Kim Hye-Jin, Kim Min-Kyung, Lee Mi-Jin, Won Hyung-Jin, Choi Si-Sun, Kim Eung-Soo
Department of Biological Engineering, Inha University, Incheon, Korea.
PLoS One. 2015 Apr 7;10(4):e0123270. doi: 10.1371/journal.pone.0123270. eCollection 2015.
A novel polyene compound NPP identified in a rare actinomycetes, Pseudonocardia autotrophica KCTC9441, was shown to contain an aglycone identical to nystatin but to harbor a unique di-sugar moiety, mycosaminyl-(α1-4)-N-acetyl-glucosamine, which led to higher solubility and reduced hemolytic activity. Although the nppDI was proved to be responsible for the transfer of first polyene sugar, mycosamine in NPP biosynthesis, the gene responsible for the second sugar extending glycosyltransferase (GT) as well as NPP post-PKS tailoring mechanism remained unknown. Here, we 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. These results set the stage for the biotechnological application of sugar diversification for the biosynthesis of novel polyene compounds in actinomycetes.
在一种罕见的放线菌——自养拟诺卡氏菌KCTC9441中鉴定出的一种新型多烯化合物NPP,被证明含有与制霉菌素相同的苷元,但带有独特的二糖部分,即霉菌氨基糖基-(α1-4)-N-乙酰葡糖胺,这导致其具有更高的溶解度和更低的溶血活性。尽管已证明nppDI负责NPP生物合成中第一种多烯糖(霉菌胺)的转移,但负责第二种糖延伸的糖基转移酶(GT)基因以及NPP的聚酮合酶后修饰机制仍然未知。在此,我们鉴定出一个位于NPP生物合成基因簇边缘的NPP特异性第二种糖延伸GT基因,命名为nppY。靶向nppY基因缺失及其互补实验证明,nppY确实负责NPP生物合成中第二种糖N-乙酰葡糖胺的转移。对nppY进行定点诱变还揭示了几个对NppY GT功能至关重要的氨基酸残基。此外,对参与NPP聚酮合酶后生物合成的两个GT基因(nppDI和nppY)和一个P450羟化酶基因(nppL)进行缺失和互补组合实验表明,NPP苷元分别由nppDI和nppY编码的两种不同GT依次修饰,随后由nppL驱动在NPP的C10位置进行区域特异性羟基化。这些结果为放线菌中新型多烯化合物生物合成的糖多样化生物技术应用奠定了基础。