| pubmed-article:21568297 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:21568297 | lifeskim:mentions | umls-concept:C0314911 | lld:lifeskim |
| pubmed-article:21568297 | lifeskim:mentions | umls-concept:C0030004 | lld:lifeskim |
| pubmed-article:21568297 | lifeskim:mentions | umls-concept:C0030956 | lld:lifeskim |
| pubmed-article:21568297 | lifeskim:mentions | umls-concept:C0039859 | lld:lifeskim |
| pubmed-article:21568297 | lifeskim:mentions | umls-concept:C1883254 | lld:lifeskim |
| pubmed-article:21568297 | lifeskim:mentions | umls-concept:C0678594 | lld:lifeskim |
| pubmed-article:21568297 | pubmed:issue | 12 | lld:pubmed |
| pubmed-article:21568297 | pubmed:dateCreated | 2011-6-10 | lld:pubmed |
| pubmed-article:21568297 | pubmed:abstractText | The structures of the ribosomally synthesized peptide antibiotics from Bacillus amyloliquefaciens FZB42, plantazolicin A and B, have been elucidated by high resolving ESI-MSMS, 2D (1)H-(13)C-correlated NMR spectroscopy as well as (1)H-(15)N-HMQC/(1)H-(15)N-HMBC NMR experiments. (15)N-labeling prior to the experiments facilitated the structure determination, unveiling a hitherto unusual number of thiazoles and oxazoles formed from a linear 14mer precursor peptide. This finding further extends the number of known secondary metabolites from B. amyloliquefaciens and represents a new type of secondary metabolites from the genus Bacillus. | lld:pubmed |
| pubmed-article:21568297 | pubmed:language | eng | lld:pubmed |
| pubmed-article:21568297 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21568297 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:21568297 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21568297 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21568297 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21568297 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21568297 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:21568297 | pubmed:month | Jun | lld:pubmed |
| pubmed-article:21568297 | pubmed:issn | 1523-7052 | lld:pubmed |
| pubmed-article:21568297 | pubmed:author | pubmed-author:SüssmuthRoder... | lld:pubmed |
| pubmed-article:21568297 | pubmed:author | pubmed-author:BorrissRainer... | lld:pubmed |
| pubmed-article:21568297 | pubmed:author | pubmed-author:VaterJoachimJ | lld:pubmed |
| pubmed-article:21568297 | pubmed:author | pubmed-author:ScholzRomyR | lld:pubmed |
| pubmed-article:21568297 | pubmed:author | pubmed-author:NachtigallJon... | lld:pubmed |
| pubmed-article:21568297 | pubmed:author | pubmed-author:HelalySoleima... | lld:pubmed |
| pubmed-article:21568297 | pubmed:author | pubmed-author:KalyonBaharB | lld:pubmed |
| pubmed-article:21568297 | pubmed:copyrightInfo | © 2011 American Chemical Society | lld:pubmed |
| pubmed-article:21568297 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:21568297 | pubmed:day | 17 | lld:pubmed |
| pubmed-article:21568297 | pubmed:volume | 13 | lld:pubmed |
| pubmed-article:21568297 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:21568297 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:21568297 | pubmed:pagination | 2996-9 | lld:pubmed |
| pubmed-article:21568297 | pubmed:meshHeading | pubmed-meshheading:21568297... | lld:pubmed |
| pubmed-article:21568297 | pubmed:meshHeading | pubmed-meshheading:21568297... | lld:pubmed |
| pubmed-article:21568297 | pubmed:meshHeading | pubmed-meshheading:21568297... | lld:pubmed |
| pubmed-article:21568297 | pubmed:meshHeading | pubmed-meshheading:21568297... | lld:pubmed |
| pubmed-article:21568297 | pubmed:meshHeading | pubmed-meshheading:21568297... | lld:pubmed |
| pubmed-article:21568297 | pubmed:meshHeading | pubmed-meshheading:21568297... | lld:pubmed |
| pubmed-article:21568297 | pubmed:meshHeading | pubmed-meshheading:21568297... | lld:pubmed |
| pubmed-article:21568297 | pubmed:meshHeading | pubmed-meshheading:21568297... | lld:pubmed |
| pubmed-article:21568297 | pubmed:meshHeading | pubmed-meshheading:21568297... | lld:pubmed |
| pubmed-article:21568297 | pubmed:year | 2011 | lld:pubmed |
| pubmed-article:21568297 | pubmed:articleTitle | Plantazolicin A and B: structure elucidation of ribosomally synthesized thiazole/oxazole peptides from Bacillus amyloliquefaciens FZB42. | lld:pubmed |
| pubmed-article:21568297 | pubmed:affiliation | Institut fu?r Chemie, Technische Universita?t Berlin, 10623 Berlin, Germany. | lld:pubmed |
| pubmed-article:21568297 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:21568297 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
