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| Open AccessA selective and atom-economic rearrangement of uridine by cascade biocatalysis for production of pseudouridine
Pseudouridine (Ψ), the C-nucleoside isomer of uridine, and its 1-N-methyl derivative, are incorporated in mRNA vaccines and essential for their efficiency, but difficult to synthetically access. Here, the authors report on selective and atom-economic 1N-5C rearrangement of β-d-ribosyl on uracil to obtain Ψ from unprotected U in quantitative yield
- Martin Pfeiffer
- , Andrej Ribar
- & Bernd Nidetzky
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Article
| Open AccessThe evolutionary advantage of an aromatic clamp in plant family 3 glycoside exo-hydrolases
Barley β-d-glucan glucohydrolase is a glycoside hydrolase family 3 (GH3) enzyme critical for growth and development. Here the authors carryout mutagenesis, structural analyses and multi-scale molecular dynamics to examine the binding and conformational behaviour of several β-d-glucosides during the substrate-product assisted catalysis that operates in GH3 hydrolases.
- Sukanya Luang
- , Xavier Fernández-Luengo
- & Maria Hrmova
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Article
| Open AccessReverse C-glycosidase reaction provides C-nucleotide building blocks of xenobiotic nucleic acids
C-nucleosides are analogues of the canonical N-nucleosides and, despite their synthetic value, biocatalysis has not targeted them yet. Here, the authors report a pseudouridine monophosphate C-glycosidase enzyme for selective 5-β-C-glycosylation of uracil and its derivatives from pentose 5- phosphate substrates.
- Martin Pfeiffer
- & Bernd Nidetzky
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Article
| Open AccessStructure and dynamics of an α-fucosidase reveal a mechanism for highly efficient IgG transfucosylation
AlfC transfucosidase is used to modulate fucosylation of glycans decorating monoclonal antibodies. Herein, structural and biophysical characterization reveals the enzymatic mechanism of AlfC and a blueprint for the design of AlfC mutants with novel specificities and functions.
- Erik H. Klontz
- , Chao Li
- & Eric J. Sundberg
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Article
| Open AccessExploring and applying the substrate promiscuity of a C-glycosyltransferase in the chemo-enzymatic synthesis of bioactive C-glycosides
C-glycosides are of pharmaceutical interest due to their stability against in vivo hydrolysis, however their enzymatic synthesis faces challenges. Here, the authors report a C-glycosyltransferase from Aloe barbadensis catalysing the C-glycosylation of drug-like acceptors to generate bioactive C-glycosides.
- Kebo Xie
- , Xiaolin Zhang
- & Jungui Dai
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Article
| Open AccessHierarchical and programmable one-pot synthesis of oligosaccharides
The software Optimer has aided the programmable one-pot oligosaccharide synthesis with a library of 50 Building BLocks (BBLs). Here, the authors expanded Optimer's validated and virtual libraries of BBLs and developed Auto-CHO, a software which allows the one-pot programmable synthesis of more complex glycans.
- Cheng-Wei Cheng
- , Yixuan Zhou
- & Chi-Huey Wong
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Article
| Open AccessEnergy efficiency trade-offs drive nucleotide usage in transcribed regions
Substantial cellular resources are devoted to nucleotide biosynthesis. Here the authors propose that transcribed regions prefer ‘cheaper’ nucleotides, which appears true for synonymous sites, although more expensive nucleotides coding for cheaper amino acids are selected for at non-synonymous sites.
- Wei-Hua Chen
- , Guanting Lu
- & Martin J. Lercher