記事
Biomolecular chemistry heterologous production of asperipin-2a: proposal for sequential oxidative macrocyclization
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CiNii Research
Biomolecular chemistry heterologous production of asperipin-2a: proposal for sequential oxidative macrocyclization
- 資料種別
- 記事
- 著者
- Ye, Yingほか
- 出版者
- Royal Society of Chemistry
- 出版年
- 2019-01-07
- 資料形態
- デジタル
- 掲載誌名
- Organic & biomolecular chemistry 17 1
- 掲載ページ
- p.39-43
資料詳細
要約等:
- Asperipin-2a is a ribosomally synthesized and post-translationally modified peptide isolated from Asperigillus flavus. Herein, we report the heterolog...
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デジタル
- 資料種別
- 記事
- 著者標目
- 出版年月日等
- 2019-01-07
- 出版年(W3CDTF)
- 2019-01-07
- タイトル(掲載誌)
- Organic & biomolecular chemistry
- 巻号年月日等(掲載誌)
- 17 1
- 掲載巻
- 17
- 掲載号
- 1
- 掲載ページ
- 39-43
- 掲載年月日(W3CDTF)
- 2019-01-07
- ISSN(掲載誌)
- 14770520
- 出版事項(掲載誌)
- Royal Society of Chemistry
- 本文の言語コード
- en
- 対象利用者
- 一般
- 標準番号(その他)
- HDL : http://hdl.handle.net/2115/76469
- DOI
- 10.1039/c8ob02824a
- オンライン閲覧公開範囲
- インターネット公開
- 参照
- Biosynthesis of Cyclochlorotine: Identification of the Genes Involved in Oxidative Transformations and Intramolecular <i>O</i>,<i>N</i>-TransacylationUstiloxin biosynthetic machinery is not compatible between Aspergillus flavus and Ustilaginoidea virensNew developments in RiPP discovery, enzymology and engineeringPromoter tools for further development of Aspergillus oryzae as a platform for fungal secondary metabolite productionPeptides derived from Kex2-processed repeat proteins are widely distributed and highly diverse in the Fungi kingdomHow to improve the production of peptidyl compounds in filamentous fungiBiosynthetic Studies of Phomopsins Unveil Posttranslational Installation of Dehydroamino Acids by UstYa Family Proteins真核生物由来リボソーム環状ペプチド研究の最前線
- 参照
- Unveiling the Biosynthetic Pathway of the Ribosomally Synthesized and Post‐translationally Modified Peptide Ustiloxin B in Filamentous FungiRapid Reconstitution of Biosynthetic Machinery for Fungal Metabolites in <i>Aspergillus oryzae</i>: Total Biosynthesis of AflatremClass of cyclic ribosomal peptide synthetic genes in filamentous fungiHeterologous expression of highly reducing polyketide synthase involved in betaenone biosynthesisUstiloxins, fungal cyclic peptides, are ribosomally synthesized in <i>Ustilaginoidea virens</i>Expression of ustR and the Golgi protease KexB are required for ustiloxin B biosynthesis in Aspergillus oryzaeA Nonempirical Method Using LC/MS for Determination of the Absolute Configuration of Constituent Amino Acids in a Peptide: Elucidation of Limitations of Marfey's Method and of Its Separation MechanismRibosomally synthesized and post-translationally modified peptide natural products: overview and recommendations for a universal nomenclatureA Cyclopeptide and a Tetrahydroisoquinoline Alkaloid from <i>Ophiorrhiza nutans</i>Gene family encoding the major toxins of lethal <i>Amanita</i> mushroomsA Nonempirical Method Using LC/MS for Determination of the Absolute Configuration of Constituent Amino Acids in a Peptide: Combination of Marfey's Method with Mass Spectrometry and Its Practical ApplicationMIDDAS-M: Motif-Independent De Novo Detection of Secondary Metabolite Gene Clusters through the Integration of Genome Sequencing and Transcriptome DataA Self‐Sacrificing <i>N</i>‐Methyltransferase Is the Precursor of the Fungal Natural Product OmphalotinBiosynthetic investigation of phomopsins reveals a widespread pathway for ribosomal natural products in AscomycetesA novel family of cyclic oligopeptides derived from ribosomal peptide synthesis of an in planta-induced gene, gigA, in Epichloë endophytes of grassesDetermination ofD-amino acids. II. Use of a bifunctional reagent, 1,5-difluoro-2,4-dinitrobenzeneAlkaloide aus rhamnaceen, V franganin und frangufolin, zwei weitere peptid-alkaloide aus L.Strained cyclophane natural products: Macrocyclization at its limitsCharacterization of the biosynthetic gene cluster for the ribosomally synthesized cyclic peptide ustiloxin B in Aspergillus flavusAlkaioide aus sterculiaceen, IAutocatalytic backbone N-methylation in a family of ribosomal peptide natural products
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- NII論文ID
- 120006776812