A biosynthetic pathway for the red-antibiotic, prodigiosin, was proposed over a decade ago but not all the suggested intermediates could be detected experimentally. Here we show that a thioester that was not originally included in the pathway is an intermediate. In addition, the enzyme PigE was originally described as a transaminase but we present evidence that it also catalyses the reduction of the thioester intermediate to its aldehyde substrate.BBSRC, UK, awards BB/N008081/1 and BB/K001833/1 Frances and Augustus Newman foundation Cambridge Commonwealth Trust Emmanuel College, Cambridg
The Bohlmann-Rahtz intermediates (aminodienones) have provided a viable route to 2,3,6- trisubstitut...
The intermolecular asymmetric Stetter reaction is an almost unexplored transformation for biocatalys...
Phosphinothricin tripeptide (PTT) is a peptide antibiotic produced by Streptomyces viridochromogenes...
In the biosynthesis of the tripyrrolic pigment prodigiosin, PigB is a predicted flavin-dependent oxi...
Prodiginines are a class of red-pigmented natural products with immunosuppressant, anticancer, and a...
Prodigiosin ligase PigC catalyses the final condensation step in the prodigiosin biosynthesis of Ser...
Prodigiosin synthetase PigC is an ATP-dependent membrane-associated ligase that catalyzes the final ...
The deeply red-colored natural compound prodigiosin is a representative of the prodiginine alkaloid ...
The prodiginine antibiotics exhibit antitumor and immunosuppressive activity. In this issue of Chemi...
The biosynthetic pathway to 4-methoxy-2,2'-bipyrrole-5-carboxaldehyde (MBC), a key intermediate in t...
Increased antimicrobial resistance combined with the lack of new antibiotics, is leading towards a r...
SummaryThe enzyme RedP is thought to initiate the biosynthesis of the undecylpyrolle component of th...
The tripyrrolic products of the prodiginine class of natural products are signature antibiotics of S...
Prodiginines, which are tripyrrole alkaloids displaying a wide array of bioactivities, occur as line...
The growing demand to fulfill the needs of present-day medicine in terms of novel effective molecule...
The Bohlmann-Rahtz intermediates (aminodienones) have provided a viable route to 2,3,6- trisubstitut...
The intermolecular asymmetric Stetter reaction is an almost unexplored transformation for biocatalys...
Phosphinothricin tripeptide (PTT) is a peptide antibiotic produced by Streptomyces viridochromogenes...
In the biosynthesis of the tripyrrolic pigment prodigiosin, PigB is a predicted flavin-dependent oxi...
Prodiginines are a class of red-pigmented natural products with immunosuppressant, anticancer, and a...
Prodigiosin ligase PigC catalyses the final condensation step in the prodigiosin biosynthesis of Ser...
Prodigiosin synthetase PigC is an ATP-dependent membrane-associated ligase that catalyzes the final ...
The deeply red-colored natural compound prodigiosin is a representative of the prodiginine alkaloid ...
The prodiginine antibiotics exhibit antitumor and immunosuppressive activity. In this issue of Chemi...
The biosynthetic pathway to 4-methoxy-2,2'-bipyrrole-5-carboxaldehyde (MBC), a key intermediate in t...
Increased antimicrobial resistance combined with the lack of new antibiotics, is leading towards a r...
SummaryThe enzyme RedP is thought to initiate the biosynthesis of the undecylpyrolle component of th...
The tripyrrolic products of the prodiginine class of natural products are signature antibiotics of S...
Prodiginines, which are tripyrrole alkaloids displaying a wide array of bioactivities, occur as line...
The growing demand to fulfill the needs of present-day medicine in terms of novel effective molecule...
The Bohlmann-Rahtz intermediates (aminodienones) have provided a viable route to 2,3,6- trisubstitut...
The intermolecular asymmetric Stetter reaction is an almost unexplored transformation for biocatalys...
Phosphinothricin tripeptide (PTT) is a peptide antibiotic produced by Streptomyces viridochromogenes...