Oligomerization of 3-substituted quinolines by catalytic activity of soybean peroxidase as a wastewater treatment. Product formation and computational studies

被引:14
作者
Mashhadi, Neda [1 ]
Taylor, Keith E. [1 ]
Biswas, Nihar [2 ]
Meister, Paul [1 ]
Gauld, James W. [1 ]
机构
[1] Univ Windsor, Dept Chem & Biochem, 401 Sunset Ave, Windsor, ON N9B 3P4, Canada
[2] Univ Windsor, Dept Civil & Environm Engn, 401 Sunset Ave, Windsor, ON N9B 3P4, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Wastewater treatment; Soybean peroxidase; Computational analysis; Product; Quinoline; HORSERADISH-PEROXIDASE; ELECTROCHEMICAL OXIDATION; AROMATIC-HYDROCARBONS; REMOVAL; POLYMERIZATION; DERIVATIVES; POTENTIALS; METABOLISM; PROTONS; LACCASE;
D O I
10.1016/j.cej.2019.01.184
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Although heterocyclic aromatics make up a vast group of water contaminants, the effect of enzyme on this class of recalcitrant compounds is largely unknown. Here, the feasibility of treatment of selected quinolines with soybean peroxidase is demonstrated and the effects of the most important parameters; pH, enzyme concentration, and peroxide concentration are optimized for each compound. 3-hydroxy and 3-aminoquinoline were found to be substrates amenable to >= 94% removal with pH optima of 8.6 and 5.6, respectively. In order to identify the transformation products of such treatment, the solution and precipitate after enzymatic treatment were analyzed by mass spectrometry to find that the dominant products were dimers and trimers from oxidative radical coupling. In addition, for 3-aminoquinoline azo-linked dimers and trimers were found. Computational techniques used to investigate the influence of redox potential and ionization energy of pollutants on their treatability by SBP showed a possible threshold between substrates and non-substrates. Computed spin densities were used to predict the regiochemistry of the radical coupling reaction.
引用
收藏
页码:340 / 348
页数:9
相关论文
共 58 条
  • [1] Alva KS, 1998, J APPL POLYM SCI, V70, P1257, DOI 10.1002/(SICI)1097-4628(19981114)70:7<1257::AID-APP2>3.0.CO
  • [2] 2-L
  • [3] OZONATION OF PYRIDINE IN AQUEOUS-SOLUTION - MECHANISTIC AND KINETIC ASPECTS
    ANDREOZZI, R
    INSOLA, A
    CAPRIO, V
    DAMORE, MG
    [J]. WATER RESEARCH, 1991, 25 (06) : 655 - 659
  • [4] Effects of phenanthrene and its nitrogen-heterocyclic analogues aged in soil on the earthworm Eisenia fetida
    Anyanwu, Ihuoma N.
    Semple, Kirk T.
    [J]. APPLIED SOIL ECOLOGY, 2016, 105 : 151 - 159
  • [5] OXIDATIVE COUPLING OF PHENOLS .8. A THEORETICAL-STUDY OF THE COUPLING OF PHENOXYL RADICALS
    ARMSTRONG, DR
    CAMERON, C
    NONHEBEL, DC
    PERKINS, PG
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, 1983, (05): : 575 - 579
  • [6] Nitrogen-containing organic compounds: Origins, toxicity and conditions of their photocatalytic mineralization over TiO2
    Bamba, Drissa
    Coulibaly, Mariame
    Robert, Didier
    [J]. SCIENCE OF THE TOTAL ENVIRONMENT, 2017, 580 : 1489 - 1504
  • [7] BOYD JA, 1987, CANCER RES, V47, P4007
  • [8] METABOLISM OF AROMATIC-AMINES BY PROSTAGLANDIN-H SYNTHASE
    BOYD, JA
    ELING, TE
    [J]. ENVIRONMENTAL HEALTH PERSPECTIVES, 1985, 64 : 45 - 51
  • [9] Application of Radical Cation Spin Density Maps toward the Prediction of Photochemical Reactivity between N-Methyl-1,2,4-triazoline-3,5-dione and Substituted Benzenes
    Breton, Gary W.
    Hoke, Kevin R.
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 2013, 78 (10) : 4697 - 4707
  • [10] Heterocyclic Aromatic Hydrocarbons Show Estrogenic Activity upon Metabolization in a Recombinant Transactivation Assay
    Brinkmann, Markus
    Maletz, Sibylle
    Krauss, Martin
    Bluhm, Kerstin
    Schiwy, Sabrina
    Kuckelkorn, Jochen
    Tiehm, Andreas
    Brack, Werner
    Hollert, Henner
    [J]. ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2014, 48 (10) : 5892 - 5901