about
Characterization of the biosynthesis gene cluster for the pyrrole polyether antibiotic calcimycin (A23187) in Streptomyces chartreusis NRRL 3882Biosynthesis of oxygen and nitrogen-containing heterocycles in polyketidesNonprocessive [2 + 2]e- off-loading reductase domains from mycobacterial nonribosomal peptide synthetasesHeterologous expression and structural characterisation of a pyrazinone natural product assembly lineSecondary metabolism and biotrophic lifestyle in the tomato pathogen Cladosporium fulvumComplete genome sequence and transcriptomics analyses reveal pigment biosynthesis and regulatory mechanisms in an industrial strain, Monascus purpureus YY-1The Role of a Nonribosomal Peptide Synthetase in l-Lysine Lactamization During Capuramycin Biosynthesis.Oxidative dearomatisation: the key step of sorbicillinoid biosynthesis†Electronic supplementary information (ESI) available: Containing all experimental details. See DOI: 10.1039/c3sc52911hClick here for additional data file.How to kill the honey bee larva: genomic potential and virulence mechanisms of Paenibacillus larvae.The reductase domain in a Type I fatty acid synthase from the apicomplexan Cryptosporidium parvum: restricted substrate preference towards very long chain fatty acyl thioestersInsights into the complex biosynthesis of the leupyrrins in Sorangium cellulosum So ce690.Identification and characterization of the anti-methicillin-resistant Staphylococcus aureus WAP-8294A2 biosynthetic gene cluster from Lysobacter enzymogenes OH11.Spliceostatin hemiketal biosynthesis in Burkholderia spp. is catalyzed by an iron/α-ketoglutarate-dependent dioxygenase.Recent advancements in the biosynthetic mechanisms for polyketide-derived mycotoxins.Enzymatic processing of fumiquinazoline F: a tandem oxidative-acylation strategy for the generation of multicyclic scaffolds in fungal indole alkaloid biosynthesis.Characterization of the lnmKLM genes unveiling key intermediates for β-alkylation in leinamycin biosynthesis.Biosynthesis of HSAF, a tetramic acid-containing macrolactam from Lysobacter enzymogenesA sea of biosynthesis: marine natural products meet the molecular age.Various mechanisms in cyclopeptide production from precursors synthesized independently of non-ribosomal peptide synthetases.New insights into the formation of fungal aromatic polyketides.Vitroprocines, new antibiotics against Acinetobacter baumannii, discovered from marine Vibrio sp. QWI-06 using mass-spectrometry-based metabolomics approachGenome analyses of the sunflower pathogen Plasmopara halstedii provide insights into effector evolution in downy mildews and Phytophthora.Interrogation of global active site occupancy of a fungal iterative polyketide synthase reveals strategies for maintaining biosynthetic fidelity.The complete genome sequence of the acarbose producer Actinoplanes sp. SE50/110.Unusual Biosynthesis and Structure of Locillomycins from Bacillus subtilis 916Biosynthesis of Antibiotic Leucinostatins in Bio-control Fungus Purpureocillium lilacinum and Their Inhibition on Phytophthora Revealed by Genome Mining.Polyketide proofreading by an acyltransferase-like enzyme.Divergent biosynthesis yields a cytotoxic aminomalonate-containing precolibactinMetagenomic Analysis of the Sponge Discodermia Reveals the Production of the Cyanobacterial Natural Product Kasumigamide by 'Entotheonella'.Directed evolution of the tryptophan synthase β-subunit for stand-alone function recapitulates allosteric activation.Cyclization of fungal nonribosomal peptides by a terminal condensation-like domainAnalysis of the cercosporin polyketide synthase CTB1 reveals a new fungal thioesterase functionMolecular modeling of the reaction pathway and hydride transfer reactions of HMG-CoA reductase.Development of Genetic Dereplication Strains in Aspergillus nidulans Results in the Discovery of Aspercryptin.Conserved biosynthetic pathways for phosalacine, bialaphos and newly discovered phosphonic acid natural products.Proteomics guided discovery of flavopeptins: anti-proliferative aldehydes synthesized by a reductase domain-containing non-ribosomal peptide synthetase.Thioesterase domains of fungal nonreducing polyketide synthases act as decision gates during combinatorial biosynthesis.A hybrid polyketide-nonribosomal peptide in nematodes that promotes larval survivalHarnessing the potential of halogenated natural product biosynthesis by mangrove-derived actinomycetes.Structural analysis of protein-protein interactions in type I polyketide synthases
P2860
Q24630070-4B3DCD30-5DF5-4478-91F6-9E89E9D9DAB8Q26738945-6961F4C2-32DF-4274-B20E-1DDBFE32CDC4Q27678223-63AC2CF1-663F-437E-981F-3347E7EE5318Q27682818-CAFBBA41-6694-4658-B304-1FF5F0123F47Q28538826-985FA509-589C-4E2F-AABB-E3ECDB22787FQ28650289-8778DA94-0458-4E09-83F4-7CE8CCC76708Q30781109-0B4F683D-68E8-448D-84DC-BD60D7EA40CDQ30884081-644F4A16-74A3-44B8-8BBF-3D3B273534F1Q31152705-7DA31226-E0B0-4EF6-9D50-E9F59A4A3739Q33751992-874B1DEC-D82C-4EBE-9F64-9ABF07105EA9Q33834252-3B04D739-F3A3-4C37-A8D4-D4FE6EB243D8Q34022733-28A76526-60F0-434E-B603-88DDF7A38AE8Q34082976-BFA37C34-B58E-4CE4-990F-58CA645CCA4EQ34122684-B3790DA1-4605-4E3D-B41B-F3749074A661Q34425191-A207AA80-AC3B-43B4-91FF-6639A721C136Q34782058-7D065ED8-F59B-40F1-A204-9DDF07093F6FQ34806456-296F9B0E-3B26-4763-9FF1-ED740166D186Q35006338-76D9251D-C697-4A12-9513-BFC4456FE543Q35232648-7120EA78-2952-48C3-AF2F-A0F855CA29F4Q35235074-DBCE8B07-BF8F-4681-89D1-652517C0864DQ35735860-DA487F7A-5A56-4FDE-B19F-750D52275E06Q35800038-6D05E6CF-220C-4CF9-AFD2-EAC8410E9EE8Q35906588-3BE2A81D-3CDC-4C6F-B6A4-659DC35F4327Q36000509-0D51E49F-3723-4B99-877E-71E26D597DDAQ36033311-0B146C54-3A06-4AED-A359-473BF3074A67Q36077749-CA6CCCBA-C4DF-49A5-BC46-9F5B6AD39426Q36104031-187D8971-0A35-4DE7-86E9-83909F0FBDD4Q36108894-28302078-45F3-4E45-AF9D-276C2C06F7E9Q36161540-D50CE179-4D4F-443D-BC65-EF1021343A5EQ36332051-ADEFDD61-F5A6-408D-89CD-7573C1C06D40Q36420193-BC7E1FE6-BFF5-4C32-ACDB-7BEC020C456DQ36421477-9568A0BF-0B94-4F76-A9AC-6FCA43F98D4AQ36467657-2AD0D328-EEA9-4FFA-B348-168B5EE794EBQ36494186-37C629F5-CA6C-4B0E-87C0-E893670F3023Q36515391-B75E64CE-22B0-4A98-B4AB-326EC1B596AEQ37119622-BC0C25B9-F9C0-4F4D-8400-4938573E72BFQ37191237-0FF281E4-E81B-47AD-B409-06E9E104ED6DQ37270504-A8110883-4BCA-40F8-B64F-F9F1DA546C7FQ37304016-63246462-20D1-47F9-85AD-55698C0E85A7Q37352218-1197E2E1-832D-4D28-B26E-89BFA916B566
P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 04 December 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
PKS and NRPS release mechanisms.
@en
PKS and NRPS release mechanisms.
@nl
type
label
PKS and NRPS release mechanisms.
@en
PKS and NRPS release mechanisms.
@nl
prefLabel
PKS and NRPS release mechanisms.
@en
PKS and NRPS release mechanisms.
@nl
P2860
P356
P1476
PKS and NRPS release mechanisms.
@en
P2093
Liangcheng Du
P2860
P304
P356
10.1039/B912037H
P577
2009-12-04T00:00:00Z