Kinetic Consequences of Replacing the Internucleotide Phosphorus Atoms in DNA with Arsenic

被引:33
作者
Fekry, Mostafa I. [1 ,3 ]
Tipton, Peter A. [2 ]
Gates, Kent S. [1 ,2 ]
机构
[1] Univ Missouri, Dept Chem, Columbia, MO 65211 USA
[2] Univ Missouri, Dept Biochem, Columbia, MO 65211 USA
[3] Cairo Univ, Fac Pharm, Dept Pharmacognosy, Cairo 11562, Egypt
关键词
PURINE NUCLEOSIDE PHOSPHORYLASE; TRANSITION-STATE ANALYSIS; HYDROLYSIS; REDUCTION; PHOSPHODIESTERS; PHOSPHATASES; ARSENOLYSIS; EXCHANGE; REPAIR; WATER;
D O I
10.1021/cb2000023
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
It was claimed in a recent publication that a strain of Halomonadacea bacteria (GFAJ-1) isolated from the arsenic-rich waters of Mono Lake, California is able to substitute arsenic for phosphorus in its macromolecules and small molecule metabolites. In this short Perspective, we consider chemical and biochemical issues surrounding the central claim that Halomonadacea GFAJ-1 is able to survive while incorporating kinetically labile arsenodiester linkages into the backbone of its DNA. Chemical precedents suggest that arsenodiester linkages in the putative arsenic-containing DNA of GFAJ-1 would undergo very rapid hydrolytic cleavage in water at 25 degrees C with an estimated half-life of 0.06 s. In contrast, the phosphodiester linkages of native DNA undergo spontaneous hydrolysis with a half-life of approximately 30,000,000 y at 25 degrees C. Overcoming such dramatic kinetic instability in its genetic material would present serious challenges to Halomonadacea GFAJ-1.
引用
收藏
页码:127 / 130
页数:4
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