Bormann C, Aberle K, Fiedler H P, Schrempf H
Universität Tübingen, Biologie II, Tübingen, Federal Republic of Germany.
Appl Microbiol Biotechnol. 1990 Jan;32(4):424-30. doi: 10.1007/BF00903777.
Streptomyces tendae Tü 901 produces the nucleoside peptide antibiotic nikkomycin. In shot-gun cloning experiments using pIJ699 as vector we isolated a 9.4-kb DNA fragment from S. tendae which complemented the nikkomycin nonproducing mutant NP9 to the formation of nikkomycin C/Cx and Kx. Nikkomycins were identified by HPLC analyses and their characteristic UV spectra. In Southern hybridization experiments the cloned DNA exclusively reacted with S. tendae DNA sequences. As shown by Northern dot blotting, transcripts of the isolated DNA fragment were only detected during stationary growth and correlated with the extent of nikkomycin production. When the recombinant plasmid pNP113 containing the 9.4-kb DNA fragment was transferred into the over-producing mutant Tü901/S2566, transformants exhibited a significantly decreased capacity for forming nikkomycin. Southern analysis of genomic DNA of these transformants revealed that severe rearrangements occurred in DNA sequences homologous to the 9.4-kb insert of pNP113.
天蓝色链霉菌Tü 901产生核苷肽抗生素多氧霉素。在以pIJ699为载体的鸟枪法克隆实验中,我们从天蓝色链霉菌中分离出一个9.4 kb的DNA片段,该片段使多氧霉素不产生突变体NP9恢复合成多氧霉素C/Cx和Kx。通过高效液相色谱分析及其特征紫外光谱鉴定了多氧霉素。在Southern杂交实验中,克隆的DNA仅与天蓝色链霉菌的DNA序列发生反应。如Northern斑点印迹所示,仅在稳定生长期检测到分离的DNA片段的转录本,且与多氧霉素的产生程度相关。当将含有9.4 kb DNA片段的重组质粒pNP113转入高产突变体Tü901/S2566时,转化体形成多氧霉素的能力显著下降。对这些转化体的基因组DNA进行Southern分析表明,与pNP113的9.4 kb插入片段同源的DNA序列发生了严重重排。