Special seminar on “Actinomycetes Genome Mining and Post-PKS Engineering of a Novel Disaccharide-containing Polyene in Pseudonocardia autotrophica”
Department of Genetics would like to invite you to a special seminar on
“Actinomycetes Genome Mining and Post-PKS Engineering of a Novel
Disaccharide-containing Polyene in Pseudonocardia autotrophica”
by Prof. Dr.Eung-Soo Kim, Department of Biological Engineering, Inha University,
Incheon, Korea, (abstract attached)
on Thursday 6 July 2017, 10:00-11:00,
at room 4521, 5th floor, Microbiology-Genetic Building, Department of Genetics,
Faculty of Science, Kasetsart University.
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Actinomycetes Genome Mining and Post-PKS Engineering of a Novel Disaccharide-containing Polyene in Pseudonocardia autotrophica
Department of Biological Engineering, Inha University, Incheon 22212, Korea
E-mail : email@example.com
Introduction. Polyene antibiotics such as nystatin are a large family of very valuable antifungal polyketide compounds typically produced by soil actinomycetes. Using a polyene cytochrome P450 hydroxylase-specific genome mining, Pseudonocardia autotrophica KCTC9441 was determined to contain an approximately 125.7-kb region of contiguous DNA with a total of 23 open reading frames, which are involved in the biosynthesis and regulation of a structurally unique polyene natural product named NPP (1). The complete structure of NPP, which contains an aglycone identical to nystatin and harbors a unique di-sugar moiety, mycosaminyl-(α1-4)-N-acetyl-glucosamine, which led to higher solubility and reduced hemolytic activity (1).
Results. To understand and engineer post-PKS tailoring steps, we first identified a NPP-specific second sugar extending GT gene named nppY, located at the edge of the NPP biosynthetic gene cluster. Targeted nppY gene deletion and its complementation proved that nppY is indeed responsible for the transfer of second sugar, N-acetyl-glucosamine in NPP biosynthesis. Site-directed mutagenesis on nppY also revealed several amino acid residues critical for NppY GT function. Moreover, a combination of deletions and complementations of two GT genes (nppDI and nppY) and one P450 hydroxylase gene (nppL) involved in the NPP post-PKS biosynthesis revealed that NPP aglycone is sequentially modified by the two different GTs encoded by nppDI and nppY, respectively, followed by the nppL-driven regio-specific hydroxylation at the NPP C10 position (2). These results set the stage for the biotechnological application of sugar diversification for the biosynthesis of novel polyene compounds in actinomycetes.
- 1. Lee MJ, Kong D, Han KB, Sherman DH, Bai L, Deng Z, Lin S, Kim ES. (2012). Appl Microbiol Biotechnol. 95:157-168
- 2. Kim HJ, Kim MK, Lee MJ, Won HJ, Choi SS, Kim ES. (2015). PLoS One. 10(4)