Zirkle Ross, Black Todd A, Gorlach Joern, Ligon James M, Molnár István
Syngenta Biotechnology Inc., 3054 Cornwallis Road, Research Triangle Park, NC 27709, USA.
DNA Seq. 2004 Apr;15(2):123-34. doi: 10.1080/1042517042000208167.
A 108-kb genomic DNA region of Saccharopolyspora spinosa NRRL 18395, producer of the agriculturally important insecticidal antibiotics spinosyns, has been cloned, sequenced and analyzed to reveal clustered genes encoding a type I polyketide synthase (PKS) complex. The genes for the PKS are flanked by genes encoding homologs of enzymes that are involved in the urea cycle, valine, leucine and isoleucine biosynthesis and energy metabolism. While the disruption of the PKS genes by insertional inactivation was not expected to abolish the production of spinosyns, no differences were found in the antibacterial, antifungal, or insecticidal activities either of the parental and the knockout mutant strains under the growth conditions tested. Deduction of the most likely structure of the polyketide core of the cryptic metabolite, termed obscurin, from the predicted modules and domains of the PKS suggests the formation of a highly unsaturated substituted C22 carboxylic acid that might undergo further processing after its release from the PKS.
多杀菌素是一类具有重要农业价值的杀虫抗生素,由刺糖多孢菌NRRL 18395产生。已对该菌108 kb的基因组DNA区域进行克隆、测序和分析,以揭示编码I型聚酮合酶(PKS)复合体的成簇基因。PKS基因两侧是编码参与尿素循环、缬氨酸、亮氨酸和异亮氨酸生物合成以及能量代谢的酶的同源物的基因。虽然预期通过插入失活破坏PKS基因不会消除多杀菌素的产生,但在测试生长条件下,亲本菌株和敲除突变菌株的抗菌、抗真菌或杀虫活性均未发现差异。根据PKS预测的模块和结构域推断出神秘代谢产物(称为obscurin)聚酮核心的最可能结构,表明形成了一种高度不饱和的取代C22羧酸,其从PKS释放后可能会经历进一步加工。