About: Biosynthesis of the antibiotic maduramicin. Origin of the carbon and oxygen atoms as well as the 13C NMR assignments

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About: Biosynthesis of the antibiotic maduramicin. Origin of the carbon and oxygen atoms as well as the 13C NMR assignments Goto Sponge NotDistinct Permalink

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scientific article published on 01 December 1984

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в грудні 1984 (uk) im Dezember 1984 veröffentlichter wissenschaftlicher Artikel (de) scientific article published on 01 December 1984 (en) artículu científicu espublizáu n'avientu de 1984 (ast)
publication date	wds:Q70755739-5514D053-5307-4C25-8C2B-D4660E604EAB
publication date	1984-12-01 00:00:00Z (xsd:dateTime)
cites work	wds:Q70755739-9ED83BB2-B83A-4A29-AD5B-C3AE5CC10DFC wds:Q70755739-A4AC7F59-4B2D-4DB1-AAC3-EF070AF660FA
cites work	Novel polyether antibiotics X-14868A, B, C, and D produced by a Nocardia. Discovery, fermentation, biological as well as ionophore properties and taxonomy of the producing culture. Studies on the ionophorous antibiotics. XXI. Structural elucidation of a new polyether antibiotic 6016 by application of the empirical rules in 13C-NMR spectroscopy
author name string	wds:Q70755739-1FA8805C-2254-4942-8B2D-23D70A3D4399 wds:Q70755739-26F55770-C26F-4EED-B24F-841EA62AF07C wds:Q70755739-5A38E51C-857D-4731-8CBE-530474F19A4A wds:Q70755739-607A30BB-1E41-421E-84E6-02AB560B28F4 wds:Q70755739-6C966441-46B0-45EE-BC3F-ACC801EFF66D wds:Q70755739-7EFB1EB6-9E54-42B1-B850-B56FA400CB07 wds:Q70755739-9E89A8AE-F21D-47BD-A40E-52E072B45425 wds:Q70755739-AB1144BD-6EA1-4768-8C3E-647AF390D138 wds:Q70755739-E1AF29CF-1332-4D87-94DC-31E076C4ED9D
author name string	S Rajan R Fiala J H Martin J C James D B Borders M W Bullock G O Morton P C Mowery H Tsou
rdfs:label	Biosynthesis of the antibiotic maduramicin. Origin of the carbon and oxygen atoms as well as the 13C NMR assignments (en) Biosynthesis of the antibiotic maduramicin. Origin of the carbon and oxygen atoms as well as the 13C NMR assignments (nl)
skos:prefLabel	Biosynthesis of the antibiotic maduramicin. Origin of the carbon and oxygen atoms as well as the 13C NMR assignments (en) Biosynthesis of the antibiotic maduramicin. Origin of the carbon and oxygen atoms as well as the 13C NMR assignments (nl)
name	Biosynthesis of the antibiotic maduramicin. Origin of the carbon and oxygen atoms as well as the 13C NMR assignments (en) Biosynthesis of the antibiotic maduramicin. Origin of the carbon and oxygen atoms as well as the 13C NMR assignments (nl)
title	wds:Q70755739-A081128C-60A8-4B0B-9A51-22CF8319AF15
title	Biosynthesis of the antibiotic maduramicin. Origin of the carbon and oxygen atoms as well as the 13C NMR assignments (en)
page(s)	wds:Q70755739-2AE41695-E2E9-4016-956E-1FE6A0763406
page(s)	1651-1663
instance of	wds:Q70755739-35C9AB6E-88BC-4852-AF41-DE06867018F2
instance of	scholarly article
PubMed ID	wds:Q70755739-726A8405-3B97-4D74-844D-77C3437D2262
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/6526733
PubMed ID	6526733
published in	wds:Q70755739-EC79BBEF-A342-4276-9284-4D0B2EEC68BD
published in	The Journal of Antibiotics
issue	wds:Q70755739-3279462A-587A-4263-8253-C2A0AF967325
volume	wds:Q70755739-1A977856-C02C-4AB1-BDAE-B8978285F7CD
issue	12
volume	37
DOI	wds:Q70755739-4FAD3EB1-04C4-4C6A-8AE3-CF14982A0808
DOI	http://dx.doi.org/10.7164/ANTIBIOTICS.37.1651
DOI	10.7164/ANTIBIOTICS.37.1651
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q70755739
is cites work of	Biosynthesis of the polyether antibiotic narasin origins of the oxygen atoms and the mechanisms of ring formation A comprehensive review of glycosylated bacterial natural products. Anticoccidial evaluation of halofuginone, lasalocid, maduramicin, monensin and salinomycin Selection of a specifically blocked mutant of Streptomyces cinnamonensis: isolation and synthesis of 26-deoxymonensin A The utilization of molecular oxygen during the biosynthesis of maduramicin. Maduramicin inhibits proliferation and induces apoptosis in myoblast cells Isolation and characterization of three novel polyether antibiotics and three novel actinomycins as cometabolites of the same Streptomyces sp. X-14873, ATCC 31679 Astonishing diversity of natural surfactants: 2. Polyether glycosidic ionophores and macrocyclic glycosides Antibiotic biosynthesis Chemical and Biochemical Aspects of Polyether-Ionophore Antibiotic Biosynthesis
is cites work of	wds:Q68985543-852398A5-7021-4B54-9F92-551B68D6DB66 wds:Q68427202-50355046-BAAE-4176-8C43-794EDB0CE204 wds:Q36929109-9539C4E4-DB41-422E-A66C-0AEAB8D1F1FF wds:Q79144072-8DAF3BEA-5BB9-4362-9206-0A79B718F4C1 wds:Q36029831-E6E91517-817A-4BC3-9AA4-6A1A2551AAA0 wds:Q36163711-46BF89B7-93EF-40F5-9201-F66C418BEAA1 wds:Q35532104-342D82B2-5F8A-4AD2-8243-E6B4D25BE6EA wds:Q43761646-E607C17B-EF09-4CB1-B6A4-EDC6770D1603 wds:Q105286470-FB8CFD6D-2989-4E51-A22B-591BCE21337D wds:Q69666430-7B0DE13C-6818-4930-8E4D-F56D3EF2D176

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