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Label-free, non-invasive, rapid absorbance spectral imaging  A ( x , y ,λ) microscopy of single live cells at 1.2  μ m × 1.2  μ m resolution with an NA = 0.85 objective was developed and applied to unicellular green algae  Chlamydomonas reinhardtii . By introducing the fiber assembly to rearrange a two-dimensional image to the one-dimensional array to fit the slit of an imaging spectrograph equipped with a CCD detector, scan-free acquisition of three-dimensional information of  A ( x , y ,λ) was realized. The space-resolved absorbance spectra of the eyespot, an orange organelle about 1  μ m, were extracted from the green-color background in a chlorophyll-rich single live cell absorbance image. Characteristic absorbance change in the cell suspension after hydrogen photoproduction in  C. reinhardtii  was investigated to find a single 715-nm absorption peak was locally distributed within single cells. The formula to calculate the absorbance of cell suspensions from that of single cells was presented to obtain a quantitative, parameter-free agreement with the experiment. It is quantitatively shown that the average number of chlorophylls per cell is significantly underestimated when it is evaluated from the absorbance of the cell suspensions due to the package effect.

Scan-Free Absorbance Spectral Imaging A(x, y, λ) of Single Live Algal Cells for Quantifying Absorbance of Cell Suspensions