Wang Peng, Zhang Wenjun, Zhan Jixun, Tang Yi
Laboratory of Microbial Metabolism and School of Life Science and Biotechnology, Shanghai Jiaotong University, Shanghai 200030, China.
Chembiochem. 2009 Jun 15;10(9):1544-50. doi: 10.1002/cbic.200900122.
The double hydroxylation of 6-pretetramid to 4-keto-anhydrotetracycline is a key tailoring reaction during the biosynthesis of the broad-spectrum antibiotic tetracyclines. It has been shown previously by heterologous reconstitution that OxyL is a dioxygenase and is the only enzyme required to catalyze the insertion of oxygen atoms at the C-12a and C-4 positions. We report here that OxyE, a flavin adenine dinucleotide (FAD)-dependent hydroxylase homologue, is an ancillary mono-oxygenase for OxyL during oxytetracycline biosynthesis in Streptomyces rimosus. By using both gene disruption and heterologous reconstitution approaches, we demonstrated that OxyE plays a nonessential, but important role in oxytetracycline biosynthesis by serving as a more efficient C-4 hydroxylase. In addition, we demonstrated that partially oxidized biosynthetic intermediates can undergo various glycosylation modifications in S. rimosus. Our results indicate that the synergistic actions of OxyE and OxyL in the double hydroxylation step prevent accumulation of shunt products during oxytetracycline biosynthesis in S. rimosus.
6-预四环素向4-酮-脱水四环素的双羟基化反应是广谱抗生素四环素生物合成过程中的关键修饰反应。先前通过异源重组已表明,OxyL是一种双加氧酶,是催化在C-12a和C-4位插入氧原子所需的唯一酶。我们在此报告,黄素腺嘌呤二核苷酸(FAD)依赖性羟化酶同源物OxyE是龟裂链霉菌中四环素生物合成过程中OxyL的辅助单加氧酶。通过使用基因破坏和异源重组方法,我们证明OxyE作为更有效的C-4羟化酶,在四环素生物合成中发挥非必需但重要的作用。此外,我们证明部分氧化的生物合成中间体在龟裂链霉菌中可进行各种糖基化修饰。我们的结果表明,OxyE和OxyL在双羟基化步骤中的协同作用可防止龟裂链霉菌中四环素生物合成过程中旁路产物的积累。