TY - JOUR
T1 - Unusual transformations in the biosynthesis of the antibiotic phosphinothricin tripeptide
AU - Blodgett, Joshua A V
AU - Thomas, Paul M.
AU - Li, Gongyong
AU - Velasquez, Juan E.
AU - Van Der Donk, Wilfred A.
AU - Kelleher, Neil L.
AU - Metcalf, William W.
N1 - Funding Information:
This work was supported by US National Institute of General Medical Sciences grants GM59334 and GM067725 and US National Institute of Health Chemical Biology Interface Training Grant 5T32 GM070421. The authors wish to thank A. Salyers (University of Illinois, Urbana-Champaign) for the gift of Bacteroides fragilis NCTC9343 genomic DNA and M.J. Thomas (University of Wisconsin, Madison) for plasmids pOJ260 and pKC1139. We also thank V. Mainz and P. Molitor for NMR advice and C. Wenger for developing custom data analysis software for MS (University of Illinois, Urbana-Champaign).
PY - 2007/8
Y1 - 2007/8
N2 - Phosphinothricin tripeptide (PTT, phosphinothricylalanylalanine) is a natural-product antibiotic and potent herbicide that is produced by Streptomyces hygroscopicus ATCC 21705 (ref. 1) and Streptomyces viridochromogenes DSM 40736 (ref. 2). PTT has attracted widespread interest because of its commercial applications and unique phosphinic acid functional group. Despite intensive study since its discovery in 1972 (see ref. 3 for a comprehensive review), a number of steps early in the PTT biosynthetic pathway remain uncharacterized. Here we report a series of interdisciplinary experiments involving the construction of defined S. viridochromogenes mutants, chemical characterization of accumulated intermediates, and in vitro assay of selected enzymes to examine these critical steps in PTT biosynthesis. Our results indicate that early PTT biosynthesis involves a series of catalytic steps that to our knowledge has not been described so far, including a highly unusual reaction for carbon bond cleavage. In sum, we define a pathway for early PTT biosynthesis that is more complex than previously appreciated.
AB - Phosphinothricin tripeptide (PTT, phosphinothricylalanylalanine) is a natural-product antibiotic and potent herbicide that is produced by Streptomyces hygroscopicus ATCC 21705 (ref. 1) and Streptomyces viridochromogenes DSM 40736 (ref. 2). PTT has attracted widespread interest because of its commercial applications and unique phosphinic acid functional group. Despite intensive study since its discovery in 1972 (see ref. 3 for a comprehensive review), a number of steps early in the PTT biosynthetic pathway remain uncharacterized. Here we report a series of interdisciplinary experiments involving the construction of defined S. viridochromogenes mutants, chemical characterization of accumulated intermediates, and in vitro assay of selected enzymes to examine these critical steps in PTT biosynthesis. Our results indicate that early PTT biosynthesis involves a series of catalytic steps that to our knowledge has not been described so far, including a highly unusual reaction for carbon bond cleavage. In sum, we define a pathway for early PTT biosynthesis that is more complex than previously appreciated.
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U2 - 10.1038/nchembio.2007.9
DO - 10.1038/nchembio.2007.9
M3 - Article
C2 - 17632514
AN - SCOPUS:34447544332
SN - 1552-4450
VL - 3
SP - 480
EP - 485
JO - Nature Chemical Biology
JF - Nature Chemical Biology
IS - 8
ER -