Yin Min, Jiang Mingxing, Ren Zhen, Dong Yilong, Lu Tao
School of Medicine, Yunnan University, 2 North Cui Hu Road, Kunming, Yunnan 650091, China.
Yunnan Institute of Microbiology, School of Life Sciences, Yunnan University, 2 North Cui Hu Road, Kunming, Yunnan 650091, China.
J Biotechnol. 2017 Jun 20;252:27-31. doi: 10.1016/j.jbiotec.2017.04.037. Epub 2017 May 2.
Streptomyces autolyticus CGMCC 0516 produces the anti-tumor benzoquinone ansamycins geldanamycin, autolytimycin, and reblastatin and the 16-membered macrodiolide elaiophylin. Here, we report the complete genome sequence of S. autolyticus CGMCC 0516, which consists of a 10,029,028bp linear chromosome and seven circular plasmids. Fifty-seven putative biosynthetic gene clusters for secondary metabolites were found. The geldanamycin, autolytimycin, and reblastatin biosynthetic gene clusters were located on the left arm (2.06-2.15Mb) of the chromosome, and the elaiophylin gene cluster was located on the right arm (9.45-9.53Mb). Twenty-one putative gene clusters with high or moderate similarity to important antibiotic biosynthetic gene clusters were found, including the antitumor agents echoside, bafilomycin, hygrocin, and toxoflavin; the antibacterial/antifungal agents nigericin, skyllamycin, kanamycin, naphthomycin, eco-02301, and bottromycin A2; the immunosuppressants meridamycin and brasilicardin A; the anti-inflammatory agent cyclooctatin; and the acute iron poisoning medication desferrioxamine B. The genome sequence reported here will enable us to study the biosynthetic mechanism of these important antibiotics and will facilitate the discovery of novel secondary metabolites with potential applications to human health.
自溶链霉菌CGMCC 0516可产生抗肿瘤苯醌安莎霉素格尔德霉素、自溶霉素和瑞布拉他汀以及16元大环二内酯伊索菌素。在此,我们报道了自溶链霉菌CGMCC 0516的完整基因组序列,其由一条10,029,028bp的线性染色体和七个环状质粒组成。发现了57个假定的次生代谢物生物合成基因簇。格尔德霉素、自溶霉素和瑞布拉他汀生物合成基因簇位于染色体的左臂(2.06 - 2.15Mb),伊索菌素基因簇位于右臂(9.45 - 9.53Mb)。发现了21个与重要抗生素生物合成基因簇具有高度或中度相似性的假定基因簇,包括抗肿瘤剂回声糖苷、巴弗洛霉素、潮霉素和毒黄素;抗菌/抗真菌剂尼日利亚菌素、斯库拉霉素、卡那霉素、萘霉素、eco - 02301和波卓霉素A2;免疫抑制剂美里达霉素和巴西卡定A;抗炎剂环辛他汀;以及急性铁中毒药物去铁胺B。本文报道的基因组序列将使我们能够研究这些重要抗生素的生物合成机制,并将有助于发现对人类健康有潜在应用价值的新型次生代谢物。