Park Heung-Soon, Park Ji-Hee, Kim Hye-Jin, Kang Seung-Hoon, Choi Si-Sun, Kim Eung-Soo
Department of Biological Engineering, Inha University, Incheon, South Korea.
Front Bioeng Biotechnol. 2022 Aug 15;10:964765. doi: 10.3389/fbioe.2022.964765. eCollection 2022.
Polyene natural products including nystatin A1, amphotericin B, ECO-02301, and mediomycin belong to a large family of valuable antifungal polyketide compounds typically produced by soil actinomycetes. A previous study (Park et al., Front. Bioeng. Biotechnol., 2021, 9, 692340) isolated Inha501 with strong antifungal activity and analyzed a large-sized biosynthetic gene cluster (BGC) of a linear polyene compound named Inha-neotetrafibricin (I-NTF) using whole genome sequencing and bioinformatics. In the present study, an entire I-NTF BGC (∼167 kb) was isolated through construction and screening of BAC library. Overexpression of the cloned I-NTF BGC in the wild-type Inha501 and its heterologous expression in led to 2.6-fold and 2.8-fold increase in I-NTF yields, respectively. The qRT-PCR confirmed that the transcription levels of I-NTF BGC were significantly increased in both homologous and heterologous hosts containing the BAC integration of I-NTF BGC. In addition, the I-NTF aglycone-producing strains were constructed by a target-specific deletion of glycosyltransferase gene present in I-NTF BGC. A comparison of the biological activities of I-NTF and I-NTF aglycone confirmed that the rhamnose sugar motif of I-NTF plays a critical role in both antifungal and antibacterial activities. These results suggest that the BAC cloning of a large-sized natural product BGC is a valuable approach for natural product titer improvement and biological activity screening of natural product in actinomycetes.
包括制霉菌素A1、两性霉素B、ECO - 02301和medimycin在内的多烯类天然产物属于一大类有价值的抗真菌聚酮化合物,通常由土壤放线菌产生。先前的一项研究(Park等人,《生物工程与生物技术前沿》,2021年,9卷,692340)分离出了具有强抗真菌活性的Inha501,并使用全基因组测序和生物信息学分析了一种名为Inha - neotetrafibricin(I - NTF)的线性多烯化合物的大型生物合成基因簇(BGC)。在本研究中,通过构建和筛选BAC文库分离出了完整的I - NTF BGC(约167 kb)。在野生型Inha501中克隆的I - NTF BGC的过表达及其在异源宿主中的表达分别导致I - NTF产量提高了2.6倍和2.8倍。qRT - PCR证实,在含有I - NTF BGC的BAC整合体的同源和异源宿主中,I - NTF BGC的转录水平均显著提高。此外,通过对I - NTF BGC中存在的糖基转移酶基因进行靶向特异性缺失,构建了I - NTF苷元生产菌株。I - NTF和I - NTF苷元的生物活性比较证实,I - NTF的鼠李糖基序在抗真菌和抗菌活性中都起着关键作用。这些结果表明,大型天然产物BGC的BAC克隆是提高放线菌中天然产物效价和筛选天然产物生物活性的一种有价值的方法。