Tao Zhanhua, Zhang Pengfei, Qin Zhaojun, Li Yong-Qing, Wang Guiwen
Guangxi Academy of Sciences, Laboratory of Biophysics, 98 Daling Road, Nanning, Guangxi 530007, China.
Washington University in St. Louis, Department of Biomedical Engineering, Optical Imaging Laboratory, One Brookings Drive, Campus Box 1097, St. Louis, Missouri 63130, United States.
J Biomed Opt. 2016 Sep 1;21(9):97005. doi: 10.1117/1.JBO.21.9.097005.
Cupriavidus necator accumulates large amounts of poly(3-hydroxybutyrate) (PHB), a biodegradable substitute for petroleum-based plastics, under certain nutrient conditions. Conventional solvent-extraction-based methods for PHB quantification only obtain average information from cell populations and, thus, mask the heterogeneity among individual cells. Laser tweezers Raman spectroscopy (LTRS) was used to monitor dynamic changes in the contents of PHB, nucleic acids, and proteins in <italic<C. necator</italic< at the population and single-cell levels when the microorganism cells were cultivated at various carbon-to-nitrogen ratios. The biosynthetic activities of nucleic acids and proteins were maintained at high levels, and only a small amount of PHB was produced when the bacterial cells were cultured under balanced growth conditions. By contrast, the syntheses of nucleic acids and proteins were blocked, and PHB was accumulated in massive amount inside the microbial cells under nitrogen-limiting growth circumstances. Single-cell analysis revealed a relatively high heterogeneity in PHB level at the early stage of the bacterial growth. Additionally, bacterial cells in populations at certain cultivation stages were composed of two or three subpopulations on the basis of their PHB abundance. Overall, LTRS is a reliable single-cell analysis tool that can provide insights into PHB fermentation.
在特定营养条件下,食酸戴尔福特菌(Cupriavidus necator)会积累大量聚(3-羟基丁酸酯)(PHB),这是一种可生物降解的石油基塑料替代品。传统的基于溶剂萃取的PHB定量方法只能从细胞群体中获取平均信息,因此掩盖了单个细胞之间的异质性。当微生物细胞在不同碳氮比下培养时,利用激光镊子拉曼光谱(LTRS)在群体和单细胞水平上监测食酸戴尔福特菌中PHB、核酸和蛋白质含量的动态变化。在平衡生长条件下培养细菌细胞时,核酸和蛋白质的生物合成活性维持在较高水平,仅产生少量PHB。相比之下,在氮限制生长条件下,核酸和蛋白质的合成被阻断,PHB在微生物细胞内大量积累。单细胞分析显示,在细菌生长早期,PHB水平存在相对较高的异质性。此外,在某些培养阶段,群体中的细菌细胞根据其PHB丰度由两个或三个亚群组成。总体而言,LTRS是一种可靠的单细胞分析工具,可用于深入了解PHB发酵过程。