Guranowski A, Starzyńska E, Taylor G E, Blackburn G M
Katedra Biochemii, Akademia Rolnicza, Poznań, Poland.
Biochem J. 1989 Aug 15;262(1):241-4. doi: 10.1042/bj2620241.
Six new methylenephosphonate analogues of P1P4-bis-(5',5'''-adenosyl) tetraphosphate, Ap4A, having P2-P3 carbon bridges CF2, CCl2 and CH2CH2 or P1-P2 and P3-P4 carbon bridges CF2, CCl2 and CH2CH2 in the tetraphosphate chain, were examined as substrates or inhibitors for two specific Ap4A-degrading enzymes: (asymmetrical) Ap4A hydrolase (EC 3.6.1.17) from yellow-lupin seeds and (symmetrical) Ap4A hydrolase (EC 3.6.1.41) from Escherichia coli. All analogues in which the central oxygen atom was replaced by a stable carbon bridge were hydrolysed by the asymmetrical hydrolase (CF2 greater than CCl2 greater than O greater than CHBr greater than CH2 greater than CH2CH2). As expected, these analogues were not hydrolysed by the symmetrical hydrolase, which was also unable to act on analogues having P1-P2 and P3-P4 carbon bridges.
研究了六种新的P1P4 - 双 -(5',5'''-腺苷)四磷酸(Ap4A)的亚甲基膦酸酯类似物,它们在四磷酸链中具有P2 - P3碳桥CF2、CCl2和CH2CH2或P1 - P2和P3 - P4碳桥CF2、CCl2和CH2CH2,作为两种特定Ap4A降解酶的底物或抑制剂:来自黄羽扇豆种子的(不对称)Ap4A水解酶(EC 3.6.1.17)和来自大肠杆菌的(对称)Ap4A水解酶(EC 3.6.1.41)。所有中心氧原子被稳定碳桥取代的类似物都被不对称水解酶水解(CF2>CCl2>O>CHBr>CH2>CH2CH2)。正如预期的那样,这些类似物不会被对称水解酶水解,对称水解酶也无法作用于具有P1 - P2和P3 - P4碳桥的类似物。