首页> 外文期刊>Biological & pharmaceutical bulletin >Induction of Viable but Non-culturable (VBNC) State in Salmonella Cultured in M9 Minimal Medium Containing High Glucose
【24h】

Induction of Viable but Non-culturable (VBNC) State in Salmonella Cultured in M9 Minimal Medium Containing High Glucose

机译:在含高糖M9最小培养基中培养的沙门氏菌中诱导有活力但不可培养(VBNC)状态

获取原文
获取原文并翻译 | 示例
           

摘要

An environmental isolate of Salmonella enterica serovar Enteritidis (SE) clone, SE Cl#15-1, loses its culturability during 72-h culture in M9 minimal medium containing 0.8% glucose, a concentration twice higher than that in normal M9 medium, whereas the bacterium retains its culturability in normal M9 medium. Live/dead analysis using the 5-cyano-2,3-di(p-tolyl) tetrazolium chloride (CTC)-reduction assay revealed that SE cells cultured in M9 medium containing 0.8% glucose died with time when in the "viable but nonculturable" (VBNC) state. Assay of the culturability of SE cells in the used supernatant (0.4 spent M9 or 0.8 spent M9) also indicated that 0.8 spent M9 soon showed a lethal effect on intact SE cells. These results suggest that large amounts of glucose metabolites might have been responsible for the toxicity. Analysis of the 0.8 spent M9 revealed that formate rapidly accumulated in the medium. The pH of the medium rapidly dropped to 4.7, leading to conversion of formate to formic acid, which might have damaged the bacterial cell membrane. These results suggest that the excessive amount of glucose in the M9 medium might have injured SE cells in the VBNC state by being metabolized to formic acid and other acidic compounds.
机译:肠炎沙门氏菌肠炎沙门氏菌(SE Cl#15-1)的环境分离株在含0.8%葡萄糖的M9基本培养基中72小时培养期间丧失了可培养性,其浓度比正常M9培养基高两倍。细菌在正常的M9培养基中保持其可培养性。使用5-氰基-2,3-二(对甲苯基)氯化四氮唑(CTC)还原法进行的生/死分析表明,在“有活力但不可培养的”条件下,含有0.8%葡萄糖的M9培养基中培养的SE细胞随时间死亡。 ”(VBNC)状态。对用过的上清液(0.4用过的M9或0.8用过的M9)中SE细胞的可培养性的测定也表明0.8用过的M9很快对完整的SE细胞显示出致死作用。这些结果表明,大量的葡萄糖代谢产物可能是造成毒性的原因。对0.8消耗的M9的分析表明,甲酸盐在培养基中迅速积累。培养基的pH值迅速下降到4.7,导致甲酸转化为甲酸,这可能已经损坏了细菌细胞膜。这些结果表明,M9培养基中过量的葡萄糖可能通过代谢为甲酸和其他酸性化合物而以VBNC状态损伤了SE细胞。

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