Hill Laura S, Richardson Tammi L, Profeta Luisa T M, Shaw Timothy J, Hintz Christopher J, Twining Benjamin S, Lawrenz Evelyn, Myrick Michael L
Department of Chemistry and Biochemistry, University of South Carolina, Columbia, South Carolina 29208, USA.
Rev Sci Instrum. 2010 Jan;81(1):013103. doi: 10.1063/1.3270251.
Characterization of phytoplankton community composition is critical to understanding the ecology and biogeochemistry of the oceans. One approach to taxonomic characterization takes advantage of differing pigmentation between algal taxa and thus differences in fluorescence excitation spectra. Analyses of bulk water samples, however, may be confounded by interference from chromophoric dissolved organic matter or suspended particulate matter. Here, we describe an instrument that uses a laser trap based on a Nikon TE2000-U microscope to position individual phytoplankton cells for confocal fluorescence excitation spectroscopy, thus avoiding interference from the surrounding medium. Quantitative measurements of optical power give data in the form of photons emitted per photon of exposure for an individual phytoplankton cell. Residence times for individual phytoplankton in the instrument can be as long as several minutes with no substantial change in their fluorescence excitation spectra. The laser trap was found to generate two-photon fluorescence from the organisms so a modification was made to release the trap momentarily during data acquisition. Typical signal levels for an individual cell are in the range of 10(6) photons/s of fluorescence using a monochromated 75 W Xe arc lamp excitation source with a 2% transmission neutral density filter.
浮游植物群落组成的表征对于理解海洋生态和生物地球化学至关重要。一种分类表征方法利用藻类分类群之间不同的色素沉着,进而利用荧光激发光谱的差异。然而,对大量水样的分析可能会因发色溶解有机物或悬浮颗粒物的干扰而混淆。在此,我们描述了一种仪器,它基于尼康TE2000-U显微镜使用激光阱来定位单个浮游植物细胞,用于共聚焦荧光激发光谱分析,从而避免周围介质的干扰。光功率的定量测量给出的数据形式为单个浮游植物细胞每曝光一个光子所发射的光子数。单个浮游植物在仪器中的停留时间可长达几分钟,其荧光激发光谱无实质性变化。发现激光阱会使生物体产生双光子荧光,因此在数据采集期间对仪器进行了修改,使其能瞬间释放阱。使用带有2%透射率中性密度滤光片的75 W单色氙弧灯激发源时,单个细胞的典型信号水平在10⁶ 个荧光光子/秒的范围内。