Bailly V, Verly W G, O'Connor T, Laval J
Laboratoire de Biochimie, Faculté des Sciences, Université de Liège, Belgium.
Biochem J. 1989 Sep 1;262(2):581-9. doi: 10.1042/bj2620581.
Escherichia coli [formamidopyrimidine]DNA glycosylase catalyses the nicking of both the phosphodiester bonds 3' and 5' of apurinic or apyrimidinic sites in DNA so that the base-free deoxyribose is replaced by a gap limited by 3'-phosphate and 5'-phosphate ends. The two nickings are not the results of hydrolytic processes; the [formamidopyrimidine]DNA glycosylase rather catalyses a beta-elimination reaction that is immediately followed by a delta-elimination. The enzyme is without action on a 3'-terminal base-free deoxyribose or on a 3'-terminal base-free unsaturated sugar produced by a beta-elimination reaction nicking the DNA strand 3' to an apurinic or apyrimidinic site.
大肠杆菌[甲酰胺嘧啶]DNA糖基化酶催化DNA中无嘌呤或无嘧啶位点3'和5'处的磷酸二酯键断裂,使得无碱基的脱氧核糖被一个由3'-磷酸和5'-磷酸末端限定的缺口所取代。这两次断裂并非水解过程的结果;[甲酰胺嘧啶]DNA糖基化酶反而催化一个β-消除反应,该反应紧接着发生一个δ-消除反应。该酶对由β-消除反应在无嘌呤或无嘧啶位点3'端切断DNA链所产生的3'-末端无碱基脱氧核糖或3'-末端无碱基不饱和糖不起作用。