The biosynthetic pathway to 4-methoxy-2,2'-bipyrrole-5-carboxaldehyde (MBC), a key intermediate in the biosynthesis of prodiginine antibiotics in Streptomyces coelicolor, has been elucidated using a combination of gene replacements and feeding experiments with chemically synthesised MBC and a synthetic analogue of a pathway intermediate
AbstractActinomycetes are a rich source for the synthesis of medically and technically useful natura...
Tailoring enzymes catalyze reactions that modify natural product backbone structures before, during,...
The tripyrrolic products of the prodiginine class of natural products are signature antibiotics of S...
Background: Prodiginines are a large family of pigmented oligopyrrole antibiotics with medicinal pot...
Background: Prodiginines are a large family of pigmented oligopyrrole antibiotics with medicinal pot...
The last step of proline biosynthesis is typically catalysed by the enzyme Delta(1)-pyrroline-5-carb...
How is the extraordinarily dense array of functional groups adorning the cyclopentane rings of the a...
SummaryThe enzyme RedP is thought to initiate the biosynthesis of the undecylpyrolle component of th...
The 2,5-Diketopiperazines (DKPs) constitute a large family of natural products with important biolog...
Actinomycetes make a wealth of complex, structurally diverse natural products, and a key challenge i...
SummaryThe red gene cluster of Streptomyces coelicolor directs production of undecylprodiginine. Her...
Part I. Studies on a Red Pigment from Streptomyces. The mechanism of antibiotic biosynthesis was exa...
The function of RedH from Streptomyces coelicolor as an enzyme that catalyses the condensation of 4-...
All of the genetic elements necessary for the production of the antibiotic methylenomycin (Mm) and i...
SummaryThe gene cluster for the bipyridyl compound collismycin was characterized from Streptomyces s...
AbstractActinomycetes are a rich source for the synthesis of medically and technically useful natura...
Tailoring enzymes catalyze reactions that modify natural product backbone structures before, during,...
The tripyrrolic products of the prodiginine class of natural products are signature antibiotics of S...
Background: Prodiginines are a large family of pigmented oligopyrrole antibiotics with medicinal pot...
Background: Prodiginines are a large family of pigmented oligopyrrole antibiotics with medicinal pot...
The last step of proline biosynthesis is typically catalysed by the enzyme Delta(1)-pyrroline-5-carb...
How is the extraordinarily dense array of functional groups adorning the cyclopentane rings of the a...
SummaryThe enzyme RedP is thought to initiate the biosynthesis of the undecylpyrolle component of th...
The 2,5-Diketopiperazines (DKPs) constitute a large family of natural products with important biolog...
Actinomycetes make a wealth of complex, structurally diverse natural products, and a key challenge i...
SummaryThe red gene cluster of Streptomyces coelicolor directs production of undecylprodiginine. Her...
Part I. Studies on a Red Pigment from Streptomyces. The mechanism of antibiotic biosynthesis was exa...
The function of RedH from Streptomyces coelicolor as an enzyme that catalyses the condensation of 4-...
All of the genetic elements necessary for the production of the antibiotic methylenomycin (Mm) and i...
SummaryThe gene cluster for the bipyridyl compound collismycin was characterized from Streptomyces s...
AbstractActinomycetes are a rich source for the synthesis of medically and technically useful natura...
Tailoring enzymes catalyze reactions that modify natural product backbone structures before, during,...
The tripyrrolic products of the prodiginine class of natural products are signature antibiotics of S...