Structural diversity, biosynthesis, and biological functions of lipopeptides from Streptomyces

S Zhang, Y Chen, J Zhu, Q Lu, MJ Cryle… - Natural Product …, 2023 - pubs.rsc.org
Covering: up to 2022 Streptomyces are ubiquitous in terrestrial and marine environments,
where they display a fascinating metabolic diversity. As a result, these bacteria are a prolific …

The structural diversity of acidic lipopeptide antibiotics

M Strieker, MA Marahiel - ChemBioChem, 2009 - Wiley Online Library
Resisting resistance: Acidic lipopeptide antibiotics are very effective in fighting multidrug‐
resistant Gram‐positive bacteria, including methicillin‐resistant Staphylococcus aureus and …

Introduction of a non-natural amino acid into a nonribosomal peptide antibiotic by modification of adenylation domain specificity.

J Thirlway, R Lewis, L Nunns, M Al Nakeeb… - … (International ed. in …, 2012 - europepmc.org
Calcium-dependent antibiotics (CDA) are cyclic lipopeptides assembled by nonribosomal
peptide synthetase (NRPS) enzymes. Active site modification of the 3-methyl glutamate …

Novel cyclic hexapeptides from marine-derived fungus, Aspergillus sclerotiorum PT06-1

J Zheng, H Zhu, K Hong, Y Wang, P Liu, X Wang… - Organic …, 2009 - ACS Publications
Two novel cyclic hexapeptides containing both anthranilic acid and dehydroamino acid
units, sclerotides A (1) and B (2), were isolated from the marine-derived halotolerant …

Total Synthesis of α‐and β‐Amanitin

C Lutz, W Simon, S Werner‐Simon… - Angewandte Chemie …, 2020 - Wiley Online Library
Abstract α‐Amanitin and related amatoxins have been studied for more than six decades
mostly by isolation from death cap mushrooms. The total synthesis, however, remained …

Bulky α, β-dehydroamino acids: their occurrence in nature, synthesis, and applications

J Jiang, Z Ma, SL Castle - Tetrahedron, 2015 - Elsevier
α, β-Dehydroamino acids (ΔAAs) are nonproteinogenic residues that occur in both natural
and synthetic peptides. Their planar geometry at the α and β carbons profoundly impacts the …

Catalytic Vilsmeier–Haack Reactions for C1-Deuterated Formylation of Indoles

J Xue, YS Zhang, Z Huan, JD Yang… - The Journal of Organic …, 2022 - ACS Publications
The Vilsmeier–Haack reaction is a powerful tool to introduce formyl groups into electron-rich
arenes, but its wide application is significantly restricted by stoichiometric employment of …

Mycetoindole, an N-acyl dehydrotryptophan with plant growth inhibitory activity from an actinomycete of the genus Actinomycetospora

S Saito, N Oku, Y Igarashi - The Journal of Antibiotics, 2022 - nature.com
A rare actinomycetal strain of the genus Actinomycetospora was found to produce a new
tryptophan derivative, designated mycetoindole (1). The structure of 1 was determined to be …

Convergent synthesis of calcium-dependent antibiotic CDA3a and analogues with improved antibacterial activity via late-stage serine ligation

D Chen, KHL Po, P Blasco, S Chen, X Li - Organic Letters, 2020 - ACS Publications
A convergent synthesis via the late-stage serine ligation of naturally occurring calcium-
dependent antibiotic CDA3a and its analogues has been developed, which allowed us to …

The chemo- enzymatic synthesis of labeled l-amino acids and some of their derivatives

M Pająk, K Pałka, E Winnicka, M Kańska - Journal of Radioanalytical and …, 2018 - Springer
This review compiles the combined chemical and enzymatic synthesis of aromatic l-amino
acids (l-phenylalanine, l-tyrosine, l-DOPA, l-tryptophan, and their derivatives and precursors) …