Goto Yuki, Ito Yumi, Kato Yasuharu, Tsunoda Shotaro, Suga Hiroaki
Department of Chemistry, Graduate School of Science, The University of Tokyo, Tokyo 113-0033, Japan; JST, PRESTO, Tokyo 113-0033, Japan.
Department of Chemistry and Biotechnology, Graduate School of Engineering, The University of Tokyo, Tokyo 113-8656, Japan.
Chem Biol. 2014 Jun 19;21(6):766-74. doi: 10.1016/j.chembiol.2014.04.008. Epub 2014 May 22.
Azoline moieties in the backbones of peptidic natural products are important structural motifs that contribute to diverse bioactivities. Some azoline-containing peptides (Az-peptides) are produced from ribosomally synthesized precursor peptides, in which cysteine, serine, and threonine residues are converted to their corresponding azolines by posttranslational modification through a cyclodehydratase. We have devised an in vitro biosynthesis system of Az-peptides, referred to as the FIT-PatD (flexible in vitro translation) system, by the integration of a cell-free translation system with the posttranslational cyclodehydratase PatD. This system enabled the "one-pot" synthesis of a wide variety of Az-peptide derivatives expressed from synthetic DNA templates. The FIT-PatD system also facilitated mutagenesis studies on a wide array of precursor peptide sequences, unveiling unique in vitro substrate tolerance of PatD.
肽类天然产物主链中的唑啉部分是重要的结构基序,有助于产生多种生物活性。一些含唑啉的肽(Az肽)由核糖体合成的前体肽产生,其中半胱氨酸、丝氨酸和苏氨酸残基通过环化脱水酶的翻译后修饰转化为相应的唑啉。我们通过将无细胞翻译系统与翻译后环化脱水酶PatD整合,设计了一种Az肽的体外生物合成系统,称为FIT-PatD(灵活体外翻译)系统。该系统能够从合成DNA模板“一锅法”合成多种Az肽衍生物。FIT-PatD系统还促进了对多种前体肽序列的诱变研究,揭示了PatD独特的体外底物耐受性。