| pubmed-article:19275222 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:19275222 | lifeskim:mentions | umls-concept:C0002062 | lld:lifeskim |
| pubmed-article:19275222 | lifeskim:mentions | umls-concept:C0220781 | lld:lifeskim |
| pubmed-article:19275222 | lifeskim:mentions | umls-concept:C0449445 | lld:lifeskim |
| pubmed-article:19275222 | pubmed:issue | 4 | lld:pubmed |
| pubmed-article:19275222 | pubmed:dateCreated | 2009-4-24 | lld:pubmed |
| pubmed-article:19275222 | pubmed:abstractText | To determine the biosynthesis pathway of the atisine-type diterpenoid alkaloids spiramines A/B and C/D, feeding experiments in in vitro cultured plantlets and enzymatic transformations in cell-free extracts were performed in combination with LCMS and tandem MS analyses. L-[2-(13)C,(15)N]Serine was used in the feeding experiments and enzymatic transformations, and the diterpene spiraminol was identified as a biosynthetic precursor of spiramine alkaloids. The LCMS and tandem MS spectra of the extracts from these experiments indicated that L-[2-(13)C,(15)N]serine was incorporated into spiramines A/B and C/D. The labeled reaction products show that l-serine is the one possible nitrogen source involved in the biosynthesis of atisine-type DAs. | lld:pubmed |
| pubmed-article:19275222 | pubmed:language | eng | lld:pubmed |
| pubmed-article:19275222 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19275222 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:19275222 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19275222 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19275222 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19275222 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19275222 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19275222 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:19275222 | pubmed:month | Apr | lld:pubmed |
| pubmed-article:19275222 | pubmed:issn | 1520-6025 | lld:pubmed |
| pubmed-article:19275222 | pubmed:author | pubmed-author:RauJ LJLJr | lld:pubmed |
| pubmed-article:19275222 | pubmed:author | pubmed-author:HeHong-PingHP | lld:pubmed |
| pubmed-article:19275222 | pubmed:author | pubmed-author:ShenYue-MaoYM | lld:pubmed |
| pubmed-article:19275222 | pubmed:author | pubmed-author:HaoXiao-Jiang... | lld:pubmed |
| pubmed-article:19275222 | pubmed:author | pubmed-author:ZengYingY | lld:pubmed |
| pubmed-article:19275222 | pubmed:author | pubmed-author:ZhaoPei-JiPJ | lld:pubmed |
| pubmed-article:19275222 | pubmed:author | pubmed-author:FanLi-MingLM | lld:pubmed |
| pubmed-article:19275222 | pubmed:author | pubmed-author:NieJing-LeiJL | lld:pubmed |
| pubmed-article:19275222 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:19275222 | pubmed:volume | 72 | lld:pubmed |
| pubmed-article:19275222 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:19275222 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:19275222 | pubmed:pagination | 645-9 | lld:pubmed |
| pubmed-article:19275222 | pubmed:meshHeading | pubmed-meshheading:19275222... | lld:pubmed |
| pubmed-article:19275222 | pubmed:meshHeading | pubmed-meshheading:19275222... | lld:pubmed |
| pubmed-article:19275222 | pubmed:meshHeading | pubmed-meshheading:19275222... | lld:pubmed |
| pubmed-article:19275222 | pubmed:meshHeading | pubmed-meshheading:19275222... | lld:pubmed |
| pubmed-article:19275222 | pubmed:meshHeading | pubmed-meshheading:19275222... | lld:pubmed |
| pubmed-article:19275222 | pubmed:meshHeading | pubmed-meshheading:19275222... | lld:pubmed |
| pubmed-article:19275222 | pubmed:meshHeading | pubmed-meshheading:19275222... | lld:pubmed |
| pubmed-article:19275222 | pubmed:year | 2009 | lld:pubmed |
| pubmed-article:19275222 | pubmed:articleTitle | Approach to the biosynthesis of atisine-type diterpenoid alkaloids. | lld:pubmed |
| pubmed-article:19275222 | pubmed:affiliation | State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, People's Republic of China. | lld:pubmed |
| pubmed-article:19275222 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:19275222 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
