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PMID: 17002325 Published · ppublish English Journal Article Research Support, N.I.H., Extramural

Protein assembly line components in prodigiosin biosynthesis: characterization of PigA,G,H,I,J.

Journal of the American Chemical Society ·Vol. 128 ·No. 39 ·2006-10-04 ·Pages 12600-1

Garneau-Tsodikova S, Dorrestein PC, Kelleher NL, Walsh CT

Abstract

The red streptomycete metabolite prodigiosin has a unique tripyrrolic structure with two of the three pyrrolyl moieties in tandem. Five enzymes, PigA,G,H,I, and J, are involved in dipyrrole (rings A and B) formation. We have heterologously expressed and purified from Escherichia coli these five enzymes. At first, pyrrole ring A is formed on the peptidyl carrier protein PigG by one of two possible ways: (i) by action of the adenylation domain PigI that transforms l-proline into l-prolyl-AMP and by the flavoprotein dehydrogenase PigA responsible for the four-electron oxidation reaction; (ii) by loading with the pyrrolyl-2-carboxyl-(S)-pantetheinyl moiety from synthetic pyrrolyl-CoA using the phosphopantetheinyl transferase Sfp. Subsequently, pyrrole ring B is constructed by PigH after the transfer of ring A to the ketosynthase of PigJ. PigH consists of three domains: two acyl carrier proteins (ACPs) and a seryltransferase (SerT). Using HPLC and nanospray-Fourier Transform Mass Spectrometry (nFTMS), we established that all three domains of PigH undergo post-translational modifications and gained insight into the machinery involved in 2,2-dipyrrole biosynthesis.

MeSH Terms
Carrier Proteins/biosynthesis,metabolism Escherichia coli/enzymology,genetics Mass Spectrometry Phenylpropionates Prodigiosin/biosynthesis Proline/metabolism Pyrroles/metabolism Recombinant Proteins/biosynthesis,genetics,metabolism Serratia/enzymology,metabolism
Chemicals
Carrier Proteins Phenylpropionates Pyrroles Recombinant Proteins 4-hydroxyphenyllactic acid Proline Prodigiosin
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Garneau-Tsodikova Sylvie
Department of Biological Chemistry & Molecular Pharmacology, Harvard Medical School, 240 Longwood Avenue, Boston, MA 02115, USA.
Dorrestein Pieter C
Kelleher Neil L
Walsh Christopher T
Article Info
Journal
Journal of the American Chemical Society
Abbr.
J Am Chem Soc
ISSN
0002-7863
Published
2006-10-04
Pages
12600-1
Language
English
Region
United States
NLM ID
7503056
Subset
IM
Grants
NIGMS NIH HHS · F32 GM 073323-01 · United States
NIGMS NIH HHS · GM 067725 · United States
NIGMS NIH HHS · GM 49338 · United States
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