Comparison of catalytic activities of new La(III) and Ce(III) complexes with different diaza-crown ether ligands for DNA hydrolytic cleavage. (1st September 2016)

• Record Type: Journal Article
• Authors: Li, Fang-zhen; Xie, Jia-qing; Cai, Shu-lan; Feng, Fa-mei
• Is Part Of: Progress in reaction kinetics and mechanism. Volume 41:Number 3(2016)
• Page Start: 309
• Page End: 318
• Publication Date: 2016-09-01
• Subjects: Chemical kinetics -- Periodicals; 541.39405
• DOI: 10.3184/146867816X14698928943442
• Languages: English
• ISSNs: 1468-6783

Abstract

A new diaza-crown ether with double hydroxypropyl branches (L = 1, 1'-(1, 4, 10, 13-tetraoxa-7, 16-diazacyclooctadecane-7, 16-diyl)dipropan-2-ol) and its two lanthanide complexes (LaL and CeL) were synthesised and characterised. Their nuclease activities on pUC19 DNA cleavage were investigated using agarose gel electrophoresis, and pseudo-first-order rate constants kobs of 0.067 h–1 for LaL, 0.041 h–1 for CeL, 0.013 h–1 or LaL0, and 0.027 h–1 CeL0 were obtained (L0 = 1, 4, 10, 13-tetraoxa-7, 16-diazacyclooctadecane). The results indicated that the CeL complex was more efficient than the LaL complex for DNA cleavage at low concentrations, but the LaL complex was more efficient than the CeL complex at high concentrations. Moreover, kinetic studies demonstrated that introducing hydroxypropyl side arms in the ring of the diazacrown ether can improve the catalytic ability of the complexes in DNA cleavage, which may be due to the hydroxypropyl side arms enhancing the bonding interaction between the complex and the DNA molecule by hydrogen bonding. A hydrolytic mechanism for DNA cleavage was demonstrated by applying several oxygen scavengers to the DNA catalytic cleavage. A proposed mechanism for the DNA cleavage shows that the hydroxypropyl side groups can recognise and bind the phosphodiester bond of DNA by hydrogen bonding and electrostatic interaction.