Stanišić Aleksa, Hüsken Annika, Kries Hajo
Independent Junior Research Group Biosynthetic Design of Natural Products , Leibniz Institute for Natural Product Research and Infection Biology e.V. , Hans Knöll Institute (HKI Jena) , Beutenbergstr. 11a , 07745 Jena , Germany . Email:
Chem Sci. 2019 Oct 3;10(44):10395-10399. doi: 10.1039/c9sc04222a. eCollection 2019 Nov 28.
Adenylation enzymes selecting substrates for ribosomal and nonribosomal protein and peptide biosynthesis have been popular targets of enzyme engineering. Previous standard assays for adenylation specificity have been cumbersome and failed to reflect the competition conditions inside a cell because they measure substrates one at a time. We have developed an adenylation assay based on hydroxamate quenching and LC-MS/MS detection of hydroxamate products testing dozens of competing amino acid substrates in parallel. Streamlined specificity profiling of adenylation enzymes will facilitate engineering and directed evolution of ribosomal and nonribosomal peptide synthesis.
为核糖体和非核糖体蛋白质及肽生物合成选择底物的腺苷酸化酶一直是酶工程的热门靶点。以前用于腺苷酸化特异性的标准检测方法繁琐,且由于一次只检测一种底物,无法反映细胞内的竞争情况。我们开发了一种基于异羟肟酸淬灭和异羟肟酸产物的液相色谱-串联质谱检测的腺苷酸化检测方法,可同时检测数十种竞争性氨基酸底物。简化腺苷酸化酶的特异性分析将有助于核糖体和非核糖体肽合成的工程改造和定向进化。