TY - JOUR
T1 - The Earlier the Better
T2 - Structural Analysis and Separation of Lanthanides with Pyrroloquinoline Quinone
AU - Lumpe, Henning
AU - Menke, Annika
AU - Haisch, Christoph
AU - Mayer, Peter
AU - Kabelitz, Anke
AU - Yusenko, Kirill V.
AU - Guilherme Buzanich, Ana
AU - Block, Theresa
AU - Pöttgen, Rainer
AU - Emmerling, Franziska
AU - Daumann, Lena J.
N1 - Publisher Copyright:
© 2020 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.
PY - 2020/8/6
Y1 - 2020/8/6
N2 - 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, Eu2PQQ2, 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, 151Eu-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.
AB - 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, Eu2PQQ2, 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, 151Eu-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.
KW - PQQ
KW - coordination chemistry
KW - lanthanides
KW - rare earth elements
KW - separations
UR - http://www.scopus.com/inward/record.url?scp=85087552426&partnerID=8YFLogxK
U2 - 10.1002/chem.202002653
DO - 10.1002/chem.202002653
M3 - Article
C2 - 32497263
AN - SCOPUS:85087552426
SN - 0947-6539
VL - 26
SP - 10133
EP - 10139
JO - Chemistry - A European Journal
JF - Chemistry - A European Journal
IS - 44
ER -