Strovas Tim J, Sauter Linda M, Guo Xiaofeng, Lidstrom Mary E
Department of Chemical Engineering, University of Washington, Box 352125, Seattle, WA 98195, USA.
J Bacteriol. 2007 Oct;189(19):7127-33. doi: 10.1128/JB.00746-07. Epub 2007 Jul 20.
Cell-to-cell heterogeneity in gene expression and growth parameters was assessed in the facultative methylotroph Methylobacterium extorquens AM1. A transcriptional fusion between a well-characterized methylotrophy promoter (P(mxaF)) and gfp(uv) (encoding a variant of green fluorescent protein [GFPuv]) was used to assess single-cell gene expression. Using a flowthrough culture system and laser scanning microscopy, data on fluorescence and cell size were obtained over time through several growth cycles for cells grown on succinate or methanol. Cells were grown continuously with no discernible lag between divisions, and high cell-to-cell variability was observed for cell size at division (2.5-fold range), division time, and growth rate. When individual cells were followed over multiple division cycles, no direct correlation was observed between the growth rate before a division and the subsequent growth rate or between the cell size at division and the subsequent growth rate. The cell-to-cell variability for GFPuv fluorescence from the P(mxaF) promoter was less, with a range on the order of 1.5-fold. Fluorescence and growth rate were also followed during a carbon shift experiment, in which cells growing on succinate were shifted to methanol. Variability of the response was observed, and the growth rate at the time of the shift from succinate to methanol was a predictor of the response. Higher growth rates at the time of the substrate shift resulted in greater decreases in growth rates immediately after the shift, but full induction of P(mxaF)-gfp(uv) was achieved faster. These results demonstrate that in M. extorquens, physiological heterogeneity at the single-cell level plays an important role in determining the population response to the metabolic shift examined.
在兼性甲基营养菌嗜甲基甲基杆菌AM1中评估了基因表达和生长参数的细胞间异质性。利用一个特征明确的甲基营养启动子(P(mxaF))与gfp(uv)(编码绿色荧光蛋白变体[GFPuv])之间的转录融合来评估单细胞基因表达。使用流通培养系统和激光扫描显微镜,在几个生长周期内,针对在琥珀酸盐或甲醇上生长的细胞,随着时间的推移获取了荧光和细胞大小的数据。细胞持续生长,分裂之间没有明显的停滞期,并且在分裂时的细胞大小(2.5倍范围)、分裂时间和生长速率方面观察到了较高的细胞间变异性。当跟踪单个细胞经过多个分裂周期时,在一次分裂前的生长速率与随后的生长速率之间,或者在分裂时的细胞大小与随后的生长速率之间,均未观察到直接相关性。来自P(mxaF)启动子的GFPuv荧光的细胞间变异性较小,范围约为1.5倍。在碳源转换实验中也跟踪了荧光和生长速率,在该实验中,在琥珀酸盐上生长的细胞被转换到甲醇上。观察到了反应的变异性,并且从琥珀酸盐转换到甲醇时的生长速率是反应的一个预测指标。底物转换时较高的生长速率导致转换后立即出现更大的生长速率下降,但P(mxaF)-gfp(uv)的完全诱导更快实现。这些结果表明,在嗜甲基甲基杆菌中,单细胞水平的生理异质性在决定群体对所研究的代谢转换的反应中起着重要作用。