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Benchmarking Various Green Fluorescent Protein Variants in Bacillus subtilis, Streptococcus pneumoniae, and Lactococcus lactis for Live Cell Imaging

机译:对枯草芽孢杆菌,肺炎链球菌和乳酸乳球菌中的各种绿色荧光蛋白变异进行基准,以进行活细胞成像

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Green fluorescent protein (GFP) offers efficient ways of visualizing promoter activity and protein localization in vivo , and many different variants are currently available to study bacterial cell biology. Which of these variants is best suited for a certain bacterial strain, goal, or experimental condition is not clear. Here, we have designed and constructed two “superfolder” GFPs with codon adaptation specifically for Bacillus subtilis and Streptococcus pneumoniae and have benchmarked them against five other previously available variants of GFP in B. subtilis , S. pneumoniae , and Lactococcus lactis , using promoter- gfp fusions. Surprisingly, the best-performing GFP under our experimental conditions in B. subtilis was the one codon optimized for S. pneumoniae and vice versa . The data and tools described in this study will be useful for cell biology studies in low-GC-rich Gram-positive bacteria.
机译:绿色荧光蛋白(GFP)提供了可视化启动子活性和体内蛋白定位的有效方法,并且目前有许多不同的变体可用于研究细菌细胞生物学。目前尚不清楚哪种变体最适合某种细菌菌株,目标或实验条件。在这里,我们设计并构建了两个具有密码子适应性的“超级文件夹” GFP,专门针对枯草芽孢杆菌和肺炎链球菌,并将它们与枯草芽孢杆菌,肺炎链球菌和乳酸乳球菌中其他五个可用的GFP变体进行了基准比较,使用启动子- gfp融合。令人惊讶的是,在我们的实验条件下,枯草芽孢杆菌中表现最佳的GFP是针对肺炎链球菌优化的一种密码子,反之亦然。这项研究中描述的数据和工具将对富含低GC的革兰氏阳性细菌的细胞生物学研究有用。

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