Results 11 to 20 of about 526,871 (218)

Engineering and elucidation of the lipoinitiation process in nonribosomal peptide biosynthesis

open access: yesNature Communications, 2021
Nonribosomal lipopeptides contain an acyl chain important for bioactivity, but its incorporation into the peptidyl backbone, mediated by the starter condensation (Cs) domain of nonribosomal peptide synthases, is not fully understood.
Lin Zhong   +10 more
doaj   +2 more sources

Nonribosomal Peptide Synthesis Definitely Working Out of the Rules [PDF]

open access: yesMicroorganisms, 2022
Nonribosomal peptides are microbial secondary metabolites exhibiting a tremendous structural diversity and a broad range of biological activities useful in the medical and agro-ecological fields.
Matthieu Duban   +2 more
doaj   +2 more sources

Nonribosomal Peptides

open access: yes, 2009
Nonribosomal peptides are a diverse group of compounds synthesized via modular nonribosomal peptide synthetase (NRPS) enzyme complexes. They are produced by a variety of prokaryotes, including streptomycetes, bacillus, and cyanobacteria, and lower-order eukaryotes such as fungi and sponges.
Roberts, Alexandra A.   +2 more
core   +4 more sources

Decoding and reprogramming fungal iterative nonribosomal peptide synthetases [PDF]

open access: yesNature Communications, 2017
Nonribosomal peptides are important bioactive molecules that are synthetized by enzymes containing several catalytic domains. Here the authors describe the catalytic mechanism of fungal nonribosomal peptide synthetases and present an approach to modify ...
Dayu Yu   +3 more
doaj   +2 more sources

Polyketide Synthase and Nonribosomal Peptide Synthetase Gene Clusters in Type Strains of the Genus Phytohabitans

open access: yesLife, 2020
(1) Background: Phytohabitans is a recently established genus belonging to rare actinomycetes. It has been unclear if its members have the capacity to synthesize diverse secondary metabolites.
Hisayuki Komaki, Tomohiko Tamura
doaj   +2 more sources

Identification of a Nonribosomal Peptide Analog With Activity Against Multiple Gram‐Positive Bacteria via a Synthetic Bioinformatic Natural Product Discovery Approach [PDF]

open access: yesAdvanced Science
Nonribosomal peptide (NRP) antibiotics exhibit potent biological activities and are broadly used in clinical therapy. Because most microorganisms are difficult to culture and many antibiotic biosynthetic genes are silent, traditional activity tracking ...
Keyi Chen   +9 more
doaj   +2 more sources

Synthesis of the Nonribosomal Peptide Phevalin and Analogs [PDF]

open access: yesThe Journal of Organic Chemistry, 2019
Phevalin, a cyclic nonribosomal peptide produced by Staphylococcus aureus, has intriguing biological properties. A synthetic route to access phevalin and similar pyrazinone natural products tyrvalin, leuvalin, phileucin, and a few synthetic analogs is described.
Remya Ramesh   +3 more
openaire   +3 more sources

Nonribosomal Peptides from Marine Microbes and Their Antimicrobial and Anticancer Potential

open access: yesFrontiers in Pharmacology, 2017
Marine environments are largely unexplored and can be a source of new molecules for the treatment of many diseases such as malaria, cancer, tuberculosis, HIV etc.
Shivankar Agrawal   +5 more
doaj   +2 more sources

Functional Diversity and Engineering of the Adenylation Domains in Nonribosomal Peptide Synthetases [PDF]

open access: yesMarine Drugs
Nonribosomal peptides (NRPs) are biosynthesized by nonribosomal peptide synthetases (NRPSs) and are widely distributed in both terrestrial and marine organisms. Many NRPs and their analogs are biologically active and serve as therapeutic agents.
Mengli Zhang   +5 more
doaj   +2 more sources

Development of a chemical scaffold for inhibiting nonribosomal peptide synthetases in live bacterial cells [PDF]

open access: yesBeilstein Journal of Organic Chemistry
The adenylation (A) domain is essential for non-ribosomal peptide synthetases (NRPSs), which synthesize various peptide-based natural products, including virulence factors, such as siderophores and genotoxins.
Fumihiro Ishikawa   +3 more
doaj   +2 more sources

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