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Imaging Escherichia coli using functionalized core/shell CdSe/CdS quantum dots

机译:使用功能化的核/壳CdSe / CdS量子点对大肠杆菌进行成像

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摘要

The internalization of a series of water-soluble CdSe/CdS quantum dots (QDs) stabilized by citrate, isocitrate, succinate, and malate by Escherichia coli is established by epifluorescence and confocal fluorescence scanning microscopy, fluorimetry, and UV-vis spectroscopy on whole and lysed bacterial cells. The organic-acid-stabilized QDs span a range in size from 3.8 +/- 1.1 to 6.0 +/- 2.4 nm with emission wavelengths from 540 to 630 nm. QDs of different sizes (i.e., 3.8-6 nm) can enter the bacterium and be detected on different fluorescence channels with little interference from other QDs as a result of the distinct emission profiles (i.e., 540-630 nm, respectively). Costaining QD-labeled E. coli with 4',6-diamidino-2-phenylindole dihydrochloride (DAPI) demonstrates that the QDs and DAPI are colocalized within E. coli, whereas costaining QD-labeled E. coli with membrane dye FM4-64 shows that the FM4-64 is localized in the outer bacterial membrane and that the QDs are inside.
机译:通过落射荧光和共聚焦荧光扫描显微镜,荧光法和紫外可见分光光度法,通过大肠杆菌建立了柠檬酸,异柠檬酸,琥珀酸和苹果酸稳定的一系列水溶性CdSe / CdS量子点(QD)的内在化。裂解细菌细胞。稳定的有机酸量子点的尺寸范围为3.8 +/- 1.1至6.0 +/- 2.4 nm,发射波长为540至630 nm。大小不同(即3.8-6 nm)的QD可以进入细菌,并在不同的荧光通道上被检测到,而由于不同的发射曲线(分别为540-630 nm)而不受其他QD的干扰。用4',6-二mid基-2-苯基吲哚二盐酸盐(DAPI)修饰QD标记的大肠杆菌表明QD和DAPI在大肠杆菌内共定位,而共染色QD标记的大肠杆菌与膜染料FM4-64显示FM4-64位于细菌外膜中,并且QD位于内部。

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