Janović Barbara S, Mićić Vićovac Milica Lj, Vujčić Zoran M, Vujčić Miroslava T
Department of Chemistry, Institute of Chemistry, Technology, and Metallurgy, Njegoševa 12, P.O. Box 815, Belgrade, 11000, Serbia.
Faculty of Chemistry, University of Belgrade, Studentski trg 12-16, Belgrade, 11000, Serbia.
Environ Sci Pollut Res Int. 2017 Feb;24(4):3923-3933. doi: 10.1007/s11356-016-8100-4. Epub 2016 Dec 1.
Peroxidases (EC 1.11.1.7) have enormous biotechnological applications. Usage of more abundant, basic isoforms of peroxidases in diagnostic kits and/or in immunochemistry has led to under exploitation and disregard of horseradish peroxidase (HRP) acidic isoforms. Therefore, acidic horseradish peroxidase (HRP-A) isoenzyme was used for the preparation of a biocatalyst with improved ability in dye decolorization. Ten biocatalysts were prepared by covalent binding of enzyme to chitosan and alginate, adsorption followed by cross-linking on inorganic support (aluminum oxide), and encapsulation in spherical calcium alginate beads via polyethylene glycol. Model dyes of 50 to 175 mg l were removed by the biocatalysts. Among the tested biocatalysts, the three with the highest specific activity and biodegradation rate were further studied (Chitosan-HRP, Al-Gel-HRP and Al-HRP-Gel). The impact of hydrogen peroxide concentration on dye decolorization was examined on the Chitosan-HRP biocatalyst, since the HRP is susceptible to inhibition/inactivation by high HO. On the other hand, HO is needed as a co-substrate for the HRP, and the HO/dye ratio can greatly influence decolorization efficiency. Concentrations of HO ranging from 0.22 to 4.4 mM showed no difference in terms of impact on the biocatalyst decolorization efficiency. The high decolorization efficiency of the biocatalysts was validated by the removal of 25 and 100 mg l anthraquinone (Remazol Brilliant Blue R (RBBR)), triphenylmethane (Coomassie Brilliant Blue (CBB)), acridine (Acridine Orange (AO)), and formazan metal complex dye (Reactive Blue 52 (RB52)). After the seven consecutive decolorization cycles, the decolorization was still 53, 78, and 67% of the initial dye for the Al-HRP-Gel, Al-Gel-HRP, and Chitosan-HRP immobilizate, respectively. The results obtained showed potential of otherwise neglected acidic HRP isoforms as a cost-effective biocatalyst with significant potential in wastewater dyestuff treatment.
过氧化物酶(EC 1.11.1.7)具有巨大的生物技术应用价值。在诊断试剂盒和/或免疫化学中使用更为丰富的碱性过氧化物酶同工型,导致辣根过氧化物酶(HRP)酸性同工型未得到充分开发和重视。因此,酸性辣根过氧化物酶(HRP-A)同工酶被用于制备具有更强染料脱色能力的生物催化剂。通过将酶与壳聚糖和海藻酸盐共价结合、在无机载体(氧化铝)上吸附后交联以及通过聚乙二醇封装在球形海藻酸钙珠粒中,制备了十种生物催化剂。这些生物催化剂去除了浓度为50至175 mg/L的模型染料。在测试的生物催化剂中,对三种比活性和生物降解率最高的催化剂(壳聚糖-HRP、铝凝胶-HRP和铝-HRP-凝胶)进行了进一步研究。由于HRP易受高浓度H₂O₂的抑制/失活作用,因此在壳聚糖-HRP生物催化剂上研究了过氧化氢浓度对染料脱色的影响。另一方面,H₂O₂作为HRP的共底物是必需的,H₂O₂/染料比例会极大地影响脱色效率。浓度范围为0.22至4.4 mM的H₂O₂对生物催化剂脱色效率的影响没有差异。通过去除25和100 mg/L的蒽醌(活性艳蓝R(RBBR))、三苯甲烷(考马斯亮蓝(CBB))、吖啶(吖啶橙(AO))和甲臜金属络合染料(活性蓝52(RB52)),验证了生物催化剂的高脱色效率。在连续七个脱色循环后,铝-HRP-凝胶、铝凝胶-HRP和壳聚糖-HRP固定化产物对初始染料的脱色率分别仍为53%、78%和67%。所得结果表明,原本被忽视的酸性HRP同工型作为一种具有成本效益的生物催化剂在废水染料处理中具有巨大潜力。