About: Isolation and structure of a new antibiotic, indolizomycin, produced by a strain SK2-52 obtained by interspecies fusion treatment

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About: Isolation and structure of a new antibiotic, indolizomycin, produced by a strain SK2-52 obtained by interspecies fusion treatment Goto Sponge NotDistinct Permalink

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scientific article published on 01 November 1984

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в листопаді 1984 (uk) im November 1984 veröffentlichter wissenschaftlicher Artikel (de) scientific article published on 01 November 1984 (en) artículu científicu espublizáu en payares de 1984 (ast)
publication date	wds:Q70817559-195F7119-8868-4AC4-AEE4-298677D11BEA
publication date	1984-11-01 00:00:00Z (xsd:dateTime)
access restriction status	wds:Q70817559-1D9A19A4-B539-429C-828A-21D971E99542
access restriction status	open access
author name string	wds:Q70817559-1171BC0E-DD85-407B-9A66-B246A0878933 wds:Q70817559-1EA6B012-6EAC-499F-9BD1-FBB3F2B58C90 wds:Q70817559-46131695-D46A-4389-9CD2-D96EBF366B4C wds:Q70817559-49A8B246-E78C-4547-A038-4F9DEDE0089F wds:Q70817559-78801205-043B-4B9E-AEB9-1E8F2A17CF43 wds:Q70817559-8DD08234-AEC0-4C5F-8114-20D1014F3B23 wds:Q70817559-B6679FCA-038B-433E-AC2B-60114167BAE2 wds:Q70817559-D2E6402E-12EA-4A42-85B5-8112EF7640F2 wds:Q70817559-DDB37069-C030-48A7-8413-564B27CA5206 wds:Q70817559-F2F0DBED-4C6A-4E16-8DD0-C4388F89B9C8
author name string	H Nakamura K Hotta S Gomi Y Okami S Kondo D Ikeda F Yamashita H Umezawa H Naganawa Y Iitaka
rdfs:label	Isolation and structure of a new antibiotic, indolizomycin, produced by a strain SK2-52 obtained by interspecies fusion treatment (en) Isolation and structure of a new antibiotic, indolizomycin, produced by a strain SK2-52 obtained by interspecies fusion treatment (nl)
skos:prefLabel	Isolation and structure of a new antibiotic, indolizomycin, produced by a strain SK2-52 obtained by interspecies fusion treatment (en) Isolation and structure of a new antibiotic, indolizomycin, produced by a strain SK2-52 obtained by interspecies fusion treatment (nl)
name	Isolation and structure of a new antibiotic, indolizomycin, produced by a strain SK2-52 obtained by interspecies fusion treatment (en) Isolation and structure of a new antibiotic, indolizomycin, produced by a strain SK2-52 obtained by interspecies fusion treatment (nl)
title	wds:Q70817559-805E9CE2-277C-497F-A7FE-76054979D286
title	Isolation and structure of a new antibiotic, indolizomycin, produced by a strain SK2-52 obtained by interspecies fusion treatment (en)
page(s)	wds:Q70817559-E67F03EE-D1B8-43B7-ABDB-616E74E2F189
page(s)	1491-1494
instance of	wds:Q70817559-0D1898B9-B468-4C6F-BE55-6C8AC1295452
instance of	scholarly article
main subject	wds:Q70817559-015F91F4-DB1D-4D5F-9505-307BE64EE84B wds:Q70817559-49629F96-F5CF-4959-9297-A59ACC9EC7B4
main subject	Streptomyces griseus Indolizomycin
PubMed ID	wds:Q70817559-22907964-C311-4C96-87A6-EE9EC49B3692
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/6549003
PubMed ID	6549003
published in	wds:Q70817559-E046811C-66BD-4B10-BA9E-FC56F2C636B9
full work available at URL	wds:Q70817559-C754C7C3-6472-4B05-916C-28E41349B911
published in	The Journal of Antibiotics
full work available at URL	https://www.jstage.jst.go.jp/article/antibiotics1968/37/11/37_11_1491/_pdf
issue	wds:Q70817559-8F930761-D939-4CF6-941D-78CA4F6D590B
volume	wds:Q70817559-F08B9A09-A373-4C71-B6EC-CBE5E5DF5FB0
issue	11
volume	37
DOI	wds:Q70817559-6F9345AC-9CF4-4172-8D21-831EE29094D1
DOI	http://dx.doi.org/10.7164/ANTIBIOTICS.37.1491
DOI	10.7164/ANTIBIOTICS.37.1491
online access status	wds:Q70817559-41EB2681-74EF-40EA-9AE8-0968C4ADDAE7
online access status	open access
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q70817559
is cites work of	Recombinant organisms for production of industrial products Small molecule natural products in the discovery of therapeutic agents: the synthesis connection Genetic improvement of processes yielding microbial products Biosynthesis and Metabolism of Cyclopropane Rings in Natural Compounds Production of novel antibiotic, dopsisamine, by a new subspecies of Nocardiopsis mutabilis with multiple antibiotic resistance. Identification of the Polyketide Biosynthetic Machinery for the Indolizidine Alkaloid Cyclizidine Total synthesis of (+)-ent-cyclizidine: absolute configurational confirmation of antibiotic M146791 Iminimycin A, the new iminium metabolite produced by Streptomyces griseus OS-3601. Drug discovery and development through the genetic engineering of antibiotic-producing microorganisms Mutants of Streptomyces roseosporus that express enhanced recombination within partially homologous genes. Intramolecular alkynylcyclopropanation of olefins catalyzed by Bi(OTf)3: stereoselective synthesis of 1-alkynyl-3-azabicyclo[3.1.0]hexanes Efficient synthesis of cyclopropane-fused heterocycles with bromoethylsulfonium salt Enantioselective C-H Functionalization-Addition Sequence Delivers Densely Substituted 3-Azabicyclo[3.1.0]hexanes. Thioester reduction and aldehyde transamination are universal steps in actinobacterial polyketide alkaloid biosynthesis Deciphering Piperidine Formation in Polyketide-Derived Indolizidines Reveals a Thioester Reduction, Transamination, and Unusual Imine Reduction Process. Simple indolizidine and quinolizidine alkaloids Cyclizidine-Type Alkaloids from Streptomyces sp. HNA39. Nitrosopyridine probe to detect polyketide natural products with conjugated alkenes: Discovery of novodaryamide and nocarditriene Use of Permanent Wall-Deficient Cells as a System for the Discovery of New-to-Nature Metabolites New antibiotic-producing streptomycetes, selected by antibiotic resistance as a marker. I. New antibiotic production generated by protoplast fusion treatment between Streptomyces griseus and S. tenjimariensis Essential role of genetics in the advancement of biotechnology Efficient synthesis of substituted 3-azabicyclo[3.1.0]hexan-2-ones from 2-iodocyclopropanecarboxamides using a copper-free Sonogashira coupling Prospects for the discovery of new (hybrid) antibiotics by genetic engineering of antibiotic-producing bacteria Novel synthesis of 3-azabicyclo[3.1.0]hexanes by unusual palladium(0)-catalyzed cyclopropanation of allenenes Pyridoxal phosphate-dependent reactions in the biosynthesis of natural products Protoplast fusion: a tool for intergeneric gene transfer in bacteria. Search for new compounds from Kitasato microbial library by physicochemical screening Absolute configuration of iminimycin B, a new indolizidine alkaloid, from Streptomyces griseus OS-3601 Biological methods for studying the biosynthesis of natural products Discovery of novel bioactive natural products driven by genome mining Natural products from thioester reductase containing biosynthetic pathways Biologically active indolizidine alkaloids Identification and Analysis of the Biosynthetic Gene Cluster for the Indolizidine Alkaloid Iminimycin in Streptomyces griseus A Systematic Review of Recently Reported Marine Derived Natural Product Kinase Inhibitors Direct cyclopropanation of activated N-heteroarenes via site- and stereoselective dearomative reactions Silver oxide mediated novel SET oxidative cyclization: stereoselective synthesis of 3-azabicyclo[n.1.0]alkanes Advancement of Biotechnology by Genetic Modifications

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