...
首页> 外文期刊>Mycoses: Diagnosis, therapy and prophylaxis of fungal diseases >Candida albicans inactivation and cell membrane integrity damage by microwave irradiation.
【24h】

Candida albicans inactivation and cell membrane integrity damage by microwave irradiation.

机译:白色念珠菌的失活和细胞膜完整性受到微波辐射的破坏。

获取原文
获取原文并翻译 | 示例
           

摘要

In indicating the microwave irradiation for disinfecting dentures it is necessary to see how this procedure influences Candida albicans integrity and viability. The aim of this study was to evaluate the ability of microwaves to inactivate C. albicans and damage cell membrane integrity. Two 200-ml C. albicans (ATCC 10231) suspensions were obtained. A sterile denture was placed in a beaker containing the Experimental (ES) or the Control suspension (CS). ES was microwaved at 650 W for 6 min. Suspensions were optically counted using methylene blue dye uptake as indicative of membrane-damaged cells; spread on Agar Sabouraud dextrose (ASD) for viability assay; or spectrophotometrically measured at 550 nm. Cell-free solutions were submitted to content analyses of protein (Bradford and Pyrogallol red methods); Ca(++) (Cresolftaleine complexone method); DNA (spectrophotometer measurements at 260 nm) and K(+) (selective electrode technique). Data were analysed by Student's t- or Wilcoxon z-tests (alpha 0.05). All ES cells demonstrated cell membrane damage. Viable cells were non-existent in the ES ASD plates. No significant difference in optical density between ES and CS was observed (P = 0.272). ES cells released significantly high protein (P < 0.001, Bradford; P = 0.005, Pyrogallol red), K(+) (P < 0.001), Ca(++) (P = 0.012) and DNA (P = 0.046) contents. Microwaves inactivated C. albicans and damaged cell membrane integrity.
机译:在指示用于消毒假牙的微波辐照时,有必要了解该程序如何影响白色念珠菌的完整性和生存能力。这项研究的目的是评估微波灭活白色念珠菌和破坏细胞膜完整性的能力。获得了两个200 ml白色念珠菌(ATCC 10231)悬浮液。将无菌义齿放置在装有实验(ES)或对照悬浮液(CS)的烧杯中。 ES在650 W下微波处理6分钟。使用亚甲基蓝染料摄取量对悬浮液进行光学计数,以指示细胞受损。铺在琼脂沙氏葡萄糖(ASD)上进行活力测定;或在550 nm处用分光光度法测量。将无细胞溶液提交蛋白质含量分析(Bradford和Pyrogallol红法); Ca(++)(Cresolftaleine complexone method); DNA(分光光度计在260 nm处测量)和K(+)(选择性电极技术)。数据通过Student's t检验或Wilcoxon z检验(α0.05)进行分析。所有ES细胞均表现出细胞膜损伤。 ES ASD板中不存在活细胞。在ES和CS之间没有观察到光密度的显着差异(P = 0.272)。 ES细胞释放出明显较高的蛋白质(P <0.001,Bradford; P = 0.005,邻苯三酚红),K(+)(P <0.001),Ca(++)(P = 0.012)和DNA(P = 0.046)含量。微波灭活白色念珠菌并破坏细胞膜完整性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号