜放射菌属、黄杆菌纲和放线菌科组成。三种富集了氟苯胺的培养物中的香农-威纳指数随着氟取代度的增加而降低,表明氟取代对微生物多样性有显著影响。这些发现为三种氟苯胺在好氧环境中的归宿及其降解系统中的细菌群落提供了重要信息。