Hydroxamate-based colorimetric assay to assess amide bond formation by adenylation domain of nonribosomal peptide synthetases

被引:15
|
作者
Hara, Ryotaro [1 ]
Suzuki, Ryohei [2 ]
Kino, Kuniki [1 ,2 ]
机构
[1] Waseda Univ, Res Inst Sci & Engn, Tokyo 1698555, Japan
[2] Waseda Univ, Fac Sci & Engn, Dept Appl Chem, Tokyo 1698555, Japan
基金
日本学术振兴会;
关键词
Nonribosomal peptide synthetase; Adenylation domain; Aminoacyl-AMP; Hydroxylamine; Colorimetric assay; Amide bond; COMBINATORIAL BIOSYNTHESIS; FORMING DOMAIN; EXPRESSION; EXCHANGE; ENZYMES;
D O I
10.1016/j.ab.2015.01.006
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We demonstrated the usefulness of a hydroxamate-based colorimetric assay for predicting amide bond formation (through an aminoacyl-AMP intermediate) by the adenylation domain of nonribosomal peptide synthetases. By using a typical adenylation domain of tyrocidine synthetase (involved in tyrocidine biosynthesis), we confirmed the correlation between the absorbance at 490 nm of the L-Trp-hydroxamate-Fe3+ complex and the formation of L-Trp-L-Pro, where L-Pro was used instead of hydroxylamine. Furthermore, this assay was adapted to the adenylation domains of surfactin synthetase (involved in surfactin biosynthesis) and bacitracin synthetase (involved in bacitracin biosynthesis). Consequently, the formation of various aminoacyl L-Pro formations was observed. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:89 / 91
页数:3
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