Zincophorin - biosynthesis in Streptomyces griseus and antibiotic properties.

GMS infectious diseases Pub Date : 2016-11-28 eCollection Date: 2016-01-01 DOI:10.3205/id000026
Elisabeth Walther, Sabrina Boldt, Hirokazu Kage, Tom Lauterbach, Karin Martin, Martin Roth, Christian Hertweck, Andreas Sauerbrei, Michaela Schmidtke, Markus Nett
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引用次数: 4

Abstract

Zincophorin is a polyketide antibiotic that possesses potent activity against Gram-positive bacteria, including human pathogens. While a number of total syntheses of this highly functionalized natural product were reported since its initial discovery, the genetic basis for the biosynthesis of zincophorin has remained unclear. In this study, the co-linearity inherent to polyketide pathways was used to identify the zincophorin biosynthesis gene cluster in the genome of the natural producer Streptomyces griseus HKI 0741. Interestingly, the same locus is fully conserved in the streptomycin-producing actinomycete S. griseus IFO 13350, suggesting that the latter bacterium is also capable of zincophorin biosynthesis. Biological profiling of zincophorin revealed a dose-dependent inhibition of the Gram-positive bacterium Streptococcus pneumoniae. The antibacterial effect, however, is accompanied by cytotoxicity. Antibiotic and cytotoxic activities were completely abolished upon esterification of the carboxylic acid group in zincophorin.

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灰色链霉菌中的锌磷合成及其抗生素特性。
锌磷是一种聚酮类抗生素,对革兰氏阳性细菌,包括人类病原体具有有效的活性。虽然这种高度功能化的天然产物自最初发现以来已被报道了许多全合成,但锌磷生物合成的遗传基础仍不清楚。在本研究中,利用聚酮途径固有的共线性,鉴定了天然生产者链霉菌HKI 0741基因组中的锌磷生物合成基因簇。有趣的是,同样的位点在产链霉素的放线菌S. griseus IFO 13350中完全保守,这表明后者也能够生物合成锌磷。锌磷蛋白的生物学分析显示了对革兰氏阳性细菌肺炎链球菌的剂量依赖性抑制。然而,抗菌作用伴随着细胞毒性。锌磷中羧酸基的酯化完全消除了抗生素和细胞毒活性。
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