Recent highlights in biosynthesis research using stable isotopesHedycaryol synthase in complex with nerolidol reveals terpene cyclase mechanismInduced-fit mechanism in class I terpene cyclasesIdentification and characterization of a periplasmic aminoacyl-phosphatidylglycerol hydrolase responsible for Pseudomonas aeruginosa lipid homeostasisBiochemistry and Crystal Structure of Ectoine Synthase: A Metal-Containing Member of the Cupin SuperfamilyComparative "Omics" of the Fusarium fujikuroi Species Complex Highlights Differences in Genetic Potential and Metabolite Synthesis.Experimental and Theoretical Studies on Corvol Ether Biosynthesis.Mechanistic investigations on six bacterial terpene cyclasesTerpenoids are widespread in actinomycetes: a correlation of secondary metabolism and genome data.The Sfp-type 4'-phosphopantetheinyl transferase Ppt1 of Fusarium fujikuroi controls development, secondary metabolism and pathogenicity.Genome mining of Streptomyces ambofaciens.Volatile terpenes from actinomycetes: a biosynthetic study correlating chemical analyses to genome data.Bacterial volatiles: the smell of small organisms.Terpene synthase genes in eukaryotes beyond plants and fungi: Occurrence in social amoebae.[(2)H26]-1-epi-Cubenol, a completely deuterated natural product from Streptomyces griseusQuorum sensing and bacterial biofilms.Isoprenoids in three-dimensional space: the stereochemistry of terpene biosynthesis.Capturing volatile natural products by mass spectrometry.The chemical biology of dimethylsulfoniopropionate.Bacterial terpene cyclases.Chemical differentiation of three DMSP lyases from the marine Roseobacter group.Fungal volatiles - a survey from edible mushrooms to moulds.The Ecological Role of Volatile and Soluble Secondary Metabolites Produced by Soil Bacteria.The EIMS fragmentation mechanisms of the sesquiterpenes corvol ethers A and B, epi-cubebol and isodauc-8-en-11-ol.Biosynthesis and function of secondary metabolites.Novel fatty acid methyl esters from the actinomycete Micromonospora aurantiaca.Two separate key enzymes and two pathway-specific transcription factors are involved in fusaric acid biosynthesis in Fusarium fujikuroi.antiSMASH 4.0-improvements in chemistry prediction and gene cluster boundary identification.Conformational Analysis, Thermal Rearrangement, and EI-MS Fragmentation Mechanism of (1(10)E,4E,6S,7R)-Germacradien-6-ol by (13)C-Labeling Experiments.The AngFus3 Mitogen-Activated Protein Kinase Controls Hyphal Differentiation and Secondary Metabolism in Aspergillus niger.Structural Revision and Elucidation of the Biosynthesis of Hypodoratoxide by (13) C,(13) C COSY NMR Spectroscopy.Volatiles from nineteen recently genome sequenced actinomycetes.Streptopyridines, volatile pyridine alkaloids produced by Streptomyces sp. FORM5.18-Hydroxydolabella-3,7-diene synthase - a diterpene synthase from Chitinophaga pinensis.Algicidal lactones from the marine Roseobacter clade bacterium Ruegeria pomeroyi.A detailed view on 1,8-cineol biosynthesis by Streptomyces clavuligerus.Natural products in synthesis and biosynthesis.Biological activity of volatiles from marine and terrestrial bacteriaIsotopically labeled sulfur compounds and synthetic selenium and tellurium analogues to study sulfur metabolism in marine bacteria.Genetic analysis of the upper phenylacetate catabolic pathway in the production of tropodithietic acid by Phaeobacter gallaeciensis
P50
Q26770626-DB87564F-CF5D-4100-91F3-2AD63B0ED111Q27688099-E05FCB20-5B77-4103-A30F-5602F40FE521Q27690639-280AD83B-B1BA-425C-A1AA-20C45BE68C2EQ28492987-EF0D0D8C-9CA1-4F03-B719-5F85BE1751DDQ28550791-54F9C23F-8925-45CC-B033-8D593F508307Q28818303-FC90B652-C9D6-47E9-9EA0-1250AA36373CQ31030129-DB54F367-52B5-4620-B407-6EE7E571316BQ31141683-4D0DFCDF-CCE3-4D75-8228-2212CAC004CEQ34115976-F42FFB23-C4D9-4BE7-A1E1-7E34F5F105D8Q34291040-C189E5E4-A081-405F-8C39-9E0984875923Q34386573-83C52C9A-F755-4EF0-A6DE-A095EA9BE3ABQ35045304-C5D68713-64C1-4AA4-ABF4-33F9EAD1D905Q36892012-80B941EF-0E1F-4AC8-A22A-576558636DF8Q37379799-0D38DFB5-A295-46C7-B2B2-4AAAF210E095Q37406339-26646E8F-8CD1-46F0-ACBB-DEACB1D32B94Q37697576-9878808C-982A-4E94-995D-165A5F700533Q37943241-1800DAEC-4EDA-47BC-AA81-5F0F476C24F6Q38190402-A2B3FAF2-CEEC-4315-B076-EC8F82B31137Q38305499-0C8959E4-7B76-4C71-81EE-7D8946C19BC9Q38632052-1AD9D8EF-0214-4A7B-9A16-2B77A0EBC6E0Q38796303-8C29CA82-0346-4D3B-911E-FA8BD004FD86Q38958139-AF5CBCE0-5B63-4C77-84D0-D715A558DA59Q39063223-11F2F5EF-A308-408E-9017-97E827C74A87Q39455223-0993F1DB-2CF8-49B6-B9F8-C79C6D2AC27CQ40214274-799FE4A8-2474-4D83-94EB-114AC73BE03BQ40214602-064A32E1-DBF0-41FD-A129-6E63B12007A0Q40216446-6B902C98-C777-4898-85B0-55D022184E0BQ40231155-576639A8-5070-4559-91AD-7CCD962E179FQ40549126-A47A07E4-FCFF-4440-8F54-43D6D04E573FQ41048766-07F710D5-FE32-4D7F-97D4-8600CC45A756Q41069472-5DFFFE28-4DF2-4CB1-846F-BF5BBD652493Q41588119-5D0BD19D-DB14-4D90-AE27-160BAF584833Q41589057-2853296B-338B-4393-97DA-A8FDACA80196Q41595476-EC932371-ED88-4759-BBF5-250BDBC5CEDEQ41860728-5FEA6779-CC46-4481-BBB2-4262038A7406Q41915006-18B4398C-2DCB-4B78-AC5E-C624D2108FA7Q42107315-70D5BE90-7E94-4B47-A278-55E09B9BAD55Q42117267-40CA4E5C-0865-43F9-B48F-55FB2BFE8409Q42149323-10EA2EE5-244D-4C88-AF47-EC9B91077661Q42151213-352F8F32-0A60-409A-B107-514E589518E1
P50
description
deutscher Chemiker und Hochschullehrer
@de
scheikundige
@nl
name
Jeroen S. Dickschat
@ast
Jeroen S. Dickschat
@de
Jeroen S. Dickschat
@es
Jeroen S. Dickschat
@nl
type
label
Jeroen S. Dickschat
@ast
Jeroen S. Dickschat
@de
Jeroen S. Dickschat
@es
Jeroen S. Dickschat
@nl
prefLabel
Jeroen S. Dickschat
@ast
Jeroen S. Dickschat
@de
Jeroen S. Dickschat
@es
Jeroen S. Dickschat
@nl
P214
P227
P106
P19
P21
P214
P227
P31
P569
1977-06-03T00:00:00Z
P7859
viaf-47868034