PT  - JOURNAL ARTICLE
AU  - Alexander A. Vinogradov
AU  - Morito Shimomura
AU  - Yuki Goto
AU  - Taro Ozaki
AU  - Shumpei Asamizu
AU  - Yoshinori Sugai
AU  - Hiroaki Suga
AU  - Hiroyasu Onaka
TI  - Minimal lactazole scaffold for <em>in vitro</em> production of pseudo-natural thiopeptides
AID  - 10.1101/807206
DP  - 2019 Jan 01
TA  - bioRxiv
PG  - 807206
4099  - http://biorxiv.org/content/early/2019/10/16/807206.short
4100  - http://biorxiv.org/content/early/2019/10/16/807206.full
AB  - Lactazole A is a cryptic thiopeptide from Streptomyces lactacystinaeus, encoded by a compact 9.8 kb biosynthetic gene cluster. Here, we established a platform for in vitro biosynthesis of lactazole A, referred to as the FIT-Laz system, via a combination of the flexible in vitro translation (FIT) system with recombinantly produced lactazole biosynthetic enzymes. Systematic dissection of lactazole biosynthesis revealed remarkable substrate tolerance of the biosynthetic enzymes, and led to the development of the “minimal lactazole scaffold”, a construct requiring only 6 post-translational modifications for macrocyclization. Efficient assembly of such minimal thiopeptides with FIT-Laz enabled access to diverse lactazole analogs with 10 consecutive mutations, 14- to 62-membered macrocycles, and up to 18 amino acid-long tail regions. Moreover, utilizing genetic code reprogramming, we demonstrated synthesis of pseudo-natural lactazoles containing 4 non-proteinogenic amino acids. This work opens possibilities in exploring novel sequence space of pseudo-natural thiopeptides.