4.3 Article

Biodegradation of microcystin-LR by an amino acid-degrading anaerobic bacterium

期刊

DESALINATION AND WATER TREATMENT
卷 57, 期 2, 页码 870-880

出版社

DESALINATION PUBL
DOI: 10.1080/19443994.2014.969316

关键词

Anaerobic bacterium; Microcystin-LR; Biodegradation products; Enzymatic degradation; mlrA gene

资金

  1. National Science Fund for Distinguished Young Scholars [51225901]
  2. Outstanding Youth Fund of Jiangsu Province [BK2012037]
  3. Research Fund for Innovation Team of Ministry of Education [IRT13061]
  4. Fundamental Research Funds for the Central Universities [2014B03814]
  5. QingLan Project for Innovation Team of Jiangsu Province

向作者/读者索取更多资源

Recent studies have proved that microcystins (MCs) can be degraded by sediment under anaerobic conditions, suggesting that anaerobic biodegradation is an important pathway to remove MCs in water treatment. In this study, the potential for biodegradation of microcystin-LR (MCLR) by an amino acid-degrading anaerobic bacterium ALA-1 was investigated. Under mesophilic conditions (20, 25 and 30 degrees C), MCLR was dropped from 4mg/L to below the detection limit in 10d without lag phase. While at cold temperatures (10 and 15 degrees C), MCLR degraded completely in 14 and 19d with a delay time reaching 6 and 8d, respectively. Under alkaline conditions (pH 8.0, 9.0), MCLR was degraded completely within 10d without a lag phase. While MCLR was degraded completely within 12d under neutral condition (pH 7.0). A lag time of 8 and 20d was needed prior to the onset of MCLR degradation under two slightly acidic conditions (pH 6.0, 5.0), respectively, and MCLR was completely consumed until day 22 and day 38. In addition, extra carbon or nitrogen sources had no significant effect on the degradation ability of ALA-1. Linearized MCLR (m/z 1,013.3729, C49H77N10O13), tetrapeptide (m/z 616.1208, C32H48N4O8) and Adda (m/z 332.0186, C20H30NO3), commonly known as aerobic biodegradation products of MCLR, were detected as the intermediate products. The mlrA gene homologue, known for its degradation potential of MCLR, was absent in strain ALA-1, implying that other enzymes which were not encoded by the mlrA gene cluster might have been involved in metabolizing MCLR in the present study.

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