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首页> 外文期刊>Applied and Environmental Microbiology >Quantifying Substrate Uptake by Individual Cells of Marine Bacterioplankton by Catalyzed Reporter Deposition Fluorescence In Situ Hybridization Combined with Microautoradiography
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Quantifying Substrate Uptake by Individual Cells of Marine Bacterioplankton by Catalyzed Reporter Deposition Fluorescence In Situ Hybridization Combined with Microautoradiography

机译:催化记者沉积荧光原位杂交结合微放射成像技术定量分析海洋浮游细菌单个细胞的底物吸收

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摘要

Catalyzed reporter deposition fluorescence in situ hybridization combined with microautoradiography (MICRO-CARD-FISH) is increasingly being used to obtain qualitative information on substrate uptake by individual members of specific prokaryotic communities. Here we evaluated the potential for using this approach quantitatively by relating the measured silver grain area around cells taking up 3H-labeled leucine to bulk leucine uptake measurements. The increase in the silver grain area over time around leucine-assimilating cells of coastal bacterial assemblages was linear during 4 to 6 h of incubation. By establishing standardized conditions for specific activity levels and concomitantly performing uptake measurements with the bulk community, MICRO-CARD-FISH can be used quantitatively to determine uptake rates on a single-cell level. Therefore, this approach allows comparisons of single-cell activities for bacterial communities obtained from different sites or growing under different ecological conditions.
机译:结合微放射自显影技术(MICRO-CARD-FISH)的催化报告基因沉积荧光原位杂交技术正越来越多地用于获取有关特定原核生物个体成员摄取底物的定性信息。在这里,我们通过将摄取3H标记亮氨酸的细胞周围的银颗粒面积与大量亮氨酸摄取量的测量值相关联,来评估使用这种方法的潜力。在孵育的4至6小时内,沿海细菌集合的亮氨酸同化细胞周围的银粒面积随时间的增加呈线性变化。通过为特定活动水平建立标准条件并与整体社区同时进行摄取测量,MICRO-CARD-FISH可定量用于确定单细胞水平的摄取率。因此,这种方法可以比较从不同地点获得或在不同生态条件下生长的细菌群落的单细胞活性。

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