Department of Chemistry, Ludwig-Maximilians-University Munich, Butenandtstraße 5-13, 81377, München, Germany.
Chair of Analytical Chemistry and Water Chemistry, Technical University of Munich, Marchioninistraße 17, 81377, München, Germany.
Chemistry. 2020 Aug 6;26(44):10133-10139. doi: 10.1002/chem.202002653. Epub 2020 Jul 7.
Lanthanides (Ln) are critical raw materials, however, their mining and purification have a considerable negative environmental impact and sustainable recycling and separation strategies for these elements are needed. In this study, the precipitation and solubility behavior of Ln complexes with pyrroloquinoline quinone (PQQ), the cofactor of recently discovered lanthanide (Ln) dependent methanol dehydrogenase (MDH) enzymes, is presented. In this context, the molecular structure of a biorelevant europium PQQ complex was for the first time elucidated outside a protein environment. The complex crystallizes as an inversion symmetric dimer, Eu PQQ , with binding of Eu in the biologically relevant pocket of PQQ. LnPQQ and Ln1Ln2PQQ complexes were characterized by using inductively coupled plasma mass spectrometry (ICP-MS), infrared (IR) spectroscopy, Eu-Mössbauer spectroscopy, X-ray total scattering, and extended X-ray absorption fine structure (EXAFS). It is shown that a natural enzymatic cofactor is capable to achieve separation by precipitation of the notoriously similar, and thus difficult to separate, lanthanides to some extent.
镧系元素(Ln)是关键的原材料,但它们的开采和提纯对环境有相当大的负面影响,因此需要可持续的回收和分离策略。本研究介绍了与吡咯并喹啉醌(PQQ)形成配合物的镧系元素的沉淀和溶解度行为,PQQ 是最近发现的镧系元素(Ln)依赖甲醇脱氢酶(MDH)酶的辅因子。在这种情况下,首次在蛋白质环境之外阐明了生物相关的铕 PQQ 配合物的分子结构。该配合物结晶为具有对称中心的二聚体 EuPQQ,Eu 结合在 PQQ 的生物相关口袋中。通过使用电感耦合等离子体质谱(ICP-MS)、红外(IR)光谱、Eu-Mössbauer 光谱、X 射线总散射和扩展 X 射线吸收精细结构(EXAFS)对 LnPQQ 和 Ln1Ln2PQQ 配合物进行了表征。结果表明,天然酶辅因子在一定程度上能够通过沉淀来实现对 notoriously similar,且因此难以分离的镧系元素的分离。