Aalborg University Esbjerg, Department of Chemistry and Bioscience, Niels Bohrs Vej 8, 6700 Esbjerg, Denmark.
Aalborg University Aalborg, Department of Chemistry and Bioscience, Fredrik Bajers Vej 7H, 9220 Aalborg, Denmark.
Int J Mol Sci. 2020 Oct 14;21(20):7601. doi: 10.3390/ijms21207601.
Through stepwise recreation of the biosynthetic gene cluster containing from , it was possible to produce the core scaffold compound of bostrycoidin, a red aza-anthraquinone pigment in . This was achieved through sequential transformation associated recombination (TAR) cloning of , , , and into the pESC-vector system, utilizing the inducible bidirectional galactose promoter for heterologous expression in . The production of the core metabolite bostrycoidin was investigated through triplicate growth cultures for 1-4 days, where the maximum titer of bostrycoidin was achieved after 2 days of induction, yielding 2.2 mg/L.
通过逐步重建包含 的生物合成基因簇,有可能产生红氮杂蒽醌类色素博斯提库丁的核心支架化合物。这是通过将 、 、 和 顺序转化相关重组(TAR)克隆到 pESC-载体系统中,利用诱导性双向半乳糖启动子在 中进行异源表达来实现的。通过 1-4 天的重复生长培养来研究核心代谢物博斯提库丁的生产,在诱导后 2 天达到博斯提库丁的最大滴度,产量为 2.2mg/L。