| Literature DB >> 26840634 |
Xiaodong Liu1, Yuanyuan Jin2, Zheng Cui1, Koichi Nonaka3, Satoshi Baba3, Masanori Funabashi4, Zhaoyong Yang2, Steven G Van Lanen5.
Abstract
Capuramycins are one of several known classes of natural products that contain an l-Lys-derived l-α-amino-ɛ-caprolactam (l-ACL) unit. The α-amino group of l-ACL in a capuramycin is linked to an unsaturated hexuronic acid component through an amide bond that was previously shown to originate by an ATP-independent enzymatic route. With the aid of a combined in vivo and in vitro approach, a predicted tridomain nonribosomal peptide synthetase CapU is functionally characterized here as the ATP-dependent amide-bond-forming catalyst responsible for the biosynthesis of the remaining amide bond present in l-ACL. The results are consistent with the adenylation domain of CapU as the essential catalytic component for l-Lys activation and thioesterification of the adjacent thiolation domain. However, in contrast to expectations, lactamization does not require any additional domains or proteins and is likely a nonenzymatic event. The results set the stage for examining whether a similar NRPS-mediated mechanism is employed in the biosynthesis of other l-ACL-containing natural products and, just as intriguingly, how spontaneous lactamization is avoided in the numerous NRPS-derived peptides that contain an unmodified l-Lys residue.Entities:
Keywords: antibiotics; biosynthesis; natural products; nonribosomal peptides; nucleosides
Mesh:
Substances:
Year: 2016 PMID: 26840634 PMCID: PMC4933962 DOI: 10.1002/cbic.201500701
Source DB: PubMed Journal: Chembiochem ISSN: 1439-4227 Impact factor: 3.164