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Early events of lethal action by tobramycin in Pseudomonas aeruginosa.

机译:铜绿假单胞菌中妥布霉素致死作用的早期事件。

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摘要

The immediate activities of the aminoglycoside antibiotic, tobramycin, were investigated in Pseudomonas aeruginosa PAO1. The influence of carbon growth substrate and the antibiotic exposure environment in the magnitude of activity were examined. Lethality by 8 ug/ml tobramycin occurred rapidly (1 to 3 minutes). The release of specific cellular components into the supernatant was associated with lethality. This material was initially detected as an increase in UV-absorbance. Magnesium in the reaction mixture provided protection against lethality and leakage, but did not reverse lethal damage after a 3 minute tobramycin treatment. Also, uptake of {dollar}sp3{dollar}H-tobramycin was reduced in the presence of magnesium. Cells grown with glucose as a carbon source were more susceptible than organic acid grown cells as was the rapidity and amount of cell damage. Analyses of the leakage material revealed a 2-fold increase of protein in the supernatant after a 1-3 minute treatment which paralleled lethality. A prominent 29kDa protein was observed by SDS-PAGE in the released material, which has been identified as the periplasmic enzyme, {dollar}beta{dollar}-lactamase. Tobramycin also elicited an increase of certain amino acids in the supernatant, particularly, basic amino acids. The immediate activities of tobramycin did not involve (i) release of overall cell protein, (ii) massive loss of total pool amino acids, (iii) cell lysis, (iv) inhibition of proline uptake, (v) release of lipopolysaccharide, or (vi) leakage of ATP. Electron microscopy showed no apparent damage after a 3 minute exposure. Forty percent inhibition of protein synthesis had occurred by 3 minutes of exposure, while release of UV-absorbing material and lethality were detectable after only 1 minute. These data suggest that leakage occurs at least simultaneously, if not prior, to ribosomal interference. Resistant cystic fibrosis isolates of P. aeruginosa did not leak under the same experimental conditions, but one of two susceptible strains examined did show increased UV-absorbance following treatment.
机译:在铜绿假单胞菌PAO1中研究了氨基糖苷类抗生素妥布霉素的即时活性。研究了碳生长底物和抗生素暴露环境对活性大小的影响。迅速发生8ug / ml妥布霉素致死率(1至3分钟)。特定细胞组分向上清液的释放与致死性相关。最初检测到该材料是紫外线吸收率的增加。反应混合物中的镁提供了防止致死性和泄漏的保护作用,但在妥布霉素处理3分钟后并未逆转致死性损害。另外,在镁存在下,{dol} sp3 {dol} H-妥布霉素的摄取减少。葡萄糖作为碳源生长的细胞比有机酸生长的细胞更敏感,细胞的速度和损伤程度也更高。泄漏材料的分析表明,经过1-3分钟的处理后,上清液中的蛋白质增加了2倍,与致死性平行。通过SDS-PAGE在释放的物质中观察到突出的29kDa蛋白质,该物质已被鉴定为周质酶,{beta} {beta}-内酰胺酶。妥布霉素还引起上清液中某些氨基酸,特别是碱性氨基酸的增加。妥布霉素的即时活性不涉及(i)释放总细胞蛋白,(ii)总池氨基酸大量损失,(iii)细胞裂解,(iv)脯氨酸摄取抑制,(v)脂多糖释放或(vi)ATP泄漏。电子显微镜显示暴露3分钟后没有明显的损伤。暴露3分钟对蛋白质合成的抑制作用为40%,而仅1分钟后就可以检测到吸收紫外线的物质的释放和致死性。这些数据表明,如果不是在核糖体干扰之前,至少会同时发生泄漏。铜绿假单胞菌的抗性囊性纤维化分离株在相同的实验条件下不会泄漏,但是所检测的两个敏感菌株之一确实显示出治疗后紫外线吸收增加。

著录项

  • 作者

    Raulston, Jane Elizabeth.;

  • 作者单位

    The University of Tennessee.;

  • 授予单位 The University of Tennessee.;
  • 学科 Biology Microbiology.
  • 学位 Ph.D.
  • 年度 1988
  • 页码 160 p.
  • 总页数 160
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 微生物学;
  • 关键词

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