Garforth S J, Patel D, Feng M, Sayers J R
Division of Genomic Medicine, University of Sheffield, Royal Hallamshire Hospital, Sheffield S10 2RX, UK.
Nucleic Acids Res. 2001 Jul 1;29(13):2772-9. doi: 10.1093/nar/29.13.2772.
T5 5'-3' exonuclease is a member of a homologous group of 5' nucleases which require divalent metal co-factors. Structural and biochemical studies suggest that single-stranded DNA substrates thread through a helical arch or hole in the protein, thus bringing the phosphodiester backbone into close proximity with the active site metal co-factors. In addition to the expected use of Mg(2+), Mn(2+) and Co(2+) as co-factors, we found that divalent zinc, iron, nickel and copper ions also supported catalysis. Such a range of co-factor utilisation is unusual in a single enzyme. Some co-factors such as Mn(2+) stimulated the cleavage of double-stranded closed-circular plasmid DNA. Such endonucleolytic cleavage of circular double-stranded DNA cannot be readily explained by the threading model proposed for the cleavage of substrates with free 5'-ends as the hole observed in the crystal structure of T5 exonuclease is too small to permit the passage of double-stranded DNA. We suggest that such a substrate may gain access to the active site of the enzyme by a process which does not involve threading.
T5 5'-3'核酸外切酶是一类需要二价金属辅助因子的5'核酸酶同源家族的成员。结构和生化研究表明,单链DNA底物穿过蛋白质中的螺旋拱或孔,从而使磷酸二酯主链与活性位点金属辅助因子紧密靠近。除了预期使用Mg(2+)、Mn(2+)和Co(2+)作为辅助因子外,我们发现二价锌、铁、镍和铜离子也支持催化作用。如此广泛的辅助因子利用情况在单一酶中是不常见的。一些辅助因子,如Mn(2+),刺激双链闭环质粒DNA的切割。这种环状双链DNA的内切核酸酶切割不能轻易地用为切割具有游离5'-末端的底物所提出的穿线模型来解释,因为在T5核酸外切酶的晶体结构中观察到的孔太小,无法允许双链DNA通过。我们认为,这样的底物可能通过一个不涉及穿线的过程进入酶的活性位点。