首页> 美国卫生研究院文献>Antimicrobial Agents and Chemotherapy >Feasibility of Screening for Penicillinase-Producing Neisseria gonorrhoeae from Primary Culture Plates by Using a Rapid Microacidometric Test
【2h】

Feasibility of Screening for Penicillinase-Producing Neisseria gonorrhoeae from Primary Culture Plates by Using a Rapid Microacidometric Test

机译:快速微量酸法从原代培养板中筛选产生青霉素酶的淋病奈瑟氏球菌的可行性

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

We have shown that it is possible to screen for penicillinase-producing Neisseria gonorrhoeae directly from primary culture plates. Experiments involving the cocultivation of four genera of beta-lactamase-positive (β-lac+) bacteria and a beta-lactamase-negative (β-lac) N. gonorrhoeae on modified Thayer-Martin medium indicated that suppressed or inhibited β-lac+ bacteria did not give false-positive results when isolated β-lac colonies of gonococci were tested. Colonies were assayed for β-lac production by an adaptation of a microacidometric method in which bacteria could be tested before or after the addition of oxidase reagent.
机译:我们已经表明,可以直接从原代培养板中筛选出产生青霉素酶的淋病奈瑟氏球菌。涉及将四个属的β-内酰胺酶阳性(β-lac + )细菌和β-内酰胺酶阴性(β-lac-)淋病奈瑟氏球菌共培养的实验在改良的Thayer-Martin培养基上检测到,经测试分离的淋球菌的β-lac-菌落时,抑制或抑制的β-lac + 细菌未给出假阳性结果。通过改型的微酸法测定菌落的β-lac生成量,其中可以在添加氧化酶试剂之前或之后测试细菌。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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