Santos-Beneit Fernando, Errington Jeff
Centre for Bacterial Cell Biology, Institute for Cell and Molecular Biosciences, Medical School, Newcastle University, Newcastle upon Tyne, UK.
Arch Microbiol. 2017 Aug;199(6):875-880. doi: 10.1007/s00203-017-1358-1. Epub 2017 Mar 22.
Polyketides constitute a large group of structurally diverse natural products with useful biological activities. Insights into their biosynthetic mechanisms are crucial for developing new structures. One of the most studied model polyketide is the blue-pigmented antibiotic actinorhodin, produced by Streptomyces coelicolor. This aromatic polyketide is synthesized by minimal type II polyketide synthases and tailoring enzymes. The ActIII actinorhodin ketoreductase is a key tailoring enzyme in actinorhodin biosynthesis. Previous papers have reported contradictory findings for localization of the protein in the cytoplasmic fraction or associated with the cell wall. We have now used green fluorescent protein as a reporter to analyse the spatial and temporal expression of actIII (SCO5086) in S. coelicolor under actinorhodin producing and non-producing conditions. We provide evidence in support of ActIII being a cytosolic protein, with limited if any association with the membrane or cell wall.
聚酮化合物是一大类结构多样且具有有益生物活性的天然产物。深入了解它们的生物合成机制对于开发新结构至关重要。研究最多的模型聚酮化合物之一是由天蓝色链霉菌产生的蓝色色素抗生素放线紫红素。这种芳香族聚酮化合物由最小型II型聚酮合酶和修饰酶合成。ActIII放线紫红素酮还原酶是放线紫红素生物合成中的关键修饰酶。先前的论文报道了该蛋白定位于细胞质部分或与细胞壁相关的相互矛盾的结果。我们现在使用绿色荧光蛋白作为报告基因,分析了在产生和不产生放线紫红素的条件下,天蓝色链霉菌中actIII(SCO5086)的时空表达。我们提供的证据支持ActIII是一种胞质蛋白,与膜或细胞壁的关联有限(如果有的话)。