Yang C C, Leong J
Antimicrob Agents Chemother. 1981 Oct;20(4):558-62. doi: 10.1128/AAC.20.4.558.
The free ligand, deferroviridomycin A, and its iron(II) complex, viridomycin A, were detected in culture supernatant fluids of Streptomyces viridans 1671 and were structurally characterized as 4-hydroxy-3-nitrosobenzaldehyde and tris(4-hydroxy-3-nitrosobenzaldehydato-N3,O4)ferrate(II), respectively. We investigated the antibiotic activity of the above compounds and of the chemically synthesized bis copper(II), tris cobalt(III), and tris nickel(II) complexes against Escherichia coli NIHJ, Salmonella typhimurium LT-2Z, Staphylococcus aureus 209P, Streptococcus faecium 10541, and Bacillus cereus, T. The free ligand and its kinetically labile copper(II) and nickel(II) complexes displayed activity against all of the above organisms, whereas the kinetically inert iron(II) and cobalt(III) complexes displayed activity only against S. aureus and B. cereus. The antibiotic activity of the substitutionally labile metal complexes was attributed to dissociation of the free ligand. The mode of antibiotic action of the free ligand against E. coli appears to be interference with the structural and functional integrity of the cell membrane.
在绿色链霉菌1671的培养上清液中检测到了游离配体去铁绿霉素A及其铁(II)配合物绿霉素A,其结构分别被表征为4-羟基-3-亚硝基苯甲醛和三(4-羟基-3-亚硝基苯甲醛-N3,O4)铁(II)。我们研究了上述化合物以及化学合成的双铜(II)、三钴(III)和三镍(II)配合物对大肠杆菌NIHJ、鼠伤寒沙门氏菌LT-2Z、金黄色葡萄球菌209P、粪肠球菌10541和蜡样芽孢杆菌的抗菌活性。游离配体及其动力学不稳定的铜(II)和镍(II)配合物对上述所有微生物均表现出活性,而动力学惰性的铁(II)和钴(III)配合物仅对金黄色葡萄球菌和蜡样芽孢杆菌表现出活性。取代不稳定金属配合物的抗菌活性归因于游离配体的解离。游离配体对大肠杆菌的抗菌作用方式似乎是干扰细胞膜的结构和功能完整性。