Triandafilova Galina, Smirnova Galina, Krasnykh Olga, Boteva Anastasija, Oktyabrsky Oleg
Laboratory of Physiology and Genetics of Microorganisms, Institute of Ecology and Genetics of Microorganisms, Perm Federal Research Center, Russian Academy of Sciences, Perm, Russia.
Scientific and Educational Center for Applied Chemical and Biological Research, Perm National Research Polytechnic University, Perm, Russia.
Indian J Microbiol. 2024 Jun;64(2):482-491. doi: 10.1007/s12088-023-01158-6. Epub 2023 Dec 13.
We investigated antimicrobial and antioxidant activity of nitrogen-containing heterocycles and their acyclic analogues, some of which can be considered as promising in terms of biological activity. Based on structure, 26 tested compounds were divided into 4 groups. In the test with 2,2-diphenyl-1-picrylhydrazyl (DPPH), the compounds of the group 2 had the highest radical-binding activity (RBA) (53-78%), while those of group 3 had the lowest values (1.5-5.2%). In oxygen radical absorbance capacity assay, all compounds from groups 1, 2 and 3 showed high RBA: 44-94% at 50 µM. The highest bacteriostatic activity against was found for four compounds in group 2 (MIC = 0.25-1 mM) and low bacteriostatic activity for group 3 (MIC > 4 mM). Some relationships between the structure of compounds and the values of the MIC are revealed. It was also found that four substances from different groups had the ability to inhibit the formation of colonies in from 1.3 to 5.7 times. Four compounds reduced specific biofilm formation by 40-60%. The tested substances did not induce the expression of the gene controlled by the SOS system, which indicates the lack of genotoxic activity. None of the tested compounds had pro-oxidant activity. This was shown by both the absence of production hydrogen peroxide in a bacteria-free medium and inability to induce expression of the gene encoding HPI catalase in growing . The data obtained could be useful in the development of new drugs.
我们研究了含氮杂环及其无环类似物的抗菌和抗氧化活性,其中一些在生物活性方面被认为具有潜力。基于结构,26种受试化合物被分为4组。在与2,2-二苯基-1-苦基肼(DPPH)的测试中,第2组化合物具有最高的自由基结合活性(RBA)(53 - 78%),而第3组化合物的值最低(1.5 - 5.2%)。在氧自由基吸收能力测定中,第1、2和3组的所有化合物均表现出较高的RBA:在50 μM时为44 - 94%。第2组中的四种化合物对[具体细菌名称未给出]具有最高的抑菌活性(MIC = 0.25 - 1 mM),而第3组的抑菌活性较低(MIC > 4 mM)。揭示了化合物结构与MIC值之间的一些关系。还发现来自不同组的四种物质能够将[具体细菌名称未给出]中的菌落形成抑制1.3至5.7倍。四种化合物使特定生物膜形成减少了40 - 60%。受试物质未诱导由SOS系统控制的[具体基因名称未给出]基因的表达,这表明缺乏遗传毒性活性。没有一种受试化合物具有促氧化活性。这在无细菌培养基中不产生过氧化氢以及在生长的[具体细菌名称未给出]中无法诱导编码HPI过氧化氢酶的[具体基因名称未给出]基因表达中均得到了证明。所获得的数据可能对新药开发有用。