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The chejuenolide biosynthetic gene cluster harboring an iterative trans-AT PKS system in Hahella chejuensis strain MB-1084

Authors
Ng, Bee GekHan, Jae WooLee, Dong WanChoi, Gyung JaKim, Beom Seok
Issue Date
May-2018
Publisher
JAPAN ANTIBIOTICS RESEARCH ASSOC
Citation
JOURNAL OF ANTIBIOTICS, v.71, no.5, pp.495 - 505
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF ANTIBIOTICS
Volume
71
Number
5
Start Page
495
End Page
505
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/75599
DOI
10.1038/s41429-017-0023-x
ISSN
0021-8820
Abstract
Hahella chejuensis MB-1084 is a Gram-negative marine bacterial strain that produces unusual 17-membered carbocyclic tetraenes, chejuenolide A and B. Two fosmid clones responsible for chejuenolide production were identified from the genomic DNA library of the MB-1084 strain. Systematic inactivation of the open reading frames (ORFs) in the sequenced region defines the boundaries of the chejuenolide (che) biosynthetic gene cluster (24.9 kbp) that encodes one non-ribosomal peptide synthase (NRPS)-polyketide synthase (PKS) hybrid protein, three modular PKSs, two PKS domains, and an amine oxidase homolog. Based on the results, we found that the che PKSs have non-canonical features such as trans-AT system and insufficient number of KS domains (five KS domains) for chejuenolide production (requires eight rounds of Claisen condensation reaction). Heterologous expression of the che PKSs in the E. coli BAP1 strain provides strong evidence of the iterative characteristic of the modular PKSs. Additionally, the phylogenetic relatedness of the KS domains of che PKSs and other trans-AT PKSs was analyzed to propose a possible pathway for chejuenolide biosynthesis.
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