Dhanaraj C Justin, Nair M Sivasankaran
Department of Chemistry, Manonmaniam Sundaranar University, Tirunelveli-627 012, India.
Mycobiology. 2008 Dec;36(4):260-5. doi: 10.4489/MYCO.2008.36.4.260. Epub 2008 Dec 31.
Cyclic voltammetric measurements were performed for Co(II), Ni(II), Cu(II) and Zn(II) complexes of 1: 1alternating copolymer, poly(3-nitrobenzylidene-1-naphthylamine-co-succinic anhydride) (L) and Ni(II) and Cu(II) complexes of 1: 1alternating copolymer, poly(3-nitrobenzylidene-1-naphthylamine-co-methacrylic acid) (L1). The in vitro biological screening effects of the investigated compounds were tested against the fungal species including Aspergillus niger, Rhizopus stolonifer, Aspergillus flavus, Rhizoctonia bataicola and Candida albicans and bacterial species including Staphylococcus aureus, Escherichia coli, Klebsiella pneumaniae, Proteus vulgaris and Pseudomonas aeruginosa by well diffusion method. A comparative study of inhibition values of the copolymers and their complexes indicates that the complexes exhibit higher antimicrobial activity. Copper ions are proven to be essential for the growth-inhibitor effect. The extent of inhibition appeared to be strongly dependent on the initial cell density and on the growth medium. The nuclease activity of the above metal complexes were assessed by gel electrophoresis assay and the results show that the copper complexes can cleave pUC18 DNA effectively in presence of hydrogen peroxide compared to other metal complexes. The degradation experiments using Rhodamine B dye indicate that the hydroxyl radical species are involved in the DNA cleavage reactions.
对1:1交替共聚物聚(3 - 硝基亚苄基 - 1 - 萘胺 - 共 - 琥珀酸酐)(L)的钴(II)、镍(II)、铜(II)和锌(II)配合物以及1:1交替共聚物聚(3 - 硝基亚苄基 - 1 - 萘胺 - 共 - 甲基丙烯酸)(L1)的镍(II)和铜(II)配合物进行了循环伏安测量。通过打孔扩散法,针对包括黑曲霉、匍枝根霉、黄曲霉、立枯丝核菌和白色念珠菌在内的真菌物种以及包括金黄色葡萄球菌、大肠杆菌、肺炎克雷伯菌、普通变形杆菌和铜绿假单胞菌在内的细菌物种,测试了所研究化合物的体外生物筛选效果。对共聚物及其配合物抑制值的比较研究表明,配合物表现出更高的抗菌活性。已证明铜离子对于生长抑制作用至关重要。抑制程度似乎强烈依赖于初始细胞密度和生长培养基。通过凝胶电泳分析评估了上述金属配合物的核酸酶活性,结果表明,与其他金属配合物相比,铜配合物在过氧化氢存在下能有效切割pUC18 DNA。使用罗丹明B染料的降解实验表明,羟基自由基参与了DNA切割反应。