Institute for Integrative Biology of the Cell (I2BC), CEA, CNRS Univ. Paris-Sud, Université Paris-Saclay, 91198 Gif-sur-Yvette cedex, France.
Nat Prod Rep. 2020 Mar 25;37(3):312-321. doi: 10.1039/c9np00036d.
Covering: Up to mid-2019 Cyclodipeptide synthases (CDPSs) catalyse the formation of cyclodipeptides using aminoacylated-tRNA as substrates. The recent characterization of large sets of CDPSs has revealed that they can produce highly diverse products, and therefore have great potential for use in the production of different 2,5-diketopiperazines (2,5-DKPs). Sequence similarity networks (SSNs) are presented as a new, efficient way of classifying CDPSs by specificity and identifying new CDPS likely to display novel specificities. Several strategies for further increasing the diversity accessible with these enzymes are discussed here, including the incorporation of non-canonical amino acids by CDPSs and use of the remarkable diversity of 2,5-DKP-tailoring enzymes discovered in recent years.
截至 2019 年年中,环二肽合酶(CDPS)使用氨酰化 tRNA 作为底物催化环二肽的形成。最近对大量 CDPS 的特征描述表明,它们可以产生高度多样化的产物,因此在生产不同的 2,5-二酮哌嗪(2,5-DKP)方面具有很大的潜力。序列相似性网络(SSN)被提出作为一种新的、有效的分类 CDPS 的方法,通过特异性和识别可能显示新特异性的新 CDPS。本文讨论了几种进一步增加这些酶可获得多样性的策略,包括 CDPS 中掺入非典型氨基酸以及利用近年来发现的 2,5-DKP 修饰酶的显著多样性。