Daum Martina, Peintner Iris, Linnenbrink Anton, Frerich Anke, Weber Monika, Paululat Thomas, Bechthold Andreas
Albert-Ludwigs-Universität, Institut für Pharmazeutische Wissenschaften, Pharmazeutische Biologie und Biotechnologie, Freiburg, Germany.
Chembiochem. 2009 Apr 17;10(6):1073-83. doi: 10.1002/cbic.200800823.
Polyketomycin is a tetracyclic quinone glycoside produced by Streptomyces diastatochromogenes Tü6028. It shows cytotoxic and antibiotic activity, in particular against Gram-positive multi-drug-resistant strains (for example, MRSA). The polyketomycin biosynthetic gene cluster has been sequenced and characterised. Its identity was proven by inactivation of a alpha-ketoacyl synthase gene (pokP1) of the "minimal polyketide synthase II" system. In order to obtain valuable information about tailoring steps, we performed further gene-inactivation experiments. The generation of mutants with deletions in oxygenase genes (pokO1, pokO2, both in parallel and pokO4) and methyltransferase genes (pokMT1, pokMT2 and pokMT3) resulted in new polyketomycin derivatives, and provided information about the organisation of the biosynthetic pathway.
聚酮霉素是由变栖链霉菌Tü6028产生的一种四环醌糖苷。它具有细胞毒性和抗菌活性,尤其对革兰氏阳性多重耐药菌株(如耐甲氧西林金黄色葡萄球菌)有效。聚酮霉素生物合成基因簇已被测序和表征。通过使“最小聚酮合酶II”系统的α-酮酰基合酶基因(pokP1)失活,证实了其身份。为了获得有关修饰步骤的有价值信息,我们进行了进一步的基因失活实验。产生了在加氧酶基因(pokO1、pokO2,两者平行以及pokO4)和甲基转移酶基因(pokMT1、pokMT2和pokMT3)中缺失的突变体,从而得到了新的聚酮霉素衍生物,并提供了有关生物合成途径组织的信息。