Acetylaszonalenin biosynthesis in Neosartorya fischeri. Identification of the biosynthetic gene cluster by genomic mining and functional proof of the genes by biochemical investigation.
about
Extrolites of Aspergillus fumigatus and Other Pathogenic Species in Aspergillus Section FumigatiRecent advances in genome mining of secondary metabolites in Aspergillus terreusAdvances in Aspergillus secondary metabolite research in the post-genomic eraThe tRNA-dependent biosynthesis of modified cyclic dipeptidesBiosynthesis of fungal indole alkaloidsThe structure of dimethylallyl tryptophan synthase reveals a common architecture of aromatic prenyltransferases in fungi and bacteriaStructure-Based Engineering Increased the Catalytic Turnover Rate of a Novel Phenazine PrenyltransferaseAn enzyme catalyzing O-prenylation of the glucose moiety of fusicoccin A, a diterpene glucoside produced by the fungus Phomopsis amygdaliNonribosomal peptide synthetase genes pesL and pes1 are essential for Fumigaclavine C production in Aspergillus fumigatusAnthranilate-activating modules from fungal nonribosomal peptide assembly linesFungal indole alkaloid biosynthesis: genetic and biochemical investigation of the tryptoquialanine pathway in Penicillium aethiopicumAminobenzoates as building blocks for natural product assembly lines.Deletion and gene expression analyses define the paxilline biosynthetic gene cluster in Penicillium paxilli.Enzymatic processing of fumiquinazoline F: a tandem oxidative-acylation strategy for the generation of multicyclic scaffolds in fungal indole alkaloid biosynthesis.A branched biosynthetic pathway is involved in production of roquefortine and related compounds in Penicillium chrysogenum.Expression, purification, crystallization and crystallographic study of the Aspergillus terreus aromatic prenyltransferase AtaPT.The 3,4-dioxygenated 5-hydroxy-4-aryl-quinolin-2(1H)-one alkaloids. Results of 20 years of research, uncovering a new family of natural products.Comparative genomics reveals high biological diversity and specific adaptations in the industrially and medically important fungal genus Aspergillus.Cyclization of fungal nonribosomal peptides by a terminal condensation-like domainAn iterative, bimodular nonribosomal peptide synthetase that converts anthranilate and tryptophan into tetracyclic asperlicins.New Cyclotetrapeptides and a New Diketopiperzine Derivative from the Marine Sponge-Associated Fungus Neosartorya glabra KUFA 0702.Short pathways to complexity generation: fungal peptidyl alkaloid multicyclic scaffolds from anthranilate building blocks.Application of an efficient gene targeting system linking secondary metabolites to their biosynthetic genes in Aspergillus terreus.Regiospecificities and prenylation mode specificities of the fungal indole diterpene prenyltransferases AtmD and PaxD.Characterization of cyclo-acetoacetyl-L-tryptophan dimethylallyltransferase in cyclopiazonic acid biosynthesis: substrate promiscuity and site directed mutagenesis studies.Prenylated indole derivatives from fungi: structure diversity, biological activities, biosynthesis and chemoenzymatic synthesis.Characterization and Engineering of the Adenylation Domain of a NRPS-Like Protein: A Potential Biocatalyst for Aldehyde Generation.Bioactive compounds synthesized by non-ribosomal peptide synthetases and type-I polyketide synthases discovered through genome-mining and metagenomics.The nonribosomal synthesis of diketopiperazines in tRNA-dependent cyclodipeptide synthase pathways.Tentative biosynthetic pathways of some microbial diketopiperazines.New insights into the echinocandins and other fungal non-ribosomal peptides and peptaibiotics.Mechanistic studies on the indole prenyltransferases.Prenyltransferases as key enzymes in primary and secondary metabolism.Impacts and perspectives of prenyltransferases of the DMATS superfamily for use in biotechnology.Oxidative Cyclization in Natural Product BiosynthesisElucidation of biosynthetic pathways of natural products.Two new asterriquinols from Aspergillus sp. CBS-P-2 with anti-inflammatory activity.Complexity generation in fungal peptidyl alkaloid biosynthesis: a two-enzyme pathway to the hexacyclic MDR export pump inhibitor ardeeminBiochemical characterization of indole prenyltransferases: filling the last gap of prenylation positions by a 5-dimethylallyltryptophan synthase from Aspergillus clavatusSynergism between genome sequencing, tandem mass spectrometry and bio-inspired synthesis reveals insights into nocardioazine B biogenesis.
P2860
Q26771471-4C10AA57-EDD5-409B-A4B8-6C797C8F4ACAQ26822407-320BC2AE-763D-4D56-BC5B-58C6CC5EABCAQ26823169-8C06E824-3661-4DE8-9396-D2C59A9DD7A3Q26850935-A0B4D6E2-C8BF-4E81-AFD6-4238E271335DQ27021412-309CAAD0-EA1A-482C-844A-CC021BFCD026Q27657177-17098218-1736-4868-BACB-B8267009DFD8Q27674945-7B643A59-BC63-42B4-90E8-5009DEDE81DBQ28258411-AFAE50DD-E9ED-4963-87A4-E28731F01671Q28384102-AF8B3996-9F4F-45C4-916F-B9693462B817Q33787584-C98E4F22-22D9-4D48-97A5-15DB146A0079Q34163017-5BD735C4-76E3-4995-A738-F8A06F5EF2EEQ34230699-4F417531-5B02-44A2-A213-DAEBEA006499Q34364254-776920B0-1EFA-4BFA-9CDC-6528F6E6A138Q34425191-EFADA78B-0ECA-4584-B7EB-FF0CBBDB4761Q34775672-2A3C5B21-ED46-4E54-B857-A01B493BDA9CQ35841524-4378E586-6089-4BEF-8F0D-A54D1676D2FBQ36156035-D2AFC1EE-51ED-4DBB-9758-88FB758FA61BQ36280437-42C8C356-5773-4DB9-8E0E-DDBE9D51C20DQ36420193-81CF2DEB-7211-461B-B0BC-FCFD9A4AEE24Q37058187-C09100D3-7821-4A75-A877-BA7C8D1FFA64Q37128427-6EBA65C5-A0FE-4863-9CC7-173A17E4F5D7Q37228644-B6DDA625-65A5-4436-8EA1-015BB9CCA940Q37323144-69C67A17-A74C-4E15-9B0B-C138752A2847Q37335423-127E2244-D1D1-4715-B688-B9B9E41E2931Q37439644-3A609C78-F192-425C-853F-E2713ABC5420Q37660095-19BF44A6-CF37-4966-81F7-A09526DB7871Q37701004-CF594B07-AE75-4BE5-86C8-8A072277B62FQ38000475-B3767A0C-4434-41CC-A471-80504008DE4EQ38023179-DB56D685-9E26-433C-A335-759F0AD0779DQ38129759-6D07135E-E88C-4C60-87E1-312EB57D5AF3Q38243255-835BCFEC-9938-4961-8FBC-BD2266423907Q38255721-6395C08A-8787-4CEE-86A6-046C6D496F45Q38555536-6E97CB01-FE28-4316-A2C5-555DDC4B414FQ38557858-4A8EFA72-8549-4F49-A7A3-3904FCB354E2Q39034361-9036D44F-918E-42CE-B627-9801C2018DE3Q39226283-1634E888-1545-437D-ABD0-2F2B3EF2EAB0Q39911727-C9BC4302-5BEB-4B08-8DA1-A26F9352610CQ39972234-6448663B-400D-4323-BD4F-34C253C7B5E8Q40355408-8C9DB932-D58B-4252-B7FF-5C3AE95814F4Q41196740-2C5F84CE-4257-4DDC-8C3C-753578561D2B
P2860
Acetylaszonalenin biosynthesis in Neosartorya fischeri. Identification of the biosynthetic gene cluster by genomic mining and functional proof of the genes by biochemical investigation.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh
2008年學術文章
@zh-hant
name
Acetylaszonalenin biosynthesis ...... by biochemical investigation.
@en
Acetylaszonalenin biosynthesis ...... by biochemical investigation.
@nl
type
label
Acetylaszonalenin biosynthesis ...... by biochemical investigation.
@en
Acetylaszonalenin biosynthesis ...... by biochemical investigation.
@nl
prefLabel
Acetylaszonalenin biosynthesis ...... by biochemical investigation.
@en
Acetylaszonalenin biosynthesis ...... by biochemical investigation.
@nl
P2093
P2860
P356
P1476
Acetylaszonalenin biosynthesis ...... by biochemical investigation.
@en
P2093
Alexander Grundmann
Shu-Ming Li
Wen-Bing Yin
P2860
P304
P356
10.1074/JBC.M807606200
P407
P577
2008-11-10T00:00:00Z