Division of Chemistry, Graduate School of Science, Hokkaido University, Sapporo, 060-0810, Japan.
Biomedicinal Information Research Center (BIRC), Japan Biological Informatics Consortium (JBIC), Koto-ku, Tokyo, 818, Japan.
Angew Chem Int Ed Engl. 2016 Jul 4;55(28):8072-5. doi: 10.1002/anie.201602611. Epub 2016 May 11.
The biosynthetic machinery of the first fungal ribosomally synthesized and post-translationally modified peptide (RiPP) ustiloxin B was elucidated through a series of gene inactivation and heterologous expression studies. The results confirmed an essential requirement for novel oxidases possessing the DUF3328 motif for macrocyclization, and highly unique side-chain modifications by three oxidases (UstCF1F2) and a pyridoxal 5'-phosphate (PLP)-dependent enzyme (UstD). These findings provide new insight into the expression of the RiPP gene clusters found in various fungi.
通过一系列基因失活和异源表达研究,阐明了第一个真菌核糖体合成和翻译后修饰肽(RiPP)ustiloxin B 的生物合成机制。结果证实了 novel oxidases 对于大环化所必需的,并且具有 DUF3328 基序,并且三个氧化酶(UstCF1F2)和一个吡哆醛 5'-磷酸(PLP)依赖性酶(UstD)对非常独特的侧链修饰。这些发现为各种真菌中发现的 RiPP 基因簇的表达提供了新的见解。