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Showing 1–5 of 5 results
Advanced filters: Author: Hans Iding Clear advanced filters
  • A motif was identified in the scaffold of an (S)-selective transaminase that enables the asymmetric synthesis of bulky chiral amines. This motif is transferable to other enzymes with as low as 70% sequence identity. The biocatalysts developed show high stereoselectivity and their synthetic potential was confirmed in preparative scale synthesis.

    • Ioannis V. Pavlidis
    • Martin S. Weiß
    • Uwe T. Bornscheuer
    Research
    Nature Chemistry
    Volume: 8, P: 1076-1082
  • Chemical and biological catalysts provide distinct advantages and disadvantages to the synthetic chemist. This Review focuses on efforts to combine chemo- and biocatalysts, outlining the opportunities achievable by this approach and also efforts to overcome any incompatibilities between these different systems.

    • Florian Rudroff
    • Marko D. Mihovilovic
    • Uwe T. Bornscheuer
    Reviews
    Nature Catalysis
    Volume: 1, P: 12-22
  • Ipatasertib is a potent Akt (protein kinase B) inhibitor synthesized via a chemoenzymatic process. Here, the authors use mutational scanning and algorithm-aided enzyme engineering to optimize a ketoreductase from Sporidiobolus salmonicolor and generate a 10-amino acid substituted variant exhibiting a 64-fold higher kcat and improved yield for the relevant alcohol intermediate, with ≥ 98% conversion and a diastereomeric excess of 99.7% (R,R-trans) from 100 g L−1 ketone after 30 h.

    • Sumire Honda Malca
    • Nadine Duss
    • Rebecca Buller
    ResearchOpen Access
    Communications Chemistry
    Volume: 7, P: 1-11