Adenoprevent Co., Ltd., Shizuoka 422-8526, Japan.
Department of Pharmaceutical Sciences, University of Shizuoka, Shizuoka 422-8526, Japan.
J Am Chem Soc. 2021 Apr 14;143(14):5526-5533. doi: 10.1021/jacs.1c01495. Epub 2021 Mar 31.
Colibactin is a polyketide-nonribosomal peptide hybrid secondary metabolite that can form interstrand cross-links in double-stranded DNA. Colibactin-producing has also been linked to colorectal oncogenesis. Thus, there is a strong interest in understanding the role colibactin may play in oncogenesis. Here, using the high-colibactin-producing wild-type strain we isolated from a clinical sample with the activity-based fluorescent probe we developed earlier, we were able to identify colibactin 770, which was recently identified and proposed as the complete form of colibactin, along with colibactin 788, 406, 416, 420, and 430 derived from colibactin 770 through structural rearrangements and solvolysis. Furthermore, we were able to trap the degrading mature colibactin species by converting the diketone moiety into quinoxaline in the crude culture extract to form colibactin 860 at milligram scale. This allowed us to determine the stereochemically complex structure of the rearranged form of an intact colibactin, colibactin 788, in detail. Furthermore, our study suggested that we were capturing only a few percent of the actual colibactin produced by the microbe, providing a crude quantitative insight into the inherent instability of this compound. Through the structural assignment of colibactins and their degradative products by the combination of LC-HRMS and NMR spectroscopies, we were able to elucidate further the fate of inherently unstable colibactin, which could help acquire a more complete picture of colibactin metabolism and identify key DNA adducts and biomarkers for diagnosing colorectal cancer.
肠菌素是一种聚酮-非核糖体肽杂合次级代谢产物,可在双链 DNA 中形成链间交联。产生肠菌素的细菌也与结直肠肿瘤发生有关。因此,人们强烈希望了解肠菌素在肿瘤发生中的可能作用。在这里,我们使用从临床样本中分离出的高肠菌素产生野生型菌株和我们之前开发的基于活性的荧光探针,能够鉴定出最近被鉴定并被提议为肠菌素完整形式的肠菌素 770,以及通过结构重排和溶剂解从肠菌素 770 衍生而来的肠菌素 788、406、416、420 和 430。此外,我们能够通过将二酮部分转化为粗培养物提取物中的喹喔啉,将成熟的降解肠菌素物种捕获到 quinoxaline 中,以毫克级规模形成肠菌素 860。这使我们能够详细确定完整肠菌素 788 的重排形式的立体化学复杂结构。此外,我们的研究表明,我们仅捕获了微生物产生的实际肠菌素的百分之几,这为该化合物的固有不稳定性提供了粗略的定量见解。通过结合 LC-HRMS 和 NMR 光谱学对肠菌素及其降解产物的结构分配,我们能够进一步阐明固有不稳定的肠菌素的命运,这有助于更全面地了解肠菌素代谢,并确定用于诊断结直肠癌的关键 DNA 加合物和生物标志物。