TY - JOUR
T1 - Toward the Sustainable Production of the Active Pharmaceutical Ingredient Metaraminol
AU - Labib, Mohamed
AU - Grabowski, Laura
AU - Brüsseler, Christian
AU - Kallscheuer, Nicolai
AU - Wachtendonk, Luisa
AU - Fuchs, Thomas
AU - Jupke, Andreas
AU - Wiechert, Wolfgang
AU - Marienhagen, Jan
AU - Rother, Dörte
AU - Noack, Stephan
N1 - Publisher Copyright:
© 2022 The Authors. Published by American Chemical Society.
PY - 2022/4/25
Y1 - 2022/4/25
N2 - Metaraminol is an active pharmaceutical ingredient for hypotension treatment and can serve as a precursor for other bioactive compounds. The production of metaraminol was shown previously in an enzymatic cascade consisting of a carboligation and transamination step using the oil-based amine donor isopropylamine. Alternatively, renewable l-alanine can be used. By iterative strain and process engineering, the microbial production of pyruvate and l-alanine with Corynebacterium glutamicum in a one-pot fermentation process was achieved. The subsequent biotransformation was realized by direct carboligation of 3-OH-benzaldehyde and biobased pyruvate to (R)-3-OH-phenylacetylcarbinol in the fermentation supernatant with high yields (≥92% conversion) and stereoselectivity (>98% ee) after optimization. The decoupled transamination step utilized biobased l-alanine for metaraminol synthesis. This study elucidates the compatibility of biocatalytic conversions in complex fermentation matrices and highlights implications for the integration of novel biobased processes.
AB - Metaraminol is an active pharmaceutical ingredient for hypotension treatment and can serve as a precursor for other bioactive compounds. The production of metaraminol was shown previously in an enzymatic cascade consisting of a carboligation and transamination step using the oil-based amine donor isopropylamine. Alternatively, renewable l-alanine can be used. By iterative strain and process engineering, the microbial production of pyruvate and l-alanine with Corynebacterium glutamicum in a one-pot fermentation process was achieved. The subsequent biotransformation was realized by direct carboligation of 3-OH-benzaldehyde and biobased pyruvate to (R)-3-OH-phenylacetylcarbinol in the fermentation supernatant with high yields (≥92% conversion) and stereoselectivity (>98% ee) after optimization. The decoupled transamination step utilized biobased l-alanine for metaraminol synthesis. This study elucidates the compatibility of biocatalytic conversions in complex fermentation matrices and highlights implications for the integration of novel biobased processes.
UR - http://www.scopus.com/inward/record.url?scp=85129117137&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/331205c2-9d8c-3689-9947-a8d2e23eaed7/
U2 - 10.1021/acssuschemeng.1c08275
DO - 10.1021/acssuschemeng.1c08275
M3 - Journal articles
AN - SCOPUS:85129117137
SN - 2168-0485
VL - 10
SP - 5117
EP - 5128
JO - ACS Sustainable Chemistry and Engineering
JF - ACS Sustainable Chemistry and Engineering
IS - 16
ER -