Kock, Iris

[["dc.bibliographiccitation.firstpage","530"],["dc.bibliographiccitation.issue","8"],["dc.bibliographiccitation.journal","The Journal of Antibiotics"],["dc.bibliographiccitation.lastpage","534"],["dc.bibliographiccitation.volume","58"],["dc.contributor.author","Kock, Iris"],["dc.contributor.author","Maskey, Rajendra P."],["dc.contributor.author","Biabani, MAF"],["dc.contributor.author","Helmke, Elisabeth"],["dc.contributor.author","Laatsch, Hartmut"],["dc.date.accessioned","2018-11-07T10:25:17Z"],["dc.date.available","2018-11-07T10:25:17Z"],["dc.date.issued","2005"],["dc.description.abstract","Cultivation of the marine-derived streptomycete isolate B8005 delivered three known antibiotics, resistomycin (1), resistoflavin (3a) and tetracenomycin (4), and a further member of the rare resistomycin class, the weakly antibiotically active 1-hydroxy-1-norresistomycin (2). From a related marine strain B4842, 1 and resistoflavin methyl ether (3b) have been isolated. The formation of 2 is of interest from a biosynthetic point of view."],["dc.identifier.isi","000231787100008"],["dc.identifier.pmid","16266127"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/42823"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Japan Antibiotics Research Assoc"],["dc.relation.issn","0021-8820"],["dc.title","1-hydroxy-1-norresistomycin and resistoflavin methyl ether: New antibiotics from marine-derived streptomycetes"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","87"],["dc.bibliographiccitation.issue","2-3"],["dc.bibliographiccitation.journal","Polymer Bulletin"],["dc.bibliographiccitation.lastpage","93"],["dc.bibliographiccitation.volume","49"],["dc.contributor.author","Maskey, Rajendra P."],["dc.contributor.author","Kock, Iris"],["dc.contributor.author","Shaaban, Mohamed"],["dc.contributor.author","Grun-Wollny, I."],["dc.contributor.author","Helmke, Elisabeth"],["dc.contributor.author","Mayer, F."],["dc.contributor.author","Wagner-Dobler, I."],["dc.contributor.author","Laatsch, Hartmut"],["dc.date.accessioned","2018-11-07T09:54:31Z"],["dc.date.available","2018-11-07T09:54:31Z"],["dc.date.issued","2002"],["dc.description.abstract","A new group of low-molecular weight channel-forming oligo(hydroxybutyric acids) (cPHBs, 1 with n = 8-30; main component MW approximate to 1300 dalton) was isolated from microorganisms of different origin. Inclusion bodies were electron-microscopically visible in cells in the state of autolysis, not. in cells in the exponential phase of growth.. cPHB and high-molecular poly(beta-hydroxybutyric acid) (sPHB) is cleaved by phenylethylamine and forms the corresponding monomeric hydroxybutyramide and - under drastic conditions, the crotylamide. One of these compounds; the 3-hydroxy-N-phenethyl-butyramide (5), was isolated as a new natural product now."],["dc.identifier.doi","10.1007/s00289-002-0084-1"],["dc.identifier.isi","000179671700001"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/36553"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Springer"],["dc.relation.issn","0170-0839"],["dc.title","Low molecular weight oligo-beta-hydroxybutyric acids and 3-hydroxy-N-phenethyl-butyramide - new products from microorganisms"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","692"],["dc.bibliographiccitation.issue","7"],["dc.bibliographiccitation.journal","Zeitschrift für Naturforschung B"],["dc.bibliographiccitation.lastpage","694"],["dc.bibliographiccitation.volume","58"],["dc.contributor.author","Maskey, Rajendra P."],["dc.contributor.author","Kock, Iris"],["dc.contributor.author","Helmke, Elisabeth"],["dc.contributor.author","Laatsch, Hartmut"],["dc.date.accessioned","2018-11-07T10:38:12Z"],["dc.date.available","2018-11-07T10:38:12Z"],["dc.date.issued","2003"],["dc.description.abstract","A new phenazine derivative, phenazostatin D (1a), was isolated from an extract of the actinomycete isolate Pseudonocardia sp. B6273 via a TLC-guided chemical screening. The structure of the compound was assigned by spectroscopic methods and found to be the meso-form of phenazostatin B (1b). Phenazostatin D was inactive against the tested bacteria and fungi. The strain also produced the known phenazine antibiotic methyl saphenate (2)."],["dc.identifier.isi","000185146400014"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/45756"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Verlag Z Naturforsch"],["dc.relation.issn","0932-0776"],["dc.title","Isolation and structure determination of phenazostatin D, a new phenazine from a marine actinomycete isolate Pseudonocardia sp B6273"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]