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Aseptic Laboratory Techniques: Plating Methods

机译:无菌实验室技术:电镀方法

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摘要

Microorganisms are present on all inanimate surfaces creating ubiquitous sources of possible contamination in the laboratory. Experimental success relies on the ability of a scientist to sterilize work surfaces and equipment as well as prevent contact of sterile instruments and solutions with non-sterile surfaces. Here we present the steps for several plating methods routinely used in the laboratory to isolate, propagate, or enumerate microorganisms such as bacteria and phage. All five methods incorporate aseptic technique, or procedures that maintain the sterility of experimental materials. Procedures described include (1) streak-plating bacterial cultures to isolate single colonies, (2) pour-plating and (3) spread-plating to enumerate viable bacterial colonies, (4) soft agar overlays to isolate phage and enumerate plaques, and (5) replica-plating to transfer cells from one plate to another in an identical spatial pattern. These procedures can be performed at the laboratory bench, provided they involve non-pathogenic strains of microorganisms (Biosafety Level 1, BSL-1). If working with BSL-2 organisms, then these manipulations must take place in a biosafety cabinet. Consult the most current edition of the Biosafety in Microbiological and Biomedical Laboratories (BMBL) as well as Material Safety Data Sheets (MSDS) for Infectious Substances to determine the biohazard classification as well as the safety precautions and containment facilities required for the microorganism in question. Bacterial strains and phage stocks can be obtained from research investigators, companies, and collections maintained by particular organizations such as the American Type Culture Collection (ATCC). It is recommended that non-pathogenic strains be used when learning the various plating methods. By following the procedures described in this protocol, students should be able to: ● Perform plating procedures without contaminating media. ● Isolate single bacterial colonies by the streak-plating method. ● Use pour-plating and spread-plating methods to determine the concentration of bacteria. ● Perform soft agar overlays when working with phage. ● Transfer bacterial cells from one plate to another using the replica-plating procedure. ● Given an experimental task, select the appropriate plating method.
机译:微生物存在于所有无生命的表面上,从而在实验室中普遍产生可能的污染源。实验上的成功取决于科学家对工作表面和设备进行消毒以及防止无菌仪器和溶液与非无菌表面接触的能力。在这里,我们介绍了实验室中常规用于分离,繁殖或枚举微生物(例如细菌和噬菌体)的几种电镀方法的步骤。所有这五种方法都结合了无菌技术或保持实验材料无菌的程序。所描述的程序包括(1)条纹电镀细菌培养物以分离单个菌落,(2)倒平板和(3)铺板以计数活细菌菌落,(4)软琼脂覆盖物以分离噬菌体并计数噬菌斑,以及( 5)复制电镀以相同的空间模式将细胞从一个板转移到另一个板。只要涉及非致病性微生物菌株(生物安全等级1,BSL-1),就可以在实验室工作台上执行这些程序。如果使用BSL-2生物,则这些操作必须在生物安全柜中进行。请查阅最新版的《微生物和生物医学实验室生物安全》(BMBL)以及《传染性物质材料安全数据表》(MSDS),以确定所涉及微生物的生物危害分类以及安全预防措施和收容设施。细菌菌株和噬菌体储备可以从研究调查者,公司和特定组织(例如美国典型培养物保藏所(ATCC))维护的收集物中获得。在学习各种接种方法时,建议使用非致病性菌株。通过遵循本协议中描述的步骤,学生应该能够:●执行电镀步骤而不会污染培养基。 ●通过条纹电镀方法分离单个细菌菌落。 ●使用灌注和扩散电镀方法确定细菌的浓度。 ●使用噬菌体时,进行软琼脂覆盖。 ●使用复制铺板程序将细菌细胞从一个板转移到另一个板。 ●根据实验任务,选择适当的电镀方法。

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