Sellami Kheireddine, Couvert Annabelle, Nasrallah Noureddine, Maachi Rachida, Tandjaoui Nassima, Abouseoud Mahmoud, Amrane Abdeltif
Laboratoire de Génie de la Réaction, Faculté de Génie Mécanique et Génie des Procédés, Université des Sciences et de la Technologie Houari Boumediene, Bab Ezzouar, Alger 16111, Algeria; Univ Rennes, Ecole Nationale Supérieure de Chimie de Rennes, CNRS, ISCR (Institut des Sciences Chimiques de Rennes)-UMR 6226, F-35000 Rennes, France.
Univ Rennes, Ecole Nationale Supérieure de Chimie de Rennes, CNRS, ISCR (Institut des Sciences Chimiques de Rennes)-UMR 6226, F-35000 Rennes, France.
J Hazard Mater. 2021 Feb 5;403:124021. doi: 10.1016/j.jhazmat.2020.124021. Epub 2020 Sep 17.
This work aimed at presenting a green method using a new source of peroxidase isolated from Raphanus sativus var. niger (RSVNP) in immobilized form, for the treatment of wastewater. To ensure stability and enzymatic activity in the biodegradation process, RSVNP was immobilized as a cross-linked enzyme aggregate (CLEAs). With more than 29% of recovered activity and 85% aggregation yield, acetone was selected as the best precipitating agent. The formed protein aggregates required 2% (v/v) of glutaraldehyde (GA) concentration and a ratio of 9:1 (v/v) enzyme (E) amount to cross-linker (E/GA). Compared to the free enzyme, RSVNP-CLEAs were found more chemically and thermally stable and exhibited good storage stability for more than 8 weeks. In addition, RSVNP-CLEAs were evaluated for their ability to remove phenol and p-cresol from aqueous solution by varying several operating conditions. A maximal yield (98%) of p-cresol conversion was recorded after 40 min; while 92% of phenol was degraded after 1 h duration time. The reusability of RSVNP-CLEAs was tested, displaying 71% degradation of phenol in the third batch carried out and more than 54% was achieved for p-cresol after four successive reuses in the presence of hydrogen peroxide at 2 mM concentration.
这项工作旨在提出一种绿色方法,该方法使用从黑萝卜(RSVNP)中分离出的一种新型过氧化物酶来源,以固定化形式处理废水。为确保生物降解过程中的稳定性和酶活性,将RSVNP固定化为交联酶聚集体(CLEAs)。丙酮的回收活性超过29%,聚集产率达到85%,因此被选为最佳沉淀剂。形成的蛋白质聚集体需要2%(v/v)的戊二醛(GA)浓度以及9:1(v/v)的酶量与交联剂的比例(E/GA)。与游离酶相比,发现RSVNP-CLEAs在化学和热方面更稳定,并且在超过8周的时间内表现出良好的储存稳定性。此外,通过改变几个操作条件,评估了RSVNP-CLEAs从水溶液中去除苯酚和对甲酚的能力。40分钟后记录到对甲酚转化的最大产率(98%);而1小时后苯酚降解了92%。测试了RSVNP-CLEAs的可重复使用性,在2 mM浓度的过氧化氢存在下,第三次批次中苯酚的降解率为71%,连续四次重复使用后对甲酚的降解率超过54%。