Department of Plant Physiology and Development, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, Gronostajowa 7, 30387 Kraków, Poland.
Department of Analytical Biochemistry, Jagiellonian University, Gronostajowa 7, 30387 Kraków, Poland.
Toxins (Basel). 2014 Aug 13;6(8):2379-92. doi: 10.3390/toxins6082379.
An important aim of white (grey) biotechnology is bioremediation, where microbes are employed to remove unwanted chemicals. Microcystins (MCs) and other cyanobacterial toxins are not industrial or agricultural pollutants; however, their occurrence as a consequence of human activity and water reservoir eutrophication is regarded as anthropogenic. Microbial degradation of microcystins is suggested as an alternative to chemical and physical methods of their elimination. This paper describes a possible technique of the practical application of the biodegradation process. The idea relies on the utilization of bacteria with a significantly enhanced MC-degradation ability (in comparison with wild strains). The cells of an Escherichia coli laboratory strain expressing microcystinase (MlrA) responsible for the detoxification of MCs were immobilized in alginate beads. The degradation potency of the tested bioreactors was monitored by HPLC detection of linear microcystin LR (MC-LR) as the MlrA degradation product. An open system based on a column filled with alginate-entrapped cells was shown to operate more efficiently than a closed system (alginate beads shaken in a glass container). The maximal degradation rate calculated per one liter of carrier was 219.9 µg h-1 of degraded MC-LR. A comparison of the efficiency of the described system with other biological and chemo-physical proposals suggests that this new idea presents several advantages and is worth investigating in future studies.
白色(灰色)生物技术的一个重要目标是生物修复,其中利用微生物去除不需要的化学物质。微囊藻毒素(MCs)和其他蓝藻毒素不是工业或农业污染物;然而,由于人类活动和水库富营养化的结果,它们的出现被认为是人为的。微生物降解微囊藻毒素被认为是消除它们的化学和物理方法的替代方法。本文描述了生物降解过程实际应用的一种可能技术。该想法依赖于利用具有显著增强的 MC 降解能力的细菌(与野生菌株相比)。负责 MC 解毒的微囊藻酶(MlrA)的大肠杆菌实验室菌株的细胞被固定在藻酸盐珠中。通过 HPLC 检测线性微囊藻 LR(MC-LR)作为 MlrA 降解产物来监测测试生物反应器的降解能力。与封闭系统(在玻璃容器中摇动的藻酸盐珠)相比,基于填充有藻酸盐包埋细胞的柱的开放系统显示出更高的效率。每升载体计算的最大降解速率为 219.9 µg h-1 降解的 MC-LR。将所描述的系统的效率与其他生物和化学物理方案进行比较表明,这个新想法具有几个优点,值得在未来的研究中进一步探讨。