Please use this identifier to cite or link to this item:
|Title:||Biosynthesis of the 3,4-dihydroxybenzoate moieties of petrobactin by Bacillus anthracis|
|Citation:||Koppisch, A.T., Hotta, K., Fox, D.T., Ruggiero, C.E., Kim, C.-Y., Sanchez, T., Iyer, S., Browder, C.C., Unkefer, P.J., Unkefer, C.J. (2008-08-01). Biosynthesis of the 3,4-dihydroxybenzoate moieties of petrobactin by Bacillus anthracis. Journal of Organic Chemistry 73 (15) : 5759-5765. ScholarBank@NUS Repository. https://doi.org/10.1021/jo800427f|
|Abstract:||(Chemical Equation Presented) The biosynthesis of the 3,4-dihydroxybenzoate moieties of the siderophore petrobactin, produced by B. anthracis str. Sterne, was probed by isotopic feeding experiments in iron-deficient media with a mixture of unlabeled and D-[13C6]glucose at a ratio of 5:1 (w/w). After isolation of the labeled siderophore, analysis of the isotopomers was conducted via one-dimensional 1H and 13C NMR spectroscopy, as well as 13C-13C DQFCOSY spectroscopy. Isotopic enrichment and 13C-13C coupling constants in the aromatic ring of the isolated siderophore suggested the predominant route for the construction of the carbon backbone of 3,4-DHB (1) involved phosphoenol pyruvate and erythrose-4-phosphate as ultimate precursors. This observation is consistent with that expected if the shikimate pathway is involved in the biosynthesis of these moieties. Enrichment attributable to phosphoenol pyruvate precursors was observed at C1 and C6 of the aromatic ring, as well as into the carboxylate group, while scrambling of the label into C2 was not. This pattern suggests 1 was biosynthesized from early intermediates of the shikimate pathway and not through later shikimate intermediates or aromatic amino acid precursors. © 2008 American Chemical Society.|
|Source Title:||Journal of Organic Chemistry|
|Appears in Collections:||Staff Publications|
Show full item record
Files in This Item:
There are no files associated with this item.
checked on Jan 21, 2019
WEB OF SCIENCETM
checked on Jan 14, 2019
checked on Jan 18, 2019
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.