Mancinelli R L, McKay C P
Appl Environ Microbiol. 1983 Jul;46(1):198-202. doi: 10.1128/aem.46.1.198-202.1983.
The effects of low concentrations of nitric oxide (NO) and nitrogen dioxide (NO2) on actively dividing cultures of Staphylococcus aureus, Micrococcus luteus, Micrococcus roseus, Serratia marcescens, Bacillus subtilis, Bacillus circulans, Bacillus megaterium, and Bacillus cereus were studied. Fresh cultures of each organism were incubated for 24 h at 25 degrees C on both nutrient agar and mineral salts glucose agar plates under atmospheres containing various low concentrations of NO in air (0 to 1.9 ppm [0 to 2.0 micrograms/g of air]), NO2 in air (0 to 5.5 ppm [0 to 8.8 micrograms/g of air]), or NO and NO2 in air. Bacteria grown under air only were used as controls. After incubation, the colonies that developed on the plates were counted. None of the bacteria tested was affected by NO or NO2 at the indicated concentrations while growing on nutrient agar. Serratia marcescens, B. circulans, B. subtilis, B. megaterium, and B. cereus grown on mineral salts glucose agar were not significantly affected by NO or NO2. Low concentrations (0 to 1.9 ppm) of NO were bacteriostatic to log-phase cultures of M. roseus, M. luteus, and Staphylococcus aureus grown on mineral salts glucose agar. Bacteriostatic activity over a 24-h interval was maximal at an initial NO concentration of 1 ppm. Appreciable amounts of NO2 were produced in 24 h at initial NO concentrations greater than 1 ppm. These results suggest that NO2 may reduce the bacteriostatic activity of NO. Low concentrations (0 to 5.5 ppm) of NO2 in air did not affect any of the bacteria tested. At these low concentrations, NO affected bacterial growth, although NO2, NO2-, and NO3- did not. In addition, it was determined that the bacteriostatic activity observed in this study was not due to an increase in the acidity of the medium.
研究了低浓度一氧化氮(NO)和二氧化氮(NO₂)对金黄色葡萄球菌、藤黄微球菌、玫瑰色微球菌、粘质沙雷氏菌、枯草芽孢杆菌、环状芽孢杆菌、巨大芽孢杆菌和蜡样芽孢杆菌等处于活跃分裂期培养物的影响。将每种微生物的新鲜培养物在含有不同低浓度空气中的NO(0至1.9 ppm [0至2.0微克/克空气])、空气中的NO₂(0至5.5 ppm [0至8.8微克/克空气])或空气中的NO和NO₂的环境下,于25℃在营养琼脂平板和无机盐葡萄糖琼脂平板上培养24小时。仅在空气中生长的细菌用作对照。培养后,对平板上形成的菌落进行计数。在所测试的细菌中,在营养琼脂上生长时,没有一种细菌受到所示浓度的NO或NO₂的影响。在无机盐葡萄糖琼脂上生长的粘质沙雷氏菌、环状芽孢杆菌、枯草芽孢杆菌、巨大芽孢杆菌和蜡样芽孢杆菌不受NO或NO₂的显著影响。低浓度(0至1.9 ppm)的NO对在无机盐葡萄糖琼脂上生长的玫瑰色微球菌、藤黄微球菌和金黄色葡萄球菌的对数期培养物具有抑菌作用。在24小时内,初始NO浓度为1 ppm时抑菌活性最大。初始NO浓度大于1 ppm时,24小时内会产生大量的NO₂。这些结果表明,NO₂可能会降低NO的抑菌活性。空气中低浓度(0至5.5 ppm)的NO₂对所测试的任何细菌均无影响。在这些低浓度下,NO会影响细菌生长,而NO₂、NO₂⁻和NO₃⁻则不会。此外,还确定本研究中观察到的抑菌活性并非由于培养基酸度增加所致。