Identification of Genes Essential for Sulfamate and Fluorine Incorporation During Nucleocidin Biosynthesis

被引:10
作者
Pasternak, A. R. Ola [1 ]
Bechthold, Andreas [2 ]
Zechel, David L. [1 ]
机构
[1] Queens Univ, Dept Chem, 90 Bader Ln, Kingston, ON K7L 2S8, Canada
[2] Albert Ludwigs Univ Freiburg, Dept Pharmaceut Biol & Biotechnol, Inst Pharmaceut Sci, Stefan Meier Str 19, D-79104 Freiburg, Germany
基金
加拿大自然科学与工程研究理事会;
关键词
biosynthesis; fluorine; gene disruption; nucleocidin; sulfamate; STREPTOMYCES-CALVUS; DISCOVERY;
D O I
10.1002/cbic.202200140
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nucleocidin is an adenosine derivative containing 4'-fluoro and 5'-O-sulfamoyl substituents. In this study, nucleocidin biosynthesis is examined in two newly discovered producers, Streptomyces virens B-24331 and Streptomyces aureorectus B-24301, which produce nucleocidin and related derivatives at titers 30-fold greater than S. calvus. This enabled the identification of two new O-acetylated nucleocidin derivatives, and a potential glycosyl-O-acetyltransferase. Disruption of nucJ, nucG, and nucI, within S. virens B-24331, specifying a radical SAM/Fe-S dependent enzyme, sulfatase, and arylsulfatase, respectively, led to loss of 5'-O-sulfamoyl biosynthesis, but not fluoronucleoside production. Disruption of nucN, nucK, and nucO specifying an amidinotransferase, and two sulfotransferases respectively, led to loss of fluoronucleoside production. Identification of S. virens B-24331 as a genetically tractable and high producing strain sets the stage for understanding nucleocidin biosynthesis and highlights the utility of using 16S-RNA sequences to identify alternative producers of valuable compounds in the absence of genome sequence data.
引用
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页数:9
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