Key Laboratory of Pesticide & Chemical Biology (CCNU), Ministry of Education, College of Chemistry, Central China Normal University, Wuhan 430079, People's Republic of China.
Environ Sci Technol. 2020 Jul 21;54(14):8811-8820. doi: 10.1021/acs.est.0c02155. Epub 2020 Jun 11.
Harmful blooms (HMBs) seriously threaten the ecology of environments and human health. Microcystins (MCs) produced by are powerful mediators of HMB induction and maintenance. In this study, microcystinase A (MlrA), an enzyme with MC-degrading ability, was successfully obtained at over 90% purity for the first time through overexpression in K12 TB1. The obtained MlrA exhibited high stability at high temperature and under alkaline conditions, while also exhibiting a long half-life. MlrA selectively inhibited MC-producing cultures, but had no effect on MC-nonproducing cultures. The inhibition mechanism of MlrA against was investigated by evaluating the morphological and physiological characteristics of cultures. MlrA effectively degraded extracellular MCs and decreased the synthesis of intracellular MCs by causing downregulation of genes involved in the microcystin biosynthesis pathway. Concomitantly, MlrA inhibited photosynthesis by causing the downregulated expression of important photosynthesis pathway genes and interrupting electron transport chain activities and pigment synthesis. Thus, MlrA achieved the inhibition of growth by reducing its photosynthetic capacity and intracellular MC contents, while also degrading extracellular MCs. On the basis of these results, we propose a new paradigm to achieve the simultaneous removal of MCs and HMBs using the single enzyme characterized here.
有害藻类水华(HMBs)严重威胁着环境生态和人类健康。微囊藻产生的微囊藻毒素(MCs)是诱导和维持 HMB 的有力介质。在这项研究中,通过在 K12 TB1 中过表达,首次成功获得了超过 90%纯度的具有 MC 降解能力的微囊藻酶 A(MlrA)。获得的 MlrA 在高温和碱性条件下具有很高的稳定性,半衰期也很长。MlrA 选择性地抑制产生 MC 的培养物,但对不产生 MC 的培养物没有影响。通过评估培养物的形态和生理特征,研究了 MlrA 对 的抑制机制。MlrA 通过下调参与微囊藻生物合成途径的基因,有效降解细胞外的 MCs,并降低细胞内 MCs 的合成。同时,MlrA 通过下调重要光合作用途径基因的表达,中断电子传递链活性和色素合成,抑制 的光合作用。因此,MlrA 通过降低其光合作用能力和细胞内 MC 含量来抑制 的生长,同时降解细胞外的 MCs。基于这些结果,我们提出了一个新的范例,即使用这里所描述的单一酶同时去除 MCs 和 HMBs。