TY - JOUR
T1 - Identification of the Biosynthetic Gene Cluster for Pyracrimycin A, an Antibiotic Produced by Streptomyces sp.
AU - Nielsen, Julie B.
AU - Gren, Tetiana
AU - Mohite, Omkar S.
AU - Jørgensen, Tue S.
AU - Klitgaard, Andreas K.
AU - Mourched, Anna-Sophie
AU - Blin, Kai
AU - Oves-Costales, Daniel
AU - Genilloud, Olga
AU - Larsen, Thomas O.
AU - Tanner, David
AU - Weber, Tilmann
AU - Gotfredsen, Charlotte H.
AU - Charusanti, Pep
PY - 2022
Y1 - 2022
N2 - Actinomycetes make a wealth of complex, structurally diverse natural products, and a key challenge is to link them to their biosynthetic gene clusters and delineate the reactions catalyzed by each of the enzymes. Here, we report the biosynthetic gene cluster for pyracrimycin A, a set of nine genes that includes a core nonribosomal peptide synthase (pymB) that utilizes serine and proline as precursors and a monooxygenase (pymC) that catalyzes Baeyer-Villiger oxidation. The cluster is similar to the one for brabantamide A; however, pyracrimycin A biosynthesis differs in that feeding experiments with isotope-labeled serine and proline suggest that a ring opening reaction takes place and a carbon is lost from serine downstream of the oxidation reaction. Based on these data, we propose a full biosynthesis pathway for pyracrimycin A.
AB - Actinomycetes make a wealth of complex, structurally diverse natural products, and a key challenge is to link them to their biosynthetic gene clusters and delineate the reactions catalyzed by each of the enzymes. Here, we report the biosynthetic gene cluster for pyracrimycin A, a set of nine genes that includes a core nonribosomal peptide synthase (pymB) that utilizes serine and proline as precursors and a monooxygenase (pymC) that catalyzes Baeyer-Villiger oxidation. The cluster is similar to the one for brabantamide A; however, pyracrimycin A biosynthesis differs in that feeding experiments with isotope-labeled serine and proline suggest that a ring opening reaction takes place and a carbon is lost from serine downstream of the oxidation reaction. Based on these data, we propose a full biosynthesis pathway for pyracrimycin A.
U2 - 10.1021/acschembio.2c00480
DO - 10.1021/acschembio.2c00480
M3 - Journal article
C2 - 36040247
SN - 1554-8929
VL - 17
SP - 2411
EP - 2417
JO - ACS chemical biology
JF - ACS chemical biology
IS - 9
ER -