在生物研究中建立细菌培养标准规程(BRIC)硬件

P. Fajardo-Cavazos, W. Nicholson
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引用次数: 8

摘要

NASA最近开发了基因实验室数据系统(GLDS),以便进行交叉实验比较,以了解微生物对人类航天环境的反应。然而,先前的航天实验已经使用各种不同的硬件、介质、培养条件和程序进行。这些混杂因素可能潜在地掩盖了航天和地面对照样本之间基因表达的真正差异。为了减轻这些混杂因素,我们在这里描述了一套标准化的硬件、介质和方案的发展,用于微生物的液体培养罐生物研究(BRIC)航天硬件,以模型细菌枯草芽孢杆菌菌株168和金黄色葡萄球菌菌株UAMS-1为例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Establishing Standard Protocols for Bacterial Culture in Biological Research in Canisters (BRIC) Hardware
Abstract The NASA GeneLab Data System (GLDS) was recently developed to facilitate cross-experiment comparisons in order to understand the response of microorganisms to the human spaceflight environment. However, prior spaceflight experiments have been conducted using a wide variety of different hardware, media, culture conditions, and procedures. Such confounding factors could potentially mask true differences in gene expression between spaceflight and ground control samples. In an attempt to mitigate such confounding factors, we describe here the development of a standardized set of hardware, media, and protocols for liquid cultivation of microbes in Biological Research in Canisters (BRIC) spaceflight hardware, using the model bacteria Bacillus subtilis strain 168 and Staphylococcus aureus strain UAMS-1 as examples.
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